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Duration

One year, part-time

Application Deadline

24 August 2025

Location

Online

Start dates

September 2025

Study our flexible online course to gain the foundational skills for a career in genomic medicine. 

Every individual is unique – our genomes and the way they respond to disease is different. By understanding what’s going on in our bodies, we can work towards a future where healthcare is personalised, and patients' needs are targeted more effectively. Genomics is evolving rapidly and making an impact across numerous disciplines.

This course follows a curriculum designed by NHS England and provides a foundation in human genomics and variant interpretation, and the role of genomics in cardiovascular and neurological disorders.

Is this course right for you?

Our online PgCert is the perfect option for anyone interested or involved in Genomic Medicine including researchers, healthcare professionals, or biomedical scientists, that are looking for a flexible training course. You’ll study four modules that will provide the foundational skills for a career in genomics. You can also study on a modular basis towards your Professional Development (CPD).

Funding update: If you work for the NHS then you may be eligible for funding from NHS England for up to four taught modules. Applications for NHSE funding are now closed - please register your interest to be notified when more NHSE funding is released.

Why St George's?

  • NHSE preferred provider – As well as extensive links with healthcare providers across London, we are also contracted as an NHSE preferred provider for this course.

  • Flexibility – Develop your skills with flexible study around existing commitments and join a global community of students.

  • Global expertise – You’ll be taught by expert lecturers with a global reputation in drug discovery and genomic testing and gain an internationally recognised qualification.

Want to know more?

Find out more about postgraduate study at St George’s, University of London by registering for our introductory email series.

Course content

You’ll learn how to interpret genomic data and how genomic data can be integrated into mainstream practice for the diagnosis of diseases such as neurological and cardiovascular disorders.

You’ll complete four modules:

  • Fundamentals of Human Genetics and Genomics
  • Genomics of Common and Rare Inherited Diseases
  • Variant Interpretation
  • Genomics of Cardiovascular Disorders or Genomics of Neurological Disorders

All modules can also be studied on a modular basis towards your Professional Development (CPD).

Interpret genomic data

You’ll look at the role of genetics in disease and how genomic information can explain disease mechanisms and biology. We’ll also share examples of both common and rare diseases from across the entire healthcare spectrum to demonstrate how to interpret genomic data.

Course structure

The online Genomic Medicine PgCert runs part-time over one year. Students are required to complete four taught modules worth 15 credits each, to a total of 60 credits. Three of the modules are compulsory, with the final module chosen from two optional modules.

Core mandatory modules (15 credits):

  • Fundamentals of Human Genetics and Genomics (term 1)
  • Genomics of Common and Rare Inherited Diseases (term 2)
  • Variant Interpretation (term 2)

Optional modules (15 credits) choosing one from the below:

  • Genomics of Cardiovascular Disorders (term 2)
  • Genomics of Neurological Disorders (term 2)

Modules run consecutively. Once a module opens, you will have ten weeks to complete it including the assessment. Completed module content will be available for you until the end of the course.

You will study on average 15 hours per week, which includes self-directed learning and preparing for assessments alongside learning materials. Depending on your level of genetics knowledge, you may need to spend less time, particularly for the fundamentals module.

2025/26 timetable (PDF)

Our modules can also be studied individually as part of Continuous Professional Development (CPD). View the above timetable for module running dates, and the apply tab for information on application deadlines and how to apply. 

You can choose to upgrade the online PgCert to the in-person PgDip or MSc Genomic Medicine following successful completion of the course.

Modules

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Fundamentals of Human Genetics and Genomics (15 credits)

Students undertaking this module will review the architecture of the human genome and the functional units embedded in it. Students will also cover aspects of gene regulation and chromatin structure and consider the importance of the epigenome. In addition, this module will cover DNA sequence variation and structural variation, exploring how this variation is “normal” but that sometimes it can be associated with disease. Students will learn about monogenic and multifactorial genetic disorders and the most appropriate methods for identifying causal and contributory variants. Students will also learn about some of the most common chromosomal abnormalities and the methods for detecting these in the laboratory. In essence, this module covers what the genome is, what variants can arise and how they arise, how best to identify these variants and what the clinical implications of these variants may be. 

