The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
Clare Turnbull(Institute of Cancer Research), Richard H. Scott(University College London), Ellen Thomas(Guy's and St Thomas' NHS Foundation Trust), J. Louise Jones(Genomics England), Nirupa Murugaesu(Genomics England), Freya Boardman Pretty(Genomics England), Dina Halai(Genomics England), Emma L. Baple(University of Exeter), C. E. H. Craig(Genomics England), Angela Hamblin(Genomics England), Shirley Henderson(NHS England), Christine Patch(King's College London), Amanda O’Neill(University of Cambridge), A. Devereau(Genomics England), Katherine R. Smith(Genomics England), Antonio Rueda Martin(Genomics England), Alona Sosinsky(Genomics England), Ellen M. McDonagh(Genomics England), Răzvan Sultana(Genomics England), Michael Mueller(Genomics England), Damian Smedley(William Harvey Research Institute), Adam Toms(Genomics England), Lisa Dinh(Genomics England), Tom Fowler(Genomics England), Mark Bale(Department of Health and Social Care), Tim Hubbard(Genomics England), Augusto Rendon(Genomics England), Sue Hill(NHS England), Mark J. Caulfield(Genomics England)
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Abstract
In partnership with NHS England, Genomics England’s ambitious plans to embed genomic medicine into routine patient care are well underway. <b>Clare Turnbull and colleagues</b> discuss its progress
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