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Detecting ultralow-frequency mutations by Duplex Sequencing.
Kennedy, Scott R; Schmitt, Michael W; Fox, Edward J; Kohrn, Brendan F; Salk, Jesse J; Ahn, Eun Hyun; Prindle, Marc J; Kuong, Kawai J; Shen, Jiang-Cheng; Risques, Rosa-Ana; Loeb, Lawrence A.
Afiliação
  • Kennedy SR; Department of Pathology, University of Washington, Seattle, USA.
  • Schmitt MW; Department of Medicine, University of Washington, Seattle, USA.
  • Fox EJ; Department of Pathology, University of Washington, Seattle, USA.
  • Kohrn BF; Department of Biology, Portland State University, Portland, Oregon, USA.
  • Salk JJ; Department of Medicine, University of Washington, Seattle, USA.
  • Ahn EH; Department of Pathology, University of Washington, Seattle, USA.
  • Prindle MJ; Department of Pathology, University of Washington, Seattle, USA.
  • Kuong KJ; Department of Pathology, University of Washington, Seattle, USA.
  • Shen JC; Department of Pathology, University of Washington, Seattle, USA.
  • Risques RA; Department of Pathology, University of Washington, Seattle, USA.
  • Loeb LA; 1] Department of Pathology, University of Washington, Seattle, USA. [2] Department of Biochemistry, University of Washington, Seattle, USA.
Nat Protoc ; 9(11): 2586-606, 2014 Nov.
Article em En | MEDLINE | ID: mdl-25299156
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Taxa de Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Protoc Ano de publicação: 2014 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: Análise Mutacional de DNA / Sequenciamento de Nucleotídeos em Larga Escala / Taxa de Mutação Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Nat Protoc Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos