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高效贝叶斯方法用于多位点关联映射,包括基因-基因相互作用。

Efficient Bayesian approach for multilocus association mapping including gene-gene interactions.

机构信息

Department of Biomedical Engineering and Computational Science, FI-02015 Helsinki University of Technology, Finland.

出版信息

BMC Bioinformatics. 2010 Sep 2;11:443. doi: 10.1186/1471-2105-11-443.

Abstract

BACKGROUND

since the introduction of large-scale genotyping methods that can be utilized in genome-wide association (GWA) studies for deciphering complex diseases, statistical genetics has been posed with a tremendous challenge of how to most appropriately analyze such data. A plethora of advanced model-based methods for genetic mapping of traits has been available for more than 10 years in animal and plant breeding. However, most such methods are computationally intractable in the context of genome-wide studies. Therefore, it is hardly surprising that GWA analyses have in practice been dominated by simple statistical tests concerned with a single marker locus at a time, while the more advanced approaches have appeared only relatively recently in the biomedical and statistical literature.

RESULTS

we introduce a novel Bayesian modeling framework for association mapping which enables the detection of multiple loci and their interactions that influence a dichotomous phenotype of interest. The method is shown to perform well in a simulation study when compared to widely used standard alternatives and its computational complexity is typically considerably smaller than that of a maximum likelihood based approach. We also discuss in detail the sensitivity of the Bayesian inferences with respect to the choice of prior distributions in the GWA context.

CONCLUSIONS

our results show that the Bayesian model averaging approach which explicitly considers gene-gene interactions may improve the detection of disease associated genetic markers in two respects: first, by providing better estimates of the locations of the causal loci; second, by reducing the number of false positives. The benefits are most apparent when the interacting genes exhibit no main effects. However, our findings also illustrate that such an approach is somewhat sensitive to the prior distribution assigned on the model structure.

摘要

背景

自可用于全基因组关联 (GWA) 研究以破译复杂疾病的大规模基因分型方法问世以来,统计遗传学面临着如何最适当地分析此类数据的巨大挑战。 10 多年来,在动植物育种中,已经有大量先进的基于模型的方法可用于性状的遗传定位。 然而,在全基因组研究的背景下,大多数此类方法在计算上都难以处理。 因此,毫不奇怪,GWA 分析在实践中主要由一次关注单个标记基因座的简单统计检验主导,而更先进的方法仅在最近才出现在生物医学和统计文献中。

结果

我们引入了一种新的贝叶斯建模框架,用于关联映射,该框架能够检测影响二分感兴趣表型的多个基因座及其相互作用。 与广泛使用的标准替代方法相比,该方法在模拟研究中表现良好,并且其计算复杂度通常明显小于基于最大似然的方法。 我们还详细讨论了在 GWA 环境中选择先验分布对贝叶斯推断的敏感性。

结论

我们的结果表明,贝叶斯模型平均方法(明确考虑基因-基因相互作用)可以在两个方面提高与疾病相关的遗传标记的检测能力:首先,通过提供因果基因座位置的更好估计;其次,通过减少假阳性数量。当相互作用的基因没有主效应时,好处最为明显。 但是,我们的发现也表明,这种方法对模型结构分配的先验分布有些敏感。

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