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Multiplex assessment of protein variant abundance by massively parallel sequencing.
Matreyek, Kenneth A; Starita, Lea M; Stephany, Jason J; Martin, Beth; Chiasson, Melissa A; Gray, Vanessa E; Kircher, Martin; Khechaduri, Arineh; Dines, Jennifer N; Hause, Ronald J; Bhatia, Smita; Evans, William E; Relling, Mary V; Yang, Wenjian; Shendure, Jay; Fowler, Douglas M.
Afiliação
  • Matreyek KA; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Starita LM; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Stephany JJ; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Martin B; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Chiasson MA; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Gray VE; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Kircher M; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Khechaduri A; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Dines JN; Department of Medical Genetics, University of Washington, Seattle, WA, USA.
  • Hause RJ; Department of Genome Sciences, University of Washington, Seattle, WA, USA.
  • Bhatia S; School of Medicine, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Evans WE; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Relling MV; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Yang W; Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Shendure J; Department of Genome Sciences, University of Washington, Seattle, WA, USA. shendure@u.washington.edu.
  • Fowler DM; Howard Hughes Medical Institute, Seattle, WA, USA. shendure@u.washington.edu.
Nat Genet ; 50(6): 874-882, 2018 06.
Article em En | MEDLINE | ID: mdl-29785012
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto Limite: Humans Idioma: En Revista: Nat Genet Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mutação de Sentido Incorreto Limite: Humans Idioma: En Revista: Nat Genet Ano de publicação: 2018 Tipo de documento: Article