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Yourgene Health

ygen · LSE Healthcare
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Employees 201-500
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FY2020 Annual Report · Yourgene Health
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ENABLING   
SCIENTIFIC   
ADVANCES 
to  POSITIVELY   
IMPACT HUMAN   
HEALTH

ANNUAL REPORT AND A CCOUNTS 2020

 
 
 
 
 
 
 
I N T RO D U C T I O N

We are an international molecular 
diagnostics Group which develops 
and commercialises genetic 
products and services

The Group works in partnership with global leaders in DNA technology  
to advance diagnostic science. Our product development, research  
service and commercial capabilities extend across the life cycle of  
DNA test development including regulatory submissions.

Through our technical expertise, commercial footprint and strong 
partnerships we are expanding across reproductive health, molecular 
genetics and now also infectious disease applications.

Financial Statements
Independent Auditor’s Report to the  
Members of Yourgene Health PLC 
Consolidated Statement of  
Comprehensive Income 
Consolidated Statement of Financial Position 
Consolidated Statement of Changes in Equity 
Consolidated Statement of Cash Flows 
Notes to the Consolidated Financial Statements 
Company Statement of Financial Position 
Company Statement of Changes in Equity 
Company Statement of Cash Flows 
Notes to the Company Financial Statements 
Glossary of Technical Terms and Measurements 
Company Information 

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84
85

Company Overview
Highlights 

Strategic Report
Providing Solutions 
At a Glance 
Our People and Culture 
Making Progress 
Business Model 
Working with Partners 
Strategy 
Strategy in Action 
Chairman’s Statement 
CEO Statement 
Financial Review 
Principal Risks and Uncertainties 

Governance
Board of Directors 
Corporate Governance Statement 
Directors’ Report 
Directors’ Responsibility Statement 

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06
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Company o verview

StrateGic report

Governance

Financial StatementS

Solutions

We h a v e a g r o w i n g p o r t f o l i o o f  c o m p e t i t i v e 
p r o d u c t s a n d s e r v i c e s t o m e e t  d i f f e r e n t 
g e o g r a p h i e s , c u s t o m e r s a n d  m a r ke t  n e e d s .

  S E E PA G E S 0 4 - 0 5 F O R M O R E I N F O R M AT I O N

Progress 

We a r e m a k i n g s t r o n g  p r o g r e s s a g a i n s t  o u r  f o u r 
p i l l a r s f o r  s t r a t e g i c g r o w t h : g e o g r a p h i c  e x p a n s i o n , 
m a r ke t p e n e t r a t i o n ,  p r o d u c t e x p a n s i o n a n d m e r g e r s 
a n d a c q u i s i t i o n s ( m & a ) .

  S E E PA G E S 10 -11 F O R M O R E I N F O R M AT I O N

Partners

St r a t e g i c p a r t n e r s h i p s w i t h o u r  key 
s u p p l i e r s , c u s t o m e r s , key o p i n i o n l e a d e r s , 
d i s t r i b u t o r s a n d  o t h e r  s t a ke h o l d e r s 
u n d e r p i n s o u r b u s i n e s s  g r o w t h .

  S E E PA G E S 14 -15 F O R M O R E I N F O R M AT I O N

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H i G H l i G H tS

We continue to execute on 
our strategy of broadening 
our product mix and 
international reach

The strong growth across all regional 
segments shown below demonstrates the 
Company’s diversified geographic base.

G EO G R A P H I C A N D M A R K E T G R O W T H

Geographic sales by region

market segment sales

2.0m

4.1m

10.5m

UK
Europe
International

2.8m

3.7m

NIPT
Reproductive Health
Molecular Genetics

10.1m

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Company o verview

StrateGic report

Governance

Financial StatementS

O P E R AT I O N A L H I G H L I G H T S

F I N A N C I A L  H I G H L I G H T S

revenue (£m)

16.6m

8.9m

6.1m

2018

2019

2020

Gross profit (£m)

10.2m

3.2m

4.6m

2018

2019

2020

adjusted eBiTDa* (£m)

(7.9)m

(3.9)m

1.3m

2018

2019

2020

•   Acquisition of Elucigene and associated 
£11.8 million (gross) equity fundraise in 
April 2019.

•   Acquisition of AGX-DPNI S.A.S.,  

a newly formed entity comprised of the 
non-invasive prenatal screening (NIPT) 
distribution business of AdGeniX the 
Company’s current French distribution 
partner for the IONA® Test.

•   Launch of first oncology CE marked 

product, the Elucigene® DPYD Assay,  
a new chemotoxicity diagnostic  
assay for precision medicine and 
subsequent regulatory approval  
in Australia.

•   First US revenues and opening of 
Yourgene Health Inc in the US.

•   Development of the Illumina-based 
IONA® Test progressing well and on 
schedule for launch (CE mark gained 
June 2020).

•   European quality accreditation 

transferred to BSI Netherlands to 
offset Brexit risks. 

•   Non-executive appointments  

Dr John Brown, CBE and Jonathan 
Seaton.

•   Post-period end launch of Yourgene 
Flex™ Analysis Software to support 
product diversification.

•   First contract manufacturing 

partnership for COVID-19 assay 
components.

•   Triple Awards win – Bionow Investment 
Deal of Year, Bionow Company of the 
Year and Medilink Outstanding 
Achievement Award.

* adjusted eBitda is the operating profit/(loss) before interest, tax, 
depreciation, amortisation, share-based payments and acquisition-
related expenses shown separately disclosed on the face of the  
income Statement.

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03

 
prov i d i n G So lu t i o n S

We continue to execute on our 
strategy of broadening our 
product and service portfolio. 
Strengthening our reproductive 
health solutions gives us a 
broader coverage of tests 
throughout the reproductive  
life cycle and we are now building 
our Molecular Genetics division.  
We are really pleased to have 
been able to utilise our expertise 
in developing clinical diagnostics 
and developed our own  
SARS-CoV-2 screening test  
and laboratory service, to make  
a contribution to the global 
COVID-19 testing demand.

Dr Jo mason
r&d director

Enabling scientific  
advances to positively  
impact human health

04

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STraTe GiC repor T

Governance

Financial StatementS

yoUr Gene HeaLTH pLC  annual report and account S 2020
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Enabling scientific  

advances to positively  

impact human health

at a G l a n c e

WHAT WE DO

WHAT WE FOCUS ON

NON-INVASIVE PRENATAL SCREENING

We have a growing range of nipt offerings to suit  
our different customer needs and different markets. 
the iona® test still remains our flagship product and 
our technology underpins many other commercial 
nipt offerings globally. 

•  the iona® test is the first ce marked in vitro diagnostic 

product for non-invasive prenatal screening. it is now routinely 
screening pregnant women across many different countries 
through our customer network of clinical laboratories, 
hospitals and clinics that offer our test. often customers 
choose to give the test their own nipt brand name but our 
reagents and our iona® Software form the nipt lab workflow. 

• 

in our clinical laboratories, the iona® test runs on the  
ion torrent suite of next Generation Sequencing (nGS) 
instruments from thermo Fisher. iona® nx nipt Workflow 
runs on the illumina nextseq nGS platform and has just 
received its ce mark ahead of european launch and roll-out. 

•  Sagetm 32 plex nipt Workflow is a new high throughput 

offering for laboratories running large numbers of samples 
each week. it provides a more efficient sequencing workflow 
and covers a broader range of clinical coverage including 
trisomies, sex chromosomal aneuploidies and autosomal 
aneuploidies.

Yourgene has a strong and 
growing portfolio of molecular 
in vitro diagnostic products  
and services across 
reproductive health including 
non-invasive prenatal screening, 
oncology and most recently 
infectious diseases. 

our products and services focus on where they can 
make a real difference.  

•  Making a clinical difference: 

• Where the screening result can improve a patient outcome.
•  enable patients to receive the correct dose or therapy  
based on their genetics.
•  early detection of disease or a genetic disorder.
•  diagnosis of the presence of an infectious agent.
•  Simple and easy to interpret clinical results.

•  Making a technical difference:

• improved workflow.
•  improved accuracy and detection rates,  
reducing false positive and false negative rates.
• user-friendly bioinformatics portals.
• tests working across different platforms.
• improving turnaround times.
• reducing technician hands-on time with automated process.
• improving cost efficiencies of running the test. 

•  Making a market difference: 

•  considering product modifications to some regions, for 
example, cystic Fibrosis country specific kits that cover 
different mutations.
•  adapting and understanding local reimbursement to ensure 
products are covered.
•  regulatory submissions for different regions. 
•  local language translations of iFu, test reports, marketing 
collateral.
•  adapting to local ethical and legal differences, for example,  
in india, fetal sex determination through nipt is illegal.

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Financial StatementS

WHAT WE FOCUS ON

REPRODUCTIVE HEALTH

MOLECULAR GENETICS 

to complement and add value to our nipt offering we 
have a range of products in the reproductive health 
life cycle that utilises different technologies. 

•  QST*r rapid aneuploidy analysis  

a market-leading test for women that have a high risk nipt 
result; they are recommended a confirmatory diagnostic test 
with a follow-up amniocentesis (14-18 weeks) or chorionic 
villus sampling (cvS) (10-12 weeks). 

•  male Factor infertility 

a polymerase chain reaction-based (pcr) assay that looks at 
mutations related to cystic Fibrosis that can be indicative of 
male infertility. the male Factor infertility Kit detects both sex 
chromosome aneuploidy and y chromosome microdeletions in 
a single tube. 

•  QST*r recurrent pregnancy Loss  

a QF- pcr-based assay used for the routine in vitro  
quantitative diagnosis of the six most common autosomal 
trisomies associated with pregnancy loss. 

•  Cystic Fibrosis Screening  

cystic Fibrosis has a frequency of 1 in 2,500 in the caucasian 
populations but is less common in asians (1 in 35,000). 
cF-eu2v1 is the only commercially available pan-european 
cystic Fibrosis testing kit designed specifically to address the 
most common mutations found across populations of 
european origin. market-leading pcr product range that has 
different mutational coverage per country, used in many 
newborn screening programmes across europe. 

as our new product and service development pipeline 
matures, we now have a molecular Genetics portfolio, 
which includes oncology and research Services  
and two new segments: infectious disease and  
core technology. 

Oncology and Research Services
our taipei service laboratory provides an oncology genetic 
analysis service with tests available predominantly for lung, 
colorectal and breast cancer. Working with a key clinical research 
organisation (cro) partner in taiwan, our lab is involved in a 
national cancer research screening study. 

the elucigene® dpyd assay is the first ce marked in vitro 
diagnostic oncology test from yourgene which was launched in 
September 2019 in europe and subsequently received approval 
for sale in australia. it detects the presence of several key 
mutations in the dpd gene which are indicative of a person’s 
toxicity response to a cancer treatment, a commonly used 
chemotherapy called 5Fu. 

Core Technology 
yourgene Flex™ analysis Software is a modular nGS analysis 
framework harnessing best in class bioinformatics pipelines to 
offer high quality, robust yet flexible nGS analysis solutions. 
enabling yourgene to support our in vitro diagnostic (ivd) product 
development partnerships and research collaborations with key 
industry players.

Infectious Disease
in response to the global covid-19 pandemic, yourgene rapidly 
reacted and utilised our r&d team’s expertise at developing highly 
accurate and reliable tests and the company is developing the 
clarigene™ SarS cov-2 test using pcr technology. the test will 
be ce marked and we are on track to launch in summer 2020. 
clarigene™ is the brand family for our infectious disease portfolio 
and we are looking at what additional tests will be developed. 

in addition, the yourgene Service laboratory in manchester has 
established a covid-19 testing service to support corporate 
institutions and organisations test their employees or private 
healthcare setting such as care homes and private Gp networks. 

yoUr Gene HeaLTH pLC  annual report and account S 2020

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o u r peo pl e  a n d  c u lt u r e

We are delivering results  
by living our values and 
developing our people

OUR CULTURE AND PERFORMANCE

at yourgene we are very proud of our value-led global culture and our people; 
we encourage an open, honest, innovative, collegiate culture that embraces 
and welcomes our local geographical and cultural diversity. communication is 
key and we have a transparent and clear leadership team and programme 
management office (pmo) that ensures accountability and delivery. 

this year we have rolled out additional programmes to enhance and support 
our culture:

Recognition:
•  cheers from peers scheme where 

Internal communication:
•  your Source – yourgene’s global intranet 

cross-functional colleagues can nominate 
each other for going above and beyond. 
•  long-term service awards to recognise the 
commitment and loyalty of colleagues.
innovation award for employees that 
submit exceptional new ideas into our 
Gateway incubator.

• 

Cheers
from
 Peers

just launched.

•  yourgene: your news – our biweekly global 

internal newsletter.

•  lyn’s blog – quarterly blog from our ceo to 

all staff.

•  Quarterly townhalls – (meetings or 

webinars) companywide events to update 
everyone on strategy, progress and to 
keep us connected.

Yourgene Social Huddle:
a team of volunteers across the Group who 
embody our values and act as champions of 
our culture:
•  compile feedback and suggestions  

from around the business. 

•  Strive to encourage engagement  

and participation.

•  organise social and wellbeing events  

and programmes.

•  organise charity fundraising across  

the Group.

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Financial StatementS

VALUES

OUR PEOPLE AND CULTURE DURING COVID-19

our values shape everything we do as a 
company, from how we develop our 
products, how we work with our customers 
and how we engage with each other.

the company quickly identified that covid-19 was a 
serious threat and established a coBra taskforce 
within the organisation to look at the risk and mitigation 
planning across the different territories and functions. 

 Recognition: Key to our success is to 
recognise our employees, our customers and 
other stakeholders that embody our values, in 
order to inspire each other to reach our goals.

 Teamwork: We know that our best work is 
not produced by individuals but by our teams. 
this team mentality also extends to our 
clients as we approach every relationship as  
a partnership.

 Trust: this is core to everything we do;  
we can’t embody the other values if we don’t 
have trust. We are driven to be a company 
with people, products and partnerships that 
are trusted. 

 Achievement: We have clear goals,  
milestones and Kpis and we are driven to 
achieve these and then to recognise our 
achievements.

 Integrity: We do the right thing.  
We are professional, ethical, honest and  
open about everything we do. 

 Commitment: We are committed and 
passionate about achieving our goals for  
the benefit of all our stakeholders.

our key priority was the health and safety of our employees and 
ensuring we were able to continue to supply our customers with our 
products. 

•  prior to government recommendations we relocated our staff to 

homeworking where appropriate.

•  enabled social and physical distancing and split shifts across our 

laboratories, manufacturing and operations teams.
• 
increased communications internally to daily updates.
•  Social Huddle organised virtual events, quizzes and social 
hangouts via Zoom and teams to keep the culture alive.

•  teams adapted and embraced new technologies and 

communication channels.

•  ensured availability of key raw materials and supply chains intact.
initiated cross-training programme across all key functions.
• 
•  customer communications and support.
•  regular 1:1 contact with customers remotely and virtual  

technical support.

in addition, the company responded to the global pandemic and our 
flexible and agile teams enabled a fast commitment in supporting the 
testing effort for the global pandemic threefold:
•  contract manufacturing of covid-19 components for a partner.
•  opening our own covid-19 testing service laboratory  

in manchester.

•  developing our own clarigene™ SarS cov-2 assay.

the company is pleased that we have been able to support the global 
pandemic with much needed covid-19 testing and that we are in a 
position to grow and hire new staff and we haven’t had to furlough any 
of our teams during this challenging time. 

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m a Ki n G pro Gr e SS

The reorientation of the 
business to focus on our 
four key strategic growth 
drivers is starting to bear 
fruit, and I remain 
convinced we have a  
very significant 
opportunity ahead of us. 
We are confident in our 
outlook and very excited 
about the prospects for 
further growth over the 
following years.

Lyn rees
chief executive officer

We are very excited  
about our strong  
commercial momentum  
and the prospects  
for further growth

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Financial StatementS

£16.6mREVENUE
87%REVENUE GROWTH

yoUr Gene HeaLTH pLC  annual report and account S 2020
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B uS i n e SS m o d el

Our strategic growth drivers are a key 
focus in our business model to enable us 
to reach our annual goals, with the aim of 
adding value to all our stakeholders 

HOW WE GENERATE GROWTH

Set and exceed  
high profit and 
performance targets

Attract and retain  
great talent to 
strengthen the  
values-led culture

Create  
innovative, agile, and 
dynamic partnerships*

growth

Invest  
in improving people, 
product development, 
and infrastructure

Develop  
‘best in class’ ivd 
products/services/
solutions that delight 
and excite customers

Construct  
scalable, quality assured, 
lean, business processes 
and capabilities that 
enable and support 
growth

Drive  
sales in territories  
and market sectors

*  partnerships include suppliers, platforms, distributors,  
key opinion leaders, co-development, in-licensing.

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PRODUCT PORTFOLIO DEVELOPED FOR GROWTH

NIPT 

Reproductive Health

Molecular Genetics:
•  Oncology
•  Research Services
Infectious Diseases
• 
•  Core Technology

Growing Technology Portfolio 

Growing Geographical Reach 

Growing Product & Service Portfolio

MARKET CHANNELS

VALUE FOR OUR STAKEHOLDERS

Indirect
yourgene has a strong and growing international 
distribution network for our channel markets. in addition 
to driving product demand and growing revenue in  
the region, they provide regulatory support, export 
logistics, first line technical assistance and local market 
understanding. We work in partnership with our 
distributors to promote our products in that region  
with co-marketing initiatives and local conference 
attendance, often organising educational launch events 
with our key customers.

Direct
across some regions we have a direct sales network 
such as uK, india, Singapore, taiwan, canada. Since the 
acquisition of aGX-dpni we now sell directly in France 
supported by a French-speaking commercial team and 
we have recently gone direct in the dacH (Germany, 
austria and Switzerland) region.

the company works directly with key strategic 
partners from the pharma, diagnostic and research 
industry to develop partnership development 
programmes or contract manufacturing opportunities.

Partners
yourgene works in close partnership with our key 
platform providers to support their laboratory 
customer base with our reproductive health and 
molecular genetics solutions. We develop targeted 
co-marketing campaigns for specific regions, working 
collaboratively to win market share. 

Employees
We want our employees to value their role at yourgene,  
to feel that we have an engaged, open culture where 
everyone’s ideas and contributions matter. We want our 
teams to feel valued, recognised and that they are pivotal to 
the company’s achievements. We want to be able to attract 
and retain great talent and invest in their future growth and 
development at yourgene. 

Shareholders
We want our investors to feel excited by our growth story  
and proud of our progress and milestones that we reach as  
a business. that we are open communicators and we share 
news in a transparent and considered manner. 

Healthcare Professionals
We develop and offer excellent quality, highly regulated in 
vitro diagnostics that give clinically relevant information  
in an easy to interpret manner to healthcare professionals. 
We have a strong ethical stance on the tests that we develop 
that they will impact patient outcomes. 

Laboratories
at yourgene we spend a lot of time talking to our lab 
customers to understand what their needs are. We then build 
this feedback into our product development roadmap and 
across our support functions to ensure our customers receive 
the highest quality products and services to meet their needs.

Partners
We work in close collaboration with key partners to develop an 
impactful, clear, open and honest relationship that focuses on 
mutual beneficial goals with key milestones outlined to give 
accountability and ensure key deliverables are on track. 

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Wo r K i n G W i t H pa rt n er S

We work in partnership
with global leaders  
in DNA technology to 
advance diagnostic science

We describe the Company as 
being partnership rich and 
strong in strategic relationships 
with our different stakeholders, 
which is the foundation of our 
growth strategy. We see our 
customers as more than 
transactional, we want to really 
understand them and their 
needs, we want to collaborate 
across different applications and 
really strengthen and grow the 
relationship into a trusted and 
valued partnership.

Hayden Jeffreys
chief operating officer

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St r at eGy

We have made sound progress in all 
four areas of our strategic growth 
priorities this year

STRATEGIC PRIORITIES

Market Penetration 
Sell more in existing channels
drive worldwide sales of our current product and 
service portfolio by targeting further expansion 
through direct and key distribution channels.

I

C
N
A
G
R
O

i

C
n
a
G
r
o
n

i

Geographic Reach
Sell into new territories
expand directly and through distributors  
and partners into new regions.

Product Expansion
New product lines and content
leverage our technical and regulatory expertise and 
partnerships to extend our genetic testing offering.

Support diagnostic majors and bioinformatics 
specialists with ivd product contract development 
partnerships.

Mergers and Acquisitions
Consolidator in the market
We are considering additional selective mergers  
and acquisitions in the future to support our  
business growth.

it’s a fragmented market with few medium-sized 
entities which presents a strong opportunity for 
consolidation.

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ACHIEVEMENTS

FUTURE PLANS

•  range selling to customers with expanded reproductive 

•  developing an advisory panel for key opinion leaders 

health & infectious disease product range.

•  Gained nipt market share across some key regions.
•  revenue growth of 87%.
•  consolidated nipt market in France with acquisition of 
aGX-dpni enabling us to get closer to the customer.
•  co-marketing partnerships with distributors and key 

platform partners.

•  Global review and alignment of distribution network.
•  Global sales organisation re-structure and strengthened 

• 

the team with key appointments.
increased digital marketing in lieu of exhibitions due to 
covid-19.

•  now in over 60 countries due to elucigene acquisition.
•  established yourgene Health inc and first customer 

revenue achieved in uS.

•  dpyd assay approved for sale in australia.
• 

iona® nx nipt Workflow received ce mark ahead of 
commercial launch.

•  Substantial expansion of nipt customers in india,  

South east asia and middle east.

•  Growing regulatory framework of submissions scheduled.

•  Science excellence internal working party.
•  Strengthened r&d team with key appointments.
•  developed the clarigene™ infectious disease portfolio  
and developing our first clarigene™ SarS cov-2 test.
•  launched elucigene® dpyd assay – our first precision 

medicine ce marked product.

•  launched yourgene Flex™ analysis Software. 
•  developed iona® nx nipt Workflow on the illumina  

nGS platform. 

and key customers.

•  Further professional development for global  

sales team.

•  Strengthening product management team to support 

growing product mix.

•  new and improved internal global crm system.
•  additional co-marketing campaigns with key  

platform leaders.

•  uK and european roll-out of iona® nx nipt Workflow.
•  emergency use Fda approval submission for 

clarigene™ SarS-cov-2 test.
•  market entry plans for latam.
•  development of cystic Fibrosis panels for new regions. 

•  develop a Scientific advisory Board.
•  expansion of the precision medicine portfolio  

with a focus on oncology initially.

•  expansion of the clarigene™ infectious  

disease portfolio. 

•  enhancements to Sage™ link cloud-based  

nipt software.

•  elucigene integration complete with synergy cost savings 

•  continue to identify m&a opportunities based on 

realised.

•  elucigene and yourgene teams merged and mostly all 
located together at refitted citylabs headquarters in 
manchester.

•  completion of acquisition of aGX-dpni – French nipt 

distributor partner. 

•  realised roadmap to profitability. 

business growth strategy.

•  position yourgene as a consolidator in the market.
•  Showcase yourgene to investors as a high growth  

story for future m&a fundraising.

•  transition aGX-dpni French customers to iona®  

nx nipt Workflow. 

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17

St r at eGy i n  ac t i o n

The acquisition of AGX-DPNI has an 
immediate and positive impact on 
earnings and is an opportunity to 
fully capitalise on our rising NIPT 
sales in this growing market

HOW THIS ACQUISITION 
SUPPORTS OUR STRATEGY

Market 
Development

Geographic 
Reach

Product 
Expansion

Mergers and 
Acquisitions

in march 2020, the company announced that we 
had acquired aGX-dpni, the nipt arm of our 
French distributor adGeniX. this was achieved by 
raising £2.5 million with BGF one of our significant 
investors. this is a timely and strategic acquisition, 
just ahead of the roll-out of iona® nx nipt 
Workflow, enabling us to be much closer to our 
growing French lab customer base. the acquisition 
is fundamentally about acquiring our French 
customers’ business and does not include facilities, 
technology or people. Following an initial period of 
integration, we will then gain direct control of this 
growing and important market.

Market Penetration in France 
France is a key growth market for nipt with 
French government reimbursement agreed 
in early 2019 and 75% growth in yourgene 
nipt volume sales in 2019. yourgene 
currently have seven established nipt labs  
in France and they are mainly large private 
laboratory networks which have nationwide 
coverage. yourgene having direct customer 
ownership as we roll-out our iona® nx nipt 
Workflow into these labs will ensure a 
smooth transition. in addition, we have over 
30 lab public hospital lab customers in France 
that use our cystic Fibrosis and other 
reproductive health products, optimising 
opportunities for range selling. 

Geographic Expansion
the acquisition will enable improved access 
to new high growth markets in the French-
speaking africa and middle east regions.  
the yourgene commercial operation has a 
dedicated French-speaking team based in the 
uK and in country to support our customers. 

Product Expansion
opens up new clinical collaborations  
with customers to develop new menu 
opportunities across the broad and growing 
product range. 

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This provides us with our first direct 
commercial presence in Europe,  
and gives us an EU-based presence 
post-Brexit. It also opens up access to  
high-growth French-speaking African 
and Middle Eastern markets not 
previously addressed by Yourgene.

Lyn rees
chief executive officer

yoUr Gene HeaLTH pLC  annual report and account S 2020
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c Ha i r m a n ’ S Stat em en t

The enlarged Yourgene  
Health is a renewed  
business, with considerable 
growth potential

i am delighted to report that the 2019/2020 financial 
year has been a defining one for your company,  
led by the ceo lyn rees. We have taken the business 
through a period of substantial change and created a 
strong foundation for future growth.

yourgene Health plc has gone from strength-to-strength and 
during the financial year 2019/20, we have reported our first year 
of positive eBitda*. the Group now has three clear areas of 
product focus:

•  non-invasive prenatal testing (nipt)
•  reproductive Health 
•  molecular Genetics, including oncology, research services 

and infectious disease (covid-19 testing)

excluding infectious disease, which was a new focus post-
period end, each of these areas grew throughout the last 
financial year, however it will be their contribution throughout 
2020 and beyond that will define the Group.

distribution channels expanded during the period and we now 
currently distribute to over 60 countries, to over 300 customers, 
either directly or via distributors. to accommodate this 
expansion we have invested in new facilities and staff, which will 
provide additional capacity for the anticipated future growth of 
the Group and to support the roll out of the iona® nx product.

the Board during this period has been strengthened by the 
appointment of dr John Brown cBe and Jonathan Seaton, who 
both have extensive experience within the life science industry 
and have made a very valuable contribution. Jonathan in 
particular has a lot of expertise in mergers and acquisitions and 
is based in the uS – this supports our strategic growth plans.

during the 2019/20 financial year we acquired and integrated 
elucigene diagnostics and in march 2020 we acquired aGX-dpni 
S.a.S, both of these acquisitions have been earnings enhancing 
during the current financial year and will continue to be so.

i would like to take this opportunity to thank all of our team at 
yourgene for their effort, dedication and loyalty to the Group 
during this period and the covid-19 pandemic. We have a 
business that has a balanced portfolio with substantial 
opportunities, which we are determined to deliver upon.

adam reynolds
non-executive chairman
27 July 2020

* adjusted eBitda is the operating profit/(loss) before interest, tax, 
depreciation, amortisation, share-based payments and acquisition-
related expenses shown separately disclosed on the face of the  
income Statement.

