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Application of clinical text data for phenome-wide association studies (PheWASs).
Hebbring, Scott J; Rastegar-Mojarad, Majid; Ye, Zhan; Mayer, John; Jacobson, Crystal; Lin, Simon.
  • Hebbring SJ; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA and Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA.
  • Rastegar-Mojarad M; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA and Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA.
  • Ye Z; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA and Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA.
  • Mayer J; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA and Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA.
  • Jacobson C; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA and Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA.
  • Lin S; Center for Human Genetics, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA and Biomedical Informatics Research Center, Marshfield Clinic Research Foundation, Marshfield, WI 54449, USA.
Bioinformatics ; 31(12): 1981-7, 2015 Jun 15.
Article en En | MEDLINE | ID: mdl-25657332
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenotipo / Enfermedad / Biología Computacional / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenotipo / Enfermedad / Biología Computacional / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Estudio de Asociación del Genoma Completo Tipo de estudio: Risk_factors_studies Límite: Humans Idioma: En Año: 2015 Tipo del documento: Article