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Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.
He, Zihuai; Liu, Linxi; Wang, Chen; Le Guen, Yann; Lee, Justin; Gogarten, Stephanie; Lu, Fred; Montgomery, Stephen; Tang, Hua; Silverman, Edwin K; Cho, Michael H; Greicius, Michael; Ionita-Laza, Iuliana.
Afiliação
  • He Z; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA. zihuai@stanford.edu.
  • Liu L; Quantitative Sciences Unit, Department of Medicine, Stanford University, Stanford, CA, USA. zihuai@stanford.edu.
  • Wang C; Department of Statistics, Columbia University, New York, NY, USA.
  • Le Guen Y; Department of Biostatistics, Columbia University, New York, NY, USA.
  • Lee J; Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.
  • Gogarten S; Quantitative Sciences Unit, Department of Medicine, Stanford University, Stanford, CA, USA.
  • Lu F; Department of Biostatistics, University of Washington, Seattle, WA, USA.
  • Montgomery S; Department of Statistics, Stanford University, Stanford, CA, USA.
  • Tang H; Department of Genetics, Stanford University, Stanford, CA, USA.
  • Silverman EK; Department of Pathology, Stanford University, Stanford, CA, USA.
  • Cho MH; Department of Statistics, Stanford University, Stanford, CA, USA.
  • Greicius M; Department of Genetics, Stanford University, Stanford, CA, USA.
  • Ionita-Laza I; Channing Division of Network Medicine and Division of Pulmonary and Critical Care Medicine Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Nat Commun ; 12(1): 3152, 2021 05 25.
Article em En | MEDLINE | ID: mdl-34035245
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Estudo de Associação Genômica Ampla / Sequenciamento Completo do Genoma / Modelos Genéticos Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Estudo de Associação Genômica Ampla / Sequenciamento Completo do Genoma / Modelos Genéticos Idioma: En Ano de publicação: 2021 Tipo de documento: Article