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An Ensemble Learning Approach Jointly Modeling Main and Interaction Effects in Genetic Association Studies

机译:集成学习方法共同建模遗传关联研究中的主效应和相互作用效应

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摘要

Complex diseases are presumed to be the results of interactions of several genes and environmental factors, with each gene only having a small effect on the disease. Thus, the methods that can account for gene-gene interactions to search for a set of marker loci in different genes or across genome and to analyze these loci jointly are critical. In this article, we propose an ensemble learning approach (ELA) to detect a set of loci whose main and interaction effects jointly have a significant association with the trait. In the ELA, we first search for “base learners” and then combine the effects of the base learners by a linear model. Each base learner represents a main effect or an interaction effect. The result of the ELA is easy to interpret. When the ELA is applied to analyze a data set, we can get a final model, an overall P-value of the association test between the set of loci involved in the final model and the trait, and an importance measure for each base learner and each marker involved in the final model. The final model is a linear combination of some base learners. We know which base learner represents a main effect and which one represents an interaction effect. The importance measure of each base learner or marker can tell us the relative importance of the base learner or marker in the final model. We used intensive simulation studies as well as a real data set to evaluate the performance of the ELA. Our simulation studies demonstrated that the ELA is more powerful than the single-marker test in all the simulation scenarios. The ELA also outperformed the other three existing multi-locus methods in almost all cases. In an application to a large-scale case-control study for Type 2 diabetes, the ELA identified 11 single nucleotide polymorphisms that have a significant multi-locus effect (P-value = 0.01), while none of the single nucleotide polymorphisms showed significant marginal effects and none of the two-locus combinations showed significant two-locus interaction effects.
机译:复杂疾病被认为是几种基因与环境因素相互作用的结果,每种基因对疾病的影响很小。因此,能够解释基因-基因相互作用以在不同基因或整个基因组中搜索一组标记基因座并共同分析这些基因座的方法至关重要。在本文中,我们提出了一种集成学习方法(ELA),以检测其主要作用和相互作用共同与该性状具有显着关联的一组基因座。在ELA中,我们首先搜索“基础学习者”,然后通过线性模型组合基础学习者的效果。每个基础学习者代表一种主要作用或一种互动作用。 ELA的结果很容易解释。当将ELA应用于分析数据集时,我们可以获得最终模型,最终模型所涉及的基因座集合与特征之间的关联测试的整体P值,以及每个基础学习者和最终模型中涉及的每个标记。最终模型是一些基础学习者的线性组合。我们知道哪个基础学习者代表主要作用,哪个代表相互作用作用。每个基础学习者或标记的重要性度量可以告诉我们基础学习者或标记在最终模型中的相对重要性。我们使用了大量的仿真研究以及真实的数据集来评估ELA的性能。我们的仿真研究表明,在所有仿真方案中,ELA均比单标记测试强大。在几乎所有情况下,ELA的性能都优于其他三种现有的多位置方法。在一项针对2型糖尿病的大规模病例对照研究的应用中,ELA鉴定出11种具有明显多位点效应的单核苷酸多态性(P值= 0.01),而单核苷酸多态性均未显示明显的边缘并且,两个位点的组合都没有显示出明显的两个位点的相互作用。

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