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YEAR IN REVIEW

March 2020 
acquisition of aGX-dpni, 
French distribution channel 

February 2020 
ce marking technical file submission 
for iona® nx nipt Workflow 

February 2020 
medilink award for outstanding achievement 

February 2020 
dpyd approved for sale in australia 

November 2019 
Bionow double award win
Winners of Bionow investment deal of year and 
Bionow company of the year at the 18th annual 
Bionow awards ceremony

November 2019 
opening of new facilities in citylabs 1.0, 
manchester and corporate HQ

October 2019 
launch of yourgene Flex™ analysis Software – 
expanding our capabilities in bioinformatics 

September 2019 
ce-ivd certification renewal with 
notified body BSi, netherlands 

September 2019 
launch of elucigene® dpyd assay
First precision medicine ce marked kit for 
chemotoxicity 

August 2019 
yourgene Health inc established and 
first uS revenue generated 

August 2019 
Jonathan Seaton appointed to the 
Board as non-executive director 

July 2019 
dr John Brown appointed to the Board 
as a Senior independent director 

April 2019
acquisition and fundraise 
£11.8 million fundraise to finance acquisition 
of elucigene diagnostics 

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c eo Stat em en t

We have continued to deliver  
on our strategy this year and  
I’m very excited about the 
prospects for further growth  
over the following years

i am absolutely delighted with the positive progress 
that we’ve made in the last 12 months, and i am equally 
excited about the opportunities we have ahead of us in 
the new financial year which will allow us to continue 
our strong commercial momentum despite the 
challenges caused by the global pandemic.  

i am also very proud of the way the team has pulled together  
to support the global covid-19 effort with the launch of our 
clarigene™ SarS-cov-2 test and also to progress the iona® nx 
nipt Workflow product (“iona nx”) through ce marking and 
towards commercial launch under difficult market conditions.

KEY STRATEGIC PRIORITIES FOR GROWTH

Product Penetration
Selling more into existing 
channels

Product Expansion
new product lines and 
content

certainly, from a financial perspective, the year ending 31 march 
2020 proved to be another year of delivering significant growth 
in line with expectations. revenues were up 87% to £16.6m 
compared to the previous year and we achieved a key milestone 
of recording a positive adjusted eBitda* for the first time, with 
adjusted eBitda of £1.3m compared to an adjusted eBitda loss 
of £3.4m last year. also, with over £2.7m of cash in the bank at 
year end we are well funded to continue to execute against our 
four key strategic priorities for growth, and which over the last 
year we made significant progress against.

Geographic Expansion
Selling more into new 
territories

Acquisitive Growth
Both earnings enhancement 
opportunities and technology 
consolidation

Product Penetration
during the year we recorded like for like organic growth from 
existing products of approximately 36%. 

the majority of this organic growth is derived from the increased 
use of our flagship non-invasive prenatal tests (nipt) for  
down’s syndrome and other genetic disorders. Sales from nipt 
products and services were up 29% over the year to just over 
£10m (up from £7.9m), although this does include three weeks’ 
contribution from our French nipt distribution business which 
was acquired in march. Whilst we are delighted with the 
continued performance of the nipt business this growth was 
held back due to anticipation by our uK and european customers 
for the new illumina-based iona nx format, which we expect  
to be a major driver of nipt sales growth in these markets  
once launched. 

* adjusted eBitda is the operating profit/(loss) before interest, tax, 
depreciation, amortisation, share-based payments and acquisition-
related expenses shown separately disclosed on the face of the  
income Statement.

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it was also pleasing to see a very strong performance over the year from our research services activities operated from taipei, which made 
a strong contribution to the performance of our molecular Genetics division (previously referred to as oncology & research services).

our strong focus on the development of key relationships has been essential to ensuring continued growth from our existing sales 
channels. We have cultivated and reinforced our direct relationships with customers in key regions and we have a well-established channel 
of distribution partners who bring the experience of local market knowledge, culture and language, networks and provide on the ground 
regulatory and logistic support. We continue to maintain and develop relationships with key instrumentation manufacturers such as 
illumina and thermo Fisher. We have established collaborations with key opinion leaders, clinicians, and scientists, to promote the need for 
high-quality and highly accurate prenatal screening.

Having already established a strong nipt footprint in india, the middle east and asia we have benefited from continued growth in these 
areas. as nipt use continues to grow in these areas, our distribution partners have successfully increased adoption of our products within 
their regions.

Geographic Expansion
We continue to make excellent progress in expanding our commercial footprint into new territories. a key achievement during the year  
was the establishment of a direct sales presence in the uS for the first time, through the establishment of yourgene Health inc, and most 
importantly the generation of our first uS revenues. We expect to see good growth from the uS market when borders open up again.

the elucigene acquisition has been a big driver of our increased geographic coverage and we now sell products into over 60 countries 
worldwide, compared to 30 countries last year. 

during the year we have entered new markets with contract wins for nipt in South east asia, eastern europe and the middle east, we have 
appointed new distributors to cover additional countries, previously not served by our distribution network. We continue to look for long 
term opportunities in china across our expanded product range and we continue to evaluate potential partners.

the result of our geographic expansion can be seen below:

Revenue Analysed by Geographical Market

regional segments

uK
europe
international

Total

year ended 
30 march 2020
£m

2.0
4.1
10.5

16.6

year ended 
30 march 2019
£m

1.2
1.8
5.9

8.9

% of total

12%
25%
63%

100%

% of total

14%
20%
66%

100%

Growth

+62%
+133%
+78%

+87%

Product Expansion
during the year we have successfully executed our plan to broaden our product lines and content beyond nipt and to establish a 
wider range of additional reproductive health products within the Group, covering many elements of the reproductive lifecycle.

during the year we launched our first oncology product, the elucigene dpyd assay, a new chemotoxicity diagnostic assay,  
a simple-to-use genotyping test that can identify cancer patients with dihydropyrimidine dehydrogenase (dpd) deficiency.  
dpd can cause severe and sometimes lethal side effects in patients being treated with chemotherapeutic drug 5-Fluorouracil 
(5-Fu), commonly used in the treatment of colon, oesophageal, stomach, pancreatic, breast and cervical cancers. uK sales are 
growing with several public sector key customers routinely using the test to pre-screen cancer patients ahead of being prescribed a 
treatment therapy. 

this year we also launched yourgene Flex™ analysis Software which allows us to work in close collaboration with product 
development partners to customise our analysis platform for their nGS applications beyond nipt. We believe that this will open up 
opportunities to develop products in other fields such as reproductive health, oncology or other clinical diagnostic fields and across 
new regions too. 

Following the successful development and ce marking of our iona nx product our talented r&d team are now able to deploy on 
developing additional new products and services, not only for us but also for any contract development partners. this is particularly 
significant given our expedited development of products and services focused on infections disease, namely covid-19, and i will 
address this opportunity in my outlook statement. our product range is more diverse, utilises broader technologies and we have 
become platform agnostic. We are the only nipt provider to offer the test for both nGS platforms.

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c eo Stat em en t CO N T I N U ED

the increased spread of our revenue base outside of nipt can be seen in the table below:

Revenue Analysed by Product Segments

product segments

nipt
reproductive Health
molecular Genetics

Total

year ended 
30 march 2020
£m

10.1
3.7
2.8

16.6

year ended 
30 march 2019
£m

7.9
0.0
1.0

8.9

% of total

61%
22%
17%

100%

% of total

89%
0%
11%

100%

Growth

+29%
n/a
+174%

+87%

Continued Expansion of People Talent
outside of the Board, we’ve been keen to invest in the future 
growth of our business by acquiring talented individuals to the 
organization, strengthening our team and developing staff’s 
expertise. Key hires this year include our first uS commercial 
recruit to support uS operations, a new research & development 
director, and a new Hr director. We have added new talent and 
skills to our service laboratory offering and have strengthened 
our quality and regulatory team. in anticipation of further 
commercial growth and the launch of new products we have also 
strengthened our marketing, sales, business development and 
customer service teams. in addition, we have grown our european 
sales team with key appointments in uK, France, Germany to 
support the commercial roll-out of the iona nx nipt Workflow. 

conscious of the fact that it is our entire team that delivers value 
to shareholders, we are in the process of identifying suitable 
ways to ensure that everyone involved in this business will be 
rewarded for success. this will align the interests of all staff with 
our investors, and with staff themselves as shareholders we will 
ensure that we all work together to deliver shareholder value.

Acquisitive Growth
during the year we completed two strategic and earnings 
enhancing acquisitions that have been a major contributor to the 
successful growth of the company and has set us up with a much 
stronger platform to deliver further growth in 2020 and beyond.

in april 2019, we acquired elucigene diagnostics, a highly 
complementary business which was immediately accretive to 
earnings. integration has gone incredibly well with the team now 
united under one management structure operating out of our 
citylabs 1.0 facilities in manchester. manufacturing is now 
concentrated on this one site and the expected synergies from 
integration have been fully realized. yourgene now has a wider 
portfolio of complementary products that can be sold to 
customers as part of a range and a broader global sales network.
Following integration we have achieved over 12% like-for-like 
growth in the elucigene business through the realisation of 
commercial synergies.

in march 2020 we announced the acquisition of our French nipt 
distribution channel, aGX-dpni, providing us with direct access 
into a key growth market given that the French Government 
agreed nipt reimbursement in early 2019 and we experience 
75% growth in our nipt volume sales in France during 2019.

We will continue to consider additional selective synergistic m&a 
opportunities that offer significant shareholder value, whether 
these might be earnings enhancement opportunities or the 
chance to acquire complementary molecular diagnostic 
technologies.

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Clarigene™ SARS CoV-2 Test
the launch of our clarigene™ SarS-cov-2 test for research use 
last month is a significant step towards the launch of our ce 
marked product.

We remain on track to achieve ce marking for our test before the 
end of this month. initial data has shown that the test shows 
competitive performance against other market leading products 
(i.e. 100% specificity) and has a quick turnaround time and low 
false negative results, given that the test only detects rna and 
not amplified patient dna. the ce-ivd version will have two viral 
targets and assay controls, making it more desirable from the 
reimbursement perspective across several european regions.

there is no doubt that there is a significant opportunity to drive 
sales of the clarigene™ SarS-cov-2 test and ce ivd kits, once 
approved. recent collaborations with partners are in place to 
provide corporate partners and healthcare settings such as care 
homes and private Gp practice with a fast and reliable covid-19 
lab testing service.  

the next key news for shareholders on our progress in this area 
will be confirmation of ce marking. We understand that the 
covid-19 testing market is dynamic and, to a certain extent, 
unpredictable as a result. With this in mind, we will commit to 
updating shareholders on a quarterly basis on the commercial 
take-up of this product, and not based on unsupported 
speculation of what the future potential uptake might be. 

market forecasts for 2021 and beyond see our growth trajectory 
continuing and heralds a move towards full profitability in the 
near term. We remain confident that we can deliver against these 
forecasts and that both iona nx and our clarigene products will 
be major contributors to this growth. there has never been a 
better time to be in this high growth molecular diagnostics 
market and i am really excited about the opportunities ahead for 
the Group.

lyn rees
chief executive officer
27 July 2020

Impact of COVID-19 on the Business
i am exceptionally proud of how the entire yourgene team  
have adapted to the new working conditions imposed by the 
coronavirus pandemic. early on in the crisis we put in place 
robust systems to continue to operate efficiently and to 
continue to provide customers with world-leading molecular 
diagnostic solutions and services. Keeping customer supplied 
was key during this period and i am pleased to say that this has 
been maintained throughout. i would certainly like to record my 
thanks to everyone for their hard work and dedication and i’m 
sure shareholders will join me in congratulating the team for 
continuing to supply customer and develop new products for 
commercial launch under such testing circumstances.

Outlook
Without doubt, the most exciting part of our business is not just 
what we have proudly achieved in 2019, but the platform that 
we’ve built to deliver future growth in 2020 and beyond. critical 
to this is the opportunity for growth that we have through the 
launch of iona nx, following successful ce-ivd marking, and 
also the launch of our clarigene™ SarS-cov-2 test.

IONA Nx
in June we were delighted to announce the ce-ivd mark for our 
illumina-based iona® test, which will be launched as the iona® 
nx nipt Workflow. this test has been developed to run on the 
illumina nextSeq 550dx next Generation Sequencing (“nGS”) 
instrument, and this is major advancement of our flagship nipt 
given that illumina’s nGS technology accounts for around 75% of 
the global nGS market. not only does it allow us for the first time 
to proactively market in our existing markets (mainly europe) but 
it will also allow us to target new markets, previously excluded to 
us for nipt, such as asia pacific and north america.

in anticipation of full commercial launch, we are soon to be 
installing the test to run as part of our own laboratory service run 
from our facilities in manchester. this will allow us to imbed best 
practice in readiness for the transition to our customer labs. 
planning and scheduling are underway with existing iona 
customers across europe to transition to the iona nx and 
market development plans are in place for the introduction of 
iona nx in new territories and discussions are progressing with 
customers in new territories for the iona nx. We expect to 
announce further details of our commercial launch and roll-out 
activities over the summer and will be working through a 
schedule of regulatory submissions to allow launch into new 
regions over the coming months. 

our iona test has a strong reputation for reliability and accuracy 
and was the first ce marked nipt product for the european 
market. the new iona nx combines this gold standard for 
reliability and accuracy with a market leading sequencer and we 
believe this will be a strong driver of growth in the future.

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Fi n a n c i a l r e v i e W

Continued progress
towards a profitable  
business of scale

Income Statement
in the trading year revenues grew 87% to £16.6 million (2019: 
£8.9 million) due to organic growth, the april 2019 acquisition of 
elucigene diagnostics in the uK and the march 2020 acquisition 
of aGX-dpni in France as described elsewhere in this report.

Gross profits grew 122% to £10.2m (2019: £4.6m) with gross 
margins increasing to 62% (2019: 52%). Gross margins benefited 
from the higher margin elucigene product mix as well as an 
increasing proportion of revenues in our international 
geographic market. General administrative expenses increased 
to £9.0m (2019: £8.1m) in particular due to the enlarged 
operational capabilities acquired in the elucigene business.  
We maintained research and development expenditure as we 
focused on the development of the new version of the iona® 
test for the illumina nGS platform. 

Separately Disclosed Items
Significant items within administrative expenses are shown 
separately in the consolidated Statement of comprehensive 
income, with further details in note 5. these separately 
disclosed items include non-cash accounting charges for 
share-based payments which reflect the improved business 
performance (ie the likelihood of achieving performance 
targets) and the increases in the company’s share price in the 
second half of the reporting period. the costs of acquisitions 
and the associated integration expenses are also shown 
separately as non-trading expenses and for greater 
transparency. note that the integration expenses are largely 
related to the acquisition of elucigene diagnostics in april 2019, 
and are largely offset in cash terms by renegotiated property 
leases and operational synergies realised which will flow through 
the income Statement in future years.

We recorded our first adjusted eBitda profit of £1.3 million  
(2019: £3.4 million loss). adjusted eBitda is measured as  
the operating loss before depreciation, amortisation, and 
separately disclosed items. operating lease commitments are 
now classified as right of use assets and financial liabilities under 
iFrS16, which we have adopted for the first time (see note 2).

Operating Loss
there is a resultant much-reduced operating loss after total 
administrative expenses of £3.2 million (2018: £4.8 million loss) 
driven by rising revenues and gross profits, whilst controlling 
administrative expenses and despite the significant non-cash 
separately disclosed items.

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Financial StatementS

Finance Income/(Expenses)
during the period the Group incurred net finance expenses of 
£0.1m (2019: net finance income of £8.2m). the 2019 figure was 
principally due to a one-off restructured relationship with life 
technologies which involved a significant debt cancellation in 
February 2019 (see note 30).

Taxation and Foreign Exchange
the resulting loss on ordinary activities of £2.4m (2019: 3.4m 
profit) reflects a £0.9m tax credit which is described in note 12 
and is primarily the recognition of a deferred tax asset from 
historic losses to offset the deferred tax liability arising on 
acquisition of elucigene’s intangible assets. there are still 
significant historic tax losses in the uK which have not yet been 
recognised which will help offset taxes arising on future 
anticipated profits.

the Group made a small gain of £0.1 million (2019: gain less than 
£0.1 million) on translation of its foreign subsidiaries and foreign 
currency balances to the presentational currency.

Total Comprehensive Loss
the Group recorded a total comprehensive loss of £2.3m (2019: 
profit of £3.4m).

Earnings per Share
earnings per share were a loss of 0.4 pence (2019: earnings of  
0.9 pence).

Statement of Financial Position
at the balance sheet date the Group had total assets of £37.7m 
(2019: £15.6m). intangible assets and goodwill increased to 
£10.2m and £10.8m respectively (2019: £1.2m and £7.0m 
respectively) as a result of acquiring customer relationships and 
intellectual property with elucigene diagnostics and customer 
relationships with aGX-dpni. property, plant and equipment 
was stable at £2.0m (2019: £2.1m) with physical assets being 
maintained. the adoption of iFrS16 has led to the recognition of 
a right of use asset of £3.0m relating to the properties occupied 
by the Group in its various operating facilities and their 
renegotiated leases post the elucigene acquisition.

total current assets increased to £10.0m (2019: £5.3m) with 
rapid revenue growth leading to increased trade and other 
receivables and a smaller increase in inventories.

total equity and liabilities increased to £37.7m (2019: £15.6m) 
due to the equity-based fundraising to support acquisitions, and 
due to the recognition of a £2.7m lease liability under iFrS16. 

Statement of Cash Flows
the Group had an opening cash position of £1.3m (2019: £0.3m) 
and a net cash increase of £1.5m (2019: £1.0m). cash and cash 
equivalents at the end of the period were £2.8m (2019: £1.3m). 
during the period the Group used £2.1m (2019: £4.0m) of cash in 
operating activities due to working capital movements arising 
from business growth. cash used in investing activities was 
£9.0m (2019: £0.6m) reflecting acquisitions during the year, 
capital expenditure in the year and capitalisation of internally 
generated intangible assets.

Financing activities generated a surplus of £12.6m (2019: £5.6m) 
with equity fundraises in april 2019 and march 2020 to support 
the respective acquisitions of elucigene diagnostics and 
aGX-dpni described in note 18.

as with all businesses at this early stage of development,  
the Board assesses carefully the Group’s ability to operate  
as a going concern and has detailed plans for revenue growth, 
margin improvement and cash flow control which are intended 
to achieve positive cash flows in the near future. more detail on 
these plans can be found in the notes to the accounts.

Dividends
no dividend is recommended (2019: £nil) due to the growth 
stage nature of the Group.

Capital Management
the Board’s objective is to maintain a balance sheet that is both 
efficient at delivering long-term shareholder value and also 
safeguards the Group’s financial position in light of variable 
economic cycles and the principal risks and uncertainties 
outlined in this report. as at 31 march 2020 the Group had net 
cash of £2.4m (2019: £1.0m) after borrowings of £0.4m (2019: 
£0.3m) but before lease liabilities arising under iFrS16 (with their 
offsetting right of use assets). Business growth and the 
increased scale achieved through the post-period elucigene 
acquisition are expected to enable the Group to operate as a 
going concern for the foreseeable future.

Post-balance Sheet Events
in may 2020 warrants and share options were exercised 
generating proceeds of £0.8m. on 3 July the Group expanded its 
research services activities by acquiring a small uK company 
with capabilities in that area. the Group has also been 
contending with the global covid-19 pandemic and has 
responded effectively despite some logistical disruption in the 
early stages of the pandemic and is now targeting commercial 
opportunities for covid-19 testing for further risk mitigation.

Barry Hextall
chief Financial officer
27 July 2020

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pr i n c i pa l r i S K S a n d  u n c erta i n t i e S

there are a number of risks and uncertainties associated with the Group’s activities. the Board 
believes the following are the principal risks, along with the mitigation actions being pursued.

r i S K 

i m pac t 

Legal & regulatory risks

m i t i G at i o n 

Intellectual 
Property (IP) 
Litigation

Patents

Changes in 
Legislation and 
Regulatory 
Regimes

Brexit

market risks

Competition

the life sciences industry is characterised by significant 
litigation from patent-holders and their licensees who 
try to erect legal barriers to entry via ip rights. 
non-invasive prenatal testing, in particular, has seen a 
high level of activity in the uSa, europe and elsewhere, 
primarily involving illumina inc who have acquired or 
licensed ip in this sector.

the Group is focused on protecting its ip. to protect its 
key products the Group has secured and is seeking to 
secure patents. However, there remains the risk that 
the Group may face opposition from third parties to 
patents that it seeks to have granted. the Group also 
faces the risk of third parties infringing its ip. no such 
situations have arisen during the reporting period or 
since.

changes in laws, legislation and international relations 
affecting the diagnostics market could have a negative 
impact on the Group’s business activities and 
consequently may have a detrimental effect upon the 
trading performance of the Group. the international 
diagnostics industry is highly regulated by 
governmental authorities across the world where the 
Group intends to market its products. no assurance 
can be given that the Group’s products will successfully 
obtain any necessary regulatory approvals in these 
territories.

in carrying out its activities the Group may also face 
contractual and statutory claims, or other types of 
claim from customers, suppliers, employees and/or 
investors. in addition, the Group is exposed to potential 
product liability risks that are inherent in the research, 
development, production and supply of its products.

the Brexit question has now been resolved but the 
timing and nature of Britain’s exit from the eu still have 
significant uncertainty. the implications for the Group 
are equally unknowable at this time but could 
potentially affect the costs and effort associated with 
sales to the eu and purchases from it, the way in which 
ce marked product registrations are managed, the 
impact on indirect taxation and customs duties and 
Brexit-influenced exchange rate movements.

in September 2018 the Group settled a long-running patent 
infringement dispute with illumina in the uK and entered into  
a licence and Supply agreement covering the uK and other 
international territories where nipt patents are granted.  
Since this agreement was signed the Group has been developing 
an updated version of its iona® test, which received ce-ivd 
certification in June 2020 and is being rolled out in the relevant 
territories.

the Group engages reputable legal advisers to mitigate the  
risk of patent infringement and to advise on the protection of the 
Group’s ip.

the Group has implemented, and proactively manages, quality 
assurance and health and safety systems to meet regulatory 
requirements and to ensure ongoing compliance. during the 
reporting period the Group appointed a director of Quality and 
regulatory affairs to further strengthen the Group’s capabilities 
in this area.

the Group also monitors closely the regulatory rules which apply 
to the Group’s products in order to anticipate changes and ensure 
the Group’s products are available for sale.

the Group retains a suite of insurance policies to protect it from 
the most likely areas of claim, and undertakes risk management 
practices to minimise the number and size of claims arising.

the Group has made significant preparations for a ‘hard’ Brexit 
scenario by changing its regulatory notified Body to one based in 
the eu, and also through the acquisition of a French trading 
company which can act as a bridge into the eu’s simplified vat 
regime for example. 

the Group is in competition with other nipt providers 
of services and products. there is a risk that they 
achieve greater than expected market penetration and/
or continue with aggressive price discounting and 
bundling of nipt with other genetic or clinical service 
offerings.

the Group’s continuing product development, marketing 
activities and collaboration with nGS platform providers are 
designed to ensure that the iona® test remains at the forefront 
of the nipt market. the acquisition of elucigene and the product 
development pipeline also diversify the Group’s product range.

Procurement

there is a risk that uK and international procurement 
practices may create market segments in which the 
Group is unable to effectively offer its products and 
services.

the Group works with policymakers, trade organisations and 
legal advisers to monitor and influence any changes in such 
practices, and also to highlight areas where procurement 
practices may not be fair and transparent.

Similarly, competitors may seek to influence 
procurement practices to the disadvantage of the 
Group.

Increased risk

Decreased risk

 No change

28

yoUr Gene HeaLTH pLC  annual report and account S 2020

company o vervieW

STraTe GiC repor T

Governance

Financial StatementS

r i S K 

Financial risks

Future Funding 
Requirements

Third-party 
Reimbursement

operational risks

Dependence on 
Key Personnel

Technology

Contracts

COVID-19

i m pac t 

m i t i G at i o n 

the Group may need to raise additional funding to 
continue to invest in the activities of the Group. there 
is no certainty that this will be possible at all or on 
acceptable terms. in addition, the terms of any such 
financing may be dilutive to, or otherwise adversely 
affect, shareholders.

the Group may be adversely affected by third-party 
reimbursement decisions. the Group may not be able 
to sell its products profitably if reimbursement from 
these sources is unavailable or limited. third-party 
payers are increasingly attempting to contain costs 
through measures that could impact the Group’s nipt 
products, including challenging the prices charged for 
products and services, limiting both coverage and the 
amount of reimbursement for new diagnostics’ 
products and services, and denying or limiting coverage 
for products that are approved by the regulatory 
agencies but are considered experimental by third-
party payers.

the Group has a global leadership team and the future 
success of the Group, in common with other businesses 
of a similar size, will be highly dependent on the 
expertise and experience of the Board and key 
management. However, the retention of such key 
personnel cannot be guaranteed. the loss of any key 
personnel, or the inability to attract appropriate 
personnel could materially adversely impact the Group’s 
business, prospects, financial condition or results  
of operations.

technologies used within the diagnostics marketplace 
are constantly evolving and improving. therefore there 
is a risk that the Group’s products may become 
outdated as improvements in technology are made.

there can be no certainty that third parties will 
perform, or be able to perform, their obligations under 
various contracts with the Group or that the Group will 
be able to recover damages for breach of contract. the 
insolvency of third parties or their default under the 
terms of such contracts could have a material adverse 
effect on the Group and its operations.

the global pandemic of covid-19 created significant 
operating risks to all businesses towards the end of this 
reporting period and into the new financial year. risks 
include the inability for staff to access Group facilities, 
for ill-health to reduce the available capacity in the 
business, for products to be shipped to new and 
existing customers, for suppliers to maintain supply of 
critical raw materials and for staff to travel to support 
existing and potential accounts or engage in business 
development activities. customers are diagnostic 
laboratory groups who may be affected by diverting 
resources towards covid-19 testing activities and 
away from the Group’s core product portfolio.

to manage this risk the Group is actively building its revenue 
generating capabilities and monitors its cash flow requirements 
closely. activities are adjusted according to available funding 
through its periodic business planning process to control cash 
consumption, whilst maintaining a dialogue with potential future 
funders. the fundraise concluded in april 2019 and march 2020 
alongside the elucigene and France acquisitions respectively 
providing significant funding runway as the Group nears self-
sufficiency in operating cash flows.

the Group proactively engages with the clinical community to 
align its product offering with the best current medical 
requirements in order to ensure its commercial model is 
supported by reimbursement regimes as they reach their 
decisions on nipt screening in the coming years. to date, 
reimbursement has been more of an opportunity than a risk as 
coverage increases nipt testing volumes.

the Group provides attractive remuneration incentives, including 
share options, and endeavours to maintain an empowering 
culture to encourage retention of key individuals, as well as 
recruiting suitable deputies over time. the acquisition of 
elucigene has also strengthened the breadth and depth of 
leadership within the Group.

the Group has a research and development function which seeks 
to keep up with the latest developments in the genetic-testing 
sector.

the acquisition of elucigene adds pcr-based products to spread 
this technological risk, deepen the Group’s r&d capabilities and 
extend the Group’s access to insights into how international 
markets are evolving.

the Group monitors its contractual commitments and 
outstanding exposures closely, supplier strength and 
outstanding debtor exposures closely, developing specific plans 
where the potential impacts would be significant.

the Group’s it infrastructure is primarily cloud-based which 
enabled the business to move to remote working for all but 
laboratory-based staff very efficiently. laboratory safety 
protocols have been implemented to minimise the risks of 
infection, and thankfully the Group’s employees have not been 
significantly affected. Some supply difficulties have been caused by 
international lockdowns but close management of the situation by a 
senior ‘coBra’ committee has ensured the business has been able 
to continue to trade effectively throughout the pandemic. to 
offset potential demand weakness where customers are diverted 
to covid-19 testing, the Group has launched its own testing 
service and announced in June 2020 the launch of clarigene™, its 
own testing product. it has also partnered with other organisations 
in the global pandemic response.

