利用多性状识别全基因组关联研究中潜在的遗传交互作用

IF 10.4 1区 生物学 Q1 GENETICS & HEREDITY
Andrew J. Bass, Shijia Bian, Aliza P. Wingo, Thomas S. Wingo, David J. Cutler, Michael P. Epstein
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引用次数: 0

摘要

复杂性状的遗传率 "缺失 "的部分原因可能是遗传变异与其他基因或环境的相互作用,而这些基因或环境很难指定、观察和检测。我们提出了一种新的基于核的方法,称为潜在相互作用测试(LIT),用于筛选遗传相互作用,这种方法利用了多个相关性状的多向性,而不需要指定或观察相互作用变量。通过模拟数据,我们证明与单变量方法相比,LIT 提高了潜在遗传交互作用的检测能力。然后,我们将 LIT 应用于英国生物库中与肥胖相关的性状,并检测已知肥胖相关基因附近具有交互效应的变体(网址:https://CRAN.R-project.org/package=lit )。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identifying latent genetic interactions in genome-wide association studies using multiple traits
The "missing" heritability of complex traits may be partly explained by genetic variants interacting with other genes or environments that are difficult to specify, observe, and detect. We propose a new kernel-based method called Latent Interaction Testing (LIT) to screen for genetic interactions that leverages pleiotropy from multiple related traits without requiring the interacting variable to be specified or observed. Using simulated data, we demonstrate that LIT increases power to detect latent genetic interactions compared to univariate methods. We then apply LIT to obesity-related traits in the UK Biobank and detect variants with interactive effects near known obesity-related genes (URL: https://CRAN.R-project.org/package=lit ).
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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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