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Clinical whole-genome sequencing from routine formalin-fixed, paraffin-embedded specimens: pilot study for the 100,000 Genomes Project.
Robbe, Pauline; Popitsch, Niko; Knight, Samantha J L; Antoniou, Pavlos; Becq, Jennifer; He, Miao; Kanapin, Alexander; Samsonova, Anastasia; Vavoulis, Dimitrios V; Ross, Mark T; Kingsbury, Zoya; Cabes, Maite; Ramos, Sara D C; Page, Suzanne; Dreau, Helene; Ridout, Kate; Jones, Louise J; Tuff-Lacey, Alice; Henderson, Shirley; Mason, Joanne; Buffa, Francesca M; Verrill, Clare; Maldonado-Perez, David; Roxanis, Ioannis; Collantes, Elena; Browning, Lisa; Dhar, Sunanda; Damato, Stephen; Davies, Susan; Caulfield, Mark; Bentley, David R; Taylor, Jenny C; Turnbull, Clare; Schuh, Anna.
  • Robbe P; Oxford Molecular Diagnostics Centre, Radcliffe Department of Medicine, University of Oxford, Oxford, UK. pauline.robbe@ndcls.ox.ac.uk.
  • Popitsch N; Wellcome Trust Centre of Human Genetics, University of Oxford, Old Road Campus Research Building, Oxford, UK.
  • Knight SJL; Wellcome Trust Centre of Human Genetics, University of Oxford, Old Road Campus Research Building, Oxford, UK.
  • Antoniou P; Oxford Molecular Diagnostics Centre, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Becq J; Illumina Cambridge Ltd., Chesterford Research Park, Saffron Walden, UK.
  • He M; Illumina Cambridge Ltd., Chesterford Research Park, Saffron Walden, UK.
  • Kanapin A; Department of Oncology, University of Oxford, Oxford, UK.
  • Samsonova A; Department of Oncology, University of Oxford, Oxford, UK.
  • Vavoulis DV; Oxford Molecular Diagnostics Centre, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Ross MT; Illumina Cambridge Ltd., Chesterford Research Park, Saffron Walden, UK.
  • Kingsbury Z; Illumina Cambridge Ltd., Chesterford Research Park, Saffron Walden, UK.
  • Cabes M; Oxford Molecular Diagnostics Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Ramos SDC; Oxford Molecular Diagnostics Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Page S; Oxford Molecular Diagnostics Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Dreau H; Oxford Molecular Diagnostics Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Ridout K; Oxford Molecular Diagnostics Centre, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Jones LJ; Genomics England, William Harvey Research Institute, Queen Mary University of London, London, UK.
  • Tuff-Lacey A; Genomics England, William Harvey Research Institute, Queen Mary University of London, London, UK.
  • Henderson S; Oxford Molecular Diagnostics Centre, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxford, UK.
  • Mason J; Genomics England, William Harvey Research Institute, Queen Mary University of London, London, UK.
  • Buffa FM; Computational Biology and Integrative Genomics, Department of Oncology, University of Oxford, Oxford, UK.
  • Verrill C; Nuffield Department of Surgical Sciences, University of Oxford, John Radcliffe Hospital, Oxford, UK.
  • Maldonado-Perez D; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Roxanis I; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Collantes E; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Browning L; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Dhar S; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Damato S; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Davies S; Department of Cellular Pathology, Oxford University Hospital Foundation Trust, Oxford, UK.
  • Caulfield M; Genomics England, William Harvey Research Institute, Queen Mary University of London, London, UK.
  • Bentley DR; NIHR Biomedical Research Centre at Barts Health NHS Trust, London, UK.
  • Taylor JC; Illumina Cambridge Ltd., Chesterford Research Park, Saffron Walden, UK.
  • Turnbull C; Wellcome Trust Centre of Human Genetics, University of Oxford, Old Road Campus Research Building, Oxford, UK.
  • Schuh A; NIHR Comprehensive Biomedical Research Centre, Oxford, UK.
Genet Med ; 20(10): 1196-1205, 2018 10.
Article en En | MEDLINE | ID: mdl-29388947
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genoma Humano / Variaciones en el Número de Copia de ADN / Secuenciación Completa del Genoma / Neoplasias Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article
Texto completo
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XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Genoma Humano / Variaciones en el Número de Copia de ADN / Secuenciación Completa del Genoma / Neoplasias Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Female / Humans / Male Idioma: En Año: 2018 Tipo del documento: Article