All analysis on the Genomics England dataset happens within a secure, cloud workspace called the Research Environment. To access the data, researchers must first apply to become a member of either the ...

Genomics England's very first initiative – sequencing 100,000 genomes from around 85,000 NHS patients affected by rare disease or cancer – is leading to groundbreaking insights and continued findings ...

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 ...

We have developed a machine learning tool for scanning large volumes of scientific literature to find reports of gene-disease ...

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 ...

Our vision is that all patients, regardless of their background, receive the same quality of genomics-enabled personalised medicine, supported by the latest research on people like them.

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 ...

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 ...

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 ...

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 Participant Panel is made up of a diverse group of people whose data is held in the National Genomic Research Library. Members come from different walks of life and bring their life experiences of ...