Your browser doesn't support javascript.
loading
CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.
Johansson, Lennart F; van Dijk, Freerk; de Boer, Eddy N; van Dijk-Bos, Krista K; Jongbloed, Jan D H; van der Hout, Annemieke H; Westers, Helga; Sinke, Richard J; Swertz, Morris A; Sijmons, Rolf H; Sikkema-Raddatz, Birgit.
Afiliação
  • Johansson LF; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • van Dijk F; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands.
  • de Boer EN; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • van Dijk-Bos KK; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands.
  • Jongbloed JD; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • van der Hout AH; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Westers H; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Sinke RJ; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Swertz MA; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Sijmons RH; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
  • Sikkema-Raddatz B; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.
Hum Mutat ; 37(5): 457-64, 2016 May.
Article em En | MEDLINE | ID: mdl-26864275
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Predisposição Genética para Doença / Variações do Número de Cópias de DNA / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Predisposição Genética para Doença / Variações do Número de Cópias de DNA / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article