Abstract

Backgrounds: Although many disease-associated common variants have been discovered through genome-wide association studies, much of the genetic effects of complex diseases have not been explained. Population-based association studies are vulnerable to population stratification. A possible solution is to use family-based tests. However, if tests only estimate the genetic effect from the within-family variation to avoid population stratification, they may ignore the useful genetic information from between-family variation and lose power. Methods: We have developed an adaptive weighted sum test for family-based association studies. The new test uses data driven weights to combine two test statistics, and the weights measure the strength of population stratification. When population stratification is strong, the proposed test will automatically put more weight on one statistic derived from within-family variation to maintain robustness against spurious positives. On the other hand, when the effect of population stratification is relatively weak, the proposed test will automatically put more weight on the other statistic derived from both within-family and between-family variation to make use of both sources of genetic variation; and at the same time, the degrees of freedom of the test will be reduced and power of the test will be increased. Results: In our study, the proposed method achieves a higher power in most scenarios of linkage disequilibrium structure as well as Hap Map data from different genes under different population structures while still keeping its robustness against population stratification.

Highlights

  • We compare the power of the proposed test Proposed test in this article (FBATWS) with the following three family-based association tests (FBAT) tests: 1) the single-marker test with Bonferroni multiple testing adjustment Single-marker test with Bonferroni multiple testing adjustment (FBATB) the Bonferroni adjusted p-value

  • 2) the multi-marker test Multi-marker family-based association test (FBATMM) [10], which is similar to the Hotelling T 2 test, 3) the multi-marker test Linearly combined single-marker test statistics (FBATLC) [11] that linearly combines the single-marker test statistics using data-driven weights

  • A target region with eight observed Single-nucleotide polymorphism (SNP) and an unobserved causative SNP in the middle is simulated. Both parental haplotypes for nine correlated SNP markers are simulated on the basis of a multivariate normal distribution with linkage disequilibrium (LD) structure ΣkLD (i, j ) where k = 1, 6 Each allele on the haplotype is generated with the cut-off of the minor allele frequency which is obtained from a uniform distribution between 0.1 and 0.3

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Summary

Introduction

Recent advances in next-generation sequencing technologies provide new opportunities to study the genetic effects of lowfrequency variants and rare variants. Many of those complex-trait rare-variant association studies are population based [1]. A recently developed program GIGI is efficient to impute genotypes in a large pedigree [5], and it is used for rare-variant family association studies [6]. We introduce an adaptive weighted sum association test to capture more important information from multiple loci in family-based studies by considering the genetic effect from both within-family and between-family variation while maintaining robustness to population stratification

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