Evidence map›Paper›PMID 29726908›Full record

ArticleBioinformatics (Oxford, England)2018

VarExp: estimating variance explained by genome-wide GxE summary statistics.

Vincent Laville, Amy R Bentley, Florian Privé, Xiaofeng Zhu, Jim Gauderman, Thomas W Winkler, Mike Province, D C Rao, Hugues Aschard

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Gene-lifestyle interactions in the genomics of human complex traits.European journal of human genetics : EJHG · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

9 authors.

Vincent LavilleGroupe de Génétique Statistique, Département de Génomes and Génétique, C3BI, Institut Pasteur, Paris, France.
Amy R BentleyCenter for Research on Genomics and Global Health, NHGRI, NIH, Bethesda, MD, USA.
Florian PrivéGroupe de Génétique Statistique, Département de Génomes and Génétique, C3BI, Institut Pasteur, Paris, France.
Xiaofeng ZhuDepartment of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, OH, USA.
Jim GaudermanDivision of Biostatistics, Department of Preventive Medicine, University of Southern California, Los Angeles, CA, USA.
Thomas W WinklerDepartment of Genetic Epidemiology, University of Regensburg, Regensburg, Germany.
Mike ProvinceDivision of Statistical Genetics, Washington University in St. Louis, St. Louis, MO, USA.
D C RaoDivision of Biostatistics, School of Medicine, Washington University in St. Louis, St. Louis, MO, USA.
Hugues AschardGroupe de Génétique Statistique, Département de Génomes and Génétique, C3BI, Institut Pasteur, Paris, France.

Funding

Translational Research Support CoreP30ES007048 · NIEHS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Joseph Leo Wiemels · 1996 to 2026
$46.4M
Statistical Methods for Integrative Genomics in CancerP01CA196569 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI David V Conti · 2016 to 2026
$25.5M
A Multi-Ethnic Study of Gene-Lifestyle Interactions in Cardiovascular TraitsR01HL118305 · NHLBI · WASHINGTON UNIVERSITY · PI RAO, DABEERU C · 2014 to 2017
$8.3M
Genetic epidemiology of complex diseasesZ01HG200362 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI ROTIMI, CHARLES · 2008 to 2008
$1.7M
Identifying Genome-scale Interaction Effects in Human Traits and DiseasesR21HG007687 · NHGRI · HARVARD SCHOOL OF PUBLIC HEALTH · PI ASCHARD, HUGUES · 2015 to 2016
$444k
Intramural NIH HHS Z01 HG200362NCI NIH HHS P01 CA196569NHGRI NIH HHS R21 HG007687NHLBI NIH HHS R01 HL118305NIEHS NIH HHS P30 ES007048
6 · The paper itself

Abstract

Summary: Many genome-wide association studies and genome-wide screening for gene-environment (GxE) interactions have been performed to elucidate the underlying mechanisms of human traits and diseases. When the analyzed outcome is quantitative, the overall contribution of identified genetic variants to the outcome is often expressed as the percentage of phenotypic variance explained. This is commonly done using individual-level genotype data but it is challenging when results are derived through meta-analyses. Here, we present R package, 'VarExp', that allows for the estimation of the percentage of phenotypic variance explained using summary statistics only. It allows for a range of models to be evaluated, including marginal genetic effects, GxE interaction effects and both effects jointly. Its implementation integrates all recent methodological developments and does not need external data to be uploaded by users. Availability and implementation: The R package is available at https://gitlab.pasteur.fr/statistical-genetics/VarExp.git. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

Genome-Wide Association StudyGenotypeSoftwareComputational BiologyHumansPhenotype

Identifiers

PMID29726908
PMCPMC6157079

What OpenQuestion holds

Textmetadata
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.