You can use the form below to sign up for email alerts about new positions as they open. Fields marked with an asterisk (*) are required. Genomics England partners with the NHS to provide whole genome ...

Genomics England’s Generation Study has now enrolled 25,000 babies - a major milestone in one of the world’s largest research ...

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 ...

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 Privacy Notice gives general information about who we are, what we do and who to contact if you want more information (such as to exercise your information rights ...

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

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 ...

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.

Our mission is to continue refining, scaling, and evolving our ability to enable others to deliver genomic healthcare and conduct genomic research.

As a group of UK and international scientific experts, our Science Advisory Committee advises us on the development and delivery of Genomics England's research programmes. This committee plays a key ...

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 ...

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.