Homepage | Genomics England
网页Genomics England analyses sequenced genomes for the NHS and then equips researchers to use data to help find the cause of disease.
About Us | Genomics England
网页Powering the future of healthcare. Our mission is to continue refining, scaling, and evolving our ability to enable others to deliver genomic healthcare and conduct genomic research. How it all started.
Genomics England announces list of rare conditions to be …
网页Today (2 October 2023), Genomics England have published an initial list of over 200 rare conditions that will be looked for as part of its world-leading Generation Study, which aims to start in NHS hospitals in late 2023. The Generation Study is an NHS-embedded research study which aims to understand whether sequencing babies’ genomes can help to discover rare genetic conditions earlier. It ...
10 years | Genomics England
网页July 2023 marks 10 years of Genomics England. Over the past decade, our partnership with the NHS has brought life-changing discoveries to those living with cancer and rare conditions . This year, we celebrate the achievements of the past 10 years.
Academic research | Genomics England
网页Our Research Network for academics, clinicians, and students worldwide to carry out research on the world's largest whole genome dataset to gain novel disease and patient-related insights.
Genomic Medicine - Genomics England
网页Genomic medicine uses an individual's genomic information as part of their clinical care. Advances in science and technology, along with collaboration with the NHS Genomic Medicine Service (GMS), provides a unique way to integrate genomic medicine into routine care. Here at Genomics England, we focus on developing analytical and IT systems that ...
Newborn Genomes Programme - Genomics England
网页The Generation Study is a groundbreaking research study which will sequence the genomes of 100,000 newborn babies. We are running our study in partnership with the NHS to understand whether we can improve our ability to diagnose and treat genetic conditions. Our study has been developed following extensive consultation with the public, parents ...
Genomics in the UK
网页The UK has often led the world in scientific breakthroughs and DNA was no exception. Crick and Watson won the Nobel Prize for discovering the double helix structure of DNA. And it was a British double Nobel Prize winning scientist, Fred Sanger, who discovered how to sequence it. Today, the UK continues to maintain its position as a world-leader in genomic research and healthcare.
COVID-19 Study - Genomics England
网页Read about our partnership with the GenOMICC consortium, led by the University of Edinburgh, to analyse the whole genome sequences of those affected by COVID-19.
Understanding genomics - Genomics England
网页Learn about genomics including: what is a genome, how genome sequencing works, and why we sequence genomes.
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