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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Structured Genome-Wide Association Studies with Bayesian Hierarchical Variable Selection
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Structured Genome-Wide Association Studies with Bayesian Hierarchical Variable Selection

机译:贝叶斯等级变量选择结构化基因组协会研究

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It becomes increasingly important in using genome-wide association studies (GWAS) to select important genetic information associated with qualitative or quantitative traits. Currently, the discovery of biological association among SNPs motivates various strategies to construct SNP-sets along the genome and to incorporate such set information into selection procedure for a higher selection power, while facilitating more biologically meaningful results. The aim of this paper is to propose a novel Bayesian framework for hierarchical variable selection at both SNP-set (group) level and SNP (within group) level. We overcome a key limitation of existing posterior updating scheme in most Bayesian variable selection methods by proposing a novel sampling scheme to explicitly accommodate the ultrahigh-dimensionality of genetic data. Specifically, by constructing an auxiliary variable selection model under SNP-set level, the new procedure utilizes the posterior samples of the auxiliary model to subsequently guide the posterior inference for the targeted hierarchical selection model. We apply the proposed method to a variety of simulation studies and show that our method is computationally efficient and achieves substantially better performance than competing approaches in both SNP-set and SNP selection. Applying the method to the Alzheimers Disease Neuroimaging Initiative (ADNI) data, we identify biologically meaningful genetic factors under several neuroimaging volumetric phenotypes. Our method is general and readily to be applied to a wide range of biomedical studies.
机译:在利用基因组 - 范围内研究(GWA)来选择与定性或定量性状相关的重要遗传信息变得越来越重要。目前,SNP中的生物关联发现激发了各种策略,以构建沿着基因组的SNP-套,并将这些设置信息纳入选择过程中,以便更高的选择能力,同时促进更具生物学上有意义的结果。本文的目的是在SNP-Set(组)级别和SNP(组内)级别提出一种新的贝叶斯框架。我们通过提出新的采样方案来克服大多数贝叶斯变量选择方法中现有后更新方案的关键限制,以明确地容纳遗传数据的超高维度。具体地,通过在SNP设定级别下构造辅助变量选择模型,新过程利用辅助模型的后部样本来随后引导针对目标分层选择模型的后部推理。我们将建议的方法应用于各种仿真研究,并表明我们的方法是在计算上有效的,而不是SNP集合和SNP选择中的竞争方法的性能大得比。将方法应用于阿尔茨海默病神经影像序列(ADNI)数据,我们在几种神经影像体积体内表型下鉴定生物学上有意义的遗传因素。我们的方法是一般的,容易应用于各种各样的生物医学研究。

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