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Identification of missing variants by combining multiple analytic pipelines.
Ren, Yingxue; Reddy, Joseph S; Pottier, Cyril; Sarangi, Vivekananda; Tian, Shulan; Sinnwell, Jason P; McDonnell, Shannon K; Biernacka, Joanna M; Carrasquillo, Minerva M; Ross, Owen A; Ertekin-Taner, Nilüfer; Rademakers, Rosa; Hudson, Matthew; Mainzer, Liudmila Sergeevna; Asmann, Yan W.
Afiliação
  • Ren Y; Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Reddy JS; Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Pottier C; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Sarangi V; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
  • Tian S; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
  • Sinnwell JP; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
  • McDonnell SK; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
  • Biernacka JM; Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA.
  • Carrasquillo MM; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Ross OA; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Ertekin-Taner N; Department of Clinical Genomics, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Rademakers R; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Hudson M; Department of Neurology, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Mainzer LS; Department of Neuroscience, Mayo Clinic, Jacksonville, FL, 32224, USA.
  • Asmann YW; National Center for Supercomputing Applications, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.
BMC Bioinformatics ; 19(1): 139, 2018 04 16.
Article em En | MEDLINE | ID: mdl-29661148
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Biologia Computacional Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: BMC Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos
Texto completo
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Biologia Computacional Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: BMC Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos