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

Job Description Build, develop and manage detailed economic models based on theories of change to explain and understand GELs benefit across ...

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 ...

Greater diversity is needed in genetic research to make genomics’ use in cancer care and screening more accurate and reliable for all, according to a new study. The research, led by Genomics England ...

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 ...

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 ...

In this explainer episode, we’ve asked Mathilde Leblond, Senior Design Researcher for the Generation Study at Genomics England, to answer some frequently asked questions that we received from parents ...

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

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 ...

Volunteer recruitment has begun for a new collaborative research programme focused on improving our knowledge and understanding of health conditions and their unique impacts on UK Black communities.

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 ...