Increased risk

Decreased risk

 No change

yoUr Gene HeaLTH pLC  annual report and account S 2020

29

BoA R d o F d I R ec to Rs

Adam Reynolds
non-executive chairman

dr stephen little
Vice chairman

dr John Brown 
senior Independent director

nicholas Mustoe
non-executive director

Jonathan seaton
non-executive director

lyn Rees
chief executive officer

dr Bill chang
chief scientific officer

Barry Hextall
chief Financial officer

Hayden Jeffreys
chief operating officer

30

YOURGENE HEALTH PLC  AnnuAl RepoR t And Accounts 2020

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Adam Reynolds
non-executive chairman
Adam began his career as a stockbroker and 
established his own pR/IR and corporate 
Finance firm, Hansard group plc which sold  
in 2004. In 2005, Adam became executive 
chairman of International Brand licensing plc, 
today it is known as eKF diagnostics plc. Adam 
is a non-executive director and a substantial 
shareholder of eKF diagnostics plc and is 
non-executive chairman of concepta plc  
and optibiotix plc. Adam is a non-executive 
director of online fashion giant sosandar. 
Adam has been named as one of the fifty most 
influential people in the city by growth 
company Investor. Adam chairs the combined 
nominations and Remuneration committee 
and is a member of the Audit committee at 
yourgene Health.

dr stephen little
Vice chairman
stephen is a successful serial biotechnology 
entrepreneur. He is the former ceo of dxs,  
an innovator in the field of personalised 
medicine. dxs was funded with £3.5 million  
in 2001 and was sold to QIAgen BV in 2009  
for £85 million. dxs pioneered the use of 
molecular diagnostic tests such as KRAs  
and egFR to predict the use of novel cancer 
therapies. At QIAgen stephen became  
Vp of personalised Healthcare, responsible  
for developing companion diagnostic 
partnerships with the pharma industry.  
prior to this he spent 20 years in various  
senior positions in the diagnostic divisions of 
Astra Zeneca and IcI. 

dr John Brown 
senior Independent director
John has over 20 years’ capital markets 
experience in the healthcare and life sciences 
sector. He is currently a senior Independent 
director of Biocity and Acacia pharma and is 
chairman of the cell and gene therapy 
catapult and synpromics. Additionally, he has 
previous significant board experience with 
roles including chairman of Axis-shield, 
chairman of Btg, non-executive director  
of Vectura and chief executive officer of 
Acambis. John is a member of the 
nominations/Remuneration and Audit 
committees at yourgene Health.

nicholas Mustoe
non-executive director
nick started his career in london in 
advertising agency Foote cone and Belding 
and at lowe Howard spink, before 
establishing his own agency, Mustoes 
Merriman levy (Mustoes). In 2008 Mustoes 
merged with a leading pR agency geronimo  
to form Kindred, the first fully integrated pR  
& Advertising agency. nick subsequently led  
an MBo of Kindred in 2010. He is currently 
chairman of charity starlight children’s 
Foundation and chairman of Big sofa 
technology plc, as well as a non-executive 
director of Hub capital. nick is a member of 
the nominations/Remuneration and chairs 
the Audit committee at yourgene Health.

Jonathan seaton
non-executive director
Jonathan has extensive experience working 
for leading global life sciences and diagnostic 
companies having worked on > 40 merger  
and acquisition transactions. At Roche 
diagnostics he held the position of Vice 
director, global Business development, 
advising leading merger and acquisition 
activity and strategic partnerships. Jonathan 
also held key strategic roles as a healthcare 
investment banker at deutsche Bank 
securities, a strategic senior role at Becton, 
dickinson and company and Head of 
corporate and Business development and 
government Affairs at Illumina.

lyn Rees
chief executive officer
lyn is a seasoned executive in global 
healthcare and IVd markets. prior to joining 
yourgene Health, lyn was group ceo at the 
BBI group for over 9 years. lyn has completed 
7 acquisitions during his tenure at BBI group, 
all of which have been successfully integrated. 
He founded BBI detection and BBI Animal 
Health and has demonstrated a strong track 
record of organic and acquisitive growth. 
Before this role, he spent several years as  
the Managing director and founder of BBI 
Healthcare. He first began his business career 
as the european Marketing Manager at 
shimano europe BV. 

dr Bill chang
chief scientific officer
Bill is the Founder of yourgene Bioscience in 
taipei which he was ceo for several years 
before it was acquired by yourgene Health. 
Bill’s first role after his phd was with Academia 
sinica in 2007 as a research specialist and he 
established the bioinformatics core facility  
at the Institute of plant and Microbial Biology. 
He co-founded sofiva genomics in 2012 to 
provide prenatal genetic testing services.  
Bill has a phd and is now also an Honorary 
Fellow at the Faculty of Veterinary science, 
university of Melbourne. Bill actively  
presents technical results at many 
international conferences. 

Barry Hextall
chief Financial officer
Barry is a chartered Management Accountant 
with over 25 years’ experience in senior 
financial roles, including with international 
AIM-listed organisations. He has managed 
many businesses through major changes and 
rapid growth, and has significant experience 
working in the global medical devices and  
in vitro diagnostic sectors. His previous 
employers include Immunodiagnostic 
systems plc, JRI orthopaedics ltd,  
c J garland & co ltd, ernst & young llp  
and Zeneca plc (originally IcI). Barry holds  
a diploma in company direction from  
the Iod, and an MBA from cranfield  
school of Management.

Hayden Jeffreys
chief operating officer
Hayden has over 20 years’ experience in the 
clinical diagnostics industry and he has a 
proven track record of formulating and 
implementing commercial strategy and 
driving the next stage of global growth for 
businesses. prior to joining yourgene Health, 
Hayden was chief operating officer at 
cambridge epigenetix. Hayden has also held 
several international senior positions within 
the eRBA group, ceo and Head of corporate 
Business development and strategy. Hayden 
received a Msc in Management studies from 
the university of oxford. 

YOURGENE HEALTH PLC  AnnuAl RepoR t And Accounts 2020

31

co R p o R At e go Ve R nAn c e  s t At eM en t
FO R T H E Y E A R EN D ED 31 M A RCH 2020

the Board recognises the importance of sound corporate governance 
and has elected to implement the corporate governance code for 
small and Mid-size Quoted companies, as published by the Quoted 
companies Alliance (the QcA code), to the extent it is considered 
appropriate in light of the group’s size, stage of development, risk 
profile and resources. the company is also subject to the uK city  
code on takeovers and Mergers. Further information on the group’s 
governance practices, the business model and strategy can be found  
in the company overview, strategic Report and governance sections 
in this Annual Report and Accounts.

this governance statement was last reviewed and updated on  
22 July 2020.

Strategy and Business Model (QCA Principle 1)
yourgene develops molecular diagnostic products and services that 
will have a positive impact on human health and deliver long-term 
shareholder value. the group has a clear strategy to increase 
penetration of sales in the markets in which it operates, to expand the 
geographic markets in which it operates and to launch new products 
and services into these markets. this strategy is being driven 
organically, and through acquisitions where target companies are 
found which support one or more of these four strategic ‘pillars’.

the group is currently focused on delivering high-quality reproductive 
health screening products and services to support a growing 
international customer base of laboratories and healthcare 
professionals. the group provides customers with further clinical and 
research genetic testing services across different fields such as 
oncology, predominantly from taiwan. yourgene has also established a 
contract development partnership programme for customers, building 
on our expertise in developing in vitro diagnostic products. In June 2020, 
yourgene also launched its first infectious disease product which is a 
coVId-19 diagnostic test, clarigene™ and at the same time launched 
an in-house coVId-19 testing service.

the IonA® test is a ce-IVd marked test for prenatal screening which 
enables clinical laboratories around the world to establish their own 
quality assured non-invasive prenatal screening service. In other 
regions we offer the sage™ prenatal screen which provides a greater 
clinical depth of data that is reported and allows labs and clinics greater 
flexibility with the analysis work package. By having these two 
complementary prenatal screening solutions we meet a wider scope of 
customer and market needs. the group continues to expand the range 
of in vitro diagnostic products into different fields as demonstrated  
by the April 2019 acquisition of elucigene diagnostics and its product 
portfolio. the group also invested in stronger penetration of the 
French market through the acquisition of its French distribution 
business in March 2020.

the group also has two clinical laboratories running high throughput 
services in Manchester, uK and taipei, taiwan. Both service labs offer an 
nIpt provision where customer clinicians will send blood samples for 
analysis with the IonA® test and sage™ prenatal screen. new laboratory 
customers will often use the service lab during the installation and 
training phase where they need to begin their nIpt offering as soon  
as possible. In addition, the taipei laboratory offers a range of both 
research and clinical genetic testing for a range of cancer screening tests 
including breast, lung and colon cancer and other non-oncology tests.

Meeting Shareholder Needs (QCA Principle 2)
the company places a great deal of importance on communicating 
with its shareholders. All shareholders are given at least 21 days’ notice 
of the Annual general Meeting and are encouraged to attend. An 
opportunity is provided for them to ask questions at the meeting. 

32

YOURGENE HEALTH PLC  AnnuAl RepoR t And Accounts 2020

throughout the year the chairman, chief executive officer and  
chief Financial officer are in regular contact with the company’s major 
investors and respond to queries from private investors through an 
investor contact email or via the company’s financial pR firm, walbrook 
pR. the ceo is responsible for ensuring that shareholders’ views are 
communicated to the Board as a whole. the group appointed stifel 
nicolaus in April 2019 to act as sole broker to the company, to further 
improve the quality and quantity of investor relations activities.

Manage our Responsibilities to Wider Stakeholders  
(QCA Principle 3)
we take seriously our responsibilities to our staff, trading partners, 
neighbours, the clinical, research and laboratory communities we supply 
and the pregnant and patient populations we support. we operate a 
high standard of quality management to ensure we comply with the 
appropriate regulations in the various territories in which we operate, and 
that we thoroughly investigate any occurrences which fall below our high 
standards so we can implement corrective and improvement actions.

Family-friendly and flexible employee policies, rigorous health, safety 
and environmental practices are very important additions to the 
quality management system in ensuring we manage our stakeholder 
and social responsibilities appropriately.

Risk Management (QCA Principle 4)
the environment in which we operate presents certain general risks  
as well as particular risks that are specific to our own circumstances. 
the Board monitors the key legal, regulatory, market, financial and 
operational risk areas to identify relevant risks, assess their potential 
impact and to develop mitigation strategies that will enable the group to 
flourish. principal risks and uncertainties are described in the appropriate 
section in this Annual Report and Accounts and are set out below.

the Audit committee monitors key risks and is responsible for:
• 

reviewing the company’s external reporting process, including  
the financial statements, reports and announcements and  
the accounting policies and judgements that underline them,  
and making recommendations to the Board before release;
•  monitoring the statutory audit of the annual accounts; and
•  monitoring of the independence of the external auditors and the 

establishment of a policy for their use for non-audit work.

Maintain a Well-functioning Board (QCA Principle 5)
the chairman has considerable experience of Boards operating in the 
AIM environment and ensures the Board has an appropriate composition 
of skills. with the appointment of two new non-executive directors in 
July / August 2019 the company has moved closer to meeting the QcA 
guidance of more non-executives than executives. the Board now 
comprises four non-executive directors, four executive directors and  
a Vice chairman who is partly non-executive and partly executive.

the role of the Board
the directors collectively bring a broad range of business experience 
to the Board which is considered essential for the effective 
management of the company. the Board is responsible for strategic 
and major operational issues affecting the company. It reviews 
financial performance, regulatory compliance, monitors key 
performance indicators and will consider any matters of significance  
to the company, including corporate activity. certain matters can only 
be decided by the Board and these are contained in the schedule of 
matters reserved to the Board. the day-to-day management of the 
company’s business is delegated to the chief executive officer and 
executive directors of the company. during the reporting period the 
Board held eight meetings and there were three Audit committee 
meetings. All directors eligible to participate attended all meetings.

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the composition of the Board and division  
of responsibilities
the Board currently consists of a non-executive chairman, a Vice 
chairman, two non-executive directors, a chief executive officer 
and three other executive directors. the composition of the Board 
ensures that no single individual or group of individuals is able to 
dominate the decision-making process. Board composition remains 
under review going forward to move towards QcA compliance. 
details of the individual directors and their biographies are set  
out in this Annual Report and Accounts and on the website  
www.yourgene-health.com

Roles of chairman and chief executive officer
the roles of the chairman and the chief executive officer are 
separate to ensure a clear division of authority and responsibility  
at the most senior level within the company.

Ensure Directors have Necessary, Up-to-date Skills  
(QCA Principle 6)
directors are provided with access to the company’s nominated 
Adviser and corporate lawyers who provide briefings on necessary 
legislation and regulations from time to time. directors are 
supported if required to ensure their skills remain up to date, 
including training and continuing professional development and 
participation in peer networks via the Institute of directors, the 
Quoted companies Alliance and external advisers.

Evaluate Board Performance (QCA Principle 7)
the Board to date has operated an informal performance review and 
succession planning process but is committed to implementing 
formal procedures. the focus is currently on psychometric profiling 
and performance management of the senior management team 
which may be extended to the Board in due course.

Promote a Value-based Corporate Culture  
(QCA Principle 8)
the Board sets great store by its values-based corporate culture and 
ethical reputation which is crucial to the group’s reputation in the 
highly regulated field in which it operates. the company manages  
a highly regarded quality management system which is used to 
monitor any complaints or deviations from expected behaviours. 
the Board monitors any significant non-compliance matters that 
may arise. In addition, ethical considerations are factored into 
debates on Board matters as and when this is relevant. Recruitment 
practices are heavily focused on recruiting people with similarly 
strong values, and the group’s senior management team are 
currently re-evaluating the values, behaviours and communication 
practices to ensure they remain fit-for-purpose as the group 
continues to expand.

Maintain Fit-for-purpose Governance Structures  
(QCA Principle 9)
the company has adopted and operates a share-dealing code 
governing the share dealings of the directors and applicable 
employees to ensure compliance with the AIM Rules.

Chairman: the chairman is responsible for the leadership of the 
Board and ensuring the effective running and management of the 
Board. He is also responsible for the Board’s oversight of the 
company’s affairs, which includes ensuring that the directors 
receive accurate, timely and clear information, ensuring the 
effective contribution of the non-executive directors and 
implementing effective communication with shareholders.

Chief Executive Officer: the chief executive officer is responsible  
for the day-to-day management and the executive leadership of  
the business. His other responsibilities include the progress and 
development of objectives for the company, managing the company’s 
risk exposure, implementing the decisions of the Board and ensuring 
effective communication with shareholders and regulatory bodies.

Non-executive Directors and independence: non-executive 
directors are required to allocate sufficient time to the company to 
discharge their responsibilities effectively. the Board considers the 
non-executive directors to be sufficiently independent to provide 
appropriate oversight and scrutiny.

Re-election of Directors: in accordance with the company’s Articles 
of Association all serving directors are subject to re-election every 
three years, and a minimum of one-third of directors are subject to 
re-election each year. newly appointed directors are re-elected at the 
first Annual general Meeting after their appointment.

Board meetings and information to the Directors: before each Board 
meeting the directors receive, on a timely basis, comprehensive 
papers and reports on the issues to be discussed at the meeting.  
In addition to Board papers, directors are provided with relevant 
information between meetings. the Board has regular scheduled 
meetings which occur at least quarterly and often monthly.

Board committees and senior Independent director
the Board has two committees, namely the Audit committee and a 
combined nominations and Remuneration committee. In addition,  
it has identified a senior Independent director (sId).

Audit Committee: the Audit committee is chaired by nicholas Mustoe 
with Adam Reynolds and dr John Brown as members.

Nominations and Remuneration Committee: due to the size of the Board 
and the infrequency of senior appointments these two committees have 
been merged. the committee has delegated responsibility from the Board 
for identifying and appointing executive directors, and for developing the 
remuneration policy of the company and for setting the remuneration of 
its executive directors and senior managers. Adam Reynolds chairs the 
committee which is also attended by nick Mustoe and dr John Brown. the 
committee’s activities were reported to the Board throughout the period.

Senior Independent Director: nick Mustoe fulfilled the duties of the 
senior Independent director until the appointment of dr John Brown 
who then assumed the sId role from July 2019. the senior 
Independent director provides an alternative contact point for 
directors and shareholders for matters where they do not wish to 
approach the chairman directly.

Communicate Governance and Performance with 
Shareholders (QCA Principle 10)
the Board communicates regularly with shareholders providing updates 
on group performance to shareholders via interim and annual financial 
reports, trading updates, investor presentations and a regular news flow 
of significant developments for the group. governance practices are 
described fully in this Annual Report and Accounts and the company’s 
website is maintained to be up-to-date and informative.

the enhanced Audit Report in these accounts is representative of the 
Audit committee’s focus areas.

Adam Reynolds
chairman
27 July 2020

YOURGENE HEALTH PLC  AnnuAl RepoR t And Accounts 2020

33

d I Rec to Rs’ Rep o Rt
FO R T H E Y E A R EN D ED 31 M A RCH 2020

the corporate governance statement set out on pages 32 and 33 forms part of this report.

Results and Dividends
the results for the year are set out on page 42.

no ordinary dividends were paid. the directors do not recommend payment of a final dividend.

Directors
the directors who held office during the year and up to the date of signature of the financial statements were as follows:

Adam Reynolds
dr stephen little
dr John Brown cBe (appointed 29 July 2019)
nicholas Mustoe
Jonathan seaton (appointed 15 August 2019)
lyn Rees
dr Bill chang
Barry Hextall
Hayden Jeffreys
Keng Hsu (resigned 10 July 2019)

Directors’ Beneficial Interests and Share Options
details of directors’ beneficial interests in the issued share capital of the company as at 31 March 2020 were as follows (and see also note 9):

Adam Reynolds
nicholas Mustoe
dr John Brown (appointed 29 July 2019)
Jonathan seaton (appointed 15 August 2019)
dr stephen little
lyn Rees
dr Bill chang
Keng Hsu (resigned 9 July 2019)
Hayden Jeffreys
Barry Hextall

details of directors’ share options are as follows:

Adam Reynolds

nicholas Mustoe

dr stephen little

Jonathan seaton (appointed 15 August 2019)

lyn Rees

dr Bill chang

Barry Hextall

Keng Hsu (resigned 9 July 2019)

Hayden Jeffreys

ordinary shares 
of £0.01 each

percentage held

5,449,656
8,186,869
100,000
0
6,278,283
500,000
74,855,996
4,002,729
389,372
432,498

1.2%
1.8%
0.0%
0.0%
1.4%
0.1%
16.3%
0.9%
0.1%
0.1%

At 1 April 2019 At 31 March 2020

date from which 
exercisable

expiry date

591,666

591,666

591,666

19/03/2018

19/03/2024

591,666

19/03/2018

19/03/2024

1,500,000
10,555,984
1,700,000

1,500,000
10,555,984
1,700,000

14/07/2017
04/09/2016
01/07/2019

14/07/2025
05/09/2024
30/06/2028

0

1,500,000

01/07/2020

30/10/2029

10,000,000

10,000,000
4,000,000

01/07/2019
01/07/2020

30/06/2028
01/06/2029

300,000
400,000

1,000,000
4,000,000

250,000
3,300,000

3,000,000

300,000
400,000
400,000

1,000,000
4,000,000
400,000

31/03/2019
01/07/2019
01/07/2020

14/07/2017
01/07/2019
01/07/2019

01/03/2027
30/06/2028
01/06/2019

14/07/2025
30/06/2028
01/06/2029

250,000
3,300,000

31/03/2019
01/07/2019

01/03/2027
30/06/2028

3,000,000
2,400,000

01/07/2019
01/07/2019

30/06/2028
01/06/2019

Qualifying Third-party Indemnity Provisions
the group has arranged qualifying third-party indemnity for directors and officers liability insurance for the sum of £5 million.

34

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Stakeholder responsibility 
In line with section 172(1) of the companies Act 2006 we are pleased to 
describe the ways we engage with stakeholders to both fulfil our 
obligations and achieve our vision. these are described in various parts 
of our strategic Report.

Supplier Payment Policy
the company’s current policy concerning the payment of trade 
creditors is to:
•  settle the terms of payment with suppliers when agreeing the terms 

of each transaction;

•  ensure that suppliers are made aware of the terms of payment by 

inclusion of the relevant terms in contracts; and

•  pay in accordance with the company’s contractual and other legal 

obligations.

Principal Activities, Trading Review and 
Future Developments
A detailed review of the business, post reporting date events and likely 
future developments is given in the strategic Report on pages 4 to 29.

Key Performance Indicators
the key performance indicators are discussed in the company 
overview on page pages 1 to 3.

Financial Instruments
details and required disclosure of the financial instruments used by the 
group are contained in notes 24 and 25 of the financial statements.

Auditor
saffery champness llp were re-appointed at the group’s Annual 
general Meeting in september 2019 and in accordance with the 
company’s articles, a resolution proposing that saffery champness 
llp be reappointed as auditor of the company will be put at a  
general Meeting.

Events After the Reporting Date
significant events that have occurred since the reporting date are 
described in the strategic Report on page 21 and within note 34 of 
these financial statements.

Risks and Uncertainties
the principal risks and uncertainties facing the group are discussed  
in the principal risks and uncertainties section of this report on  
pages 28 and 29.

Donations and Political Contributions
the group made no donations or political contributions in the current 
or prior periods.

Going Concern
In their assessment of the group’s ability to continue as a going 
concern, the directors have focused on the implications of the organic 
growth of the existing business plus the in-year acquisitions of the 
profitable elucigene diagnostics in April 2019, and the profit-enhancing 
customer relationships acquired in March 2020 from the group’s French 
distributor AdgeniX sarl. For the enlarged group the directors have 
assessed the market dynamics in which it operates, the historic and 
anticipated rate of growth of gross profits, decisions available to them 
for management of the cost base of the group and the potential for 
future fundraising.

the group operates a strategic planning process which has delivered 
strong progress on its ambitious multi-year business plan.

As described in the strategic Report, the group has made progress 
towards achieving positive cash flows through growth in revenues 
since launching the IonA® test in February 2015, acquiring yourgene 
Bioscience in March 2017, acquiring elucigene diagnostics (elucigene) 
in April 2019 and acquiring the customer relationships of its French 
distributor in March 2020. the group has reported a positive adjusted 
eBItdA for the first time, however, it continues to use cash in its 
trading operations albeit at a much-reduced level; which reflects that 
break-even levels of revenues have not yet been reached. the group’s 
forecasts include assumptions of further growth in revenue, which are 
key in achieving positive cash flows. the directors have also assessed 
the group’s cost structure as part of the strategic planning process 
and are investing in a scalability programme aimed at ensuring costs 
growth can be contained below gross profit increases.

there is an ongoing commitment to keep costs and working capital 
under control so that increasing gross profits can drive positive cash 
flows. detailed sensitivity analysis has been performed to assess the 
potential impact on the group’s liquidity caused by delays in revenue 
growth against expected levels along with potential mitigating actions 
which can be taken to safeguard the group’s cash position. these 
include working capital controls and reductions in discretionary 
spending. these sensitivities have been applied more aggressively  
this year in light of the coVId-19 pandemic, although to mitigate its 
potential negative impacts the group is generating revenues through 
its contract manufacturing services, the development of its own 
coVId-19 diagnostic product (launched June 2020) and launching its 
own coVId-19 testing services (July 2020). 

If events transpire differently to this assessment, for example,  
if revenues fail to grow at the anticipated pace, then there could be 
lower cash headroom. given the successful fundraise which took place 
alongside the acquisitions of elucigene and the French customer 
relationships, the directors believe there is sufficient cash available to 
avoid a cash shortfall.

the directors have concluded that considering the circumstances 
described above and mitigation strategies in place, the directors  
have a reasonable expectation that the group and company will have 
adequate resources to continue in operational existence for the 
foreseeable future. For these reasons, they continue to adopt the 
going concern basis in preparing the Annual Report and Accounts.

