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Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.
Regier, Allison A; Farjoun, Yossi; Larson, David E; Krasheninina, Olga; Kang, Hyun Min; Howrigan, Daniel P; Chen, Bo-Juen; Kher, Manisha; Banks, Eric; Ames, Darren C; English, Adam C; Li, Heng; Xing, Jinchuan; Zhang, Yeting; Matise, Tara; Abecasis, Goncalo R; Salerno, Will; Zody, Michael C; Neale, Benjamin M; Hall, Ira M.
Afiliação
  • Regier AA; McDonnell Genome Institute, Washington University School of Medicine, St. Louis, 63108, MO, USA.
  • Farjoun Y; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Larson DE; McDonnell Genome Institute, Washington University School of Medicine, St. Louis, 63108, MO, USA.
  • Krasheninina O; Human Genome Sequencing Center, Baylor College of Medicine, Houston, 77030, TX, USA.
  • Kang HM; Department of Biostatistics, University of Michigan, Ann Arbor, 48109, MI, USA.
  • Howrigan DP; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Chen BJ; New York Genome Center, New York, 10013, NY, USA.
  • Kher M; Google, New York, 10011, NY, USA.
  • Banks E; New York Genome Center, New York, 10013, NY, USA.
  • Ames DC; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • English AC; DNAnexus Inc, Mountain View, 94040, CA, USA.
  • Li H; Spiral Genetics, Seattle, 98104, WA, USA.
  • Xing J; Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
  • Zhang Y; Department of Genetics, Rutgers University, Piscataway, 08854, NJ, USA.
  • Matise T; Department of Genetics, Rutgers University, Piscataway, 08854, NJ, USA.
  • Abecasis GR; Department of Genetics, Rutgers University, Piscataway, 08854, NJ, USA.
  • Salerno W; Department of Biostatistics, University of Michigan, Ann Arbor, 48109, MI, USA.
  • Zody MC; Human Genome Sequencing Center, Baylor College of Medicine, Houston, 77030, TX, USA.
  • Neale BM; New York Genome Center, New York, 10013, NY, USA.
  • Hall IM; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, 02142, MA, USA.
Nat Commun ; 9(1): 4038, 2018 10 02.
Article em En | MEDLINE | ID: mdl-30279509
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequenciamento Completo do Genoma / Genética Humana Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sequenciamento Completo do Genoma / Genética Humana Limite: Humans Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos