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

All analysis on the Genomics England dataset happens within a secure, cloud workspace called the Research Environment. To access the data, researchers must first apply to become a member of either the ...

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 ...

The Participant Panel is made up of a diverse group of people whose data is held in the National Genomic Research Library. Members come from different walks of life and bring their life experiences of ...

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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 ...

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 ...

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 series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, we explain the term ‘non-coding DNA’, and the important role it plays in ...