A recent study found that around 14,000 patients with cancer could have reduced risk of harmful side effects from cancer ...

A new study led by Genomics England and Queen Mary University of London estimates that genetic testing could identify approximately 14,540 patients per year on any of 5 commonly prescribed drugs who ...

In this explainer episode, we’ve asked Callum Morris, Pharmaceutical Research and Development Insights Manager at Genomics England, to explain what happens in a clinical trial. You can also find a ...

In this explainer episode, we’ve asked Nicole Chai, Research and Development Bioinformatician at Genomics England, to explain what X-linked inheritance is. You can also find a series of short videos ...

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 term personalised medicine, and how it is transforming our ...

You can use the form below to sign up for email alerts about new positions as they open. Genomics England partners with the NHS to provide whole genome sequencing diagnostics. We also equip ...

We use cookies to personalize content and to analyze our traffic and improve our website.

A rare disease is defined as one that affects less than 1 in 2,000 of the general population. There are between 5,000 and 8,000 known rare diseases. In the UK, a single rare disease may affect up to ...

You can use the form below to sign up for email alerts about new positions as they open. Genomics England partners with the NHS to provide whole genome sequencing diagnostics. We also equip ...

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 ...

We have developed a machine learning tool for scanning large volumes of scientific literature to find reports of gene-disease associations using AWS Cloud services and Large Language Models. This will ...