The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
Clare Turnbull(Institute of Cancer Research), Mark J. Caulfield(Queen Mary University of London), Damian Smedley(University of Iowa), Sue Hill(National Health Service), A. Devereau(Genomics England), Dina Halai(Genomics England), Richard H. Scott(Genomics England), Katherine R. Smith(Murdoch Children's Research Institute), Michael Mueller(Genomics England), Freya Boardman Pretty(Genomics England), Ellen M. McDonagh(Wellcome Sanger Institute), Tom Fowler(UK Health Security Agency), Mark Bale(Department of Health and Social Care), Augusto Rendon(University of Cambridge), Răzvan Sultana(Genomics England), Angela Hamblin(Genomics England), Alona Sosinsky(Genomics England), Lisa Dinh(Genomics England), Antonio Rueda Martin(Genomics England), J. Louise Jones(Queen Mary University of London), Christine Patch(Wellcome Connecting Science), Emma L. Baple(University of Exeter), Amanda O’Neill(University of Cambridge), Adam Toms(Genomics England), C. E. H. Craig(Genomics England), Ellen Thomas(Guy's and St Thomas' NHS Foundation Trust), Tim Hubbard(King's College London), Shirley Henderson(Genomics England), Nirupa Murugaesu(University of Pavia)
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