Evidence map›Paper›PMID 24482837›Full record

ArticleGenetic epidemiology2014

A versatile omnibus test for detecting mean and variance heterogeneity.

Ying Cao, Peng Wei, Matthew Bailey, John S K Kauwe, Taylor J Maxwell

Abstract read
In one paragraph

Article in Genetic epidemiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  18. High-Order Association Mapping for Expression Quantitative Trait Loci.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  19. Article
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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

5 authors.

Ying Cao *Human Genetics Center, UT School of Public Health, Houston, TX 77030, USA.
Peng Wei *Human Genetics Center, UT School of Public Health, Houston, TX 77030, USA.
Matthew BaileyDepartment of Biology, Brigham Young University, Provo, UT 84602, USA.
John S K KauweDepartment of Biology, Brigham Young University, Provo, UT 84602, USA.
Taylor J MaxwellHuman Genetics Center, UT School of Public Health, Houston, TX 77030, USA.

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
RECRUITMENT COREU19AG010483 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FELDMAN, HOWARD · 2013 to 2020
$80.6M
Association analysis of rare variants with sequencing dataR01HL116720 · NHLBI · UNIVERSITY OF MINNESOTA · PI PAN, WEI, WEI, PENG · 2013 to 2020
$3.3M
Research Supplements to Promote Diversity in Health-Related ResearchR01AG042611 · NIA · BRIGHAM YOUNG UNIVERSITY · PI KAUWE, JOHN SAI KEONG · 2012 to 2017
$1.5M
Impact of Amino Acid Variants and Interactions on Lipid Profiles and Incident CHDR01HL105502 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MAXWELL, TAYLOR J · 2011 to 2015
$1.1M
Genetic Susceptibility and Risk Model for Pancreatic CancerR01CA169122 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI WEI, PENG · 2013 to 2016
$1.1M
NCI NIH HHS R01 CA169122NCI NIH HHS R01CA169122NHLBI NIH HHS R01 HL105502NHLBI NIH HHS R01HL105502NHLBI NIH HHS R01 HL116720NHLBI NIH HHS R01HL116720NIA NIH HHS R01 AG042611NIA NIH HHS U19 AG010483NIA NIH HHS U24 AG021886
6 · The paper itself

Abstract

Recent research has revealed loci that display variance heterogeneity through various means such as biological disruption, linkage disequilibrium (LD), gene-by-gene (G × G), or gene-by-environment interaction. We propose a versatile likelihood ratio test that allows joint testing for mean and variance heterogeneity (LRT(MV)) or either effect alone (LRT(M) or LRT(V)) in the presence of covariates. Using extensive simulations for our method and others, we found that all parametric tests were sensitive to nonnormality regardless of any trait transformations. Coupling our test with the parametric bootstrap solves this issue. Using simulations and empirical data from a known mean-only functional variant, we demonstrate how LD can produce variance-heterogeneity loci (vQTL) in a predictable fashion based on differential allele frequencies, high D', and relatively low r² values. We propose that a joint test for mean and variance heterogeneity is more powerful than a variance-only test for detecting vQTL. This takes advantage of loci that also have mean effects without sacrificing much power to detect variance only effects. We discuss using vQTL as an approach to detect G × G interactions and also how vQTL are related to relationship loci, and how both can create prior hypothesis for each other and reveal the relationships between traits and possibly between components of a composite trait.

Indexed as

Models, GeneticAlzheimer DiseaseGene FrequencyGenesGenotypeHumansLikelihood FunctionsLinkage DisequilibriumMatrix Metalloproteinase 3PhenotypeQuantitative Trait LociResearch DesignMatrix Metalloproteinase 3MMP3 protein, human

Identifiers

PMID24482837
PMCPMC4019404

What OpenQuestion holds

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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.