Homepage | Genomics England
Genomics England analyses sequenced genomes for the NHS and then equips researchers to use data to help find the cause of disease.
Conditions list - Genomics England
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 …
About Us | Genomics England
Who we are and what we do at Genomics England, from our origin to the current mission and beyond.
Newborn Genomes Programme - Genomics England
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 …
NHS Genomic Medicine Service - Genomics England
If you're a patient of the NHS Genomic Medicine Service, you may be offered whole genome sequencing as part of your clinical care.You will be asked if you want to donate genome …
Data - Genomics England
Through our secure Research Environment, approved researchers can access and analyse data in the National Genomic Research Library (NGRL). The NGRL is a repository of genomic and …
Origins - Genomics England
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 …
Publications - Genomics England
We collect data on the user’s navigation and behaviour on our website. These are known as analytic cookies. This data is used to compile statistical reports and heatmaps to improve the …
Governance - Genomics England
The Genomics England Board oversees all of our activities, ratifies all major decisions and sets the overall strategy for the organisation. Genomics England has several independent advisory …
Engagement | Genomics England
In 2021, Genomics England and the UK National Screening Committee commissioned a public dialogue to explore the implications of whole genome sequencing for newborns.