Abstract

In recent years, there has been an increasing interest in detecting disease-related rare variants in sequencing studies. Numerous studies have shown that common variants can only explain a small proportion of the phenotypic variance for complex diseases. More and more evidence suggests that some of this missing heritability can be explained by rare variants. Considering the importance of rare variants, researchers have proposed a considerable number of methods for identifying the rare variants associated with complex diseases. Extensive research has been carried out on testing the association between rare variants and dichotomous, continuous or ordinal traits. So far, however, there has been little discussion about the case in which both genotypes and phenotypes are ordinal variables. This paper introduces a method based on the γ-statistic, called OV-RV, for examining disease-related rare variants when both genotypes and phenotypes are ordinal. At present, little is known about the asymptotic distribution of the γ-statistic when conducting association analyses for rare variants. One advantage of OV-RV is that it provides a robust estimation of the distribution of the γ-statistic by employing the permutation approach proposed by Fisher. We also perform extensive simulations to investigate the numerical performance of OV-RV under various model settings. The simulation results reveal that OV-RV is valid and efficient; namely, it controls the type I error approximately at the pre-specified significance level and achieves greater power at the same significance level. We also apply OV-RV for rare variant association studies of diastolic blood pressure.

Highlights

  • Genome-wide association studies (GWAS) have identified thousands of common variants associated with complex diseases or traits

  • Due to the low mutation rate of rare variants, traditional methods used to test single common variants usually lead to substantial bias and low power in rare variant association analysis (Li & Leal, 2008)

  • They showed that sequence kernel association test’ (SKAT) allows for different directions and magnitudes of rare variant effects and achieves greater efficiency compared with burden tests

Read more

Summary

Introduction

Genome-wide association studies (GWAS) have identified thousands of common variants associated with complex diseases or traits. They showed that SKAT allows for different directions and magnitudes of rare variant effects and achieves greater efficiency compared with burden tests. We put forward a method based on the γ-statistic, called OV-RV, for detecting disease-related rare variants when both genotypes and phenotypes are ordinal. We introduce a measure called γ for detecting the association between two ordinal variables and show that the asymptotic distribution of the γ-statistic is no longer applicable in rare variant association studies. To address this issue, a detailed permutation approach is provided.

Method
The cross-contingency table
The γ-statistic
Simulation studies
Simulation I
Simulation II
Application to the detection of disease-related genes
Discussion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call