Evidence map›Paper›PMID 30165584›Full record

ArticleBioinformatics (Oxford, England)2019

PolyQTL: Bayesian multiple eQTL detection with control for population structure and sample relatedness.

Biao Zeng, Greg Gibson

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Biao ZengSchool of Biological Sciences and Center for Integrative Genomics, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Greg GibsonSchool of Biological Sciences and Center for Integrative Genomics, Georgia Institute of Technology, Atlanta, GA 30332, USA.

Funding

eQTL mega-analysis for functional assessment of multi-enhancer gene regulationR01HG008146 · NHGRI · GEORGIA INSTITUTE OF TECHNOLOGY · PI GIBSON, GREGORY C · 2016 to 2018
$2.3M
NHGRI NIH HHS R01 HG008146
6 · The paper itself

Abstract

motivationExpression quantitative loci (eQTL) are being used widely to annotate and interpret GWAS hits. Recent studies have demonstrated that individual gene expression is often regulated by multiple independent cis-acting eQTL. Diverse methods, frequentist and Bayesian, have already been developed to simultaneously detect and fine-map such multiple eQTL, but most of these ignore sample relatedness and potential population structure. This can result in false positives and disrupt the accuracy of fine-mapping. Here we introduce PolyQTL software for identifying and estimating eQTL effects. The package incorporates a genetic relatedness matrix to remove the influence of population structure and sample relatedness, while utilizing a Bayesian multiple eQTL detection pipeline to identify the most plausible candidate causal variants at one or more independent loci influencing abundance of a transcript.

resultsSimulations demonstrate that our approach improves the rate of discovery of causal variants relative to methods that do not account for relatedness. AVAILABILITY AND IMPLEMENTATION: The software is written in C++, and freely available for download at https://github.com/jxzb1988/PolyQTL.

Indexed as

Genome-Wide Association StudyQuantitative Trait LociBayes TheoremGene ExpressionPolymorphism, Single NucleotideSoftware

Identifiers

PMID30165584
PMCPMC6419993

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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.