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A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.
Liu, Yuwen; Liang, Yanyu; Cicek, A Ercument; Li, Zhongshan; Li, Jinchen; Muhle, Rebecca A; Krenzer, Martina; Mei, Yue; Wang, Yan; Knoblauch, Nicholas; Morrison, Jean; Zhao, Siming; Jiang, Yi; Geller, Evan; Ionita-Laza, Iuliana; Wu, Jinyu; Xia, Kun; Noonan, James P; Sun, Zhong Sheng; He, Xin.
Afiliación
  • Liu Y; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Liang Y; Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15123, USA.
  • Cicek AE; Computational Biology Department, School of Computer Science, Carnegie Mellon University, Pittsburgh, PA 15123, USA; Computer Engineering Department, Bilkent University, Ankara 06800, Turkey.
  • Li Z; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang 325000, China.
  • Li J; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China; National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, Hunan 410078, China.
  • Muhle RA; Child Study Center, Yale Medicine, New Haven, CT 06520, USA.
  • Krenzer M; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
  • Mei Y; Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100000, China.
  • Wang Y; Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100000, China.
  • Knoblauch N; Committee on Genetics, Genomics and Systems Biology, The University of Chicago, Chicago, IL 60637, USA.
  • Morrison J; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Zhao S; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA.
  • Jiang Y; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang 325000, China; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
  • Geller E; Department of Genetics, Yale School of Medicine, New Haven, CT 06520, USA; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
  • Ionita-Laza I; Department of Biostatistics, Columbia University, New York, NY 10027, USA.
  • Wu J; Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100000, China; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang 325000, China.
  • Xia K; Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan 410078, China.
  • Noonan JP; Department of Genetics, Yale School of Medicine, New Haven, CT 06520, USA; Kavli Institute for Neuroscience, Yale School of Medicine, New Haven, CT 06520, USA.
  • Sun ZS; Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing 100000, China; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang 325000, China. Electronic address: sunzs@mail.biols.ac.cn.
  • He X; Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA. Electronic address: xinhe@uchicago.edu.
Am J Hum Genet ; 102(6): 1031-1047, 2018 06 07.
Article en En | MEDLINE | ID: mdl-29754769
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estadística como Asunto / Mapeo Cromosómico / Predisposición Genética a la Enfermedad / Secuenciación Completa del Genoma / Mutación Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Estadística como Asunto / Mapeo Cromosómico / Predisposición Genética a la Enfermedad / Secuenciación Completa del Genoma / Mutación Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos