Evidence map›Paper›PMID 29029013›Full record

ArticleBiostatistics (Oxford, England)2018

An empirical Bayes approach for multiple tissue eQTL analysis.

Gen Li, Andrey A Shabalin, Ivan Rusyn, Fred A Wright, Andrew B Nobel

Abstract read
In one paragraph

Article in Biostatistics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Article
  7. Distributed eQTL analysis with auxiliary information.Journal of statistical planning and inference · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Where Are the Disease-Associated eQTLs?Trends in genetics : TIG · 2021
    Review
  15. Article
  16. Article
  17. Article
  18. Expression Quantitative Trait Loci Analysis in Multiple Tissues.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  19. Article
  20. 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

5 authors.

Gen LiDepartment of Biostatistics, Mailman School of Public Health, Columbia University, 722 W 168th St, New York, NY, 10032 USA gl2521@cumc.columbia.edu.
Andrey A ShabalinCenter for Biomarker Research and Personalized Medicine, Virginia Commonwealth University, 1112 East Clay Street, Richmond, VA, 23298 USA.
Ivan RusynTexas Veterinary Medical Center, Texas A & M University, 660 Raymond Stotzer Pkwy, College Station, TX, 77843 USA.
Fred A WrightDepartment of Statistics and Biological Sciences, North Carolina State University, 1 Lampe Drive, Raleigh, NC, 27695 USA.
Andrew B NobelDepartment of Statistics and Operations Research, University of North Carolina at Chapel Hill, 318 E Cameron Ave, Chapel Hill, NC, 27599 USA.

Funding

Single cell, multi-parametric high throughput platform to classify endocrine disruptor potential of mixturesP42ES027704 · NIEHS · TEXAS A&M UNIVERSITY · PI Weihsueh A Chiu · 2017 to 2026
$21.2M
Genes, genomes, and genotoxicity: in vivo epigenetic toxicology of 1,3-butadieneR01ES023195 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CRAWFORD, GREGORY E, FUREY, TERRENCE S. · 2013 to 2016
$2.2M
Multi-tissue and network models for next-generation EQTL studiesR01HG009125 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NOBEL, ANDREW B, WRIGHT, FRED A. · 2016 to 2018
$1.1M
FACILITATING GTEx, DISEASE, AND GxE ANALYSES VIA FAST EXPRESSION (e)QTL MAPPINGR01MH090936 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NOBEL, ANDREW B, RUSYN, IVAN · 2010 to 2012
$847k
NHGRI NIH HHS R01 HG009125NIEHS NIH HHS P42 ES027704NIEHS NIH HHS R01 ES023195NIMH NIH HHS R01 MH090936
6 · The paper itself

Abstract

Expression quantitative trait locus (eQTL) analyses identify genetic markers associated with the expression of a gene. Most up-to-date eQTL studies consider the connection between genetic variation and expression in a single tissue. Multi-tissue analyses have the potential to improve findings in a single tissue, and elucidate the genotypic basis of differences between tissues. In this article, we develop a hierarchical Bayesian model (MT-eQTL) for multi-tissue eQTL analysis. MT-eQTL explicitly captures patterns of variation in the presence or absence of eQTL, as well as the heterogeneity of effect sizes across tissues. We devise an efficient Expectation-Maximization (EM) algorithm for model fitting. Inferences concerning eQTL detection and the configuration of eQTL across tissues are derived from the adaptive thresholding of local false discovery rates, and maximum a posteriori estimation, respectively. We also provide theoretical justification of the adaptive procedure. We investigate the MT-eQTL model through an extensive analysis of a 9-tissue data set from the GTEx initiative.

Indexed as

Gene ExpressionModels, StatisticalQuantitative Trait LociBayes TheoremBiostatisticsGenomicsGenotyping TechniquesHumans

Identifiers

PMID29029013
PMCPMC6366007

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.