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, ...

Information on the 100,000 Genomes Project, including an overview of the project, participant resources, getting results, and additional findings from the… ...

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 ...

New research using data from the 100,000 Genomes Project has identified a genetic change that drives osteosarcoma, an aggressive childhood bone cancer.

Genomics England began as a vessel to execute the UK Government's bold plan to sequence 100,000 whole genomes and incorporate genomic medicine into routine care in the NHS, a feat we achieved in 2018 ...

An explanation of how the Newborns Programme has explored and decided which conditions to screen for in newborns.

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 ...

Recent research has discovered a common cause for neurodevelopmental disorders in the non-coding genome, providing a diagnosis to hundreds of people… ...