Whole genome sequencing in psychiatric disorders: the WGSPD consortium

被引:0
|
作者
Stephan J. Sanders
Benjamin M. Neale
Hailiang Huang
Donna M. Werling
Joon-Yong An
Shan Dong
Goncalo Abecasis
P. Alexander Arguello
John Blangero
Michael Boehnke
Mark J. Daly
Kevin Eggan
Daniel H. Geschwind
David C. Glahn
David B. Goldstein
Raquel E. Gur
Robert E. Handsaker
Steven A. McCarroll
Roel A. Ophoff
Aarno Palotie
Carlos N. Pato
Chiara Sabatti
Matthew W. State
A. Jeremy Willsey
Steven E. Hyman
Anjene M. Addington
Thomas Lehner
Nelson B. Freimer
机构
[1] University of California,Department of Psychiatry, UCSF Weill Institute for Neurosciences
[2] San Francisco,Analytic and Translational Genetics Unit, Department of Medicine
[3] Massachusetts General Hospital and Harvard Medical School,Stanley Center for Psychiatric Research and Program in Medical and Population Genetics
[4] Broad Institute of Harvard and MIT,Department of Biostatistics, School of Public Health
[5] University of Michigan,South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley
[6] National Institute of Mental Health,Department of Neurology, David Geffen School of Medicine
[7] School of Medicine,Center for Autism Research and Treatment, Semel Institute, David Geffen School of Medicine
[8] University of California Los Angeles,Department of Psychiatry
[9] University of California,Institute for Genomic Medicine, Columbia University Medical Center
[10] Los Angeles,Department of Psychiatry, Neuropsychiatry Section, Perelman School of Medicine
[11] Yale University School of Medicine,Brain Center Rudolf Magnus, Department of Psychiatry
[12] Hammer Health Sciences,Center for Neurobehavioral Genetics, Semel Institute for Neuroscience and Human Behavior
[13] University of Pennsylvania,Department of Human Genetics, David Geffen School of Medicine
[14] University Medical Center Utrecht,Department of Psychiatry, Zilkha Neurogenetic Institute, Keck School of Medicine
[15] University of California Los Angeles,Department of Health Research and Policy, Division of Biostatistics
[16] University of California Los Angeles,undefined
[17] University of Southern California,undefined
[18] Stanford University,undefined
来源
Nature Neuroscience | 2017年 / 20卷
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摘要
As technology advances, whole genome sequencing (WGS) is likely to supersede other genotyping technologies. The rate of this change depends on its relative cost and utility. Variants identified uniquely through WGS may reveal novel biological pathways underlying complex disorders and provide high-resolution insight into when, where, and in which cell type these pathways are affected. Alternatively, cheaper and less computationally intensive approaches may yield equivalent insights. Understanding the role of rare variants in the noncoding gene-regulating genome through pilot WGS projects will be critical to determining which of these two extremes best represents reality. With large cohorts, well-defined risk loci, and a compelling need to understand the underlying biology, psychiatric disorders have a role to play in this preliminary WGS assessment. The Whole Genome Sequencing for Psychiatric Disorders Consortium will integrate data for 18,000 individuals with psychiatric disorders, beginning with autism spectrum disorder, schizophrenia, bipolar disorder, and major depressive disorder, along with over 150,000 controls.
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页码:1661 / 1668
页数:7
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