This module is assessed with a 15 - 25 minute pre-recorded PowerPoint presentation of a case analysis. 

Genomics of Common and Rare Inherited Diseases (15 credits)

This module will initially explore the clinical presentation, diagnosis, management and treatment of a range of common and rare inherited diseases. The principles and practice of medical genetics and genomics, and the management and treatment of patients and their families will be discussed. In addition, the role of genomics in a care pathway will be examined, including the patient and family perspective. This module will explore the traditional and current approaches used to identify genes responsible for common and rare inherited diseases, focusing on the latter. Students will explore the analytical challenges in genomics, as applied to rare inherited diseases. The module will also cover key initiatives such as the development of genomic medicine services and the infrastructure supporting incorporation of genomic testing into the NHS. 

This module is assessed with an analysis of rare and common disease cases involving exome sequencing data.

Variant Interpretation (15 credits)

This module will explore the genomic variants among individuals and populations, benign, pathological or of unknown significance, and the tools used by healthcare professionals to identify and interpret these and inform patient care. Students will cover tools used in variant interpretation, such as population databases, in silico analysis, functional data and phenotyping. Also introduced will be the national/international guidelines for genomic variant interpretation, and how variants are classified/weighted along these frameworks based on the tools learnt within the module.

Beginning with an introduction to the identification of variants using next generation sequencing, students will cover genomic transcript nomenclature, classification under recognised guidelines, and patient case studies. This will be followed by coverage of a range of clinically employed variant interpretation tools, the ethics of variant interpretation, and end with applying these in the context of ACMG/ACGS frameworks, including pathogenicity, population analysis, as well as predictive, functional and segregational data. Brought together, this module will prepare students for understanding and applying variant interpretation in a clinical setting.

This module is assessed with a Multidisciplinary Team Discussion (MDT) simulation.

Genomics of Cardiovascular Disorders (15 credits)

This module explores the burden of cardiovascular disease and the underlying contribution of genetics to these diseases. Students will receive refresher sessions focused on cardiac function as well as being introduced to the key diagnostic tools used in cardiology. They will learn about the major arrhythmias and cardiomyopathies, which can lead to premature and sudden death. By studying genetic causes of lipid disorders students will understand the impact of rare and common genetic variants on the risk of coronary heart disease. The contribution of "big data" in disease diagnosis and the development of novel drugs will be discussed to demonstrate some of the benefits that genomics can offer to this group of diseases. Students will hear about the role and challenges of genetic counselling in inherited cardiac conditions. 

This module is assessed with a 2000 - 2500 word scenario-based essay.

Genomics of Neurological Disorders (15 credits)

This module explores the contribution of genomics to neurological disorders. Students will receive refresher sessions focussed on neuroanatomy and the development of the neurological system followed by an introduction to the key diagnostic tools used in neurology. They will learn about the major neurological disorder categories which have a high genetic contribution. The module will explore the value of the multidisciplinary team in phenotyping, interpretation of results, management and family communication. 

This module is assessed with a 1500 - 2000 word scenario-based essay.

Entry criteria

To be considered for this course, you will need to:

  • meet the entry criteria
  • write a personal statement
  • provide two suitable references

Undergraduate degree or equivalent

You should have or be expected to achieve, a minimum of a second class degree (2:2) in a relevant bioscience degree with sufficient genetics content. For healthcare graduates, a pass is required. All degrees must be awarded before 1 August on the year of entry.

We may invite you to interview if are unable to make a decision directly from your application.

Alternative professional qualifications, or previous related experience, may be considered and we encourage you to apply.

Intercalating students

Applicants who do not have an undergraduate degree but are current medical students who have successfully completed 360 credits (or equivalent) including at least 120 credits at Level 6 (or equivalent) of their medical degree are also eligible to apply. 

