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Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL.
Klintman, Jenny; Barmpouti, Katerina; Knight, Samantha J L; Robbe, Pauline; Dreau, Hélène; Clifford, Ruth; Ridout, Kate; Burns, Adam; Timbs, Adele; Bruce, David; Antoniou, Pavlos; Sosinsky, Alona; Becq, Jennifer; Bentley, David; Hillmen, Peter; Taylor, Jenny C; Caulfield, Mark; Schuh, Anna H.
Afiliação
  • Klintman J; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Barmpouti K; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Knight SJL; Oxford University Hospitals, Oxford, UK.
  • Robbe P; NIHR Biomedical Research Centre, Oxford and Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK.
  • Dreau H; Oxford Biomedical Research Centre, Oxford, UK.
  • Clifford R; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Ridout K; Nuffield Department of Laboratory Sciences, University of Oxford, Oxford, UK.
  • Burns A; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Timbs A; Oxford University Hospitals, Oxford, UK.
  • Bruce D; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Antoniou P; Nuffield Department of Laboratory Sciences, University of Oxford, Oxford, UK.
  • Sosinsky A; Haematology Department, University Hospital Limerick, Limerick, Ireland.
  • Becq J; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Bentley D; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Hillmen P; Oxford University Hospitals, Oxford, UK.
  • Taylor JC; Molecular Diagnostic Centre, Department of Oncology, University of Oxford, Oxford, UK.
  • Caulfield M; Oxford University Hospitals, Oxford, UK.
  • Schuh AH; Genomics England, London, UK.
Br J Haematol ; 182(3): 412-417, 2018 08.
Article em En | MEDLINE | ID: mdl-29808933
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Sequenciamento Completo do Genoma Tipo de estudo: Diagnostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Leucemia Linfocítica Crônica de Células B / Sequenciamento Completo do Genoma Tipo de estudo: Diagnostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Haematol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido