4.7 Article

A Statistical Approach for Testing Cross-Phenotype Effects of Rare Variants

Journal

AMERICAN JOURNAL OF HUMAN GENETICS
Volume 98, Issue 3, Pages 525-540

Publisher

CELL PRESS
DOI: 10.1016/j.ajhg.2016.01.017

Keywords

-

Funding

  1. NIH [HG007508, HL086694, HL119443, MH071537, GM117946, AR060893]
  2. Div Of Biological Infrastructure
  3. Direct For Biological Sciences [1457935] Funding Source: National Science Foundation

Ask authors/readers for more resources

Increasing empirical evidence suggests that many genetic variants influence multiple distinct phenotypes. When cross-phenotype effects exist, multivariate association methods that consider pleiotropy are often more powerful than univariate methods that model each phenotype separately. Although several statistical approaches exist for testing cross-phenotype effects for common variants, there is a lack of similar tests for gene-based analysis of rare variants. In order to fill this important gap, we introduce a statistical method for cross-phenotype analysis of rare variants using a nonparametric distance-covariance approach that compares similarity in multivariate phenotypes to similarity in rare-variant genotypes across a gene. The approach can accommodate both binary and continuous phenotypes and further can adjust for covariates. Our approach yields a closed-form test whose significance can be evaluated analytically, thereby improving computational efficiency and permitting application on a genome-wide scale. We use simulated data to demonstrate that our method, which we refer to as the Gene Association with Multiple Traits (GAMuT) test, provides increased power over competing approaches. We also illustrate our approach using exome-chip data from the Genetic Epidemiology Network of Arteriopathy.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available