Abstract

Region-based association analysis is a more powerful tool for gene mapping than testing of individual genetic variants, particularly for rare genetic variants. The most powerful methods for regional mapping are based on the functional data analysis approach, which assumes that the regional genome of an individual may be considered as a continuous stochastic function that contains information about both linkage and linkage disequilibrium. Here, we extend this powerful approach, earlier applied only to independent samples, to the samples of related individuals. To this end, we additionally include a random polygene effects in functional linear model used for testing association between quantitative traits and multiple genetic variants in the region. We compare the statistical power of different methods using Genetic Analysis Workshop 17 mini-exome family data and a wide range of simulation scenarios. Our method increases the power of regional association analysis of quantitative traits compared with burden-based and kernel-based methods for the majority of the scenarios. In addition, we estimate the statistical power of our method using regions with small number of genetic variants, and show that our method retains its advantage over burden-based and kernel-based methods in this case as well. The new method is implemented as the R-function ‘famFLM’ using two types of basis functions: the B-spline and Fourier bases. We compare the properties of the new method using models that differ from each other in the type of their function basis. The models based on the Fourier basis functions have an advantage in terms of speed and power over the models that use the B-spline basis functions and those that combine B-spline and Fourier basis functions. The ‘famFLM’ function is distributed under GPLv3 license and is freely available at http://mga.bionet.nsc.ru/soft/famFLM/.

Highlights

  • Despite the massive success of genome-wide association studies (GWAS), a significant part of the heritability of quantitative traits remains unexplained

  • The statistical methods based on single genetic variant association tests commonly used in GWAS are underpowered for rare variants due to their uncommon occurrence

  • We have not seen a difference between models that use the functional data analysis (FDA) approach for the beta-smoothing function (BSF) only and for both the genetic variant functions (GVFs) and the BSF

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Summary

Introduction

Despite the massive success of genome-wide association studies (GWAS), a significant part of the heritability of quantitative traits remains unexplained. Studying the role of rare genetic variants in the etiology of complex traits may solve the problem of missing heritability [1]. Region-Based Association Test under Functional Linear Models progress in whole-exome and whole-genome sequencing technologies provides new opportunities for detecting rare variants that control complex traits. The statistical methods based on single genetic variant association tests commonly used in GWAS are underpowered for rare variants due to their uncommon occurrence. The statistical power of association analysis is expected to increase when genetic variants in a region of interest are tested simultaneously, instead of separately [2, 3]

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