Almost 90% of people would agree to genetic testing to tailor medication… New research shows almost 90% of people in England would agree to genetic testing to get the most effective medication and ...

New research using data from the 100,000 Genomes Project has identified a genetic change that drives osteosarcoma, an ...

This short video explains what the Genomics England Research Environment is, how genomic data is de-identified and added to the Research Environment, and how researchers can access this de-identified ...

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. Genomic medicine uses ...

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 ...

The data we collect is stored in the National Genomic Research Library, a platform built by us and NHS England that allows approved researchers to access samples, genomic data, and other associated ...

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 ...

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

Genomic medicine is already helping more people receive answers about their health conditions through better diagnosis, treatment, and support. By volunteering to take part in research, you'll be ...

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. The NHS Genomic Medicine ...

Watch this video on Jessica – one of the first children to be diagnosed in the 100,000 Genomes Project – and how genomic medicine narrowed her diagnosis from 6.4 million possible variants to one.