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Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approach

机译:检测与稀有和常见的SNP的数量性状的关联:基于非参数贝叶斯的方法

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摘要

We propose a nonparametric Bayes-based clustering algorithm to detect associations with rare and common single-nucleotide polymorphisms (SNPs) for quantitative traits. Unlike current methods, our approach identifies associations with rare genetic variants at the variant level, not the gene level. In this method, we use a Dirichlet process prior for the distribution of SNP-specific regression coefficients, conduct hierarchical clustering with a distance measure derived from posterior pairwise probabilities of two SNPs having the same regression coefficient, and explore data-driven approaches to select the number of clusters. SNPs falling inside the largest cluster have relatively low or close to zero estimates of regression coefficients and are considered not associated with the trait. SNPs falling outside the largest cluster have relatively high estimates of regression coefficients and are considered potential risk variants. Using the data from the Genetic Analysis Workshop 17, we successfully detected associations with both rare and common SNPs for a quantitative trait. We conclude that our method provides a novel and broadly applicable strategy for obtaining association results with a reasonably low proportion of false discovery and that it can be routinely used in resequencing studies.
机译:我们提出了一种基于非参数贝叶斯的聚类算法,以检测与稀有和常见的单核苷酸多态性(SNP)的数量性状的关联。与目前的方法不同,我们的方法在变体水平而非基因水平上鉴定与罕见遗传变异的关联。在这种方法中,我们使用Dirichlet过程先于SNP特定的回归系数的分布,使用距离度量进行层次聚类,该距离度量是从具有相同回归系数的两个SNP的后对成对概率得出的,并探索了数据驱动的方法来选择集群数。落在最大簇内的SNP对回归系数的估计值相对较低或接近零,并被认为与该性状无关。落在最大聚类之外的SNP具有相对较高的回归系数估计值,被认为是潜在的风险变体。利用来自遗传分析研讨会17的数据,我们成功地检测到与稀有和常见SNP的数量性状相关。我们得出的结论是,我们的方法提供了一种新颖且广泛适用的策略,可以以较低的错误发现比例获得关联结果,并且可以在重新测序研究中常规使用该方法。

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