Pioneering 100,000 Genomes Project reaches sequencing goal
6 Dec 2018
The 100,000 Genomes Project has reached its goal of sequencing 100,000 whole genomes from NHS patients. Established with the support of the MRC, the project began in 2012 with the goal of harnessing whole genome sequencing technology to uncover new diagnoses and improved treatments for patients with rare inherited diseases and cancer.
One in four participants with rare diseases has received a diagnosis for the first time, and up to half of cancer patients involved have been provided with findings which may allow them the opportunity to take part in a clinical trial or to receive a targeted therapy.
Genomics England worked with NHS England to create 13 NHS Genomic Medicine Centres (GMCs) to support the project, a state-of-the-art sequencing centre, and an automated analytics platform to return whole genome analyses to the NHS.
In 2014, the MRC invested £24 million to establish the Genomics England Data Centre, where participant data is securely stored for use by the research community and health professionals.
In partnership with the Devolved Governments of Scotland, Wales and Northern Ireland, the MRC also supports national ambitions in genomic sequencing and medicine with collaborative links to Genomics England to build a UK-wide partnership, asset and capability.
Professor Mark Caulfield, Chief Scientist at Genomics England, said: "The sequencing of 100,000 whole genomes marks an extraordinary UK achievement that is transforming the application of genomics in our NHS. Genomics England will continue to analyse these genomes alongside life course clinical information to reveal answers for as many participants as possible and improve their NHS care.”
Dr Nathan Richardson, Head of Molecular and Cellular Medicine at the MRC, said: “This is a truly exciting milestone in the development of genomic medicine within the NHS. Major investments from the government, including £24 million from the MRC, will build on the outstanding genomics and data science capabilities within the UK. This project is set to transform our ability to understand and diagnose genetic disease and better target treatment, and position the NHS and UK clinical genomics as the envy of the world.”
The human genome is comprised of 3.2 billion letters and is the blueprint for each of us. Genetic variation can cause rare disease and cancer, which is a disease of disordered genomes. Due to technological and analytical advances we can now read the whole genome with accuracy that can bring new diagnoses to patients with rare disease and choose therapy in cancer.
The 100,000 Genomes Project focused on 1,200 disorders with diagnostic unmet need after usual care. The disorders included in the programme have been nominated by the NHS, researchers and industry.
With the project, the UK has become the first nation in the world to apply whole genome sequencing at scale in direct healthcare, as well as providing access to high-quality de-identified clinical and genomic data for research aimed at improving patient outcomes.
The project has laid the foundations for a NHS Genomic Medicine Service, which will see all seriously ill children with a suspected disorder, including cancer, and adults with certain rare diseases or cancers, offered whole genomic sequencing as part of their routine care from 2019.