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Practical aspects of imputation-driven meta-analysis of genome-wide association studies

机译:归因驱动的全基因组关联研究的荟萃分析的实践方面

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摘要

Motivated by the overwhelming success of genome-wide association studies, droves of researchers are working vigorously to exchange and to combine genetic data to expediently discover genetic risk factors for common human traits. The primary tools that fuel these new efforts are imputation, allowing researchers who have collected data on a diversity of genotype platforms to share data in a uniformly exchangeable format, and meta-analysis for pooling statistical support for a genotype–phenotype association. As many groups are forming collaborations to engage in these efforts, this review collects a series of guidelines, practical detail and learned experiences from a variety of individuals who have contributed to the subject.
机译:在全基因组关联研究取得巨大成功的推动下,成群的研究人员正在积极工作,以交换和组合遗传数据以方便地发现人类常见性状的遗传危险因素。推动这些新努力的主要工具是归因,它使收集了各种基因型平台数据的研究人员能够以统一可交换的格式共享数据,并进行荟萃分析以收集对基因型-表型关联的统计支持。由于许多团体正在形成协作来从事这些工作,因此本综述收集了一系列为该主题做出贡献的个人的指南,实践细节和经验教训。

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  • 来源
    《Human Molecular Genetics》 |2008年第r2期|R122-R128|共7页
  • 作者单位

    Division of Genetics Department of Medicine Brigham and Women's Hospital Harvard Medical School-Partners Healthcare Systems Center for Genetics and Genomics Boston MA 02115 USA;

    Program in Medical and Population Genetics Broad Institute of Harvard and MIT Cambridge MA 02142 USA;

    Center for Human Genetic Research Massachusetts General Hospital Boston MA 02114 USA;

    Harvard-MIT Division of Health Sciences and Technology Boston MA 02115 USA;

    Division of Rheumatology Immunology and Allergy Brigham and Women's Hospital Boston MA 02115 USA;

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