Genomics England’s 2025 Research Summit welcomed a captivated audience to hear about the latest research and technological ...

This one-day, in-person event promises to be an exciting exploration of the latest research and technological innovations from Genomics England, its esteemed research community and members of the ...

The 100,000 Genomes Project was a British initiative to sequence and study the role our genes play in health and disease. Recruitment was completed in December 2018, although research and analysis is ...

Greater diversity is needed in genetic research to make genomics’ use in cancer care and screening more accurate and reliable for all, according to a new study.

There are thousands of potential conditions that can be tested for through genome sequencing. It was important for us to carefully consider which conditions should be looked for in the Generation ...

Adam Clatworthy, Vice Chair for Rare Conditions on the Participant Panel for Genomics England, shares the Panel's vision for ...

New research has uncovered two new genetic disorders through data from the National Genomic Research Library, providing new ...

A rare disease is defined as one that affects less than 1 in 2,000 of the general population. There are between 5,000 and 8,000 known rare diseases. In the UK, a single rare disease may affect up to ...

Genomics England holds data about each of the participants in its initiatives, including: Your medical records. A copy of this data is available through your GP. Information relating to your cancer or ...

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 ...

I'm submitting an abstract or poster to a conference ...