Evidence map›Paper›PMID 34787916›Full record

SynthesisGenetic epidemiology2022

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

Yi Yang, Saonli Basu, Lin Zhang

Abstract readMeta-Analysis
In one paragraph

Synthesis in Genetic epidemiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Yi YangDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0002-1471-4026
Saonli BasuDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota, USA.ORCID 0000-0003-1200-4546
Lin ZhangDivision of Biostatistics, University of Minnesota, Minneapolis, Minnesota, USA.

Funding

Statistical Methods for detection of genome-wide GxE interactions in longitudinalR01DA033958 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2013 to 2016
$1.1M
Improved Heritability Estimation by Spatial Mapping of Genetic RelationshipsR21DA046188 · NIDA · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI · 2018 to 2019
$398k
NIDA NIH HHS R01 DA033958NIDA NIH HHS R21 DA046188
6 · The paper itself

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.

Indexed as

Genome-Wide Association StudyModels, GeneticBayes TheoremHumansPhenotypePolymorphism, Single Nucleotidegene-based GWAShierarchical variable selectionmultiple traitsmultivariate GWASsummary statistics

Identifiers

PMID34787916
PMCPMC8795481

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.