Genomics England analyses sequenced genomes for the NHS and then equips researchers to use data to help find the cause of disease.

Who we are and what we do at Genomics England, from our origin to the current mission and beyond.

Through our secure Research Environment, approved researchers can access and analyse data in the National Genomic Research Library (NGRL). The NGRL is a repository of genomic and …

A world-first study using data on the 100,000 Genomes Project, and published in the New England Journal of Medicine, has demonstrated for the first time that whole genome …

Anyone who is offered whole genome sequencing as part of their care in the NHS Genomic Medicine Service (GMS) is asked to consent to having their genome sequence and health …

Jul 31, 2024 · The Generation Study will be testing babies for changes in genes linked to more than 200 rare genetic conditions. These all meet a set of four principles that have guided our …

If you're a patient of the NHS Genomic Medicine Service, you may be offered whole genome sequencing as part of your clinical care.You will be asked if you want to donate genome …

The UK has often led the world in scientific breakthroughs and DNA was no exception. Crick and Watson won the Nobel Prize for discovering the double helix structure of DNA.

Today (2 October 2023), Genomics England have published an initial list of over 200 rare conditions that will be looked for as part of its world-leading Generation Study, which aims to …

We're working in partnership with NHS England and the NHS Genomic Medicine Service to develop a personalised and predictive healthcare solution through the use of genomics. Your …