Genomics has the potential to play an increasingly important role in healthcare. It could help people receive medicines that ...

Every year, we ask researchers who use the National Genomic Research Library to tell us how their projects are progressing ...

Job Description We are looking to hire a Lead Genomic Data Scientist to join our Bioinformatics Consulting team at Genomics ...

Multiple research groups have identified a new recessive neurodevelopmental disorder which is believed to be one of the most common genetic causes of severe childhood epilepsy. The pieces of research, ...

Scientists analysing data from Genomics England’s National Genomic Research Library (NGRL) among other sources have uncovered five new genetic causes of retinitis pigmentosa (RP), an eye condition ...

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, the Sickle Cell Society, and the James Lind Alliance have co-produced a Priority Setting Partnership (PSP) for Sickle Cell and Genomics – resulting in 10 priorities for future ...

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 ...

In this series, ‘Genomics 101’, we go back to basics and explore some of the most important topics in genomics. In this blog, we answer the question: Are genetic conditions always inherited from ...

New research has uncovered 2 neurodevelopmental disorders using data from the National Genomic Research Library. These findings have led to new diagnoses for patients and families, opening doors for ...