Literature DB >> 34787916

A Bayesian hierarchically structured prior for gene-based association testing with multiple traits in genome-wide association studies.

Yi Yang1,2, Saonli Basu1, Lin Zhang1.   

Abstract

Although genome-wide association studies (GWAS) often collect data on multiple correlated traits for complex diseases, conventional gene-based analysis is usually univariate, and therefore, treating traits as uncorrelated. Multivariate analysis of multiple correlated traits can potentially increase the power to detect genes that affect some or all of these traits. In this study, we propose the multivariate hierarchically structured variable selection (HSVS-M) model, a flexible Bayesian model that tests the association of a gene with multiple correlated traits. With only summary statistics, HSVS-M can account for the correlations among genetic variants and among traits simultaneously and can also estimate the various directions and magnitudes of associations between a gene and multiple traits. Simulation studies show that HSVS-M substantially outperforms competing methods in various scenarios, particularly when variants in a gene are associated with a trait in similar directions and magnitudes. We applied HSVS-M to the summary statistics of a meta-analysis GWAS on four lipid traits from the Global Lipids Genetics Consortium and identified 15 genes that have also been confirmed as risk factors in previous studies.
© 2021 Wiley Periodicals LLC.

Entities:  

Keywords:  gene-based GWAS; hierarchical variable selection; multiple traits; multivariate GWAS; summary statistics

Mesh:

Year:  2021        PMID: 34787916      PMCID: PMC8795481          DOI: 10.1002/gepi.22437

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  36 in total

1.  A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants.

Authors:  Wei Pan; Il-Youp Kwak; Peng Wei
Journal:  Am J Hum Genet       Date:  2015-06-25       Impact factor: 11.025

2.  Powerful and efficient SNP-set association tests across multiple phenotypes using GWAS summary data.

Authors:  Bin Guo; Baolin Wu
Journal:  Bioinformatics       Date:  2019-04-15       Impact factor: 6.937

3.  Asymptotic tests of association with multiple SNPs in linkage disequilibrium.

Authors:  Wei Pan
Journal:  Genet Epidemiol       Date:  2009-09       Impact factor: 2.135

4.  Diacylglycerol acyltransferase-2 (DGAT2) and monoacylglycerol acyltransferase-2 (MGAT2) interact to promote triacylglycerol synthesis.

Authors:  Youzhi Jin; Pamela J McFie; Shanna L Banman; Curtis Brandt; Scot J Stone
Journal:  J Biol Chem       Date:  2014-08-27       Impact factor: 5.157

5.  USAT: A Unified Score-Based Association Test for Multiple Phenotype-Genotype Analysis.

Authors:  Debashree Ray; James S Pankow; Saonli Basu
Journal:  Genet Epidemiol       Date:  2015-12-07       Impact factor: 2.135

6.  An Adaptive Association Test for Multiple Phenotypes with GWAS Summary Statistics.

Authors:  Junghi Kim; Yun Bai; Wei Pan
Journal:  Genet Epidemiol       Date:  2015-10-22       Impact factor: 2.135

7.  A global reference for human genetic variation.

Authors:  Adam Auton; Lisa D Brooks; Richard M Durbin; Erik P Garrison; Hyun Min Kang; Jan O Korbel; Jonathan L Marchini; Shane McCarthy; Gil A McVean; Gonçalo R Abecasis
Journal:  Nature       Date:  2015-10-01       Impact factor: 49.962

8.  A Bayesian Gene-Based Genome-Wide Association Study Analysis of Osteosarcoma Trio Data Using a Hierarchically Structured Prior.

Authors:  Yi Yang; Saonli Basu; Lisa Mirabello; Logan Spector; Lin Zhang
Journal:  Cancer Inform       Date:  2018-05-21

9.  The FATP1-DGAT2 complex facilitates lipid droplet expansion at the ER-lipid droplet interface.

Authors:  Ningyi Xu; Shaobing O Zhang; Ronald A Cole; Sean A McKinney; Fengli Guo; Joel T Haas; Sudheer Bobba; Robert V Farese; Ho Yi Mak
Journal:  J Cell Biol       Date:  2012-08-27       Impact factor: 10.539

10.  Common variants at 30 loci contribute to polygenic dyslipidemia.

Authors:  Sekar Kathiresan; Cristen J Willer; Gina M Peloso; Serkalem Demissie; Kiran Musunuru; Eric E Schadt; Lee Kaplan; Derrick Bennett; Yun Li; Toshiko Tanaka; Benjamin F Voight; Lori L Bonnycastle; Anne U Jackson; Gabriel Crawford; Aarti Surti; Candace Guiducci; Noel P Burtt; Sarah Parish; Robert Clarke; Diana Zelenika; Kari A Kubalanza; Mario A Morken; Laura J Scott; Heather M Stringham; Pilar Galan; Amy J Swift; Johanna Kuusisto; Richard N Bergman; Jouko Sundvall; Markku Laakso; Luigi Ferrucci; Paul Scheet; Serena Sanna; Manuela Uda; Qiong Yang; Kathryn L Lunetta; Josée Dupuis; Paul I W de Bakker; Christopher J O'Donnell; John C Chambers; Jaspal S Kooner; Serge Hercberg; Pierre Meneton; Edward G Lakatta; Angelo Scuteri; David Schlessinger; Jaakko Tuomilehto; Francis S Collins; Leif Groop; David Altshuler; Rory Collins; G Mark Lathrop; Olle Melander; Veikko Salomaa; Leena Peltonen; Marju Orho-Melander; Jose M Ordovas; Michael Boehnke; Gonçalo R Abecasis; Karen L Mohlke; L Adrienne Cupples
Journal:  Nat Genet       Date:  2008-12-07       Impact factor: 38.330

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