International qualifications

We accept equivalent qualifications gained in other countries and use UKNARIC to assess international qualifications. Please see our International Student Support pages for more information.

If you have any questions, you can contact us at study@sgul.ac.uk

English Language

This is a Group 1 course.

Full details can be found on our English Language requirements webpages.

Personal statement and references

You will be asked to outline your reasons for applying for the course in a brief personal statement on the application form. You will also need to provide two satisfactory references.

Go to the ‘Apply’ tab for more information.

Teaching and learning

We are dedicated to delivering a world-class learning experience designed for today’s global audience. Our online Genomic Medicine PgCert combines flexibility, engagement, and cutting-edge technology to ensure students around the world can access high-quality education.

You will study on average 15 hours per week, which includes self-directed learning and preparing for assessments alongside learning materials. Depending on your level of genetics knowledge, you may need to spend less time, particularly for the fundamentals module.

Flexible scheduling

We understand the challenges of studying alongside other commitments in your life and we are excited to welcome a global audience as well. To accommodate our students, we offer a combination of synchronous (live) and asynchronous sessions (recorded sessions and many other directed-learning activities). The vast majority (at least 90%) of learning will be asynchronous meaning that you can complete the work at a time that suits you. Live classes are scheduled to accommodate students from diverse regions, including the Americas, Asia, Africa, and beyond.

Each module will include five live sessions set at the following suggested times 08.00, 11.00, 13.00, 16.00 and 17.00 (GMT/GMT+1). For those who cannot attend live, all sessions are recorded and made available for review at your convenience.

Self-paced learning

Modules will be designed with a clear study planner allowing you to progress at your own pace through the learning material. You will be able to see when there is an assignment coming up, allowing you to plan and manage your schedule. Miss a live session? No problem. Our platform ensures all course materials are accessible 24/7. This allows you to revisit lessons, catch up on missed classes, and study at a pace that suits you.

Interactive and engaging activities

Our online Genomic Medicine PgCert modules include a range of activities such as:

  • Scenario-based assignments allowing you to apply what you’ve learned;
  • Quizzes with in-built feedback to test your knowledge;
  • Peer-to-peer discussion and group work to foster collaboration;
  • Expert webinars and careers talks;
  • Practical assessments that mirror real-world challenges.

Networking opportunities

When you join the course, you become part of an extensive learning community. You’ll connect with students and professionals from diverse backgrounds, creating opportunities for cross-cultural exchange, inter-professional learning and networking that extend beyond the course.

Assessment

The way we assess your learning will change depending on the module but we use a variety of assessment methods, so every student has a chance to show their knowledge and strengths. You can expect a mixture of:

  • Pre-recorded presentation (case analysis)
  • Analysis of rare and common disease cases involving exome sequencing data
  • Multidisciplinary team discussion (MDT) simulation
  • Scenario based essays

Your assessments will be formative and summative. This means some won’t count towards your final grade and you’ll have the chance to improve based on our feedback.

As this is a modular course there is no final exam. Instead, each module has one online assessment.

MOOCs

To support your learning outside of classes we’ve created three non-assessed Massive Online Open Courses (MOOCs). In preparation for our course, we recommend our students take The Genomics Era: The Future of Genetics in Medicine as it provides a basic grounding in genomics.

The course also offers training and resources on academic and research skills including refreshers in laboratory techniques and academic support for assessments.

Student support

From day one, you’ll become part of a community of staff and students of different ages, ethnicities, nationalities and backgrounds. Everyone you meet will have one thing in common – a passion for healthcare, science and medicine.

Whether you’re an existing healthcare professional, returning to education after a break or joining us after graduating from an undergraduate degree, we want to help you make the most of your time here. To do this, we offer a full range of academic support and student services.

