Evidence map›Paper›PMID 27000043›Full record

ArticleBMC bioinformatics2016

Sparse regression models for unraveling group and individual associations in eQTL mapping.

Wei Cheng, Yu Shi, Xiang Zhang, Wei Wang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Wei ChengDepartment of Computer Science, UNC at Chapel Hill, 201 S Columbia St., Chapel Hill, NC 27599, USA. chengw02@gmail.com.
Yu ShiComputer Science at the University of Illinois at Urbana-Champaign, 201 North Goodwin Avenue, Urbana, IL 61801, USA.
Xiang ZhangDepartment of Elect. Eng. and Computer Science, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH 44106, USA.
Wei WangDepartment of Computer Science, University of California, Los Angeles, 3531-G Boelter Hall, Los Angeles, CA 90095, USA.

Funding

Mining the Social Web to Monitor Public Health and HIV Risk BehaviorsU01HG008488 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CONDIE, TYSON, WANG, WEI · 2015 to 2017
$1.2M
Fast and Robust Methods for Large Scale Genotype Phenotype Association StudyR01GM115833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, WEI · 2015 to 2017
$933k
NHGRI NIH HHS U01 HG008488NHGRI NIH HHS U01HG008488-01NIGMS NIH HHS R01 GM115833NIGMS NIH HHS R01GM115833-01
6 · The paper itself

Abstract

backgroundAs a promising tool for dissecting the genetic basis of common diseases, expression quantitative trait loci (eQTL) study has attracted increasing research interest. Traditional eQTL methods focus on testing the associations between individual single-nucleotide polymorphisms (SNPs) and gene expression traits. A major drawback of this approach is that it cannot model the joint effect of a set of SNPs on a set of genes, which may correspond to biological pathways.

resultsTo alleviate this limitation, in this paper, we propose geQTL, a sparse regression method that can detect both group-wise and individual associations between SNPs and expression traits. geQTL can also correct the effects of potential confounders. Our method employs computationally efficient technique, thus it is able to fulfill large scale studies. Moreover, our method can automatically infer the proper number of group-wise associations. We perform extensive experiments on both simulated datasets and yeast datasets to demonstrate the effectiveness and efficiency of the proposed method. The results show that geQTL can effectively detect both individual and group-wise signals and outperforms the state-of-the-arts by a large margin.

conclusionsThis paper well illustrates that decoupling individual and group-wise associations for association mapping is able to improve eQTL mapping accuracy, and inferring individual and group-wise associations.

Indexed as

Quantitative Trait LociAlgorithmsChromosome MappingPhenotypePolymorphism, Single NucleotideRegression AnalysisSaccharomyces cerevisiaeComputation efficiencyeQTL mappingGroup-wise association

Identifiers

PMID27000043
PMCPMC4802846

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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.