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

In this explainer episode, we’ve asked Arina Puzriakova, Scientific Curator at Genomics England, to explain what a polygenic disorder is. You can also find a series of short videos explaining some of ...

The Generation Study is a research initiative aiming to explore the use of whole genome sequencing in newborns, to screen for more than 200 rare genetic conditions. This study will recruit 100,000 ...

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 ...

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 ...

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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 ...

Hundreds of babies have begun to be tested for over 200 rare genetic conditions as part of a world-leading study in NHS hospitals that aims to screen up to 100,000 newborns in England. The Generation ...

This month Genomics England is marking Sickle Cell Awareness Month, which aims to bring greater visibility of the genetic condition and those affected by it. In recognition of sickle cell’s importance ...

Genomics England is part of a nationwide team of universities, hospitals and industry led by the Francis Crick Institute and The Royal Marsden NHS Foundation Trust, which has launched a new platform ...