Every decision, every line of code and every meeting matters. Our work changes patients' lives, shapes the future of genomic research and enables the treatments of tomorrow. We're passionate about ...

Researchers have used data from the 100,000 Genomes Project to help create a “metal detector” algorithm called PRRDetect to ...

In this blog, Scientific Curator Achchuthan Shanmugasundram shares his experience of working at Genomics England and what ...

The Access Review Committee’s (ARC) role is to provide an independent examination and response to requests for access to genomic and health data held in the Genomics England National Genomic Research ...

Jessica was one of the first children to receive a diagnosis of her rare condition from the 100,000 Genomes Project. Her diagnosis means a treatment could be recommended too. She, together with each ...

One of the main aims of the 100,000 Genomes Project was to improve cancer care for NHS patients through personalised medicine. This page covers the way the project met this aim. Cancer can be ...

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 ...

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 ...

Below are the key policies and documents that govern the processes at Genomics England.

Genomes from NHS patients affected by cancer or a rare condition collected through our 100,000 Genomes Project and the NHS Genomic Medicine Service. All participants have health data collected when ...