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GWAS Study

Genome-wide association study for multiple phenotype analysis.

Deng X, Wang B, Fisher V et al.

30263053 PubMed ID
GWAS Study Type
821 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DX
Deng X
WB
Wang B
FV
Fisher V
PG
Peloso G
CA
Cupples A
LC
Liu CT
Chapter II

Abstract

Summary of the research findings

Genome-wide association studies often collect multiple phenotypes for complex diseases. Multivariate joint analyses have higher power to detect genetic variants compared with the marginal analysis of each phenotype and are also able to identify loci with pleiotropic effects. We extend the unified score-based association test to incorporate family structure, apply different approaches to analyze multiple traits in GAW20 real samples, and compare the results. Through simulation studies, we confirm that the Type I error rate of the pedigree-based unified score association test is appropriately controlled. In marginalanalysis of triglyceride levels, we found 1 subgenome-wide significant variant on chromosome 6. Joint analyses identified several suggestive genome-wide significant signals, with the pedigree-based unified score association test yielding the greatest number of significant results.

821 individuals

Chapter III

Study Statistics

Key metrics and study information

821
Total Participants
GWAS
Study Type
No
Replicated
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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