Substantial Shareholdings
As at 27 July 2020, the following interests in 3% or more of the issued 
ordinary share capital appear in the register:

dr Bill chang
Mr steven Myers
BgF
life technologies ltd

number of shares

79,490,142
54,500,000
49,872,761
41,356,165

percentage of 
issued share 
capital

12.7%
8.7%
8.0%
6.6%

this report was approved by the Board of directors on 27 July 2020 and 
signed on its behalf by:

Adam Reynolds
chairman
27 July 2020

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35

d I R ec to Rs’ R e s p o n sI B I lI t y s t At eM en t

the directors are responsible for preparing the strategic Report and directors’ Report and the financial statements in accordance with 
applicable law and regulations.

company law requires the directors to prepare financial statements for each financial year. under that law the directors have to prepare the 
group financial statements in accordance with International Financial Reporting standards (IFRss) as adopted by the european union. the 
directors have elected to prepare the company financial statements in accordance with united Kingdom generally Accepted Accounting 
practice (united Kingdom Accounting standards and applicable laws, including FRs 101 ‘Reduced disclosure framework’). under company law 
the directors must not approve the financial statements unless they are satisfied that they give a true and fair view of the state of affairs and 
profit or loss of the company and group for that period. In preparing these financial statements, the directors are required to:
•  select suitable accounting policies and then apply them consistently;
•  make judgements and accounting estimates that are reasonable and prudent;
• 

for the consolidated financial statements state whether applicable IFRss as adopted by the european union have been followed, subject to 
any material departures disclosed and explained in the financial statements;
for the parent company financial statements state whether applicable uK Accounting standards have been followed, subject to any 
material departures disclosed and explained in the financial statements; and

• 

•  prepare the financial statements on the going concern basis unless it is inappropriate to presume that the group and company will 

continue in business.

the directors are responsible for keeping adequate accounting records that are sufficient to show and explain the company’s transactions 
and disclose with reasonable accuracy at any time the financial position of the company and enable them to ensure that the financial 
statements comply with the companies Act 2006. they are also responsible for safeguarding the assets of the company and hence for taking 
reasonable steps for the prevention and detection of fraud and other irregularities.

the directors confirm that:
•  so far as each director is aware, there is no relevant audit information of which the company’s auditor is unaware; and
• 

the directors have taken all the steps that they ought to have taken as directors in order to make themselves aware of any relevant audit 
information and to establish that the company’s auditor is aware of that information.

the directors are responsible for the maintenance and integrity of the corporate and financial information included on the company’s 
website. legislation in the united Kingdom governing the preparation and dissemination of financial statements may differ from legislation in 
other jurisdictions.

this statement was approved by the Board of directors on 27 July 2020 and signed on its behalf by:

Adam Reynolds
chairman
27 July 2020

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i n d epen d en t au d i to r ’ S r ep o rt to t H e m em B erS o F yo u rg en e H e a lt H pl C

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Opinion
we have audited the financial statements of yourgene Health plc (‘the Company’) and its subsidiaries (‘the group’) for the year ended  
31 march 2020 which comprise the Consolidated Statement of Financial position, the Consolidated Statement of Comprehensive income,  
the Consolidated Statement of Changes in equity, the Consolidated Statement of Cash Flows, the Company Statement of Financial position,  
the Company Statement of Changes in equity, the Company Statement of Cash Flows and notes to the financial statements, including a 
summary of significant accounting policies. the financial reporting framework that has been applied in their preparation is applicable law and 
international Financial reporting Standards (iFrSs) as adopted by the european union.

in our opinion:
• 

the financial statements give a true and fair view of the state of the group’s and of the Company’s affairs as at 31 march 2020 and of the 
group’s loss for the period then ended;
the group financial statements have been properly prepared in accordance with iFrSs as adopted by the european union; 
the Company financial statements have been properly prepared in accordance with united Kingdom generally accepted accounting practice; 
and
the financial statements have been prepared in accordance with the requirements of the Companies act 2006.

• 
• 

• 

Basis for opinion
we conducted our audit in accordance with international Standards on auditing (uK) (iSas (uK)) and applicable law. our responsibilities under 
those standards are further described in the auditor’s responsibilities for the audit of the financial statements section of our report. we are 
independent of the company in accordance with the ethical requirements that are relevant to our audit of the financial statements in the uK, 
including the FrC’s ethical Standard as applied to Sme listed entities, and we have fulfilled our other ethical responsibilities in accordance with 
these requirements. we believe that the audit evidence we have obtained is sufficient and appropriate to provide a basis for our opinion.

Conclusions relating to going concern
we have nothing to report in respect of the following matters in relation to which the iSas (uK) require us to report to you where:
the directors’ use of the going concern basis of accounting in the preparation of the financial statements is not appropriate; or
• 
the directors have not disclosed in the financial statements any identified material uncertainties that may cast significant doubt about the 
• 
group’s or the Company’s ability to continue to adopt the going concern basis of accounting for a period of at least twelve months from  
the date when the financial statements are authorised for issue. 

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i n d epen d en t au d i to r ’ S r ep o rt to t H e m em B erS o F yo u rg en e H e a lt H pl C CO N T I N U ED

Key audit matters
Key audit matters are those matters that, in our professional judgement, were of most significance in our audit of the financial statements of the 
current period and include the most significant assessed risks of material misstatement (whether or not due to fraud) we identified, including 
those which had the greatest effect on: the overall audit strategy, the allocation of resources in the audit; and directing the efforts of the 
engagement team. these matters were addressed in the context of our audit of the financial statement as a whole, and in forming our opinion 
thereon, and we do not provide a separate opinion on these matters. 

Key audit matter

How our audit addressed the key audit matter

acquisition of delta diagnostics (uK) limited
during the period the group acquired 100% of the shares of  
delta diagnostics (uK) limited, a uK company which trades as  
elucigene diagnostics, for £9.3m satisfied by an issue of shares  
of £3.0m and cash consideration of £6.3m.

the transaction was considered by the directors to represent a business 
combination under iFrS 3 and a fair value review exercise was performed 
in respect of the assets and liabilities acquired.

that led to the recognition of £5.4m of customer relationships and 
development work on certain diagnostic products in intangible assets 
that were not previously recorded in the delta diagnostics (uK) limited 
statement of financial position. 

goodwill of £3.8m, being the difference between the fair value of 
identifiable net assets and the consideration, was also recognised as a 
result of the transaction.

due to the significance of the transaction to the group, the accounting 
treatment of the acquisition is a key audit matter.

our audit procedures included the following:
•  obtaining and reviewing the underlying Share purchase 
agreement governing the terms of the acquisition;

•  testing the contractual cash and share consideration to bank 

payment and share issue documents;

•  obtaining management’s assessment of the fair values of 

assets and liabilities acquired;

•  reviewing the basis upon which the value of customer 

relationships and development work on diagnostic products 
was determined;

•  reviewing the mathematical accuracy of models used to 

determine the fair value of newly identified intangible assets;
•  understanding the basis for the useful life of newly identified 

intangible assets and the allocation of newly generated 
goodwill for impairment purposes; and

•  reviewing the cut-off of post-acquisition results for 

consolidation purposes.

Based on our procedures, we noted no material exceptions and 
considered management’s key assumptions to be within 
reasonable ranges. we consider that the acquisition has been 
recognised appropriately.

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Key audit matter

How our audit addressed the key audit matter

impairment assessments of goodwill and other  
intangible assets
the group held intangibles assets with a carrying value of £21.0m, 
comprising goodwill of £10.8m and other intangible assets of £10.2m.

there were significant additions of £13.4m during the year arising from 
the delta diagnostics (uK) limited acquisition £9.2m as well as the 
purchase of intangible assets held in agX-dpni SaS £1.5m.   

Brought forward intangibles relate to the 2017 acquisition of the group’s 
subsidiary in taiwan.

at the reporting date of 31 march 2020, the Covid-19 pandemic was a 
growing global crisis and world stock markets had significantly fallen  
in value.  

due to the material additions in the year, the overall significance of 
intangible assets on the Statement of Financial position and the risks of 
impairment resulting from circumstances in the local and global economy, 
the risk of impairment of intangible assets was considered a key  
audit matter.

deferred tax
the group has significant accumulated tax losses that have not 
previously been recognised as a deferred tax asset. an asset of £0.9m has 
been recognised for losses expected to reverse in yourgene Health uK 
ltd. as the group grows and develops to profitability, more of the tax 
losses will be recognised that are expected to be utilised in the 
foreseeable future.

our audit procedures included the following:
•  reviewing and challenging the cashflow forecasts produced for 

goodwill and intangible impairment assessment models;
•  evaluating and challenging the key judgements applied in 

forecast models such as the revenue growth rate, the discount 
rate, the gross margins achieved and the time period over 
which forecast cash flows are appropriate;

•  understanding the basis and rationale for the forecast growth 

in certain products and geographies;

•  assessing the directors’ assessment for the allocation of 

goodwill to Cgus and reviewing potential impairment on that 
basis;

•  reperforming amortisation calculations and assessing the 
judgement applied in assessing useful economic lives; and
•  Challenging the basis for the treatment of the acquisition of 
agX-apni SaS as an asset acquisition and assessing the 
supporting evidence for the estimation of contingent 
consideration for that acquisition.

Based on our procedures, we noted no material exceptions and 
considered the accounting and disclosure associated with this 
audit matter to be within reasonable ranges.

our audit procedures included the following:
•  reviewing the deferred tax calculations prepared by the 

directors;

•  Considering the forecasts presented in impairment 

calculations and comparing to those used in deferred tax 
calculations; and

•  Challenging the directors on the assumptions adopted.

this is a key audit matter as the amounts are significant and the area is 
judgemental.

we concluded that the deferred tax asset presented was fair  
and reasonable.

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Our application of materiality
we apply the concept of materiality in planning and performing our audit, in evaluating the effect of any identified misstatements and in forming 
our audit opinion. our overall objective as auditor is to obtain reasonable assurance that the financial statements as a whole are free from 
material misstatement, whether due to fraud or error. we consider a misstatement to be material where it could reasonably be expected to 
influence the economic decisions of the users of the financial statements.

we have determined a materiality of £160,000 for both the group and Company financial statements. this is based on 1% of revenue per draft 
financial information at the planning stage. a separate performance materiality was applied to transactions with directors and related parties.

An overview of the scope of our audit
we tailored the scope of our audit work to ensure we obtained sufficient evidence to support our opinion on the financial statements as a whole, 
taking into account the structure of the group and the Company, the accounting processes and controls and the industry in which the  
group operates.

as group auditors we carried out the audit of the Company financial statements and, in accordance with iSa (uK) 600, obtained sufficient 
evidence regarding the audit of the group’s material taiwan subsidiary, yourgene Health (taiwan) Co. ltd. we also performed a full scope audit of 
the group’s uK subsidiaries yourgene Health uK limited and delta diagnostics (uK) limited. these subsidiaries were deemed to be significant 
to the group financial statements due to their size. the group audit team directed, supervised and reviewed the work of the component auditors 
in taiwan, which involved issuing detailed instructions, holding discussions with component audit teams and performing a review of selected key 
working papers. audit work in taiwan was performed at materiality levels of £44,000, lower than group materiality.  

although not considered a significant component of the group, we also made enquiries of the work performed by the auditors of the group’s 
Singaporean subsidiary yourgene Health (Singapore) pte limited. we also performed targeted audit work on the French subsidiary  
agX-dpni SaS.

as part of designing our audit, we determined materiality and assessed the risks of material misstatement in the financial statements.  
in particular, we looked at where the directors made subjective judgements, for example in respect of significant accounting estimates that 
involved making assumptions and considering future events that are inherently uncertain. we also addressed the risk of management override of 
internal controls, including evaluating whether there was evidence of bias by the directors that represented a risk of material misstatement.

Other information
the directors are responsible for the other information. the other information comprises the information included in the annual report,  
other than the financial statements and our auditor’s report thereon. our opinion on the financial statements does not cover the other 
information and, except to the extent otherwise explicitly stated in our report, we do not express any form of assurance conclusion thereon.

in connection with our audit of the financial statements, our responsibility is to read the other information and, in doing so, consider whether  
the other information is materially inconsistent with the financial statements or our knowledge obtained in the audit or otherwise appears to be 
materially misstated. if we identify such material inconsistencies or apparent material misstatements, we are required to determine whether 
there is a material misstatement in the financial statements or a material misstatement of the other information. if, based on the work we have 
performed, we conclude that there is a material misstatement of this other information; we are required to report that fact.

we have nothing to report in this regard.

Opinions on other matters prescribed by the Companies Act 2006
in our opinion, based on the work undertaken in the course of the audit:
• 

the information given in the Strategic report and the directors’ report for the financial year for which the financial statements are prepared 
is consistent with the financial statements; and
the Strategic report and the directors’ report have been prepared in accordance with applicable legal requirements. 

• 

Matters on which we are required to report by exception
in the light of the knowledge and understanding of the company and its environment obtained in the course of the audit, we have not identified 
material misstatements in the Strategic report or the directors’ report.

we have nothing to report in respect of the following matters in relation to which the Companies act 2006 requires us to report to you if,  
in our opinion:
•  adequate accounting records have not been kept, or returns adequate for our audit have not been received from branches not visited by us; or
• 
•  certain disclosures of directors’ remuneration specified by law are not made; or
•  we have not received all the information and explanations we require for our audit. 

the financial statements are not in agreement with the accounting records and returns; or

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Responsibilities of directors
as explained more fully in the directors’ responsibilities Statement set out on page 36, the directors are responsible for the preparation of  
the financial statements and for being satisfied that they give a true and fair view, and for such internal control as the directors determine is 
necessary to enable the preparation of financial statements that are free from material misstatement, whether due to fraud or error.

in preparing the financial statements, the directors are responsible for assessing the company’s ability to continue as a going concern, 
disclosing, as applicable, matters related to going concern and using the going concern basis of accounting unless the directors either intend to 
liquidate the company or to cease operations, or have no realistic alternative but to do so.

Auditor’s responsibilities for the audit of the financial statements
our objectives are to obtain reasonable assurance about whether the financial statements as a whole are free from material misstatement, 
whether due to fraud or error, and to issue an auditor’s report that includes our opinion. reasonable assurance is a high level of assurance, but is 
not a guarantee that an audit conducted in accordance with iSas (uK) will always detect a material misstatement when it exists. misstatements 
can arise from fraud or error and are considered material if, individually or in the aggregate, they could reasonably be expected to influence the 
economic decisions of users taken on the basis of these financial statements.

a further description of our responsibilities for the audit of the financial statements is located on the Financial reporting Council’s website at: 
www.frc.org.uk/auditorsresponsibilities. this description forms part of our auditor’s report.

Use of our report
this report is made solely to the company’s members, as a body, in accordance with Chapter 3 of part 16 of the Companies act 2006. our audit 
work has been undertaken so that we might state to the company’s members those matters we are required to state to them in an auditor’s 
report and for no other purpose. to the fullest extent permitted by law, we do not accept or assume responsibility to anyone other than the 
company and the company’s members as a body, for our audit work, for this report, or for the opinions we have formed.

Simon Kite (Senior Statutory auditor)
for and on behalf of Saffery Champness llp

Chartered accountants
Statutory auditors

City tower
piccadilly plaza
manchester
m1 4Bt

27 July 2020

YOURGENE HEALTH PLC  annual report and aCC ountS 2020

41

Co n So l i dat ed S tat em en t o F Co m pr eH en S i v e i n Co m e
FO R T H E Y E A R EN D ED 31 M A RCH 2020

Revenue
Cost of sales

Gross profit

other operating income
Administrative expenses
general administrative expenses

Adjusted EBiTDA 
depreciation and amortisation
Share-based payments expense
Costs associated with subsidiary acquisition
acquisition integration expense

Total Depreciation, Amortisation and separately disclosed items

Operating loss
Financing income
Financing expenses

Profit (Loss) on ordinary activities before taxation

tax credit / (charge) on loss on ordinary activities

Profit (Loss) for the year

Other comprehensive income
exchange translation differences

Profit (Loss) and total comprehensive profit (loss) for the Year

Earnings per share
Basic: profit (loss)
diluted: profit (loss)

notes

2020

£

(2,093,808)
(1,601,746)
(264,666)
(533,358)

6
5
5
5

6
10
11

12

13

£

16,612,779 
(6,387,837)

10,224,942 

67,530 

(9,037,761)

1,254,711

(4,493,578)

(3,238,867)
19,960 
(163,203)

(3,382,110)

948,186 

(2,433,924)

139,773 

(2,294,151)

(0.4p)
(0.4p)

2019

£

(1,099,756)
(251,004)
–
– 

£

8,882,362 
(4,271,941)

4,610,421 

25,821 

(8,067,988)

(3,431,746)

(1,350,760)

(4,782,506)
9,381,761 
(1,209,554)

3,389,701 

(491)

3,389,210 

31,563 

3,420,773 

0.9p 
 0.9p 

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Co n So l i dat ed Stat em en t o F Fi n a nC i a l p o S i t i o n
A S AT 31 M A RCH 2020

Assets
Non-current assets
goodwill
intangible assets
property, plant and equipment
right-of-use asset
tax asset
deferred tax asset

Total non-current assets

Current assets
inventories
trade and other receivables
tax asset
deferred tax asset
Cash and cash equivalents

Total current assets

Total assets

Equity and liabilities attributable to equity holders of the company
Equity
Called up share capital
Share premium account
merger relief reserve
reverse acquisition reserve
Foreign exchange translation reserve
warrants reserve
retained losses

Total equity

Current liabilities
trade and other payables
lease liabilities
Current tax liabilities
Borrowings
other liabilities & provisions

Total current liabilities

Non-current liabilities
Borrowings
deferred tax liability
lease liabilities
other long term liabilities & provisions

Total non-current liabilities

Total equity and liabilities

notes

2020
£

2019
£

14
14
15
16
23
23

17
19
23
23

28
28
28
28
28
28
28

20
16

21
22

21
23
16
22

10,805,783 
10,191,889 
1,969,305 
2,996,753 
532,691
1,181,039

7,014,447 
1,228,928 
2,054,163 
–
–
–

27,677,460 

10,297,538 

1,152,308 
5,629,287 
452,485
–
2,764,117 

739,126 
2,832,695 
478,232 
–
1,250,362 

9,998,197

5,300,415 

37,675,657

15,597,953 

32,561,451 
51,179,685 
12,937,796 
(39,947,033)
(8,124)
3,069,382 
(33,494,558)

32,403,969 
37,971,265 
10,012,644 
(39,947,033)
(147,897)
3,069,382 
(32,662,380)

26,298,599

10,699,950 

4,907,813 
341,167 
433,337
277,508 
512,555 

4,172,464 
–
–
76,388 
–

6,472,380

4,248,852 

85,110 
1,153,121
2,710,123 
956,324 

4,904,678

209,302 
233,496 
–
206,353 

649,151 

37,675,657

15,597,953 

the financial statements were approved and signed by the directors and authorised for issue on 27 July 2020.

adam reynolds
Chairman
Company registration no. 03971582 

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Co n So l i dat ed S tat em en t o F C H a n g e S i n e Q u i t y
FO R T H E Y E A R EN D ED 31 M A RCH 2020

Share  
capital
£

Share 
premium 
account
£

merger  
relief 
reserve
£

warrants 
reserve
£

reverse 
acquisition 
reserve
£

Foreign 
exchange 
reserve
£

retained  
losses
£

total
£

notes

32,266,188  28,482,061  10,012,644 

4,085,546 

(39,947,033)

(179,460)

(37,318,758)

(2,598,812)

–
–

–

–
–

–

28

29
30

137,781 
–
–
–

9,716,143 
(226,939)
–
–

137,781 

9,489,204 

–
–

–

–
–
–
–

–

–
–

–

–
–
–
(1,016,164)

(1,016,164)

–
–

–

–
–
–
–

–

–
31,563 

3,389,210 
–

3,389,210 
31,563 

31,563 

3,389,210 

3,420,773 

–
–
–
–

–

–
–
251,004 
1,016,164 

9,853,924 
(226,939)
251,004 
–

1,267,168 

9,877,989 

Balance at 1 April 2018
Year ended 31 march 2019:
profit (loss) for the year
other comprehensive loss

total comprehensive 
profit for the year

Transactions with owners
issue of share capital
Share issue expenses
Share-based payments
warrants exercised

Total transactions with 

owners

Balance at 31 march 2019

32,403,969  37,971,265  10,012,644 

3,069,382 

(39,947,033)

(147,897) (32,662,380) 10,699,950 

Balance at 1 April 2019

32,403,969  37,971,265  10,012,644 

3,069,382 

(39,947,033)

(147,897) (32,662,380) 10,699,950 

Year ended 31 march 

2020:

profit (loss) for the year
other comprehensive loss

total comprehensive loss 

for the year

Transactions with owners
issue of share capital
Share issue expenses
issue of share capital on 

acquisition

Share-based payments
warrants issued

Total transactions with 

owners

–
–

–

–
–

–

132,901  14,197,534 
(989,114)

–

–
–

–

–
–

24,581 
–
–

–
–
–

2,925,152 
–
–

157,482  13,208,420 

2,925,152 

28

29
30

–
–

–

–
–

–
–
–

–

–
–

–

–
–

–
–
–

–

–
139,773 

(2,433,924)
–

(2,433,924)
139,773 

139,773 

(2,433,924)

(2,294,151)

–
–

–
–
–

–

– 14,330,435 
(989,114)
–

–
1,601,746 
–

2,949,733 
1,601,746 
–

1,601,746  17,892,800 

Balance at 31 march 2020

32,561,451  51,179,685  12,937,796 

3,069,382  (39,947,033)

(8,124) (33,494,558) 26,298,599

44

YOURGENE HEALTH PLC  annual report and aCC ountS 2020

 
 
 
 
 
 
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Co n So l i dat ed S tat em en t o F C a S H FlowS
FO R T H E Y E A R EN D ED 31 M A RCH 2020

Cash flows from operating activities
profit / (loss) for the year before tax
Adjustments for:
Finance costs
Finance income
loan payable waived
depreciation and impairment of property, plant and equipment
depreciation and impairment of right of use asset
(gain) / loss on disposal of property, plant and equipment
(gain) / loss on revaluation of right of use asset
amortisation of intangible non-current assets
impairment on financial assets (iFrS9)
Foreign exchange movements
Share based payment and warrant expense
decrease in provisions
tax (paid) / received

movements in working capital:
(increase)/decrease in inventories
(increase)/decrease in trade and other receivables
increase/(decrease) in trade and other payables
decrease/(increase) in tax asset

Cash used by operations

investing activities
purchase of subsidiaries
Cash acquired on purchase of subsidiaries
purchase of property, plant and equipment
Capitalisation of intangible assets
proceeds on disposal of property, plant and equipment
(investment)/reduction in short-term financial assets
interest received

2020

£

£

2019

£

£

(3,382,110)

163,203
(19,960)
–
949,780
467,724
67,289
(121,248)
676,304
106,511
72,127
1,601,746
(206,353)
(16,210)

26,995
(1,171,705)
(758,355)
(529,307)

(2,073,569)

(8,369,742)
684,900
(617,085)
(745,520)
13,505
–
5,010

–
–
–
–
–
–
– 

–
–
(1,066,699)
–
–
475,385
553

3,389,701

1,209,554
(35,672)
(9,346,089)
944,524
–
469
–
155,232
155,962
334,864
251,004
(756,305)
(12,933)

(462,360)
(910,663)
380,352
653,994

(4,048,366)

–
–
–
–
–
–
– 

Net cash (used in)/generated from investing activities

–

(9,028,932)

–

(590,761)

Financing activities
net proceeds from issue of shares
proceeds from borrowings
repayment of borrowings
(increase)/decrease in lease liability
repayment of lease liability obligations
interest paid

Net cash generated from financing activities

Net increase/(decrease) in cash and cash equivalents
Cash and cash equivalents at beginning of period

Cash and cash equivalents at end of period

See note 31 for analysis of change in net cash/(debt). 

13,341,321
–
(197,503)
–
(364,359)
(163,203)

–
–
–
–
–
– 

9,626,985
128,992
(4,139,100)
–
–
(9,820)

–
–
–
–
–
– 

– 

–
–

– 

12,616,256

1,513,755
1,250,362

2,764,117

– 

–
–

– 

5,607,057

967,930
282,432

1,250,362

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n ot e S to t H e C o n So l i dat ed F i n a n C i a l S tat em en t S
FO R T H E Y E A R EN D ED 31 M A RCH 2020 

1 Accounting Policies
Company information
yourgene Health plC is a public limited company incorporated and domiciled in the united Kingdom. the address of its registered office is 
Citylabs 1.0, nelson Street, manchester m13 9nQ.

the principal activity of yourgene Health plC and its subsidiaries is that of a molecular diagnostics business for research into, and the 
development and commercialisation of gene analysis techniques for prenatal screening and other clinical applications in the early detection, 
monitoring and treatment of disease.

the financial statements are presented in British pounds Sterling, the currency of the primary economic environment in which the Company’s 
headquarters is operated.

accounting convention
the financial statements have been prepared in accordance with international Financial reporting Standards (iFrS), including iFriC 
interpretations issued by the international accounting Standards Board (iaSB), as adopted for use in the european union and with those parts of 
the Companies act 2006 applicable to companies reporting under iFrS. the Company financial statements have been prepared in accordance 
with Financial reporting Standard 101 ‘reduced disclosure framework’ (FrS 101).

the financial statements have been prepared under the historical cost convention, except for those transactions recognised at fair value as 
detailed below.

the consolidated financial statements of the Company as at and for the year ended 31 march 2020 comprise the Company and its subsidiaries 
(together referred to as ‘the group’). the principal accounting policies applied in the preparation of these consolidated financial statements are 
set out below. these policies have been consistently applied to all the years presented, unless otherwise stated.

Basis of consolidation
the consolidated financial statements incorporate the financial statements of the Company and entities controlled by the Company (its 
subsidiaries, which are all owned 100%) made up to 31 march each year.

Consolidation of a subsidiary begins when the Company obtains control over the subsidiary and ceases when the Company loses control of the 
subsidiary. Specifically, the results of subsidiaries acquired or disposed of during the year are included in profit or loss from the date the 
Company gains control until the date when the Company ceases to control the subsidiary.

profit or loss and each component of other comprehensive income are attributed to the owners of the Company. total comprehensive income  
of the subsidiaries is attributed to the owners of the Company.

where necessary, adjustments are made to the financial statements of subsidiaries to bring the accounting policies used into line with the 
group’s accounting policies. all intra-group assets and liabilities, equity, income, expenses and cash flows relating to transactions between the 
members of the group are eliminated on consolidation.

going concern
in their assessment of the group’s ability to continue as a going concern, the directors have focused on the implications of the organic growth  
of the existing business plus the in-year acquisitions of the profitable elucigene diagnostics in april 2019, and the profit-enhancing customer 
relationships acquired in march 2020 from the group’s French distributor adgeniX Sarl. For the enlarged group the directors have assessed the 
market dynamics in which it operates, the historic and anticipated rate of growth of gross profits, decisions available to them for management of 
the cost base of the group and the potential for future fundraising.

the group operates a strategic planning process which has delivered strong progress on its ambitious multi-year business plan.

as described in the Strategic report, the group has made progress towards achieving positive cash flows through growth in revenues since 
launching the iona® test in February 2015, acquiring yourgene Bioscience in march 2017, acquiring elucigene diagnostics (elucigene) in april 
2019 and acquiring the customer relationships of its French distributor in march 2020. the group has reported a positive adjusted eBitda for  
the first time, however, it continues to use cash in its trading operations albeit at a much-reduced level; which reflects that break-even levels of 
revenues have not yet been reached. the group’s forecasts include assumptions of further growth in revenue, which are key in achieving positive 
cash flows. the directors have also assessed the group’s cost structure as part of the strategic planning process and are investing in a scalability 
programme aimed at ensuring costs growth can be contained below gross profit increases.

there is an ongoing commitment to keep costs and working capital under control so that increasing gross profits can drive positive cash flows. 
detailed sensitivity analysis has been performed to assess the potential impact on the group’s liquidity caused by delays in revenue growth 
against expected levels along with potential mitigating actions which can be taken to safeguard the group’s cash position. these include working 
capital controls and reductions in discretionary spending. these sensitivities have been applied more aggressively this year in light of the 
Covid-19 pandemic, although to mitigate its potential negative impacts the group is generating revenues through its contract manufacturing 
services, the development of its own Covid-19 diagnostic product (launched June 2020) and launching its own Covid-19 testing services 
(July 2020).

