Our Genomics in Sickle Cell Research Initiative is advancing this vital work with three core objectives: Building a ...

New research has identified a novel mechanism driving osteosarcoma – an aggressive paediatric bone cancer – providing ...

The Machine Learning team use machine learning and advanced data analytics to support progress for patients and research partners. Researchers and clinicians detect conditions by using different kinds ...

We use cookies to personalise content and to analyse our traffic and improve our website.

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 ...

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 ...

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 ...

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 ...

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

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 ...