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

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 ...

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.

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 ...

Genomics England's very first initiative – sequencing 100,000 genomes from around 85,000 NHS patients affected by rare disease or cancer – is leading to groundbreaking insights and continued findings ...

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 ...

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