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if events transpire differently to this assessment, for example, if revenues fail to grow at the anticipated pace, then there could be lower cash 
headroom. given the successful fundraise which took place alongside the acquisitions of elucigene and the French customer relationships,  
the directors believe there is sufficient cash available to avoid a cash shortfall.

the directors have concluded that considering the circumstances described above and mitigation strategies in place, the directors have a 
reasonable expectation that the group and Company will have adequate resources to continue in operational existence for the foreseeable 
future. For these reasons, they continue to adopt the going concern basis in preparing the annual report and accounts.

revenue
revenue from the sale of goods, equipment and related services is recognised in accordance with iFrS 15 revenue from Contracts with 
Customers in the Statement of Comprehensive income when the deemed Contractual performance obligations have been completed, which is 
determined to be at the point of despatch of the product or service unless there are specific provisions in the relevant contract. revenue from 
the provision of testing and reporting services is recognised upon delivery of the report to the customer. invoices are typically raised upon 
delivery of the products or reporting services, unless there is a different contractual requirement, for payment according to credit terms which 
are usually 30–75 days from date of invoice. For some contracts advance invoices are raised and payments received. these are held on the 
Statement of Financial position as ‘payments received on account’ (see note 20) and are only recognised as revenue once the performance 
obligations have been deemed satisfied as described above.

grant income and income for research projects is recognised when all conditions for receiving the grant or research income have been satisfied.

Separately disclosed items
Separately disclosed items are those significant items, within total administrative expense which in management’s judgement should be 
highlighted on the face of the Statement of Comprehensive income by virtue of their size or incidence to enable a full understanding of the 
group’s financial performance. Significant items in Finance income are disclosed in note 5.

property, plant and equipment
items of property, plant and equipment are initially recognised at cost. Cost includes the original purchase price, costs directly attributable to 
bringing the asset to its working condition for its intended use, dismantling and restoration costs. depreciation is provided on all items of 
property, plant and equipment to write off the carrying value of items over their expected useful lives. depreciation is applied at the 
following rates:
leasehold land and buildings  
plant and equipment  

20% straight line
20–25% straight line

the gain or loss arising on the disposal of an asset is determined as the difference between the sale proceeds and the carrying value of the asset 
and is recognised in the Statement of Comprehensive income.

leases and right-of-use assets (iFrS 16)
the group has adopted iFrS 16 from 1 april 2019 but it has not restated comparatives for the prior reporting period, as permitted under the 
specific transitional provisions in the standard. the reclassifications and the adjustments arising from the new leasing rules are therefore 
recognised in the opening Statement of Financial position on 1 april 2019. 

leases are recognised as a right-of-use asset and lease liability at the transition date of 1 april 2019 or the date of any new leases after  
1 april 2019. right-of-use assets and lease liabilities are valued on a present value basis of the lease payments over the lease term. on adoption 
of iFrS 16 the right-of-use assets and lease liability were measured at the present value of the remaining lease payments and lease term. the 
right-of-use asset is depreciated over the term or remaining term of the lease.

where there is potential for future increases in lease payments, amounts are not included in the lease liability until they implemented. the leases 
are reviewed annually and where the lease liability is increased the lease liability is reassessed and adjusted against the right-of-use asset. when 
a lease is terminated, or term amended the lease liability and right-of-use asset are recalculated and adjusted accordingly.

lease payments are divided between principal and interest expense. the interest expense is charged to finance expense in the statement of 
comprehensive income.

in adopting iFrS 16, the group has used the following practical expedients permitted by the standard:
the use of a single discount rate to a portfolio of leases with reasonably similar characteristics;
• 
reliance on previous assessments of whether leases are onerous;
• 
the accounting for operating leases, with a remaining lease term of less than 12 months as at 1 april 2019, as short-term leases;
• 
the exclusion of initial direct costs for the measurement of the right-of-use asset at the date of initial application; and
• 
the use of hindsight in determining the lease term where the contract contains options to extend or terminate the lease.
• 

the group has also elected not to reassess whether a contract is or contains a lease at the date of initial application, instead, for contracts 
entered into before the transition date, the group relied on its assessment made in applying iaS 17 and iFriC 4, ‘determining whether an 
arrangement contains a lease’.

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n ot e S to t H e C o n So l i dat ed F i n a n C i a l S tat em en t S CO N T I N U ED
FO R T H E Y E A R EN D ED 31 M A RCH 2020

1 Accounting Policies continued
accounting for acquisitions
the group assesses the acquisition of shares in a company under iFrS 3 – Business Combinations, to make an initial determination as to whether 
the acquisition meets the test for the definition “a business”. this is defined as “an integrated set of activities and assets that is capable of being 
conducted and managed for the purpose of providing goods or services to customers, generating investment income (such as dividends or 
interest) or generating other income from ordinary activities.” For acquisitions that meet the test, the accounting treatment will follow iFrS 3 
protocols to arrive at fair values. where the test for a business is not met, then the assets of the acquired company will be accounted for as 
acquired tangible or intangible assets as described in these policies.

goodwill
goodwill represents the excess of the cost of acquisition of unincorporated businesses over the fair value of net assets acquired. it is initially 
recognised as an asset at cost and is subsequently measured at cost less any accumulated impairment losses. goodwill is not amortised but is 
tested annually for impairment, or earlier if there is an indication of impairment.

acquired intangible assets
intangible assets acquired directly or as part of business combinations are capitalised at fair value at the date of acquisition. Following the  
initial recognition, the carrying amount of an intangible is its cost less accumulated amortisation and any accumulated impairment losses. 
amortisation is charged on the basis of the estimated useful life on a straight-line basis and the expense is taken to the Statement of 
Comprehensive income.

the group has recognised customer relationships as separately acquired intangible assets. the useful economic life attributed to each 
intangible asset is determined at the time of the acquisition.

impairment reviews are undertaken annually and whenever the directors consider that there has been a potential indication of impairment.

impairment of tangible and intangible assets
at each reporting end date, the group reviews the carrying amounts of its tangible assets to determine whether there is any indication that 
those assets have suffered an impairment loss. if any such indication exists, the recoverable amount of the asset is estimated in order to 
determine the extent of the impairment loss (if any). where it is not possible to estimate the recoverable amount of an individual asset,  
the group estimates the recoverable amount of the cash-generating unit to which the asset belongs.

recoverable amount is the higher of fair value less costs to sell and value in use. in assessing value in use, the estimated future cash flows are 
discounted to their present value using a pre-tax discount rate that reflects current market assessments of the time value of money and the 
risks specific to the asset for which the estimates of future cash flows have not been adjusted.

if the recoverable amount of an asset (or cash-generating unit) is estimated to be less than its carrying amount, the carrying amount of the asset 
(or cash-generating unit) is reduced to its recoverable amount. an impairment loss is recognised immediately in profit or loss, unless the relevant 
asset is carried at a revalued amount, in which case the impairment loss is treated as a revaluation decrease.

where an impairment loss subsequently reverses, the carrying amount of the asset (or cash-generating unit) is increased to the revised estimate 
of its recoverable amount, but so that the increased carrying amount does not exceed the carrying amount that would have been determined 
had no impairment loss been recognised for the asset (or cash-generating unit) in prior years. a reversal of an impairment loss is recognised 
immediately in profit or loss, unless the relevant asset is carried at a revalued amount, in which case the reversal of the impairment loss is treated 
as a revaluation increase.

inventories
inventories are stated at the lower of cost and net realisable value, after making allowance for obsolete and slow-moving items. Cost includes 
expenditure incurred in acquiring the inventories and other cost in bringing them to their existing location and condition.

Fair value measurement
iFrS 13 establishes a single source of guidance for all fair value measurements. iFrS 13 does not change when an entity is required to use fair 
value, but rather provides guidance on how to measure fair value under iFrS when fair value is required or permitted. the resulting calculations 
under iFrS 13 affected the principles that the group uses to assess the fair value, but the assessment of fair value under iFrS 13 has not 
materially changed the fair values recognised or disclosed. iFrS 13 mainly impacts the disclosures of the group. it requires specific disclosures 
about fair value measurements and disclosures of fair values, some of which replace existing disclosure requirements in other standards.

Short-term financial assets
Short-term financial assets comprise deposits placed in an escrow account which is jointly controlled by a third party.

Cash and cash equivalents
Cash and cash equivalents comprise cash on hand and demand deposits, together with other short-term, highly liquid investments maturing 
within 90 days from the date of acquisition that are readily convertible into known amounts of cash and which are subject to an insignificant risk 
of changes in value.

48

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Financial assets
Financial assets are recognised in accordance with iFrS 9 Financial instruments in the group’s Statement of Financial position when the group 
becomes party to the contractual provisions of the instrument. Financial assets are classified into specified categories. the classification 
depends on the nature and purpose of the financial assets and is determined at the time of recognition.

Financial assets are initially measured at fair value plus transaction costs, other than those classified as fair value through profit and loss,  
which are measured at fair value.

loans and receivables
these assets are non-derivative financial assets with fixed or determinable payments that are not quoted in an active market. they arise 
principally through the provision of goods and services to customers (trade receivables), but also incorporate other types of contractual 
monetary assets. they are measured subsequent to initial recognition at amortised cost using the effective interest rate method.

impairment of financial assets
Financial assets, other than those at Fvtpl, are assessed for indicators of impairment at each reporting end date.

Financial assets are impaired in either of the following situations:
(a)  where there is objective evidence that, as a result of one or more events that occurred after the initial recognition of the financial asset, the 
estimated future cash flows of the investment have been affected. the group considers a financial asset to be in default if there is explicit 
external information that indicates the debtor is unlikely to pay its creditors, including the group. in the event of a default the full value of the 
financial asset is impaired. Financial assets are written off when there is deemed to be no realistic prospect of recovery and enforcement 
activities have ceased.

(b)  where there are expected credit losses in the next reporting period as required by iFrS 9, the group recognises expected credit losses (eCl) 
for trade and other receivables. if the credit risk on a financial instrument has increased significantly since its initial recognition then eCl are 
assessed on a lifetime eCl basis. if the credit risk has not increased significantly then eCl are assessed based on the likelihood of default in 
the next 12 months. in assessing whether the credit risk on a financial instrument has increased significantly since initial recognition, the 
group considers quantitative and qualitative information including historical debt default or delinquency and forward-looking information 
that is available without undue cost or effort. Forward-looking factors include the economic and political context for the financial assets as 
well as anticipated customer-specific developments.

de-recognition of financial assets
Financial assets are de-recognised only when the contractual rights to the cash flows from the asset expire, or when there is a transfer of the 
financial asset and substantially all the risks and rewards of ownership to another entity.

Financial liabilities
Financial liabilities and equity instruments issued by the group are classified according to the substance of the contractual arrangements entered 
into and the definitions of a financial liability and an equity instrument. a financial liability is a contractual obligation to either deliver cash or 
another financial asset to another entity or to exchange a financial asset or financial liability with another entity, including obligations which may 
be settled by the group using its equity instruments. an equity instrument is any contract that evidences a residual interest in the assets of the 
Group after deducting all of its liabilities. The accounting policies adopted for specific financial liabilities and equity instruments are set out below.

Classification and subsequent measurement of financial liabilities
Financial liabilities are measured at transaction price initially and measured subsequently at amortised cost using the effective interest method, 
except for derivatives and financial liabilities designated at Fvtpl, which are carried subsequently at fair value with gains or losses recognised in 
profit or loss.

all interest-related charges and, if applicable, changes in an instrument’s fair value that are reporting in profit or loss are included within finance 
costs or finance income.

other financial liabilities
at initial recognition, financial liabilities (trade and other payables) are measured at their fair value plus, if appropriate, any transaction costs that 
are directly attributable to the issue of the financial liability. these financial liabilities are subsequently carried at amortised cost.

de-recognition of financial liabilities
Financial liabilities are de-recognised when, and only when, the group’s obligations are discharged, cancelled or they expire.

Financial liabilities recognised at fair value
Financial liabilities are classified as Fvtpl when the financial liability is held for trading. a financial liability is classified as held for trading if:
• 
•  on initial recognition it is part of a portfolio of identified financial instruments that the group manages together and has a recent actual 

it has been incurred principally for the purpose of repurchasing it in the near term, or

pattern of short-term profit taking, or
it is a derivative that is not designated and effective as a hedging instrument.

• 

Financial liabilities at Fvtpl are stated at fair value with any gains or losses arising on remeasurement recognised in profit or loss in the ‘other gains 
and losses’ category. interest paid on the financial liability is included in the finance costs line item in the Statement of Comprehensive income.

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n ot e S to t H e C o n So l i dat ed F i n a n C i a l S tat em en t S CO N T I N U ED
FO R T H E Y E A R EN D ED 31 M A RCH 2020

1 Accounting Policies continued
Compound instruments
the component parts of compound instruments issued by the group are classified separately as financial liabilities and equity in accordance with 
the substance of the contractual arrangement. at the date of issue, the fair value of the liability component is estimated using the prevailing 
market interest rate for a similar non-convertible instrument. this amount is recorded as a liability on an amortised cost basis using the effective 
interest method until extinguished upon conversion or at the instrument’s maturity date. the equity component is determined by deducting the 
amount of the liability component from the fair value of the compound instrument as a whole. this is recognised and included in equity net of 
income tax effects and is not subsequently remeasured.

equity instruments
instruments classified as equity under iaS 32 are measured at fair value on inception. Subsequent changes in the value of the instrument are not 
recognised in the financial statements.

Share capital
ordinary shares are classified as equity. incremental costs directly attributable to the issue of new shares or options are shown in equity as a deduction 
from proceeds. deferred shares arose on share splits in previous reporting periods and are not tradable and carry no economic or voting rights.

Share warrants that are issued within the scope of iFrS 2 (as detailed in note 29) are measured at fair value at each reporting period end. they are 
classified as equity instruments based on the substance of the contractual arrangements entered into.

merger relief reserve
the reserve represents a premium on the issue of the ordinary shares for the acquisition of subsidiary undertakings. the relief is only available to 
the issuing company securing at least a 90% equity holding in the acquired undertaking in pursuance of an arrangement providing for the 
allotment of equity shares in the issuing Company on terms that the consideration for the shares allotted is to be provided by the issue of equity 
shares in the other company.

warrants reserve
the warrants reserve represents the fair value of warrants issued to thermo Fisher which are in issue but not exercised at the reporting date.

taxation
the tax expense represents the sum of the tax currently payable and deferred tax.

Current tax
the tax currently payable is based on taxable profit for the year. taxable profit differs from net profit as reported in the income statement 
because it excludes items of income or expense that are taxable or deductible in other years and it further excludes items that are never taxable 
or deductible. the group’s liability for current tax is calculated using tax rates that have been enacted or substantively enacted by the 
reporting end date.

deferred tax
deferred tax is the tax expected to be payable or recoverable on differences between the carrying amounts of assets and liabilities in the 
financial statements and the corresponding tax bases used in the computation of taxable profit and is accounted for using the balance sheet 
liability method. deferred tax liabilities are generally recognised for all taxable temporary differences and deferred tax assets are recognised to 
the extent that it is probable that taxable profits will be available against which deductible temporary differences can be utilised. Such assets and 
liabilities are not recognised if the temporary difference arises from goodwill or from the initial recognition of other assets and liabilities in a 
transaction that affects neither the tax profit nor the accounting profit.

the carrying amount of deferred tax assets is reviewed at each reporting end date and reduced to the extent that it is not probable that sufficient 
taxable profits will be available to allow all or part of the asset to be recovered. where deferred tax assets not recognised in prior periods begin to 
meet the criteria for recognition, their value is assessed based on a discounted view of 5 year profit forecasts for the relevant taxable entity or 
group deferred tax is calculated at the tax rates that are expected to apply in the period when the liability is settled, or the asset is realised. 
deferred tax is charged or credited in the income statement, except when it relates to items charged or credited directly to equity, in which case 
the deferred tax is also dealt with in equity. deferred tax assets and liabilities are offset when the group has a legally enforceable right to offset 
current tax assets and liabilities and the deferred tax assets and liabilities relate to taxes levied by the same tax authority.

provisions
a provision is recognised when the group has a present obligation, legal or constructive, as a result of a past event and it is probable that an 
outflow of resources embodying economic benefits will be required to settle the obligation, and a reliable estimate can be made of the amount of 
the obligation.

provisions are reviewed at each balance sheet date and adjusted to reflect the current best estimate. if it is no longer probable that an outflow of 
economic resources will be required to settle the obligation, the provision is reversed. where the effect of the time value of money is material, 
provisions are discounted using a current pre-tax rate that reflects, where appropriate, the risks specific to the liability. when discounting is 
used, the increase in the provision due to the passage of time is recognised as a finance cost.

50

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employee benefits
the costs of short-term employee benefits are recognised as a liability and an expense, unless those costs are required to be recognised as part 
of the cost of inventories or non-current assets.

the cost of any unused holiday entitlement is recognised in the period in which the employee’s services are received.

termination benefits are recognised immediately as an expense when the group is demonstrably committed to terminate the employment of an 
employee or to provide termination benefits.

retirement benefits
the group operates a defined contribution scheme for the benefit of its employees. Contributions payable are charged to the Statement of 
Comprehensive income in the period they are payable.

Share-based payments
where share options are awarded to employees or other stakeholders, the fair value of the options at the date of grant is charged to the 
Statement of Comprehensive income over the vesting period. non-market vesting conditions are taken into account by adjusting the number of 
equity instruments expected to vest at each reporting date so that, ultimately, the cumulative amount recognised over the vesting period is 
based on the number of options that eventually vest. market vesting conditions are factored into the fair value of the options granted. as long as 
all other vesting conditions are satisfied, a charge is made irrespective of whether the market vesting conditions are satisfied. the cumulative 
expense is not adjusted for failure to achieve a market vesting condition.

where the terms and conditions of options are modified before they vest, the increase in the fair value of the options, measured immediately 
before and after the modification, is also charged to the Statement of Comprehensive income over the remaining vesting period.

where equity instruments are granted to persons other than employees, the income statement is charged with the fair value of goods and 
services received.

leases
leases are classified under iFrS 16 as lease liabilities with corresponding right of use assets in most circumstances except for leases of low value 
or a lease term of less than 12 months, in which circumstances the lease payments are expensed as incurred. lease incentives are recognised 
over the lease term.

Foreign currency
the functional currency of the parent entity is pounds Sterling. transactions entered into by group entities in a currency other than the 
reporting currency are recorded at the rates ruling when the transaction occur. Foreign currency monetary assets and liabilities are translated at 
the rates ruling at the Statement of Financial position date. exchange differences arising on the retranslation of the unsettled monetary assets 
and liabilities are similarly recognised in the income statement.

on consolidation, the results of overseas operations are translated into Sterling at rates approximating to those ruling when the transactions 
took place. 

on consolidation assets and liabilities of overseas operations are translated at the reporting date closing rate. exchange differences are charged 
or credited to other comprehensive income and recognised in the foreign exchange translation reserve. on disposal of an overseas operation 
exchange differences are recognised in the income statement as part of the gain or loss on sale.

presentation currency
these accounts have been presented in pounds Sterling as the directors consider this to be a most useful form of presentation to the 
shareholders.

operating segments
operating segments are reported in a manner consistent with the internal reporting provided to the chief operating decision maker.

Financing income and expenses
Financing expenses comprise interest payable and finance charges recognised in profit or loss using the effective interest method. Financing 
income comprises interest receivable on funds invested. interest income and interest payable is recognised within profit or loss as it is accrued, 
using the effective interest rate method.

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1 Accounting Policies continued
research and development
the group undertakes research and development activities in the uK which potentially attract a tax credit. where such activities give rise to a 
tax credit, amounts receivable are recorded in the Statement of Financial position as a tax asset and the associated credit is recorded within 
administrative expenses. the research and development tax credit is recognised in the financial statements in the same year in which the 
research and development expenditure occurred. this treatment is in line with the recognition of government grants to which the uK research 
and development tax credits scheme approximates.

2 Adoption of New and Revised Standards and Changes in Accounting Policies
adoption of new and revised standards
during the financial year, the group has adopted the following new iFrSs (including amendments thereto) and iFriC interpretations, that 
became effective for the first time.

Standard

iFrS 16 Leases

iFriC interpretation 23 – Uncertainty over Income Tax Treatments

amendments to iFrS 9 – Prepayment Features with Negative Compensation

amendments to iaS 28 – Long-term Interests in Associates and Joint Ventures

annual improvements 2015–2017 cycle

amendments to iaS 19: Plan amendment, Curtailment or Settlement

effective date, annual period 
beginning on or after

1 January 2019

1 January 2019

1 January 2019

1 January 2019

1 January 2019

1 January 2019

their adoption has not had any material impact on the disclosures or amounts reported in the financial statements except iFrS 16, the impact of 
which is described in note 16

Standards issued but not yet effective:
at the date of authorisation of these financial statements, the following standards and interpretations relevant to the group and which have not 
been applied in these financial statements, were in issue but were not yet effective. in some cases, these standards and guidance have not been 
endorsed for use in the european union. 

Standard

Conceptual Framework and amendments to references to the Conceptual Framework in iFrS Standards

amendments to iFrS 3 Business Combinations

amendments to iaS 1 and iaS 8: Definition of Material

interest rate Benchmark reform: amendments to IFRS 9, IAS 39 and IFRS 7 

Classification of liabilities as Current or non-Current: amendments to IAS 1

effective date, annual period 
beginning on or after

1 January 2020

1 January 2020

1 January 2020

1 January 2020

1 January 2022

the directors are evaluating the impact that these standards will have on the financial statements of the group. 

3 Critical Accounting Estimates and Judgements
in the application of the group’s accounting policies, the directors are required to make judgements, estimates and assumptions about the 
carrying amount of assets and liabilities that are not readily apparent from other sources. the estimates and associated assumptions are based 
on historical experience and other factors that are considered to be relevant. actual results may differ from these estimates.

the estimates and underlying assumptions are reviewed on an ongoing basis. revisions to accounting estimates are recognised in the period in 
which the estimate is revised, if the revision affects only that period, or in the period of the revision and future periods if the revision affects both 
current and future periods.

the estimates and assumptions which have a significant risk of causing a material adjustment to the carrying amount of assets and liabilities are 
outlined below.

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Critical judgements
Accounting for acquisitions of a business and intangible assets
in april 2019 the group acquired delta diagnostics uK ltd (trading as elucigene) and in march 2020 it also acquired agX-dpni SaS. the 
acquisition of elucigene was deemed to meet the iFrS 3 criteria for a business combination as it was a full standalone trading business.  
the acquisition of agX-dpni was deemed to be the acquisition of an intangible asset in the form of customer relationships, as there were no 
employees, facilities or other significant trading activities.

the acquisition of agX-dpni also contained provisions for earn-out payments to the vendors, based on achieving certain sales performance 
targets in the first year post-acquisition. these targets were based on existing business forecasts and were deemed sufficiently probable to be 
met that they are recorded as provisions rather than contingent liabilities. 

note 14 provides more information on these acquisitions including the basis on which fair values were determined for the acquired intangible assets.

Accounting for the capitalisation of development costs
the group has now been in operation for several years and has resolved some significant technical challenges in bringing its products to market. 
in certain circumstances this leads to reduced technical risk during the product development cycle. the group has also started to decouple 
some previously integrated components of its products, for example its software applications. development costs are capitalised where it is 
judged that a development project has met both of these iaS 38 criteria. 

Accounting for share-based payments
the group’s rapid growth in revenues and gross profits resulted in its first adjusted eBitda profit in this reporting period. excluding the one-off 
loan cancellation benefit in the prior reporting period, the group has therefore shown sustained growth in earnings per share, the key basis on 
which share based payments are measured. this performance trajectory is forecast to continue which increases the likelihood that share 
options will become exercisable in the future. as a result the assumptions for share-based payments have been increased and a significant 
charge recognised in the Consolidated income Statement. 

Accounting for deferred tax
the group has generated significant historic losses during its development stage, which have not been recognised as a deferred tax asset due to 
lack of visibility of future profitability within a realistic time horizon. as the group now moves towards profitability, such visibility is becoming 
more likely in the near term. the group has therefore started to recognise some of these losses where it deems it has a prudent basis on which  
to do so, including where there are deferred tax liabilities arising on acquisition that can be offset against historic tax losses.  

Key sources of estimation uncertainty
Impairment of goodwill
the group’s management undertakes an impairment review annually, or more frequently if events or changes in circumstances indicate that the 
carrying value may not be recoverable. in respect of impairment reviews, the key assumptions are as follows:

Growth rates
the value in use of the intangible assets is calculated from cash flow projections for the relevant business activities based on the latest financial 
projections covering the anticipated useful economic life of the intangible assets.

Discount rates
the pre-tax discount rate used to calculate value is determined in relation to the relevant business activities and their geographic location, using 
external benchmarks where possible to arrive at a relevant weighted average cost of capital.

Cash flow assumptions
the key assumptions for the value-in-use calculations are those regarding discount rates, growth rates and expected cash flows. Changes in 
revenues and expenditures are based on past experience and expectations of future growth.

4 Segment Reporting
in the opinion of the directors, the group has one class of business in three geographic areas; a molecular diagnostics business sells into the uK, 
europe and other countries referred to as ‘international’. the group sells into three highly interconnected clinical markets: non-invasive prenatal 
testing (nipt), reproductive health and oncology/research services. the group is therefore considered to have a single operating segment 
which is monitored by the group’s chief operating decision makers. Strategic decisions are made on the basis of unadjusted operating results.

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4 Segment Reporting continued
revenue
revenue, analysed by category, was as follows:

Turnover
Sale of goods
rendering of services

revenue analysed by geographical market

uK
europe
international

revenue analysed by clinical market

nipt
reproductive health
precision medicine

2020
£

2019
£

11,071,492
5,541,287

4,976,470
3,905,892

16,612,779

8,882,362

2020
£

1,974,632
4,142,073
10,496,074

2019
£

1,215,722
1,780,384
5,886,256

16,612,779

8,882,362

2020
£

10,144,312
3,651,142
2,817,325

2019
£

7,853,507
–
1,028,855

16,612,779

8,882,362

during the reporting period no customers represented more than 10% of group revenues (2019: two customers generated revenues of 
£2,374,372 representing a combined 27% of group revenues).

non-current assets
the group’s non-current assets are located in the following geographic regions, which support the three clinical markets in a highly 
integrated manner:

uK
europe
international
intra-group eliminations & adjustments

5 Separately Disclosed Items

Share-based payment expense
Costs associated with the acquisition of subsidiary
acquisition integration expense

2020
£

2019
£

25,327,904
2,157,093
592,449
(2,113,716))

10,845,876
–
748,352
(1,296,690)

25,963,730

10,297,538

2020
£

(1,601,746)
(264,666)
(533,358)

(2,399,770)

2019
£

(251,004)
–
–

(251,004)

Share-based payment expense relates to the provision made in accordance with iFrS 2 ‘Share-based payment’ following the issue of share 
options to employees under the Company’s share option schemes, as set out in note 29.

