In this blog, Samuel Omotosho shares his experience working as intern in the Health Data Research programme at Genomics England.

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

What do we mean by no primary findings? Not all genomic tests will result in primary findings or a diagnosis. When no primary findings are found, this means that no genetic changes have been ...

In this blog, Clinical Bioinformatician Clare Kennedy shares her experience in clinical bioinformatics and the impact of her work on patient care.

In this blog, Nadezhda Feliz, Genomics Data Scientist, shares her motivation for working in rare conditions research.

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 ...

A recent study using data from the 100,000 Genomes Project found that over 14,000 patients with cancer could have reduced risk of harmful side effects from cancer treatment by receiving a lower dose ...

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 ...

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 ...

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.