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A general framework for studying genetic effects and gene-environment interactions with missing data

机译:研究缺少数据的遗传效应和基因-环境相互作用的通用框架

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摘要

Missing data arise in genetic association studies when genotypes are unknown or when haplotypes are of direct interest. We provide a general likelihood-based framework for making inference on genetic effects and gene-environment interactions with such missing data. We allow genetic and environmental variables to be correlated while leaving the distribution of environmental variables completely unspecified. We consider 3 major study designs-cross-sectional, case-control, and cohort designs-and construct appropriate likelihood functions for all common phenotypes (e.g. case-control status, quantitative traits, and potentially censored ages at onset of disease). The likelihood functions involve both finite-and infinite-dimensional parameters. The maximum likelihood estimators are shown to be consistent, asymptotically normal, and asymptotically efficient. Expectation-Maximization (EM) algorithms are developed to implement the corresponding inference procedures. Extensive simulation studies demonstrate that the proposed inferential and numerical methods perform well in practical settings. Illustration with a genome-wide association study of lung cancer is provided.
机译:当基因型未知或单倍型直接相关时,基因关联研究中缺少数据。我们提供了一个基于总体似然性的框架,可以利用这些缺失的数据推断遗传效应和基因-环境相互作用。我们允许遗传变量和环境变量相关联,而完全不指定环境变量的分布。我们考虑了3种主要的研究设计-横断面,病例对照和队列研究-并针对所有常见表型构建适当的似然函数(例如病例对照状态,定量特征和疾病发作时的年龄限制)。似然函数涉及有限维和无限维参数。最大似然估计值被证明是一致的,渐近正态的和渐近有效的。开发了期望最大化(EM)算法以实现相应的推理过程。大量的仿真研究表明,所提出的推论和数值方法在实际环境中表现良好。提供了与肺癌的全基因组关联研究的例证。

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