Greater diversity is needed in genetic research to make genomics’ use in cancer care and screening more accurate and reliable ...

Adam Clatworthy, Vice Chair for Rare Conditions on the Participant Panel for Genomics England, shares the Panel's vision for ...

New research has uncovered two new genetic disorders through data from the National Genomic Research Library, providing new ...

In this series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, ...

A review funded as part of Genomics England’s Diverse Data initiative and led by UCL researchers has outlined how the analytical methods used to process and interpret genomic data play a critical role ...

Whole genome sequencing allows us look at lots of different genes in a person’s genome, with one single test. A genome is a person's entire genetic sequence – their bodies instruction manual. It ...

Researchers have used data from the 100,000 Genomes Project to help create a “metal detector” algorithm called PRRDetect to hunt down vulnerable tumours, in a development that could one day ...

In this series, we explore some important roles in the life sciences, and how their work impacts patients and families. In this blog, Nadezhda Feliz, Genomic Data Scientist, shares her motivation for ...

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 ...

One hundred thousand whole genomes have now been sequenced through the NHS Genomic Medicine Service (NHS GMS) – supported by Genomics England and Illumina - which has led to new diagnoses, more ...