New research published in Genetics in Medicine and led by Genomics England researchers sets out an effective framework for using genomic newborn screening to identify genetic changes linked to rare ...

Job Description Build, develop and manage detailed economic models based on theories of change to explain and understand GELs benefit across ...

Working in collaboration with researchers and the NHS, our Diverse Data initiative aims to tackle healthcare inequality and ensure the benefits of genomic… ...

A clinician is a healthcare professional who provides direct care to patients, usually in clinical settings such as hospitals ...

The Research Environment allows researchers to access one of the largest and most comprehensive genomic datasets for rare conditions and cancer. Researchers can analyse whole genome sequencing data, ...

Information on the 100,000 Genomes Project, including an overview of the project, participant resources, getting results, and additional findings from the… ...

Who we are and what we do at Genomics England, from our origin to the current mission and beyond.

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.

The Generation Study will be testing babies for changes in genes linked to more than 200 rare genetic conditions. These all meet a set of four principles that have guided our approach to choosing ...

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 ...

Find the contact, social media, service desk, and other important information for Genomics England.

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), as well as more detail about ...