Evidence map›Paper›PMID 28505156›Full record

ArticlePLoS computational biology2017

An independent component analysis confounding factor correction framework for identifying broad impact expression quantitative trait loci.

Jin Hyun Ju, Sushila A Shenoy, Ronald G Crystal, Jason G Mezey

Abstract read
In one paragraph

Article in PLoS computational biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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.

Jin Hyun JuDepartment of Genetic Medicine, Weill Cornell Medical College, New York, NY, United States of America.
Sushila A ShenoyDepartment of Genetic Medicine, Weill Cornell Medical College, New York, NY, United States of America.ORCID 0000-0002-5953-1207
Ronald G CrystalDepartment of Genetic Medicine, Weill Cornell Medical College, New York, NY, United States of America.
Jason G MezeyDepartment of Genetic Medicine, Weill Cornell Medical College, New York, NY, United States of America.ORCID 0000-0001-9250-6583

Funding

COPD Metabolome, Smoking Oxidants and Aberrant Ciliated Cell FunctionP20HL113443 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G · 2012 to 2016
$5.3M
Integrative-omics Network Model of the Disordered COPD Small Airway EpitheliumR01HL118541 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G, MEZEY, JASON G · 2014 to 2017
$3.9M
HIV Reprogrammed Airway Basal Cells Acquire a “Tissue Destructive” PhenotypeR01HL134549 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G · 2016 to 2019
$3.4M
Pulmonary Genetic Medicine Training ProgramT32HL094284 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CRYSTAL, RONALD G · 2009 to 2019
$3.0M
Medical Research CouncilNHLBI NIH HHS P20 HL113443NHLBI NIH HHS R01 HL118541NHLBI NIH HHS R01 HL134549NHLBI NIH HHS T32 HL094284Wellcome Trust
6 · The paper itself

Abstract

Genome-wide expression Quantitative Trait Loci (eQTL) studies in humans have provided numerous insights into the genetics of both gene expression and complex diseases. While the majority of eQTL identified in genome-wide analyses impact a single gene, eQTL that impact many genes are particularly valuable for network modeling and disease analysis. To enable the identification of such broad impact eQTL, we introduce CONFETI: Confounding Factor Estimation Through Independent component analysis. CONFETI is designed to address two conflicting issues when searching for broad impact eQTL: the need to account for non-genetic confounding factors that can lower the power of the analysis or produce broad impact eQTL false positives, and the tendency of methods that account for confounding factors to model broad impact eQTL as non-genetic variation. The key advance of the CONFETI framework is the use of Independent Component Analysis (ICA) to identify variation likely caused by broad impact eQTL when constructing the sample covariance matrix used for the random effect in a mixed model. We show that CONFETI has better performance than other mixed model confounding factor methods when considering broad impact eQTL recovery from synthetic data. We also used the CONFETI framework and these same confounding factor methods to identify eQTL that replicate between matched twin pair datasets in the Multiple Tissue Human Expression Resource (MuTHER), the Depression Genes Networks study (DGN), the Netherlands Study of Depression and Anxiety (NESDA), and multiple tissue types in the Genotype-Tissue Expression (GTEx) consortium. These analyses identified both cis-eQTL and trans-eQTL impacting individual genes, and CONFETI had better or comparable performance to other mixed model confounding factor analysis methods when identifying such eQTL. In these analyses, we were able to identify and replicate a few broad impact eQTL although the overall number was small even when applying CONFETI. In light of these results, we discuss the broad impact eQTL that have been previously reported from the analysis of human data and suggest that considerable caution should be exercised when making biological inferences based on these reported eQTL.

Indexed as

AlgorithmsAnxietyComputational BiologyDatabases, GeneticDepressionGene Regulatory NetworksGenome-Wide Association StudyHumansModels, GeneticModels, StatisticalNetherlandsQuantitative Trait Loci

Identifiers

PMID28505156
PMCPMC5448815

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.