Evidence map›Paper›PMID 25593000›Full record

ArticleBMC bioinformatics2015

Fast and robust group-wise eQTL mapping using sparse graphical models.

Wei Cheng, Yu Shi, Xiang Zhang, Wei Wang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Robust Multi-Network Clustering via Joint Cross-Domain Cluster Alignment.Proceedings. IEEE International Conference on Data Mining · 2015
    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

4 authors.

Wei ChengDepartment of Computer Science, UNC at Chapel Hill, 201 S Columbia St., Chapel Hill, 27599, NC, USA. weicheng@cs.unc.edu.
Yu ShiComputer Science at the University of Illinois at Urbana-Champaign, 201 North Goodwin Avenue, Urbana, 61801, IL, USA. shiyu7500@gmail.com.
Xiang ZhangDepartment of Elect. Eng. and Computer Science, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, 44106, OH, USA. xiang.zhang@case.edu.
Wei WangDepartment of Computer Science, University of California, Los Angeles, 3531-G Boelter Hall, Los Angeles, 90095, CA, USA. weiwang@cs.ucla.edu.

Funding

UNC and PERLEGEN, IncP50GM076468 · NIGMS · JACKSON LABORATORY · PI PETKOV, PETKO M · 2006 to 2015
$31.0M
Fast and Robust Methods for Large Scale Genotype Phenotype Association StudyR01GM115833 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, WEI · 2015 to 2017
$933k
Imputation and Analysis of Rare Variants in Admixed PopulationsR01HG006703 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, YUN · 2012 to 2014
$931k
NHGRI NIH HHS R01 HG006703NHGRI NIH HHS R01HG006703NIGMS NIH HHS P50 GM076468NIGMS NIH HHS P50 GM076468-08NIGMS NIH HHS R01 GM115833
6 · The paper itself

Abstract

backgroundGenome-wide expression quantitative trait loci (eQTL) studies have emerged as a powerful tool to understand the genetic basis of gene expression and complex traits. The 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 hidden biological pathways.

resultsWe introduce a new approach to identify novel group-wise associations between sets of SNPs and sets of genes. Such associations are captured by hidden variables connecting SNPs and genes. Our model is a linear-Gaussian model and uses two types of hidden variables. One captures the set associations between SNPs and genes, and the other captures confounders. We develop an efficient optimization procedure which makes this approach suitable for large scale studies. Extensive experimental evaluations on both simulated and real datasets demonstrate that the proposed methods can effectively capture both individual and group-wise signals that cannot be identified by the state-of-the-art eQTL mapping methods.

conclusionsConsidering group-wise associations significantly improves the accuracy of eQTL mapping, and the successful multi-layer regression model opens a new approach to understand how multiple SNPs interact with each other to jointly affect the expression level of a group of genes.

Indexed as

Computer GraphicsGene Regulatory NetworksModels, GeneticQuantitative Trait LociAlgorithmsChromosome MappingComputational BiologyGene OntologyGenome, FungalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSaccharomyces cerevisiae Proteins

Identifiers

PMID25593000
PMCPMC4387667

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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.