Careers service

We offer 1:1 career guidance to undergraduate and postgraduate students at every stage of your professional development, from the start of your course through to graduation and beyond. As a student, you’ll also benefit from career development activities that are specifically tailored to your course.

What we offer:

  • Career guidance: We offer 30-minute 1:1 careers guidance sessions to support you in your career planning, build your confidence, and help you identify next steps on your career journey.
  • CV and application advice: We can review your applications with you, support you in presenting yourself to potential employers, tailor your applications to a particular role and help you stand out from your competition.
  • Practice interviews: Work on the content, structure, and delivery of your answers, whether that’s motivation questions, competency questions, role-specific questions or Maximum Medical Improvement (MMI).
  • Interactive workshops: Our career education workshops are tailored and delivered within courses. Topics may include understanding the graduate job market, learning through reflection on career decision-making, making successful applications and making an impact at interviews.
  • Careers fairs: These are opportunities to explore career paths in different areas and specialities, meet with employers, and have valuable conversations to inform your career thinking.
  • Online support: We offer specific information tailored to each course, plus general careers support and resources relevant to whatever your career choices and direction via our Canvas Virtual Learning Environment.

Disability support

If you require reasonable adjustments or disability services, you can find information on our disability information for students pages. For any further information please contact the disability adviser.

Mental health support

St George’s has a confidential, free and impartial counselling service available to all students. You can also access services through our Student Life Centre and our online resources. This includes links to NHS resources, apps, podcasts and websites dedicated to mental health and wellbeing.

Personal academic tutor

When you start your course, we’ll allocate you a personal tutor. This is a member of the academic team who you’ll see regularly to monitor your progress and pick up any problems, both academic and personal. Even if they don’t have the answer, they’ll point you in the right direction towards the support you need.

Students with children

Juggling study and parenthood can be difficult, particularly if you’re taking a demanding medical or healthcare degree. Our Student Parents and Carers Empowered (SPACE) society is a group run by studying parents that meets monthly to support each other and discuss how to balance family life with studying. For more information, email the SPACE society.

Student Life Centre

Our Student Life Centre team can help you with every aspect of student life including:

  • Finances
  • Accommodation
  • Exams and assessment
  • Academic procedures
  • Admissions
  • Disability and wellbeing
  • Confidential counselling service

Your personal tutor can also signpost you to relevant support.

Students’ Union

St George's Students' Union (SU) is an independent organisation run by students for students. While many of their societies and events take place in person, the team also provides welfare support for all students, with an open-door policy.

Study+

We’re here to help you develop the academic skills you need to succeed and make the most of our library collections.

  • Sessions and tutorials on literature searches, keyword searches and using databases
  • Training materials for academic planning, reading and writing to develop key transferable skills
  • 1:1 meetings for a tailored approach to your academic support needs

Careers

Genomics is an area of rapid change. This course will upskill healthcare workers so they can apply and understand the relevance of genomic medicine to their work and enhance their career opportunities.

The course will also provide relevant knowledge and understanding applicable to careers in the pharmaceutical industry and academia.

Students can choose to upgrade the online PgCert to the in-person PgDip or MSc Genomic Medicine following successful completion of the course.

Fees and funding

In this tab you will find the financial information for this course of study, including details of financial support.

Tuition fees

2025 entry

  • PgCert: £4,500
  • Standalone Genomic Medicine module: £1,400

Additional costs

We do not expect students to incur any extra costs over and above those that we have advertised on the course page. To get the most from your studies, you will need your personal computer or laptop (Windows 10 or macOS) and an internet connection in your home. Find out more about technology requirements associated with online learning.

Funding

If you work for the NHS then you may be eligible for funding from NHS England for up to four taught modules. Applications for NHSE funding are now closed - please register your interest to be notified when more NHSE funding is released.

If you have any questions related to funding applications, please liaise with Dr George Wardley or visit the Genomics Education Programme website for more information.

How to apply

Before beginning your application please check the entry criteria of the course you wish to study to ensure you meet the required standards.

