In this series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, we explain the meaning of dominant and recessive genes, and how they are ...

Genomics England’s Generation Study has now enrolled 25,000 babies - a major milestone in one of the world’s largest research studies of its kind to explore how whole genome sequencing could be used ...

A boy born with a rare form of eye cancer, usually diagnosed in very young children, is one of numerous babies born with rare conditions who are receiving earlier diagnoses and faster, lifechanging ...

‘Airlock’ is a secure gateway used for moving data into and out of the Genomics England Research Environment. This Research Environment, sometimes shortened to ‘RE’, hosts the National Genomic ...

The pioneering Yellow Card Biobank, launched by the Medicines and Healthcare products Regulatory Agency (MHRA) and Genomics England, will today start investigating whether the risk of acute ...

New research has uncovered two new genetic disorders through data from the National Genomic Research Library, providing new diagnoses and opening the door for future treatments. - RNU2-2-related ...

In this episode of Behind the Genes, we explore the hopes, concerns and complex questions raised by the idea of a lifetime genome — a single genomic record used across a person’s life to guide ...

New research shows almost 90% of people in England would agree to genetic testing to get the most effective medication and reduce the risk of side effects 85% thought that the NHS should offer ...

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 ...

At Genomics England, we are committed to transforming health outcomes through innovation in genomics that benefit all patients, regardless of their background. Our Diverse Data Initiative is leading ...

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 ...

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 ...