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 ...

Every year hundreds of babies are born in the UK with rare genetic conditions. Early intervention can enhance the health and quality of life of many of these babies. But these conditions can be hard ...

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 ...

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 ...

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 ...

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

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 ...

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 ...

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 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 ...

In this series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, we explain the term ...

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.