If you work for the NHS and wish to be considered for NHSE funding, please make this clear on your application.

Guidance on submitting an application can be found on our how to apply webpage.

Access our online application system

Select the relevant application link and create an account:

  1. Once you have created your account, you will be able to complete an application form and upload any relevant documents. You can save a partly completed form and return to it later. Please make sure you complete all sections. Please make sure that the information you provide is accurate, including the options you select in menus.
  2. Add pgadmissions@sgul.ac.uk to your address book to ensure you do not miss any important emails from us.
  3. When you have checked that your application is complete and accurate, click ‘submit’.

You can track your application through your online account.

If you are applying to study a module please note the following:

Applications for all modules close one month before the module start date.

If you wish to do more than one module, please use the application link for the module which occurs first.  Please state in your personal statement exactly which modules you wish to do.  

Current students on a Genomic Medicine standalone module at St George's should contact genomics@sgul.ac.uk to enquire into studying further modules. Please do not use the above links.

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Guidance for completing your references

When completing your application, you will be asked to provide contact details of two referees. Please ensure these details are accurate. As soon as you have submitted your application, your referees will be contacted by the university asking them to upload a reference to your online application.

One must be a recent academic reference. The other should be either a second academic reference or a professional/employer reference. They should cover your suitability for the course and your academic ability.

Your referees should know you well enough, in an official capacity, to write about you and your suitability for higher education. We do not accept references from family, friends, partners, ex-partners or yourself.

We will send reminder emails to your referees but it is your responsibility to ensure that contact details are correct and referees are available to submit a reference. References should be uploaded within two weeks of making your application.

Find out more about our outstanding faculty of academics and clinicians.

Course director and admissions tutor

Dr Kate Everett

Reader in Human Genetics at St George’s, University of London

Dr Kate Everett read Biology at the University of York before moving to Cambridge University to pursue an MPhil in Biological Anthropology. After a year working in industry, she started her PhD at Cambridge University, funded by Cancer Research UK. The aim of this work was to elucidate the genetic basis of cutaneous malignant melanoma by using melanocytic naevi as a proxy risk measure. This was followed by a move to UCL where she stayed for 7 years before moving to St George's in 2010. Dr Everett's research now focuses primarily on neurogenetics, with an emphasis on identifying the genetic cause of neurodevelopmental disorders.

Since joining St George's in 2010, she has established research links with the clinical genetics team at St George's University Hospital NHS Trust. Her education portfolio spans many undergraduate and postgraduate courses at St George's. She has been involved in the in-person MSc Genomic Medicine since it's inception in 2015 and is currently Deputy head of the Graduate School with oversight of all taught postgraduate programmes at the Tooting campus.

Deputy course director

Dr Clara Cieza-Borrella

Senior Lecturer in Molecular Biology at St George’s, University of London

Dr Clara Cieza-Borrella is Senior Lecturer in Molecular Biology and Principal Investigator of the Prostate Cancer Biology Lab at St George's, University of London.

She graduated from University of Salamanca (Spain) with BSc Biology to later complete her master’s in Clinic and Biology of Cancer at the Centro de Investigacion del Cancer (Salamanca). She obtained her PhD in Molecular Medicine at the University of Salamanca and moved to London to carry out her postdoctoral studies on prostate cancer genetics at the Institute of Cancer Research (ICR, London). During her time there, Clara specialised in the functional validation of novel genes and variants in prostate cancer and novel technologies.

In 2019, Clara moved to St George's where she started to get involved in the St George's Genomic Medicine course, and since 2021 has been the course director of the in-person Genomic Medicine MSc.

Clara is also involved in public engagement, especially addressed to children and youth groups as part of her UK STEM Ambassador role.

Talk to Clara about: Genomic medicine, Cancer genetics, 3D Cell culture models, Targeted therapies, Liquid biopsies, Genome editing, and public engagement.

Apply now

Duration

One year, part-time

Application Deadline

24 August 2025

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