Costs associated with the acquisition of subsidiaries represents costs incurred during the acquisition of delta diagnostics uK ltd in april 2019, 
and agX-dpni in march 2020.

acquisition integration expense relates to the expense incurred integrating delta diagnostics uK ltd into the yourgene Health group.

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6 Operating Loss

operating loss for the year is stated after charging/(crediting):
research and development expense excluding salaries
research and development tax credit
depreciation of property, plant and equipment
depreciation right-of-use assets
(profit)/loss on disposal of property, plant and equipment
amortisation of intangible assets
iFrS 16 lease liability adoption (gain)/loss
impairment on financial assets iFrS 9

7 Auditor’s Remuneration
Fees payable to the group’s auditor:

For audit services
audit of the financial statements of the Company 
audit of the financial statements of the Company’s subsidiaries 

For other services 
all other assurance services
all other tax advisory services

total non-audit fees

8 Employees
the average monthly number of persons (including directors) employed by the group during the year was:

directors 
administrative
research and development 

their aggregate remuneration comprised:

wages and salaries
Social security cost
pension cost
Share-based payments (note 29)

2020
£

2019
£

518,378 
(560,204)
949,780 
467,724 
(7,564)
676,304 
(131,548)
106,511 

691,239 
(473,950)
944,524 
–
469 
155,232 
–
155,962 

2020
£

35,500 
26,250 

61,750 

14,500 
38,830

53,330

2019
£

36,000 
15,750 

51,750 

–
5,935 

5,935 

2020
Number 

2019
number 

9
81
46

136

2020
£

4,756,240 
490,802 
208,175 
1,601,746 

8
49
37

94

2019
£

3,832,974 
347,938 
150,971 
251,004 

7,056,963 

4,582,887 

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9 Directors’ Remuneration
the remuneration of the directors during the period was as follows:

Salaries 
£

Fees
£

pension 
£

BiK 
£

a reynolds
dr S little
n mustoe
l rees
dr B Chang
B Hextall
H Jeffreys
dr J Brown (appointed 29 July 2019)
J Seaton (appointed 15 august 2019)
Keng Hsu (resigned on 10 July 2019)
dr w denman (resigned 14 may 2018)
a Chang (resigned 03 July 2018)
p Collins (resigned 01 november 2018)

–
61,800
–
190,000
154,479
175,000
175,000
27,128
–
28,853
–
–
–

71,863
–
30,000
–
–
–
–
–
17,485
–
–
–
–

812,260

119,348

–
3,090
–
10,000
–
7,500
7,500
–
–
–
–
–
–

28,090

2020
£

71,863
66,751
30,000
219,739
154,479
192,968
184,074
27,128
17,485
28,853
–
–
–

2019
£

100,001
82,456
30,000
132,227
169,349
143,278
127,837
–
–
98,604
1,000
3,333
147,745

–
1,861
–
19,739

10,468
1,574
–
–
–
–
–
–

33,642

993,340 1,035,830

the number of directors to whom pension benefits are accruing under money purchase schemes is 4 (2019: 5). 

the share-based payments charge to the Consolidated Statement of Comprehensive income for directors share options was £977,670  
(2019: £155,742). during the period the directors did not exercise any options.

10 Finance Income

Interest income:
Bank deposits
loans and receivables

total interest income

Other finance income:
thermo Fisher loan waived (see note 30)
loan agreement and warrant issue expense

total other finance income

total finance income

11 Finance Expenses

interest on bank overdrafts and loans
interest on other loans and borrowings (see note 30)
iFrS 16 interest

total finance expense

12 Income Tax Expense

Current tax
uK corporation tax on profits for the current period
Foreign corporation tax

Current tax for period

Deferred tax
origination and reversal of temporary differences: uK

origination and reversal of temporary differences: foreign

deferred tax for period

total tax (credit)/charge

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YOURGENE HEALTH PLC  annual report and aCC ountS 2020

2020
£

5,010 
14,950 

19,960 

2019
£

285 
35,387 

35,672 

–
–

–

9,389,210 
(43,121)

9,346,089 

19,960 

9,381,761 

2020
£

15,673
4,656
142,874

2019
£

7,252
1,202,302
–

163,203

1,209,554

2020
£

–
328,808

328,808

2019
£

–
29,985 

29,985

(1,024,489)

(29,494)

(252,505)

–

(1,276,994)

(29,494)

(948,186)

491

 
 
 
 
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as described in the critical accounting judgements section of this report, deferred tax assets are recognised where there is deemed to be a 
reasonable probability that future taxable profits will be capable of being offset by historic tax losses.  

the charge for the year can be reconciled to the loss per the income statement as follows:

loss before taxation

expected tax credit based on a corporation tax rate of 19% (2019: 19%)
effect of expenses not deductible in determining taxable profit
unutilised tax losses carried forward
Change in unrecognised deferred tax assets
effect of overseas tax rates
effect of enhanced r&d deduction
deferred tax

Taxation (credit)/charge for the year

2020
£

2019
£

(3,382,110)

3,389,701 

(642,601)
440,168 
778,591 
86,361 
(236,400)
(349,816)
(1,024,489)

(948,186)

644,043 
(45,518)
(941,372)
78,338 
24,474 
270,020 
(29,494)

491 

the r&d tax credit of £560,204 (2019: £473,950) is shown as a deduction against general administrative expenses.

the group is required to estimate the income tax in each of the jurisdictions in which it operates. this requires an estimation of the current tax 
liability together with an assessment of the temporary differences which arise as a consequence of different accounting and tax treatments. 
these temporary differences result in deferred tax assets or liabilities which are included within the Statement of Financial position. deferred tax 
assets and liabilities are measured using substantially enacted tax rates expected to apply when the temporary differences reverse. 
management judgement is required to determine the total provision for income tax. amounts accrued are based on management’s 
interpretation of country specific tax law and the likelihood of settlement.

Factors that may affect future tax charges
the group has estimated trading losses of £15,455,325 (2019: £13,517,081), estimated excess management fees of £13,193,592 (2019: 
£11,330,723), non-trade loan relationship deficits of £1,328,796 (2019: £933,151) and capital losses of £1,934,399 (2019: £1,934,399).

the tax losses have resulted in a potential deferred tax asset of approximately £5,695,765 (2019: £4,428,392) which has been partially recognised 
(£925,364) to offset a deferred tax liability arising on the acquisition of elucigene which will be offset by historic losses. Further recognition in 
future reporting periods subject to the extent that future taxable profits will be sufficient to utilise the losses, in accordance with current and 
expected future uK tax rates.

13 Earnings Per Share
Basic
Basic earnings per share is calculated by dividing the profit or loss for the period of £2,433,924 (2019: profit £3,389,210) by the weighted average 
number of ordinary shares in issue during the period 590,467,253 (2019: 396,597,093).

diluted
diluted earnings per share dilute the basic earnings per share to take into account share options and warrants. the calculation includes the 
weighted average number of ordinary shares that would have been issued on the conversion of all the dilutive share options and warrants into 
ordinary shares. the adjusted weighted average number of shares used to calculate diluted earnings per share is 608,687,226 
(2019: 399,636,919).

26,039,443 options and warrants (2019: 92,269,091) have been excluded from this calculation as the effect would be anti-dilutive.

after the reporting period end a further 7,848,992 new ordinary shares were issued against share options and standard warrants, see note 29.

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14 Intangible Assets

Cost
at 1 april 2018
additions
at 31 march 2019

additions
exchange differences

At 31 march 2020

Amortisation and impairment
at 1 april 2018
Charge for the year
at 31 march 2019

Charge for the year
exchange differences

At 31 march 2020

Carrying amount
at 31 march 2019

At 31 march 2020

goodwill
£

7,014,447 
–
7,014,447 

3,791,336 
–

Customer 
relationships
£

1,552,328 
–
1,552,328 

6,840,696 
51,206

product ip

product 
development 
cost

total
£

–
–
–

–
–
–

8,566,775 
–
8,566,775 

2,051,699 
–

695,942 
–

13,430,879 
–

10,805,783 

8,444,230 

2,051,699 

695,942 

21,997,654 

–
–
–

–
–

–

168,168 
155,232 
323,400 

488,226 
278 

811,904 

–
–
–

188,078 
–

188,078 

7,014,447 

1,228,928 

–

–
–
–

–
–

–

–

168,168 
155,232 
323,400 

676,304 
278 

999,982 

8,243,375 

10,805,783 

7,632,326 

1,863,621 

695,942 

20,997,672 

the intangible assets arose as part of the acquisition of yourgene Health taiwan (march 2017). delta diagnostics uK ltd (april 2019) and 
agX-dpni SaS (march 2020). the assets are amortised over a useful economic life defined upon acquisition:

Customer relationships
product ip
product development cost

useful economic life

remaining useful life

10 years
10 years
5-10 years

7–10 years
9–10 years
3–10 years

amortisation has been charged to general administrative expenses in the consolidated statement of Comprehensive income.

goodwill is allocated to the group’s cash-generating units (Cgus) identified according to product segment. a product segment-level summary 
of the goodwill allocation is presented below.

nipt
reproductive health
precision medicine

2020
£

7,014,447
3,791,336
–

2019
£

7,014,447
–
–

10,805,783

7,014,447

nipt goodwill represents the goodwill arising on the acquisition of yourgene Bioscience (taiwan) in march 2017, since renamed yourgene Health 
taiwan. the reproductive Health goodwill arose on the acquisition of elucigene in april 2019.

intangible assets are subject to an annual impairment test to ascertain if the value in use is greater than the carrying value in the financial 
statements. the intangible assets arising from the acquisitions above, are tested over a five year forecast period plus a terminal value to 
represent their remaining useful economic life. a cash flow model for each business unit is used based on historical performance, in which future 
expectations of growth are forecast based on internal budgets for 12 months, and then on an initial growth rate ranging from 10% – 30% 
reducing down to 2 – 5 % per annum for the terminal value estimation, reflecting the rapid growth of the group’s markets and the opportunities 
for greater market penetration through geographic expansion. discount rates were set at 13%, being the representative cost of capital. these 
assumptions are reviewed and benchmarked to ensure they remain appropriate. 

the impairment assessments showed assessed values that exceeded the carrying values with significant headroom. in the case of elucigene a 
discount rate sensitivity of 20% did not give rise to an impairment, and the headroom for yourgene Health taiwan was even higher. 

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15 Property, Plant and Equipment

Cost
at 1 april 2018
additions
transfer
disposals
Foreign currency adjustments

at 31 march 2019
additions
Business combinations
transfer
disposals
Foreign currency adjustments

At 31 march 2020

Accumulated depreciation and impairment
at 1 april 2018
Charge for the year
transfer
eliminated on disposal
Foreign currency adjustments

at 31 march 2019
Charge for the year
transfer
eliminated on disposal
Foreign currency adjustments

At 31 march 2020

Carrying amount

At 31 march 2020

at 31 march 2019

leasehold 
land and 
buildings
£

682,641 
23,696 
–
–
258 

706,595 
150,309 
81,153 
–
(206,353)
5,635 

plant and 
equipment
£

Computer 
software
£

3,867,040 
1,043,003 
(32,755)
(1,254)
18,327 

4,894,361 
407,978 
164,863 
–
(15,827)
93,562 

24,408 
–
–
–
300 

24,708 
58,798 
40,641 
–
–
1,758 

total
£

4,574,089 
1,066,699 
(32,755)
(1,254)
18,885 

5,625,664 
617,085 
286,657 
–
(222,180)
100,955 

737,339 

5,544,937 

125,905 

6,408,181 

421,831 
120,537 
–
–
(578)

541,790 
170,764 
–
(131,548)
4,697 

2,217,360 
820,098 
(32,755)
(785)
6,242 

3,010,160 
758,220 
–
(9,838)
52,722 

15,492 
3,889 
–
–
170 

19,551 
20,796 
–
–
1,561 

2,654,683 
944,524 
(32,755)
(785)
5,834 

3,571,501 
949,780 
–
(141,386)
58,981 

585,703 

3,811,264 

41,908 

4,438,876 

151,636 

1,733,673 

83,996 

1,969,305 

164,805 

1,884,201 

5,157 

2,054,163 

Business combination refers to assets acquired in the acquisition of delta diagnostics uK ltd in april 2019, see note 18

16 Leases
lease liabilities
the Company has a number of leases for property in the uK, taiwan and Singapore. on adoption of iFrS 16, the group recognised lease liabilities 
in relation to property leases which had previously been classified as operating leases under the principles of iaS 17 leases. the group adopted 
iFrS 16 from 1 april 2019 using the modified retrospective approach, the comparative information for 2019 is not restated. the incremental 
borrowing rate applied to the lease liabilities on 1 april 2019 was based on comparable loan interest rates in the relevant jurisdiction where the 
lease is operable.

at 1 april 2019 on transition
additions
Business combinations
lease payments
interest expense
terminations and amendments
Foreign currency adjustments

At 31 march 2020

Current
non-current

At 31 march 2020

lease liability
£

1,198,368 
2,823,388 
1,557,960 
(507,233)
142,874 
(2,166,524) 
2,457 

3,051,290 

341,167 
2,710,123 

3,051,290 

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16 Leases continued
right-of-use assets
right-of-use assets for these property leases were measured at the amount equal to the lease liability as at the iFrS 16 adoption date.  
there were no onerous lease contracts that would have required an adjustment to the right-of-use assets at the date of initial application. 

Cost
at 1 april 2019 on transition
additions
Business combinations
transfer
terminations and amendments
Foreign currency adjustments

At 31 march 2020

Accumulated depreciation and impairment
Charge for the year
transfer
eliminated on termination and amendment
Foreign currency adjustments

At 31 march 2020

Carrying amount

At 31 march 2020

right-of-use asset: 
property
£

1,198,368 
2,823,388 
1,484,996 

(2,262,172)
3,729 

3,248,309 

467,724 
–
(216,897)
729 

251,556 

2,996,753 

Changes to property leases after 1 april 2019
on 26 april 2019 the Company acquired delta diagnostics uK ltd including its iFrS 16 property lease liability and right-of-use asset, as described 
in the note below. delta diagnostics uK ltd is in the process of being integrated with Company’s other uK trading subsidiary, yourgene Health 
uK ltd. as part of this integration project some uK property leases have been surrendered and others renegotiated with extended terms. the 
uK property lease restructure was completed in September 2019. a further uK property lease was taken out in march 2020 due to the integration 
and expansion of the uK business. the property lease in taiwan was extended a further six months whilst a review of alternative locations is 
undertaken to allow for expansion of operations in taiwan. 

operating lease commitments
in addition to the property leases disclosed above under iFrS 16 the group has a small number of low value asset operating leases.

minimum lease payments under operating leases 

2020
£

2019
£

91,236

205,699

2019 lease payments include property lease payments of £176,368; see above property lease liability payments for 2020.

at the reporting period date, the group had outstanding commitments for future minimum lease payments under non-cancellable operating 
leases, which fall due as follows:

within one year
Between one and five years
in over five years 

2020
£

46,316 
15,526 
–

61,842 

2019
£

227,336 
529,802 
–

757,138 

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17 Inventories

raw materials 
work in progress
Finished goods 

Finished goods recognised at cost of sales in the year amounted to £6,123,807 (2019: £4,271,941)

18 Subsidiaries
details of the Company’s subsidiaries at 31 march 2020 are shown in the table below:

name of undertaking

yourgene Health uK ltd
delta diagnostics (uK) ltd
elucigene ltd
premaitha gmbH
agX-dpni S.a.S.
yourgene Health inc
yourgene Health (taiwan) Co. ltd.
Kang Qiao Bioscience ltd
Jian Qiao Bioscience Co. ltd
yourgene Bioscience Co ltd
yourgene Health (Singapore) pte limited

2020
£

406,472
405,158
340,678

1,152,308

2019
£

200,579
286,502
252,045

739,126

Country of
incorporation

uK
uK
uK
germany
France
uSa
taiwan
taiwan
taiwan
taiwan
Singapore

ownership
interest (%)

nature of
business

100
100
100
100
100
100
100
100*
100*
100*
100*

See below
See below
non trading
See below
See below
See below
See below
See below
See below
See below
See below

yourgene Health uK ltd principal activity is that of a molecular diagnostics company employing next generation dna analysis technology to 
develop, manufacture and sell molecular diagnostic products intended to have a major beneficial impact on human health. the registered office 
is at Citylabs 1.0 nelson Street, manchester, m13 9nQ. yourgene Health uK ltd was formerly named premaitha ltd until 11 december 2019.

delta diagnostics (uK) ltd trading as elucigene is a molecular diagnostics manufacturer and developer with a suite of in vitro diagnostic Ce 
marked products focused on reproductive health and oncology. the registered office is at Citylabs 1.0 nelson Street, manchester, m13 9nQ.

premaitha gmbH is a german subsidiary whose principal activity is that of a sales office for yourgene Health uK ltd. the registered office is at 
prielmayerstraße 3, 80335 münchen, germany.

agX-dpni S.a.S. is a recently acquired subsidiary whose principal activity is that of a distributor for yourgene Health uK ltd. the registered 
office is at 20 avenue Jean Bart, 78960 voisins le Bretonneux, France.

yourgene Health inc is a uS subsidiary whose principal activity is that of a sales office and distributor for yourgene Health uK ltd. the registered 
office is at 1680 michigan ave, Suite 700 #232, miami Beach Fl 33139 uSa.

elucigene ltd is a non-trading entity, formerly named yourgene Health uK ltd until 6 december 2019. the registered office is at Citylabs 1.0 
nelson Street, manchester, m13 9nQ.

yourgene Health (taiwan) Co. ltd was formerly named yourgene Bioscience Co. ltd. it is a taiwanese subsidiary where the principal activities of 
the group headed by this Company are within the same sector as yourgene Health uK ltd. its registered office is no.376-5, Fuxing rd., Shulin 
dist., new taipei City 23871, taiwan (r.o.C.).

*  yourgene Health (taiwan) Co. ltd owns a 100% interest in each of Kang Qiao Bioscience ltd, registered office 3F., no. 3, ln. 160, Junying St., Shulin dist., new taipei City 

238, taiwan (r.o.C.); Jian Qiao Bioscience Co. ltd, registered office no.376-5, Fuxing rd., Shulin dist., new taipei City 23871, taiwan (r.o.C.); yourgene Bioscience Co. ltd, 
registered office no.376-5, Fuxing rd., Shulin dist., new taipei City 23871, taiwan (r.o.C.); and yourgene Health (Singapore) pte limited (formerly named yourgene 
Bioscience Singapore pte limited.), registered office 3 Fusionopolis place #05-54 galaxis Singapore 138523. 

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18 Subsidiaries continued
acquisition of delta diagnostics uK ltd (trading as elucigene diagnostics)
the group acquired 100% of the equity interests in delta diagnostics uK ltd on 25 april 2019 for a total consideration of £9,280,743. this 
uK-registered company is a leading molecular diagnostics manufacturer and developer of a complementary product range to that of the group. 
a summary of the net assets acquired, and the consideration paid is shown below. 

Cash and cash equivalents
intangible assets
property, plant and equipment
right-of-use asset (iFrS 16)
trade and other receivables
inventories
trade and other payables
tax liability
Borrowings
lease liability under iFrS 16
deferred tax liability

goodwill

total Fair value

Satisfied by:
Cash

issue of shares

net cash outflow arising on acquisition:
Cash consideration
Cash and cash equivalents acquired

Book value
£

627,268
–
286,657
1,484,996
1,707,060
440,177
(1,444,619)
(115,175)
(258,271)
(1,557,960)
(23,816)

1,146,317

Fair value
£

627,268
5,361,840
286,657
1,484,996
1,707,060
440,177
(1,444,619)
(115,175)
(258,271)
(1,557,960)
(1,042,566)

5,489,407
3,791,336

9,280,743

6,331,010

2,949,733
9,280,743

(6,331,010)
627,268

(5,703,742)

at the time of acquisition it was expected that all trade receivables would be collected. the goodwill arising on acquisition represents the 
perceived inherent value to the group of, for example, the additional skilled colleagues in the elucigene business, the higher grade facilities made 
available to the group as a result of the acquisition, operational synergies through combining certain business functions, the future value of 
products in development that did not meet the requirements for explicit recognition and the opportunity to offer a combined product range to 
prospective and existing customers of both businesses.

the acquisition consideration was satisfied by a combination of cash raised through an equity fundraise and the issue new shares as non-cash 
consideration. the non-cash consideration comprised 24,581,111 new ordinary shares valued at a contractual share price of 12 pence per new 
ordinary share issued which reflected the closing share price on the day prior to completion of the acquisition.

the revenue recognised in the Consolidated statement of comprehensive income for delta diagnostics uK ltd is £2,632,344 revenue, had the 
acquisition occurred on the first day of the reporting period this would have been £2,715,168. it is not practicable to state the comparable profit 
figures as there has been significant transfer of employees and leases to yourgene Health uK ltd.

acquisition of French distribution channel
the group acquired 100% of the equity interest in agX-dpni S.a.S., a newly formed entity comprised of the nipt distribution business of 
adgeniX S.a.r.l (“adgeniX”), the Company’s current French distribution partner for its iona® test, for an initial cash consideration of €2,355,000 
and up to a maximum of €1,655,000 in performance consideration payments based on sales growth performance criteria. a further two cash 
payments of €577,500 each will be payable in october 2020 and april 2021 dependent on nipt sales growth during the period, with a final cash 
bonus of up to €500,000 due in april 2021 if nipt sales exceed additional agreed targets. the acquisition has been treated as an acquisition of 
assets, and the future performance consideration payments recorded as a provision by the group due to the expected probability – based on an 
assessment of market dynamics and individual customer growth plans – that these targets will be achieved, and the ability to accurately estimate 
the value of the potential liability.

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19 Trade and Other Receivables

trade receivables
provision for doubtful trade receivables
loss allowance due to expected credit losses (under iFrS 9)

Net Trade Receivables
other receivables
vat recoverable 
other loans and receivables at amortised cost
loss allowance due to expected credit losses (under iFrS 9)

Net other loans and receivables at amortised cost

prepayments 

2020

£

£

2019

£ 

£

2,810,957
(884,349)
(48,489)

302,386
(107,473)

4,808,174
(83,161)
(101,836)

11,588
–

4,623,177
131,010
284,628

11,588

578,884

5,629,287

1,878,119
86,826
282,659

194,913

390,178

2,832,695

an amount of £nil (2019: £785,317) was provided for doubtful receivables relating to a customer which was in bankruptcy proceedings. this 
customer has now been declared bankrupt, and legal proceedings have failed to recover any outstanding monies. this amount has now been 
written off.

an amount of £80,922 (2019: £99,032) has been provided for doubtful receivable amounts overdue from specific customers.

a loss allowance against trade receivables of £101,836 (2019: £48,489) for expected credit losses has been provided for as required under iFrS 9. 
these expected credit losses were calculated after analysing the group’s receivable risks in geographic groupings which are deemed to reflect 
appropriate credit risk categories. delinquency rates and political stability are deemed to be very low in asia pacific leading to no impairment of 
receivables. in europe and america increased risk due to Covid-19 issues is reflected in a 2.5% (2019 0%) expected credit loss risk. in the middle 
east and africa region Covid-19 and general political instability have been deemed to give an expected credit loss risk rating of 5% (2019 10%). 
in india expected credit loss risk has been estimated to be greater at 15% due to specific customer delays and covid-19 issues.

other loans and receivables relate to an outstanding loan to a customer of the group, this amount has been received in the first quarter of Fy2021.

20 Trade and Other Payables

trade payables 
payments received on account
accruals
Social security and taxation
other payables

the book value of trade and other payables approximates to the fair values. See note 26 for maturity analysis.

21 Borrowings

unsecured borrowings at amortised cost
Bank loans
other loans

2020
£

2,674,449
1,170,017
612,554
167,235
283,558

2019
£

2,088,567
1,277,105
580,599
110,555
115,638

4,907,813

4,172,464

2020
£

2019
£

362,618
–

362,618

285,690
–

285,690

analysis of borrowings
Borrowings are classified based on the amounts that are expected to be settled within the next 12 months and after more than 12 months from 
the reporting date, as follows:

Current liabilities
non-current liabilities

2020
£

277,508
85,110

362,618

2019
£

76,388
209,302

285,690

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21 Borrowings continued
the continuing borrowings as at 31 march 2020 are:

asset finance facilities entered into by yourgene Health (taiwan) Co. ltd. these facilities are payable until december 2021, are secured against 
the financed equipment and incur a fixed interest rate of 1.97% per annum.

Borrowings incurred by newly acquired subsidiary, delta diagnostics (uK) ltd, payable by october 2021. the loan incurs interest at 4.94% pa over 
Base rate. the borrowings have covenants attached to them and the group has been compliant with these covenants throughout the year.

22 Provisions for Liabilities

dilapidation provision
acquisition – additional consideration 

2020
£

–
1,468,878

1,468,878

2019
£

206,353
–

206,353

analysis of provisions:
provisions are classified based on the amounts that are expected to be settled within the next 12 months and after more than 12 months from 
the reporting date, as follows:

Current liabilities
non-current liabilities

movements on provisions:

at 1 april 2019
release of provision
increase in provision 

At 31 march 2020

2020
£

512,554
956,324

1,468,878

2019
£

–
206,353

206,353

acquisition additional 
consideration
£

–
–
1,468,878

1,468,878

dilapidation 
provision
£

206,353
(206,353)
 –

total
£

206,353
(206,353)
1,468,878

–

1,468,878

dilapidation provision
as part of the group’s property leasing arrangements there was an obligation to return certain premises in the same state that they were 
received and repair damages which incur during the life of the lease, such as wear and tear. the group has adopted iFrS 16 and these costs have 
now been recognised as part of the cost of the right-of-use asset and lease liability – please see note 16.

acquisition – additional consideration
upon successful acquisition of French distribution channel for an initial cash consideration of €2.4 million a further two cash payments of  
€0.58 million each will be payable in october 2020 and april 2021 dependent on nipt sales growth during the period, with a final cash bonus of up 
to €0.5 million due in april 2021 if nipt sales exceed additional agreed targets. the executive management of adgenix are contracted during the 
earn-out period to ensure a successful transition and customer continuity, with an additional multi-year non-compete provision from completion.

