Blog articles

Looking back: Genomics in 2022 (part one)
In the first of our two-part round-up of 2022, we look back at some of this year's most exciting clinical developments in genomics

How accurate are genomic tests?
We outline five key things to consider when answering the common patient question, “How accurate is this genomic test?”

Reducing stroke risk with a genetic test
NHS Tayside introduces the UK's first routine genetic test for stroke patients, estimated to bring improved outcomes to thousands of patients each year

Detecting cancer predisposition: Finding the balance
This week, we weigh up the potential advantages and challenges of wider genomic testing for identifying cancer

The Genomics Conversation: What matters to patients
The GEP recently met with patients and their relatives to talk about their experiences of genomic testing and the key insights they want healthcare professionals to know

Rapid genomic test helps prevent newborn hearing loss
We look at how rapid pharmacogenomic testing is helping save the hearing – and lives – of newborn babies

Polygenic scores and PGT: a problematic pairing
We explore a new type of test hitting the headlines and ask whether it could ever be approved for UK clinics
News articles

The #GenomicsConversation 2023 is coming
Is genomics hidden for you? Join us in June as we uncover the many ways genomics is shaping patient care

Genomics in the NHS: A clinician’s guide to genomic testing for rare disease
Join our new two-week online course for a practical guide to the genomic testing process for rare disease

Learn and share: join our course evaluation panel
Be one of the first to complete and review our new online course for clinicians unfamiliar with requesting genomic testing

Explore genomics in health visiting
Health visitors can start or continue their genomics learning…
Events

Next Steps for Genomics in the UK
This conference will discuss the next steps for genomics in the UK.