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Genomics Conversation Week 2025 - Day 4

The theme for Day 4 of Genomics Conversation Week 2025 is 'Creating connections with the genomics community'. This article should hopefully support you to build links with genomics advisers / champions and networks, to support you further in making genomic medicine a central part of your role.

Genomic testing has increased considerably across the NHS since the NHS Genomic Medicine Service (GMS) launched in 2018.

Nationally, the NHS GMS currently delivers over 850,000 tests per year and, by 2028/29, this is expected to rise exponentially to over 2 million tests per year. From 2035, it is predicted that genomics will be part of up to 50% of all healthcare episodes/interventions.

With this increase in genomic testing comes the need to embed and mainstream genomic medicine outside of specialist clinical genetics services, within pathways and services across primary and secondary care.

Despite this, confidence in genomics among healthcare staff outside of clinical genetics services is generally low-to-moderate and varies across specialties and areas of the country. Many national surveys of healthcare professionals report high perceived importance of genomics but substantially lower confidence to order, interpret, and act on tests — especially among nurses, midwives, primary care staff and other non-genetics specialties.

Surveys of Oncology trainees and consultants have shown just 3 in 10 report having “good” knowledge of newer genetic testing technologies, whilst profession-specific surveys of pharmacists, paediatricians, midwives, nurses, GPs and clinical scientists have also identified gaps between intended and expected use and confidence/knowledge to deliver genomic medicine. Low confidence has been reported in terms of the use of genomic tests (which tests, how often, clinical contexts) and also in identifying appropriate patients, consenting, ordering tests, interpreting reports, communicating results, and using results in management.

Non-genetics specialists have also reported, through national surveys, that they want accessible decision support and local genomic MDT input.

Connecting you with the genomic community

The good news is that there are a range of networks, communities of practice, genetics clinics and multidisciplinary teams (MDTs) around the country who are providing education and training, peer support and upskilling, and supporting colleagues with genomic referrals and onward management. Below we have provided a snapshot of some of these groups across England to signpost anyone wanting to connect with the genomics community.

National genomics communities

Regional Clinical Genetics Services

Regional Clinical Genetics Services deliver speciality clinics and form part of multidisciplinary teams (MDTs) across a range of cancers and rare and inherited diseases. Many Clinical Genetics Services list the clinics they run, and include details on their Trust website (an example being Nottingham University Hospitals (opens in a new tab)). You can contact your regional Clinical Genetics service to find out more about the clinics and MDTs they run, and how to refer patients and bring cases for advice and support. You can find your regional Clinical Genetics Service here (opens in a new tab).

The Genomic Medicine Service (GMS)

The Genomic Medicine Service (GMS) host eight NHS Genomic Networks of Excellence to develop the evidence and model of adoption for cutting edge genomic advances and technology applications that will be transformative for patients. The NHS Genomic Networks of Excellence are designed to be partnerships between the NHS, academia, the third sector and industry to leverage expertise and resources from the broader genomics ecosystem, and to ensure there is a route towards rapid informing commissioning decisions. The eight GNoE are:

The GMS also monthly Lunch and Learn sessions on a range of genomics topics. Previous sessions have focussed on family history taking, genomics red flags in pregnancy and newborn screening. You can find more information on future session, including registrations and recordings of previous sessions, here.

Genomics England

Genomics England host Research Network Communities (opens in a new tab) to help research-active staff to collaborate with fellow researchers, share skills and expertise, and learn about the latest developments and opportunities in the community. You can find out more here. (opens in a new tab)

Medics for Rare Diseases

Medics for Rare Diseases have an Ambassadors programme (opens in a new tab) to work with the wider rare disease community to inform projects, identify teaching opportunities and spread the word about events and opportunities for medics.

The British Society for Genetic Medicine (BSGM)

The British Society for Genetic Medicine (BSGM) provides a forum for professionals involved in genetics and genomics as a clinical service and research. As an umbrella organisation, their membership includes a wide spectrum of clinical, laboratory and research disciplines, not only in specialist genetic services but throughout the health professions. Find out more about the benefits of joining here. (opens in a new tab)

Regional Genomics communities

NHS GMS map
The 7 regional Genomic Medicine Services across England (with East Highlighted)
East region

NHS East Genomics run a number of networks to bring Trust staff together to hear updates on genomics as it applies in their roles and services:

North West

A comprehensive range of education and training resources, developed with and by healthcare professionals, can be found here (opens in a new tab).

The North West GMS Workforce Education and Training team work collaboratively to support the integration of genomics into everyday clinical practice through tailored learning opportunities. Resources are available by area of condition or practice. In addition, links to the Workforce, Training & Education Directorate of NHS England, and the Genomic Education Programme (GEP) are provided, alongside examples of collaborative initiatives.

South East
  • Nursing & Midwifery Ambassador Network. If you are a nurse or midwife working in the Southeast with an interest in genomic medicine, join our Ambassador Network. Find out more here: Genomic Ambassador Network - South East Genomics. (opens in a new tab)
  • Nursing & Midwifery Genomic Research Forum. Are you a nurse or midwife carrying out genomic or genetic research in the Southeast? Contact Tootie Bueser to find out more: tootie.bueser@nhs.net
  • Professional Network for Pharmacy professionals. If you are a pharmacy professional in the Southeast, join our network of over 120 members from every provider Trust and ICB across the Southeast to keep up to date with pharmacogenomics news and developments. Contact Lucy Galloway to find out more: Lucy.Galloway@stgeorges.nhs.uk
  • Professional Network to bring together research and work to tackle health inequalities in genomic medicine. Contact Dr Shwetha Ramachandrappa to learn more: shwetha.ramachandrappa@nhs.net
  • Renal Genomics Community of Practice. If you are a healthcare professional working in Renal Medicine and interested in finding out more, follow the link: Renal Community of Practice - South East Genomics (opens in a new tab)
South West
  • Cancer Genomics Improvement Programme. This a collaboration between the SW GMS, the two SW Pathology Networks and the two SW Cancer Alliances. We are working to make cancer genomics available to all cancer patients who will benefit, in a timely way that supports clinical team across the SW. An important part of this is to support local pathology teams in their vital role of processing cancer samples for genomic testing and integrating genomic results into cancer care through local MDTs.
  • CTDNA (Cancer Educational Genomics Tumour Board (Cancer GTEB)). Genomic testing is now standard of care in a cancer diagnosis. The cancer multidisciplinary teams (MDT) are receiving more complex information to decide on an individual patient’s optimal treatment. Clinicians from the South West are invited to join weekly meetings to share and discuss molecular reports, both from tissue and liquid biopsies. The meeting brings together our clinical scientist team from the South West GLH with clinical genetics expertise and the clinical team caring for their patients. Our aim is to provide a forum to learn together as a team in the increasing complex world of molecular testing.
  • R208 & R210 Colleague Network. The R210 (Lynch syndrome) and R208/R444 (breast cancer) networks bring together staff who offer genomic testing in mainstream cancer care. Initially monthly meetings supported teams in setting up local test pathways and forming supportive networks. Now, with these services well established, the meetings provide a quarterly opportunity for networking, CPD and key updates on genomic testing. New members are warmly welcomed.

Connect with your regional Genomics Medicine Service

You can find out more about opportunities to create connections with the genomics community, including education, training, events and networks available to join, via the seven regional Genomic Medicine Service mailing lists:

Genomics Conversation Week 2025