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Functional Regression Models for Epistasis Analysis of Multiple Quantitative Traits

机译:多种数量性状上位性分析的功能回归模型

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摘要

To date, most genetic analyses of phenotypes have focused on analyzing single traits or analyzing each phenotype independently. However, joint epistasis analysis of multiple complementary traits will increase statistical power and improve our understanding of the complicated genetic structure of the complex diseases. Despite their importance in uncovering the genetic structure of complex traits, the statistical methods for identifying epistasis in multiple phenotypes remains fundamentally unexplored. To fill this gap, we formulate a test for interaction between two genes in multiple quantitative trait analysis as a multiple functional regression (MFRG) in which the genotype functions (genetic variant profiles) are defined as a function of the genomic position of the genetic variants. We use large-scale simulations to calculate Type I error rates for testing interaction between two genes with multiple phenotypes and to compare the power with multivariate pairwise interaction analysis and single trait interaction analysis by a single variate functional regression model. To further evaluate performance, the MFRG for epistasis analysis is applied to five phenotypes of exome sequence data from the NHLBI’s Exome Sequencing Project (ESP) to detect pleiotropic epistasis. A total of 267 pairs of genes that formed a genetic interaction network showed significant evidence of epistasis influencing five traits. The results demonstrate that the joint interaction analysis of multiple phenotypes has a much higher power to detect interaction than the interaction analysis of a single trait and may open a new direction to fully uncovering the genetic structure of multiple phenotypes.
机译:迄今为止,大多数表型的遗传分析都集中于分析单个性状或独立地分析每种表型。但是,对多个互补性状进行联合上位分析将提高统计能力,并增进我们对复杂疾病复杂遗传结构的了解。尽管它们在揭示复杂性状的遗传结构中具有重要意义,但从根本上尚未探索用于鉴定多种表型上位性的统计方法。为了填补这一空白,我们将多重定量性状分析中的两个基因之间的相互作用公式化为多功能回归(MFRG),其中将基因型功能(遗传变异图谱)定义为遗传变异的基因组位置的函数。我们使用大规模模拟来计算I型错误率,以测试具有多个表型的两个基因之间的相互作用,并通过单变量功能回归模型将其与多元成对相互作用分析和单性状相互作用分析进行比较。为了进一步评估性能,将用于上位性分析的MFRG用于来自NHLBI外显子测序项目(ESP)的外显子序列数据的五种表型,以检测多效性上位性。构成基因相互作用网络的总共267对基因显示出上位性影响五个特征的重要证据。结果表明,与单个性状的相互作用分析相比,多种表型的联合相互作用分析具有更高的检测相互作用的能力,并且可能为全面揭示多种表型的遗传结构打开新的方向。

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