New research has identified 20 genetic changes in a gene known to cause Marfan syndrome that could help to explain unsolved ...

The pioneering Yellow Card Biobank, launched by the Medicines and Healthcare products Regulatory Agency (MHRA) and Genomics ...

Genomics England will help deliver the 10 Year Health Plan through our digital systems and by generating the evidence to ...

New research has uncovered 2 neurodevelopmental disorders using data from the National Genomic Research Library. These ...

The Genomics England Research Network is a collaborative initiative, offering members opportunities to share and leverage expertise and resources, with the academic researchers, healthcare ...

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

Human genomes are 99.9% identical; however, it's differences in the 0.1% which make each of us unique – whether in terms of our hair colour, our like/dislike of certain foods, and even our sleeping ...

Genomic medicine uses insights from a human's complete set of DNA (called a genome) to inform their healthcare. But because people are very different, studying a genome by itself can't tell you very ...

The Research Environment allows researchers to access one of the largest and most comprehensive genomic datasets for rare conditions and cancer. Researchers can analyse whole genome sequencing data, ...

A survey of over 2000 British adults conducted by the Genetics Society found that trust in genetics is high and went up significantly during the pandemic. In this episode of the G Word our Head of ...

Aside from whole genome sequencing translating to better patient care, the de-identified DNA and health data from the 100,000 Genomes Project is also being used for scientific research. Approved ...

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 ...