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Genomic medicine is already helping more people receive answers about their health conditions through better diagnosis, treatment, and support. By volunteering to take part in research, you'll be ...

The Generation Study is a research initiative aiming to explore the use of whole genome sequencing in newborns, to screen for more than 200 rare genetic conditions. This study will recruit 100,000 ...

You can use the form below to sign up for email alerts about new positions as they open. Genomics England partners with the NHS to provide whole genome sequencing diagnostics. We also equip ...

Genomics England is part of a nationwide team of universities, hospitals and industry led by the Francis Crick Institute ...

Genomics England began as a vessel to execute the UK Government's bold plan to sequence 100,000 whole genomes and incorporate genomic medicine into routine care in the NHS, a feat we achieved in 2018 ...

Hundreds of babies have begun to be tested for over 200 rare genetic conditions as part of a world-leading study in NHS ...

In this explainer episode, we’ve asked Amanda Pichini, Clinical Director at Genomics England and Genetic Counsellor, to explain which healthcare professionals you may come into contact with in your ...

This month Genomics England is marking Sickle Cell Awareness Month, which aims to bring greater visibility of the genetic condition and those affected by it.