A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.

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Title: A Statistical Framework for Mapping Risk Genes from De Novo Mutations in Whole-Genome-Sequencing Studies.
Authors: 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.
Source: American journal of human genetics [Am J Hum Genet] 2018 Jun 07; Vol. 102 (6), pp. 1031-1047. Date of Electronic Publication: 2018 May 10.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1537-6605
DOI:10.1016/j.ajhg.2018.03.023