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23 Deferred Taxation and Other Tax Assets
the deferred tax liabilities and assets recognised by the group and movements thereon during the current and prior reporting period are shown 
below. the deferred tax assets and deferred tax liabilities and are not offset and are both deemed non-current.

deferred tax liability at 1 april 2018
Deferred tax movements
Credit to profit or loss

deferred tax liability at 1 april 2019

Deferred tax movements
acquired in business combination
Credit to profit or loss

Deferred tax liability at 31 march 2020

deferred tax asset at 1 april 2018
Deferred tax movements
Credit to profit or loss

deferred tax asset at 1 april 2019

Deferred tax movements
Credit to profit or loss: uK tax
Credit to profit or loss: foreign tax
Foreign exchange revaluation

Deferred tax asset at 31 march 2020

£

262,990 

(29,494)

233,496 

1,018,750 
(99,125)

1,153,121

£

–

–

–

925,364
252,505
3,170

1,181,039 

tax assets are sums arising from enhanced r&d reliefs available in the uK, and are allocated between current and non-current according to the 
Company’s view on when the benefits will arise.

tax asset at 1 april

tax movements
Business combination
refund received
Credit to profit or loss

Tax asset at 31 march

non-current tax asset
Current tax asset

As at 31 march

2020
£

2019
£

478,232

1,158,765

(48,028)
–
554,972

985,176

2020
£

532,691
452,485

985,176

–
(1,129,638)
449,105

478,232

2019
£

–
478,232

478,232

24 Financial Instruments
the principal instruments used by the group, from which the financial instrument risk arises, include cash and cash equivalents, trade 
receivables, trade payables and borrowings.

risk and sensitivity analysis
there have been no substantive changes in the group’s exposure to financial instrument risks, its objectives, policies and processes for 
managing those risks or the methods used to measure them from previous periods unless otherwise stated in this note.

the group and Company are exposed through their operations to one or more of the following financial risks: foreign currency risk, liquidity risk, 
credit risk, investment risk and interest rate risk. the policy for managing these risks is set by the Board and all such risks are managed at a group 
level within the organisation. the Board’s objective is to ensure an appropriate balance of risk and opportunity and monitors key risk factors in 
each Board meeting to determine whether that balance is deemed satisfactory. where practical risks will be mitigated, e.g. through natural 
hedging of foreign currency exposures or insurance.

there have been no changes from previous years in the way the group and Company manages risks, other than the use of forward foreign 
exchange contracts in specific situations where future currency trades can be accurately forecast. the policies for these risks are described 
further within the following notes.

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25 Financial Instruments – Market Risk
Foreign exchange risk
Foreign currency exchange risk arises because the group has asset and liabilities denominated in foreign currencies. Subsidiary operations are 
located in the uK, germany, France, uSa, Singapore and taiwan whose functional currency outside the uK is not the same as the group’s 
functional currency (Sterling). the net assets from such overseas operations are exposed to currency risk giving rise to gains or losses on 
translation to Sterling for the purposes of the consolidated financial statements. 

Subsidiaries within the group trade internationally outside their own country. the group seeks to naturally hedge its currency risk by allowing 
subsidiaries to operate multi-currency bank accounts to match foreign currency income and expenditure. the bank balances are monitored at 
group level on a weekly reporting basis, allowing the management of exchange risk across the group. when necessary any specific currency surplus 
or shortage can be transferred or translated using either spot or forward currency contracts to meet future requirements of each subsidiary.

Foreign exchange risk continued
the carrying amounts of the group’s foreign currency denominated monetary assets and liabilities at the reporting date are as follows:

gBp
euros
uS$
new taiwan dollars
Singapore dollar
other (aud/Zar/CHF/aed)

Assets

2020
£

3,527,249
1,649,019
745,177
3,011,105
526,253
175,452

2019
£

1,413,886
1,154,699
98,079
1,606,743
234,336
52,590

Liabilities

2020
£

7,001,309
721,917
178,157
2,310,766
199,541
14,678

2019
£

1,779,437
544,383
34,741
1,940,671
80,600
78,682

9,634,255

4,560,333

10,426,368

4,458,514

the following table illustrates the sensitivity of profit and equity in regard to the group’s financial assets and financial liabilities and the Sgd/
gBp, twd/gBp, uSd/gBp and euro/gBp exchange rates ‘all other things being equal’. it assumes a +/- 6% change of the Sgd/gBp, +/- 7% twd/
gBp and euro/gBp, +/- 9% uSd/gBp exchange rate for the year ended at 31 march 2020 (2019: 5%). a +/- 9% change is considered for the uSd/
gBp exchange rate (2019: 5%) and a +/-7% change is considered for the euro/gBp and twd/gBp exchange rate (2019: 5%) and +/- 6% for Sgd/
gBp (2019: 5%). all of these percentages have been determined based on the average market volatility in exchange rates in the previous 
12 months. The sensitivity analysis is based on the Group’s foreign currency financial instruments held at each reporting date. 

if the gBp had strengthened against the Sgd by 6% (2019: 5%), twd and euro by 7% (2019: 5%), uSd by 9% (2019: 5%) respectively then this 
would have had the following impact:

Sgd
£

twd
£

uSd
£

euro
£

total
£

Sgd

twd
£

31 march 2020

31 march 2019

(18,493)

(45,817)

(46,818)

(60,652)

(171,780)

(1,403)

(37,136)

(7,321)

15,901

(3,016)

(29,063)

(23,498)

(1,202)

(13,822)

uSd
£

–

–

euro
£

total
£

(141,118)

(179,657)

(269)

(15,293)

loss for the year

other equity

if the gBp had weakened against the Sgd by 6% (2019: 5%), twd and euro by 7% (2019: 5%), uSd by 9% (2019: 5%) respectively then this would 
have had the following impact:

Sgd
£

twd
£

uSd
£

euro
£

total
£

31 march 2020

31 march 2019

20,854

52,714

56,079

69,782

199,429

8,091

(17,575)

3,334

32,122

25,972

Sgd

1,582

2,530

twd
£

42,727

29,100

uSd
£

–

–

euro
£

total
£

162,362

206,671

566

32,196

loss for the year

other equity

exposures to foreign exchange rates vary during the year depending on the volume of overseas transactions. nonetheless, the analysis above is 
considered to be representative of the group’s exposure to currency risk.

interest rate risk
the group’s interest rate risk arises from interest-bearing assets and liabilities. the group has in place a policy of maximising finance income by 
ensuring that cash balances earn a market rate of interest; offsetting where possible, cash balances and by forecasting and financing its working 
capital requirements. Bank loans shown in note 21 are asset finance facilities in taiwan which are subject to fixed interest rates at 1.97% and 
interest rate of 4.94% over Base rate on loan facility for delta diagnostics (uK) ltd.

investment risk
investment risk is the risk that the fair value or future cash flows of a financial instrument will fluctuate because of changes in interest rates 
(interest rate risk), foreign exchange rates (currency risk) or other market factors (other price risk).

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the group is exposed to interest rate risk from its interest earning financial assets. the floating rate assets are held in a money market account 
earning interest at Bank of england base rate at 0.01%. the interest rate risk is mitigated by the fact cash is held in short-term deposits allowing rapid 
transfer of funds to alternative commercial banks to obtain improved interest rates. There are no financial assets earning interest at fixed rates.

Capital
as described in note 28 the group considers its capital to comprise its ordinary share capital, share premium and accumulated deficit as its 
capital reserves. in managing its capital, the group’s primary objective is to ensure its continued ability to provide a consistent return for its 
equity shareholders through capital growth. in order to achieve this objective, the group seeks to commercialise the development which has 
been undertaken to date, through major sales in a number of markets.

there have been no other significant changes to the group’s capital management objectives, policies and processes in the period nor has there 
been any change in what the group considers to be its capital.

26 Financial Instruments – Liquidity Risk
liquidity risk is the risk that the group fails to have sufficient funds to meet its debts as they become due. the liquidity risk of the group is 
managed centrally. the group holds funds in short-term bank deposits so that they are available when required.

the following table details the remaining contractual maturity for the group’s financial liabilities with agreed repayment periods. the contractual 
maturity is based on the earliest date on which the group may be required to pay.

at 31 march 2019

interest-bearing loans and borrowings
lease liabilities under iFrS 16
trade payables
accruals
other payables

At 31 march 2020

interest-bearing loans and borrowings
lease liabilities under iFrS 16
trade payables
accruals
other payables

1 year or less 
£

2 to 5 years
£

more than 5 years
£

total
£

76,388
–
2,088,567
580,599
1,392,743

4,138,297

277,508
341,167
2,674,449
612,554
1,453,574

209,302
–
–
–
–

209,302

85,110
2,710,123
–
–
–

5,359,252

2,795,233

–
–
–
–
–

–

–
–
–
–
–

–

285,690
–
2,088,567
580,599
1,392,743

4,347,599

362,618
3,051,290
2,674,449
612,554
1,453,574

8,154,485

the Board believes the current level of financial liabilities to be in line with expectations. the level of cash balances and trade and other 
receivables is sufficient to discharge the group’s financial liabilities.

27 Financial Instruments – Credit Risk
during the period, the group’s credit risk was primarily attributable to its cash balances, other loans receivable, and its trade receivables. Credit 
risk is the risk that the counterparty fails to discharge its obligation in respect of the instrument. the credit risk on liquid funds is limited as the 
funds are held at banks with high credit ratings. the risk to the group of trade receivables going bad is regarded as low to medium in most regions 
due to the current Covid-19 pandemic and medium in the middle east, africa and india regions, these are described in detail in note 19.

trade receivables consist of a large number of customers in various geographical areas. Based on historical information about customer default 
rates management consider the credit quality of trade receivables that are not past due or impaired to be good.

in march the group announced the acquisition of the French distribution channel (see note 18) from the Company’s French distributor at which 
time there was a loan outstanding of £229,770 due from the distributor. this was held within ‘other loans and receivables at amortised cost’ 
which was secured against equipment which the group bought for £57,486 as part of the acquisition of the French distribution business. the loan 
repayments were linked to the sales volume of the French distributor’s nipt business. as French nipt distribution business has now been 
acquired by the yourgene group £160,696 (2019: £107,473) of this loan has been impaired under the requirements iFrS 9. at 31 march 2020 the 
loan balance relating to outstanding receivables was £11,588 (2019: £302,386), this outstanding amount been received since 31 march 2020.

the group’s maximum exposure to credit risk by class of financial assets amounts to their carrying value of £9,634,255 (2019: £4,560,333). the 
group deems that entities from whom credit exposure arises are of adequately strong credit quality and will therefore be able to pay the 
amounts due when they arise.

the group does not hold any collateral or other credit enhancements to cover this credit risk other than the equipment security stated above.

Credit quality of financial assets
as at the balance sheet date the group had a total of £3,786,895 (2019: £1,817,747) of not impaired trade receivables which were between 
0–30 days past due and £836,282 (2019: £60,646) which were more than 30 days past due. These figures exclude amounts owing that have 
been fully provisioned due to specific impairment circumstances.

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28 Share Capital and Reserves

Ordinary shares 0.1p each

Deferred shares 0.9p each

Deferred shares 9.9p each

2020

2019

2020

2019

2020

2019

at 1 april
Shares issued placing
Shares issued warrant exercise

458,999,688
157,482,517
–

321,218,279 1,039,640,244 1,039,640,244
–
96,425,244
–
41,356,165

–
–

228,163,709
–
–

228,163,709
–
–

at 31 march

616,482,205

458,999,688 1,039,640,244 1,039,640,244

228,163,709

228,163,709

nominal value at 31 march

£616,482

£459,000

£9,356,762

£9,356,762

£22,588,207

£22,588,207

all ordinary shares in issue have equal voting rights and rights to dividends or other distributions. the deferred shares rank equally in all respects 
but do not have any voting rights or rights to receive dividends or other distributions and will not have any return on capital on a winding up.

there were three share issues during the reporting period, in april 2019, may 2019 and march 2020, for a combined total of 157.5 million new 
shares.

the following describes the nature and purpose of each reserve within shareholders’ equity: 

reserve

description and purposes

Share premium account
retained losses

merger relief reserve
reverse acquisition reserve
warrants reserve
Foreign exchange translation 

amount subscribed for share capital in excess of nominal value.
Cumulative net gains and losses recognised in the consolidated income statement.
the share option expense is recognised directly through the accumulated deficit reserve.
represents a premium on the issue of the ordinary shares for the acquisition of subsidiary undertakings.
effect on equity of the reverse acquisition of premaitha limited.
equity element of thermo Fisher warrants in issue and not yet exercised.
represents cumulative foreign exchange gains and losses arising on consolidation and exchange differences 

reserve

arising on translation of foreign operations.

29 Share-based Payment Transactions 
Share options 
the group operates two equity-settled share-based remuneration schemes for employees: an HmrC-approved emi scheme and an unapproved 
scheme, jointly known as the ‘option scheme’. under the scheme employees may be granted options to purchase shares, which vest over varying 
periods up to four years and must be exercised within 10 years from the date of grant. the options are forfeited by the employee if they leave the 
Company before the options are exercised. 

the group recognised a total share-based payment charge of £1,601,746 in the period (2019: £251,004). the increased expense is primarily due 
to the group’s increased expectations of the number of shares expected to vest. 

the exercise price of options outstanding at the end of the year ranged between 7.75p and 242p and their weighted average remaining 
contractual life was 6.8 years (2019: 7.1 years). 

the weighted average fair value of each option granted during the year was 4.65p (2019: 2.13p). 

market-based options 
the Company issued options between october 2012 and march 2014 with market-based conditions attached such that they are only exercisable 
if the share price of the Company exceeds 50p per ordinary share. in august 2019 1,183,332 options had their performance conditions modified 
to be aligned with other senior incentives, the exercise price of these options remains unchanged. 

at 31 march 2020, the following market-based options were outstanding in respect of ordinary shares: 

date of grant

31 october 2012
2 January 2013
19 march 2014

Outstanding at 31 march 2020

exercise period

1 november 2012 to 1 november 2022
3 January 2013 to 3 January 2023
18 april 2014 to 19 march 2024

2020 
Number

25,558
13,681
–

39,239

2019 
number

25,558
13,681
1,183,332

1,222,571

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the following principal assumptions were used in the valuations:

Share price
exercise price
volatility
dividend yield
risk-free interest rate
expected option life

oct 2012

Jan 2013

242p
242p
108.25%
0%
1.602%
5 years

225p
225p
108.15%
0%
1.11%
5 years

mar 2014

21.5p
10p
88.97%
0%
1.969%
5 years

earnings per share options 
the Company issued options between march 2014 and march 2020 with conditions attached such that they are only exercisable if the earnings 
per share exceeds that for the financial year preceding the grant of the option.

at 31 march 2020, the following options were outstanding in respect of ordinary shares: 

date of grant

19 march 2014
6 September 2014
15 July 2015
21 october 2016
2 march 2017
30 october 2017
2 July 2018
4 october 2018
31 may 2019
29 october 2019
27 march 2020

exercise period

18 april 2014 to 19 march 2024
4 September 2016 to 5 September 2024
14 July 2017 to 14 July 2025
1 april 2018 to 26 october 2026
31 march 2019 to 1 march 2027
28 September 2018 to 29 october 2027
1 July 2019 to 30 June 2028
1 July 2019 to 30 June 2028
31 may 2019 to 30 may 2029
29 october 2019 to 28 october 2029
27 march 2020 to 26 march 2030

Outstanding at 31 march 2020

the following principal assumptions were used in the valuations: 

2020 
Number

2019 
number

1,183,332
23,124,226
4,705,000
470,000
550,000
2,755,000
19,400,000
3,000,000
10,120,000
2,500,000
500,000

–
23,500,554
4,845,000
470,000
550,000
2,855,000
19,400,000
3,000,000
–
–
–

68,307,558

54,620,554

mar 2014

Sep 2014

Jul 2015

oct 2016

mar 2017

oct 2017

Jul 2018

oct 2018

may 2019

oct 2019

mar 2020

Share price
exercise price
volatility
dividend yield
risk-free interest rate
expected option life

10p

21.5p
10p

10.75p 21.375p
20p

14.5p
14p
88.97% 51.88% 102.79% 50.07% 54.34% 38.24% 64.00% 72.75% 46.85% 32.73% 85.55%
0%
0.71% 0.36%
5 years
5 years

0%
1.97% 1.80% 0.60% 1.00% 1.34%
5 years
5 years
5 years

0%
1.26% 1.46% 0.89%
5 years
5 years
5 years

10.05p 10.875p 12.375p
12p
10.25p

9.25p 12.875p
10p

0%
1.97%
5 years

7.75p
7.75p

7.75p
10p

5 years

5 years

20p

10p

0%

0%

0%

0%

0%

0%

0%

the fair values of the options granted were determined using a variation of the Black-Scholes model, incorporating the dilutive effects of the 
options. Share price volatility is determined by calculating the historic volatility over the prior six month period. in addition, the model was 
amended for the market-based options to incorporate the probability of the 50p trigger being met, with this being done by pricing an up & in call 
option with a barrier set at 50p. the earnings per share options are estimated to have a 50% to 100% probability of meeting the earnings per 
share conditions over the required vesting periods and this was incorporated in determining the number of options expected to vest.

options and weighted average exercise prices are as follows for the reporting periods presented: 

outstanding at 1 april 2019
granted
transferred
lapsed

Outstanding at 31 march 2020

Exercisable at 31 march 2020

market-based options

earnings per share options

number

1,222,571 
–
(1,183,332)
– 

39,239

39,239

p

17
–
10
–

236

236

number

54,620,554
13,590,000
1,183,332
(1,086,328)

68,307,558

38,412,556

p

11
10
10
11

10

11

In May 2020 employees chose to exercise 6,427,565 of the above exercisable share options. 

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69

 
n ot e S to t H e C o n So l i dat ed F i n a n C i a l S tat em en t S CO N T I N U ED
FO R T H E Y E A R EN D ED 31 M A RCH 2020

29 Share-based Payment Transactions continued
Standard warrants 
the Company issued 2,822,454 warrants as part of a share placing on 4 July 2014, of which 1,411,427 expired in July 2017. the warrants have a 
conversion price of 11p per share. 

at 31 march 2020, the following options were outstanding in respect of ordinary shares: 

date of grant

4 July 2014

exercise period

2020 
Number

2019 
number

4 July 2014 to 3 July 2020 (By agreement extended by 1 year)

1,411,427

1,411,427

the fair values of the warrants granted were determined using a variation of the Black-Scholes model, incorporating the dilutive effects of the 
warrants. the following principal assumptions were used in the valuations, based on independently sourced information:

Share price
volatility
dividend yield
risk-free interest rate
expected option life

options and weighted average exercise prices are as follows for the reporting periods presented:

outstanding at 1 april 2019
expired

Outstanding at 31 march 2020

Exercisable at 31 march 2020

Standard
warrants

11p
102.62%
0%
1.779%
3 years

number of
share
options

weighted average
exercise price
p

1,411,427
–

1,411,427

1,411,427

11
–

11

11

In May 2020 the warrants over 1,411,027 ordinary shares were exercised. 

30 Thermo Fisher Scientific Loan and Warrants 
thermo Fisher 2016 & march 2017 warrants 
on 22 September 2016, the group granted two further tranches of warrants to thermo Fisher on the same terms. these are respectively the 
2016 and march 2017 warrants. 

the 2016 warrants issued by the group on 22 September 2016 are over 17,094,018 shares with an exercise price of 11.7p per share and a term of 
7.25 years. 

the march 2017 warrants issued by the group on 31 march 2017 are over 16,913,319 shares with an exercise price of 11.825p per share and a term 
of 6.75 years. 

application of iaS 32/iaS 39 
the group assessed the accounting treatment of the warrants and concluded, having considered the terms of all of the warrants, that they 
represented equity instruments. the warrants are accounted for at fair value on inception in accordance with iaS 32. February 2019 Corporate 
and commercial restructure

in February 2019 the group agreed a corporate and commercial restructure of its relationship with thermo Fisher, through its life technologies 
subsidiary. as part of the restructure, thermo Fisher exercised some of the warrants it was holding. the notional £3.8m proceeds of this warrant 
conversion were offset against outstanding loans owed by the group to thermo Fisher. the second part of the restructure was the cancellation 
of £9.4m of debt being all remaining borrowings owing to thermo Fisher, including any accrued interest. all security held by thermo Fisher 
associated with these loans was also cancelled. the third part of the restructure was a new Commercial agreement between the parties which 
gave thermo Fisher certain exclusive commercial rights in specified South east asian countries for a period of 3 years until 2022, and thermo 
Fisher entered into a lock-in deed for its converted warrant shares for the same period. under the terms of the Commercial agreement the 
group will pay a modest sales commission, once it achieves positive cash flows. this commission is capped at £6.5m. in addition, the group 
agreed to a £6.5m contingent liability as described below. Future share gains made by thermo Fisher on the converted warrants will initially lower 
the commission cap and, once that is fully satisfied, will erode the contingent liability until that is extinguished. as at 31 march 2020, the share 
price gains achieved since the warrants were exercised was £2.7m and, if sustained, the commission cap would be reduced by this amount.

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Contingent liability 
a part of the February 2019 restructure was the creation of a £6.5 million contingent liability, which is payable by the Company to thermo Fisher 
only in the event of a sale of the Company or an insolvency event. 

warrants outstanding 
at 31 march 2020, the following warrants were outstanding in respect of ordinary shares: 

date of grant

exercise period

11 december 2015
22 September 2016
31 march 2017

11 december 2015 to 10 december 2023
22 September 2016 to 10 december 2023
31 march 2017 to 10 december 2023

2020 
Number

2019 
number

20,325,204
17,094,018
16,913,319

20,325,204
17,094,018
16,913,319

the fair values of the warrants granted were determined using a variation of the Black-Scholes model, incorporating the dilutive effects of the 
warrants. the following principal assumptions were used in the valuations: 

Share price
exercise price
volatility
dividend yield
risk-free interest rate
expected option life

options and weighted average exercise prices are as follows for the reporting periods presented: 

outstanding at 1 april 2018
granted

Outstanding at 31 march 2019

granted

Outstanding & exercisable at 31 march 2020

31 Analysis of Changes in Net Cash/(Debt) 

Cash and bank balances 
thermo Fisher loan see note 21 / 30
Bank loan see note 21

Net cash / (debt)

1 april 2018
£

1,250,362 
–
(285,690)

Cash flow
£

1,513,755 
–
197,503 

964,672 

1,711,258 

exchange
movements
£

–
–
(258,272)

(258,272)

other non-cash
movements
£

–
–
(16,159)

31 march 2019
£

2,764,117 
–
(362,618)

(16,159)

2,401,499 

32 Related Party Transactions 
Key management personnel are considered to be the directors; their emoluments are disclosed in note 9. 

during the period the group was charged £71,863 (2019: £100,001) in relation to the directors’ fees and fundraising consultancy fees of  
mr. a reynolds, a director of the Company by reyco limited. at the period end £nil (2019: £nil) was due to reyco limited in respect of  
these costs. 

during the period the group was charged £30,000 (2019: £30,000) in relation to the directors’ fees of mr. n mustoe. at the period end £nil (2019: 
£7,500) was due to mr. mustoe in respect of these costs. 

during the period the group was charged £17,485 (2019: £nil) in relation to the directors’ fees of mr. J Seaton, a director of the Company by 
Seaton life Science advisors. at the period end £2,500 (2019: £nil) was due to Seaton life Science advisors in respect of these costs. 

all services were charged on an arm’s length basis. 

YOURGENE HEALTH PLC  annual report and aCC ountS 2020

71

2015
warrants

20.63p
24.6p
68%
0%
1.74%
8 years

2016
warrants

10.625p
11.7p
48.63%
0%
0.6%
7.25 years

2017
warrants

11.625p
11.825p
59%
0%
0.979%
6.75 years

number of
share options

95,688,706
41,356,165

54,332,541

–

54,332,541

weighted average
exercise price
p

13
9

17

–

17

n ot e S to t H e C o n So l i dat ed F i n a n C i a l S tat em en t S CO N T I N U ED
FO R T H E Y E A R EN D ED 31 M A RCH 2020

33 Controlling Party 
the Company does not have an ultimate controlling party. 

34 Events After the Reporting Date 
after the reporting date 1,411,427 warrants were exercised at a price of 11 pence, and 6,437,565 share options were exercised at a price of  
10 pence. the new shares issued to satisfy these exercises raised £799k for the Company. Following the issue of these new shares on 26 may 2020 
the enlarged issued share capital of the Company comprised 624,331,197 ordinary shares of 0.1p each. on 19 June 2029 an additional 470,000 
share options under the group’s existing share option scheme issued to two employees.

on 3 July 2020 the Company completed the acquisition of ex5 genomics ltd, a small uK-based research services company for an initial cash 
consideration of £275,000, with a further potential cash earn-out potential of up to £275,000. it is anticipated that this acquisition will be 
accounted for as the purchase of property, plant and equipment and an intangible asset in the form of customer relationships, as the Company 
does not deem it meets the criteria for iFrS 3 Business Combinations.

Since the reporting date, and just prior, the group has been contending with the global Covid-19 pandemic. the effects of this on the group 
have been some logistical challenges for shipments to customers and staff travel to customer locations, as well as local adjustments required to 
allow the group’s various operating sites to adapt to local lockdowns and related disruptions. Some customers have diverted resources to 
Covid-19 testing activities. overall the group has managed this turbulence effectively in an otherwise robust sector of medical diagnostic 
testing. the group has also identified commercial opportunities to support the global response to the virus through the provision of contract 
manufacturing services to a Covid-19 test manufacturer, the launch of Covid-19 testing services from its manchester site, and from the launch  
of its own Clarigenetm SarS-Cov-2 test in June 2020.

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Co m pa n y Stat em en t o F Fi n a nC i a l p o S i t i o n 
A S AT 31 M A RCH 2020

non-current assets
property, plant and equipment
right-of-use asset
investments

Current assets
trade and other receivables
deferred tax asset
Cash and cash equivalents

Current liabilities
trade and other payables
lease liabilities
other liabilities and provisions 

net current assets

non-current liabilities
lease liabilities 
other long term liabilities and provisions 

net assets

equity
Called up share capital
Share premium account
merger relief reserve
warrants reserve
retained losses

total equity

notes

2020
£

2019
£

3
6
4

5

7
6
8

6
8

211,003
2,956,495
20,302,344

108,233
–
9,562,042

23,469,842

9,670,275

15,628,787
–
350,142

10,139,715
–
13,965

15,978,929

10,153,680

1,964,581
300,511
512,554

2,777,646

711,228
–
–

711,228

13,201,283

9,442,452

2,710,123
956,324

3,666,447

–
–

–

33,004,678

19,112,727

11
12
12
12
12

32,561,452
51,179,685
12,937,797
3,069,382
(66,743,638)

32,403,969
37,971,265
10,012,644
3,069,382
(64,344,533)

33,004,678

19,112,727

the Company has taken advantage of section 408 of the Companies act 2006 and has not included its own profit and loss account in these 
statements. the Company’s loss after tax was £4,000,851 (2019: profit £6,448,783).

the financial statements were approved by the Board of directors and authorised for issue on 27 July 2020 and are signed on its behalf by:

adam reynolds 
Chairman 
Company registration no. 03971582

YOURGENE HEALTH PLC  annual report and aCC ountS 2020

73

 
 
 
 
 
 
 
 
 
 
 
 
 
Co m pa n y S tat em en t o F C H a n g e S i n e Q u i t y 
FO R T H E Y E A R EN D ED 31 M A RCH 2020

Balance at 31 march 2018

32,266,188  28,482,061 

4,085,546  10,012,644  (72,060,484)

2,785,955 

Share
capital
£

Share 
premium 
account
£

notes

warrants
reserve
£

merger 
relief reserve
£

retained
losses
£

total
£

Year ended 31 march 2019:
profit and total comprehensive profit for the year

–

–

–

Transactions with owners
issue of share capital (cash)
warrants issued
Share-based payment
Share issue expenses

Balance at 31 march 2019

Transactions with owners
issue of share capital 
issue of share capital on acquisition 
warrants issued
Share-based payment
Share issue expenses

Balance at 31 march 2020

137,781 
–
–
–

9,716,143 
–
–
(226,939)

–
(1,016,164)
–
–

–

–
–
–
–

6,448,783 

6,448,783 

–
1,016,164 
251,004 
–

9,853,924 
–
251,004 
(226,939)

32,403,969  37,971,265 

3,069,382  10,012,644  (64,344,533) 19,112,727 

11

10

132,902  14,197,534 
–
–
–
(989,114)

24,581 
–
–
–

–

–
–
–
–
–

–

(4,000,851)

(4,000,851)

–
2,925,153 
–
–
–

– 14,330,436 
2,949,734 
–
–
–
1,601,746 
1,601,746 
(989,114)
–

32,561,452  51,179,685 

3,069,382  12,937,797  (66,743,638) 33,004,678 

Year ended 31 march 2020:
loss and total comprehensive loss for the year

–

–

74

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Co m pa n y S tat em en t o F C a S H FlowS 
FO R T H E Y E A R EN D ED 31 M A RCH 2020

Cash flow from operating activities
profit (loss) for the year before tax

Adjustments for:
Finance costs
Finance income
loan payable waived
depreciation and impairment of property, plant and equipment
depreciation and impairment of right-of-use asset
loss on disposal of property, plant and equipment
(gain) / loss on revaluation of right-of-use asset
Share-based payment and warrant expense
decrease in provisions
Foreign exchange movement

movements in working capital:
(increase)/decrease in trade and other receivables
increase/(decrease) in trade and other payables

Net cash outflow from operating activities

investing activities
purchase of property, plant and equipment
purchase of subsidiaries
(investment)/reduction in short-term financial assets
interest received

Net cash used in investing activities

Financing activities
net proceeds from issue of shares
proceeds from borrowings
repayment of borrowings
repayment of lease liability obligations
interest paid

Net cash generated from financing activities

Net decrease in cash and cash equivalents
Cash and cash equivalents at beginning of year

Cash and cash equivalents at end of year

2020
£

2019
£

(4,000,851)

6,448,783

115,072
(402,982)
–
104,521
305,437
–
(26,002)
1,601,746
–
17,978

1,247,889
(357,222)
(9,389,210)
152,791
–
469
–
251,004
(780,000)
308,948

(5,089,685)
1,253,352

(3,345,347)
(1,125,573)

(6,121,414)

(6,587,468)

(207,290)
(6,339,667)
–
3,595

(6,543,362)

–
–
475,385
357,222

832,607

13,341,321
–
–
(225,296)
(115,072)

9,626,985
128,992
(3,989,254)
–
(2,002)

13,000,953

5,764,721

336,177
13,965

350,142

9,860
4,105

13,965

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n ot e S to  t H e Co m pa n y Fi n a nC i a l Stat em en t S 
FO R T H E Y E A R EN D ED 31 M A RCH 2020

1 Accounting Policies 
Company information 
yourgene Health plC (the Company), is a public limited company incorporated and domiciled in the united Kingdom. the address of its 
registered office is Citylabs 1.0 nelson Street, manchester, england, m13 9nQ 

accounting convention 
these Financial Statements were prepared in accordance with Financial reporting Standard 101 reduced disclosure Framework (FrS 101) and in 
accordance with applicable accounting standards. 

the Financial Statements have been prepared under the historical cost convention, except for those transactions recognised at fair value as 
detailed below. 

the Company has taken advantage of the following disclosure exemptions under FrS 101: 

(a)  the requirement in paragraph 38 of iaS 1 ‘presentation of Financial Statements’ to present comparative information in respect of: 

(i)  paragraph 79(a)(iv) of iaS 1; 
(ii)  paragraph 73(e) of iaS 16 ‘property, plant and equipment’.

(b)  the requirements of paragraphs 10(d), 10(f), 39(c) and 134–136 of iaS 1 ‘presentation of Financial Statements’ and the requirements of iaS 7 

‘Statement of Cash Flows’.

(c)  the requirements of paragraphs 30 and 31 of iaS 8 ‘accounting policies, Changes in accounting estimates and errors’.

(d)  the requirements of iFrS 7 ‘Financial instruments: disclosures’.

(e)  the requirements of paragraph 17 of iaS 24 ‘related party disclosures’.

(f)  the requirements in iaS 24 ‘related party disclosures’ to disclose related party transactions entered into between two or more members of 

the group, provided that any subsidiary which is a party to the transaction is wholly owned by such a member. 

the accounting policies set out below have, unless otherwise stated, been applied consistently to all periods presented in the 
financial statements. 

the principal accounting policies adopted are set out below. 

going concern 
See note 1 to the Consolidated financial statements for the group’s going concern policy.

revenue 
revenue is recognised at the fair value of the consideration received or receivable for management services provided and is shown net of vat 
and other sales related taxes. revenue is recognised when services are provided. 

property, plant and equipment 
property, plant and equipment are initially measured at cost and subsequently measured at cost or valuation, net of depreciation and any 
impairment losses. 

depreciation is provided to write off the cost, less estimated residual values, of all non-current assets, evenly over their expected useful lives.  
it is calculated at the following rates: 
leasehold land and buildings 
plant and equipment 

20% straight line 
20%–25% straight line 

non-current investments 
investments held as fixed assets are stated at cost less any provision for impairment. the investments are reviewed for impairment at the 
balance sheet date in addition to whenever events or changes in circumstances indicate that the carrying amount may not be recoverable. if the 
expected discounted future cash flow from the use of the assets and their eventual disposition is less than the carrying amount of the assets,  
an impairment loss is recognised and measured using the asset’s fair value or discounted cash flows. 

impairment of tangible and intangible assets 
property, plant and equipment are reviewed for impairment at the balance sheet date in addition to whenever events or changes in 
circumstances indicate that the carrying amount may not be recoverable. if the expected discounted future cash flow from the use of the assets 
and their eventual disposition is less than the carrying amount of the assets, an impairment loss is recognised and measured using the asset’s fair 
value or discounted cash flows. 

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Fair value measurement 
iFrS 13 establishes a single source of guidance for all fair value measurements. iFrS 13 does not change when an entity is required to use fair 
value, but rather provides guidance on how to measure fair value under iFrS when fair value is required or permitted. the resulting calculations 
under iFrS 13 affected the principles that the Company uses to assess the fair value, but the assessment of fair value under iFrS 13 has not 
materially changed the fair values recognised or disclosed. iFrS 13 mainly impacts the disclosures of the Company. it requires specific 
disclosures about fair value measurements and disclosures of fair values, some of which replace existing disclosure requirements in 
other standards. 

Cash and cash equivalents 
Cash and cash equivalents comprise cash on hand and demand deposits, together with other short-term, highly liquid investments maturing 
within 90 days from the date of acquisition that are readily convertible into known amounts of cash and which are subject to an insignificant risk 
of changes in value. 

Financial assets 
Financial assets are recognised in the Company’s Statement of Financial position when the Company becomes party to the contractual 
provisions of the instrument. 

Financial assets are classified into specified categories. the classification depends on the nature and purpose of the financial assets and is 
determined at the time of recognition. 

Financial assets are initially measured at fair value plus transaction costs, other than those classified as fair value through profit and loss,  
which are measured at fair value. 

loans and receivables 
these assets are non-derivative financial assets with fixed or determinable payments that are not quoted in an active market. they arise 
principally through the provision of goods and services to customers (trade receivables), but also incorporate other types of contractual 
monetary asset. they are measured subsequent to initial recognition at amortised cost using the effective interest rate method. 

impairment of financial assets 
Financial assets, other than those at Fvtpl, are assessed for indicators of impairment at each reporting end date. 

Financial assets are impaired (a) where there is objective evidence that, as a result of one or more events that occurred after the initial 
recognition of the financial asset, the estimated future cash flows of the investment have been affected, or (b) where there are expected credit 
losses in the next reporting period as required by iFrS 9. 

de-recognition of financial assets 
Financial assets are de-recognised only when the contractual rights to the cash flows from the asset expire, or when it transfers the financial 
asset and substantially all the risks and rewards of ownership to another entity. 

Financial liabilities 
Financial liabilities are classified as either financial liabilities at fair value through profit or loss or other financial liabilities. 

other financial liabilities 
other financial liabilities, including borrowings, are initially measured at fair value, net of transaction costs. they are subsequently measured at 
amortised cost using the effective interest method, with interest expense recognised on an effective yield basis. 

the effective interest method is a method of calculating the amortised cost of a financial liability and of allocating interest expense over the 
relevant period. the effective interest rate is the rate that exactly discounts estimated future cash payments through the expected life of the 
financial liability to the net carrying amount on initial recognition. 

de-recognition of financial liabilities 
Financial liabilities are de-recognised when, and only when, the Company’s obligations are discharged, cancelled, or they expire. 

equity instruments 
equity instruments issued by the Company are recorded as the proceeds received, net of direct issue costs. dividends payable on equity 
instruments are recognised as liabilities once they are no longer at the discretion of the Company. 

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1 Accounting Policies continued 
provisions 
provisions are recognised when the Company has a legal or constructive present obligation as a result of a past event, it is probable that the 
Company will be required to settle that obligation and a reliable estimate can be made of the amount of the obligation. 

the amount recognised as a provision is the best estimate of the consideration required to settle the present obligation at the reporting end 
date, taking into account the risks and uncertainties surrounding the obligation. 

where a provision is measured using the cash flows estimated to settle the present obligation, its carrying amount is the present value of those 
cash flows. 

when some or all of the economic benefits required to settle a provision are expected to be recovered from a third party, a receivable is 
recognised as an asset if it is virtually certain that reimbursement will be received and the amount of the receivable can be measured reliably. 

employee benefits 
the costs of short-term employee benefits are recognised as a liability and an expense, unless those costs are required to be recognised as part 
of the cost of inventories or non-current assets. 

the cost of any unused holiday entitlement is recognised in the period in which the employee’s services are received. 

termination benefits are recognised immediately as an expense when the Company is demonstrably committed to terminate the employment 
of an employee or to provide termination benefits. 

retirement benefits 
payments to defined contribution retirement benefit schemes are charged as an expense as they fall due. 

Share-based payments 
where share options are awarded to employees, the fair value of the options at the date of grant is charged to the profit and loss account over 
the vesting period. non-market vesting conditions are taken into account by adjusting the number of equity instruments expected to vest at 
each balance sheet date so that, ultimately, the cumulative amount recognised over the vesting period is based on the number of options that 
eventually vest. market vesting conditions are factored into the fair value of the options granted. as long as all other vesting conditions are 
satisfied, a charge is made irrespective of whether the market vesting conditions are satisfied. the cumulative expense is not adjusted for failure 
to achieve a market vesting condition. 

where the terms and conditions of options are modified before they vest, the increase in the fair value of the options, measured immediately 
before and after the modification, is also charged to the statement of comprehensive income over the remaining vesting period. 

where share-based options are awarded to employees of subsidiaries the charge in respect to the share-based payments is treated as a capital 
contribution and forms part of the investment in that subsidiary. 

leases 
leases are classified as finance leases whenever the terms of the lease transfer substantially all the risks and rewards of ownership to the 
lessees. the adoption of the iFrS 16 standard has resulted in the Company recognising a right-of-use asset and related lease liability in 
connection with former operating leases except for those identified as low-value or having a remaining lease term of less than 12 months. 

Foreign exchange 
the functional currency of the Company is pounds Sterling. Foreign currency transactions are translated at the rates ruling when they occurred. 
Foreign currency monetary assets and liabilities are translated at the rates of exchange ruling at the balance sheet dates. any differences are 
taken to the income statement. 

thermo Fisher Scientific concurrent loans and warrants 
on 11 december 2015, the group entered into a share warrant agreement with thermo Fisher, issuing warrants over 20,325,204 shares to 
thermo Fisher. the warrants have an exercise price of 24.6p per share, and have a term of eight years. on 22 September 2016, the group granted 
two further tranches of warrants to thermo Fisher on the same terms. these are respectively the 2016 and march 2017 warrants. the group 
assessed the accounting treatment of the warrants based on their fair values. in February 2019 thermo Fisher converted two tranches of 
warrants into ordinary shares and cancelled all remaining loans as part of a commercial and corporate restructuring as described in note 30 to the 
consolidated financial statements.

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2 Critical Accounting Estimates and Judgements 
the preparation of the Company’s Financial Statements requires the Company to make estimates and judgements that effect the application of 
policies and reported amounts. in applying these policies the directors are required to make estimates and subjective judgements that may 
affect the reported amounts of assets and liabilities at the reporting date and reported profit or loss for the period. although the directors base 
these on a combination of past experience and any other evidence that is relevant to the particular circumstance, the actual results could 
ultimately differ from those estimates. 

included in the note are accounting policies which cover areas that the directors consider require estimates and assumptions which have a 
significant risk of causing a material adjustment to the carrying amount of assets and liabilities within the next financial period. these policies 
together with references to the related notes to the Financial Statements can be found below: 

Critical judgements 
note 3 to the consolidated financial statements describes those judgements which affect the group’s consolidated accounts.  
Company-specific critical judgements are noted below.

Impairment and investments 
investments and amounts receivable from subsidiaries are held subject to impairment review. the group’s management undertakes an 
impairment review annually, or more frequently if events or changes in circumstances indicate that the carrying value may not be recoverable. 
prior year impairments have also been reviewed to assess whether the conditions for impairment remain in place or if there are sufficient grounds 
to reverse some or all of the impairments made. no impairment reversals have been deemed appropriate in the current reporting period.

Growth rates 
the value in use of the investment is calculated from cash flow projections for the relevant entity based on financial projections covering a period 
of five years plus a terminal value, assumed growth rates and discount rates relevant to the individual entity. 

Discount rates 
the pre-tax discount rate used for the purpose of impairment assessment for yourgene Health uK ltd is 13%, derived from the average 
effective interest rate calculated over the life of the thermo Fisher loan instruments, which is deemed to be a reasonable proxy for the 
weighted average cost of capital. For the Company’s investments in Yourgene Health UK Ltd (formerly Premaitha Ltd), Yourgene Health Taiwan 
(formerly yourgene Bioscience), elucigene and agX-dpni a discount rate of 13% was also used for consistency. these discount rates were 
benchmarked against externally available cost of capital data for western europe and emerging markets respectively and are deemed to be 
therefore representative. 

Cash flow assumptions 
the key assumptions for the value in use calculations are those regarding discount rates, growth rates and expected cash flows. Changes in 
revenues and expenditures are based on past experience and expectations of future growth.

in respect of the value in use of the investments in yourgene Health taiwan, the headroom compared to the carrying value of the investment is 
£28m, and remains significantly in excess of the carrying value at discount rate sensitivities of over 30%. the investment in yourgene Health uK 
ltd was fully impaired in 2018 and despite substantial growth in the year it is deemed appropriate to retain this impairment until the subsidiary 
demonstrates sustained profitability, and after the completion of a merger with delta diagnostics uK ltd which could materially affect the 
investment values carried by the Company in its uK trading affiliate.

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FO R T H E Y E A R EN D ED 31 M A RCH 2020

3 Property, Plant and Equipment 

Cost
at 31 march 2018

disposals
at 31 march 2019
additions 

At 31 march 2020

Accumulated depreciation and impairment
at 31 march 2018
Charge for the year

eliminated on disposal
at 31 march 2019
Charge for the year
eliminated on disposal

At 31 march 2020

Carrying amount
At 31 march 2020

at 31 march 2019

4 Investments 

investments in subsidiaries

movements in non-current investments 

Cost
at 1 april 2019

investment in subsidiaries 
additions 

at 31 march 2020

Carrying amount
at 31 march 2020

at 31 march 2019

leasehold land 
and buildings
£

107,523 

–
107,523 
150,308 

257,831 

53,761 
21,505 

–
75,266 
30,931 
–

106,197 

plant and 
equipment
£

525,455 

(1,254)
524,201 
20,878 

545,079 

317,723 
131,286 

(785)
448,224 
73,590 
–

521,814 

Computer 
software 
£

–

–
–
36,104 

36,104 

–
–

–
–
–
–

–

total
£

632,978 

(1,254)
631,724 
207,290 

839,014 

371,484 
152,791 

(785)
523,490 
104,521 
–

628,011 

151,634 

32,257 

23,265 

75,977 

36,104 

–

211,003 

108,234 

Current

2020
£

–

2019
£

Non-current

2020
£

2019
£

–

20,302,344

9,562,042

Shares
£

9,562,042

10,740,302

20,302,344

20,302,344

9,562,042

refer to note 18 to the consolidated financial statements for details of subsidiary entities. 

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5 Trade and Other Receivables 

trade and other receivables
vat recoverable
amounts due from subsidiary undertakings
prepayments

Current

2020
£

123,212
115,338
15,229,426
160,810

2019
£

22,647
29,634
9,871,566
215,868

15,628,787

10,139,715

amounts due from subsidiary undertakings were assessed in accordance with iFrS 9. as all entities continue to trade and to grow revenues, all 
operate in stable economic situations and none have any significant onerous contracts which might give rise to potential impairment events, it is 
deemed that there is no significant increase in credit risk and that a 12-month expected Credit losses assessment is appropriate, as defined by 
iFrS 9. expected credit losses in the next 12 months are deemed to be zero as the conditions for partial default are not deemed to be present.

6 Leases 
lease liabilities 
the Company has a number of leases for property. on adoption of iFrS 16 it recognised lease liabilities in relation to property leases which had 
previously been classified as operating leases under the principles of iaS 17 leases. the lessee’s incremental borrowing rate applied to the lease 
liabilities on 1 april 2019 was based on comparable loan interest rates in the relevant jurisdiction where the lease is operable. 

at 1 april 2019 on transition
additions
Business combinations
lease payments
interest expense
terminations and amendments
Foreign currency adjustments

At 31 march 2020

Current
non-current

At 31 march 2020

Lease liability
£

1,104,101 
2,817,382 
–
(336,014)
110,718 
(685,553)
–

3,010,634 

300,511 
2,710,123 

3,010,634 

right-of-use assets 
right-of-use assets for these property leases were measured at the amount equal to the lease liability as at the iFrS 16 adoption date. 
There were no onerous lease contracts that would have required an adjustment to the right-of-use assets at the date of initial application. 

Cost
at 1 april 2019 on transition
additions
Business combinations
transfer
terminations and amendments
Foreign currency adjustments

At 31 march 2020

Accumulated depreciation and impairment
Charge for the year
transfer
eliminated on termination and amendment
Foreign currency adjustments

At 31 march 2020

Carrying amount
At 31 march 2020

Right-of-use 
asset: property
£

1,104,101 
2,817,382 
–
–
(777,176)
–

3,144,307 

305,437 
–
(117,626)
–

187,811 

2,956,496 

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Changes to property leases after 1 april 2019 
Some of the property leases have been surrendered and others renegotiated with extended terms. the property lease restructure was 
completed in September 2019. a further uK property lease was taken out in march 2020 due to the integration and expansion of the uK business. 

7 Trade and Other Payables 

trade payables
amounts due to fellow group undertakings
accruals
Social security and other taxation
other payables

Current 

2020
£

601,861
1,181,100
128,582
32,475
20,563

1,964,581

2019
£

530,861
–
149,603
30,764
–

711,228

refer to note 21 to the consolidated financial statements for further details on the non-current liabilities. 

8 Provisions for Liabilities 

Current liabilities
acquisition – additional consideration 

non-current liabilities
acquisition – additional consideration 

For further details on the nature of provisions see note 22 of the consolidated financial statements. 

movements on provisions 

at 1 april 2019
release of provision
increase in provision 

At 31 march 2020

Non-current

2020
£

2019
£

–
–
–
–
–

–

2020
£

512,554

956,324

–
–
–
–
–

–

2019
£

–

–

acquisition 
additional 
consideration
£

–
–
1,468,878

1,468,878

9 Retirement Benefit Schemes 
defined contribution schemes 
the Company operates a defined contribution pension scheme for all qualifying employees. the assets of the scheme are held separately from 
those of the Company in an independently administered fund. 

the total costs charged to income in respect of defined contribution plans is £38,090 (2019: £19,527). 

10 Share-based Payment Transactions 
as detailed in note 29 to the consolidated financial statements the Company issues share options and warrants to both its own employees and 
employees of its subsidiary. 

11 Share Capital 
For details of share capital see note 28 of the consolidated financial statements. 

12 Reserves 
refer to note 28 to the consolidated financial statements. 

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13 Related Party Transactions 
no guarantees have been given or received. 

the Company has taken advantage of the exemption under paragraph 8(k) of FrS101 not to disclose transactions with entities that are wholly 
owned subsidiaries of yourgene Health plC. 

there are no other related party transactions other than those relating to directors that have been disclosed in note 32 to the 
consolidated statements. 

14 Controlling party 
the Company does not have an ultimate controlling party. 

15 Events After the Reporting Date 
after the reporting date 1,411,427 warrants were exercised at a price of 11 pence, and 6,437,565 share options were exercised at a price  
of 10 pence. the new shares issued to satisfy these exercises raised £799k for the Company. Following the issue of these new shares on  
26 may 2020 the enlarged issued share capital of the Company comprised 624,331,197 ordinary shares of 0.1p each. 

on 3 July 2020 the Company completed the acquisition of ex5 genomics ltd, a small uK-based research services company for an initial cash 
consideration of £275,000, with a further potential cash earn-out potential of up to £275,000. it is anticipated that this acquisition will be 
accounted for as the purchase of property, plant and equipment and an intangible asset in the form of customer relationships, as the Company 
does not deem it meets the criteria for iFrS 3 Business Combinations.

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g loSSa ry o F t e C H n i C a l t er m S a n d m e a Su r em en t S

Autosomal aneuploidies

Amniocentesis

Cystic Fibrosis (CF)

CVS 

Fetal Fraction

iFU

iVD

aneuploidy is the presence of an abnormal number of chromosomes in a cell, but not including the 
sex chromosome aneuploidies. an extra or missing chromosome is a common cause of some 
genetic disorders. Some cancer cells also have abnormal numbers of chromosomes.

an invasive diagnostics procedure that involves removing and testing a small sample of cells from 
the amniotic fluid. it is offered to pregnant women if there is a high risk that the fetus could have a 
genetic condition, it carries a small risk of miscarriage.

Cystic Fibrosis is a genetic disorder that affects mostly the lungs, but also the pancreas, liver, 
kidneys, and intestine. long-term issues include difficulty breathing and coughing up mucus as a 
result of frequent lung infections.

Chorionic villus sampling (CvS) is a prenatal test that is used to detect birth defects, genetic 
diseases, and other problems during pregnancy. during the test, a small sample of cells (called 
chorionic villi) is taken from the placenta.

Fetal fraction is the amount of the cell-free dna in the maternal blood that is of fetal origin 
compared to maternal origin. if the fetal fraction is too small a nipt screening will not produce a 
result.

instructions For use – a detailed document that explains how to use the kit within the lab for that 
intended use

‘In vitro’ diagnostic.

male Factor infertility (mFi)

inability to conceive conception after 12 months due to the presence of some genetic mutations in 
the male partner.

microdeletion

mutation

a small, missing (or ‘deleted’) piece of a chromosome is called a microdeletion. microdeletions are 
usually not inherited from a parent. Some microdeletions cause intellectual disability and birth 
defects, while others have little impact on a child’s health and life.

a mutation is a change that occurs in our dna sequence, either due to mistakes when the dna is 
copied or as the result of environmental factors.

Next Generation Sequencing (NGS)

next generation Sequencing is also known as high-throughput sequencing, is the catch-all term 
used to describe a number of different modern sequencing technologies that has revolutionised the 
study of genomics and molecular biology.

NHS

NiPT

PCR

Plasma

Precision medicine

Sex aneuploidy

Thrombosis

national Health Service in the uK.

non-invasive prenatal test.

polymerase Chain reaction.

plasma is the largest single component of blood and makes up about 55% of total blood volume. it is 
a clear, straw-coloured liquid and it carries the dna.

precision medicine is an emerging approach for disease treatment and prevention that takes into 
account individual variability in genes, environment, and lifestyle for each person. this approach will 
allow doctors and researchers to predict more accurately which treatment and prevention 
strategies for a particular disease will work in which groups of people.

Sex chromosome aneuploidies are conditions in which there is a change from the usual two copies 
of sex chromosomes in males (Xy) or females (XX). these conditions may cause mental or physical 
defects, with different levels of severity.

the formation of a blood clot inside a blood vessel, obstructing the flow of blood through the 
circulatory system.

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Co m pa n y i n Fo r m at i o n

Directors

Company Secretary and Registered Office

Nominated Adviser

Broker

independent Auditor

Solicitors

Financial PR

Bankers

Registrars

Chairman
vice Chairman
non-executive director
non-executive director
non-executive director
Chief executive officer
Chief Scientific officer
Chief Financial officer
Chief operating officer

adam reynolds
dr Stephen little
nicholas mustoe
dr John Brown CBe
Jonathan Seaton
lyn rees
dr Bill Chang
Barry Hextall
Hayden Jeffreys

Barry Hextall
Citylabs 1.0
nelson Street
manchester m13 9nQ

Cairn Financial advisers llp
Cheyne House
Crown Court
62–63 Cheapside
london eC2v 6aX

Stifel nicolaus europe limited
150 Cheapside
london eC2v 6et

Saffery Champness llp
City tower
manchester m1 4Bt

addleshaw goddard llp
one St peter’s Square
manchester m2 3de

walbrook pr ltd
4 lombard Street
london eC3v 9Hd

the royal Bank of Scotland group
Commercial Banking
1st Floor
1 Hardman Boulevard
manchester m3 3aQ

link registrars
the registry
34 Beckenham road
Beckenham
Kent Br3 4tu

Company number

03971582

Country of incorporation of Parent Company

england

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YOURGENE HEALTH PLC

Citylabs 1.0
Nelson Street
Manchester
M13 9NQ, UK

T: +44 (0) 161 669 8122
Investors@yourgene-health.com
www.yourgene-health.com