In this blog, we spoke to Andreia Rogerio, Applied Machine Learning Engineer, about her professional journey and the ...

We use cookies to personalise content and to analyse our traffic and improve our website.

We use cookies to personalise content and to analyse our traffic and improve our website.

In this explainer episode, we’ve asked Katrina Stone, Clinical Genetics Doctor, and Clinical Fellow at Genomics England, to explain what happens when you go for whole genome sequencing for a rare ...

There are thousands of potential conditions that can be tested for through genome sequencing. It was important for us to carefully consider which conditions should be looked for in the Generation ...

Below are the key policies and documents that govern the processes at Genomics England.

Genomes from NHS patients affected by cancer or a rare condition collected through our 100,000 Genomes Project and the NHS Genomic Medicine Service. All participants have health data collected when ...

I'm submitting an abstract or poster to a conference ...

The Participant Panel is made up of a diverse group of people whose data is held in the National Genomic Research Library. Members come from different walks of life and bring their life experiences of ...

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 ...

Genomics England's very first initiative – sequencing 100,000 genomes from around 85,000 NHS patients affected by rare disease or cancer – is leading to groundbreaking insights and continued findings ...