Evidence map›Paper›PMID 36197939›Full record

SynthesisPLoS computational biology2022

Random-effects meta-analysis of effect sizes as a unified framework for gene set analysis.

Mohammad A Makrooni, Dónal O'Shea, Paul Geeleher, Cathal Seoighe

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% of its field
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 at 2 institutions in 2 countries.

Mohammad A MakrooniSchool of Mathematical and Statistical Sciences, University of Galway, Galway, Ireland.
Dónal O'SheaSchool of Mathematical and Statistical Sciences, University of Galway, Galway, Ireland.
Paul GeeleherDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, Tennessee, United States of America.
Cathal SeoigheSchool of Mathematical and Statistical Sciences, University of Galway, Galway, Ireland.ORCID 0000-0003-0496-4029
Ollscoil na Gaillimhe – University of Galway · IESt. Jude Children's Research Hospital · US

Funding

Computational tools for estimating cell-type-specific effects in bulk RNA-seq and spatial transcriptomics data, using reference single-cell RNA-seq datasetsR35GM138293 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GEELEHER, PAUL · 2020 to 2024
$2.2M
Novel computational approaches for pharmacogenomic discoveryR00HG009679 · NHGRI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI GEELEHER, PAUL · 2019 to 2021
$739k
NHGRI NIH HHS R00 HG009679NIGMS NIH HHS R35 GM138293
6 · The paper itself

Abstract

Gene set analysis (GSA) remains a common step in genome-scale studies because it can reveal insights that are not apparent from results obtained for individual genes. Many different computational tools are applied for GSA, which may be sensitive to different types of signals; however, most methods implicitly test whether there are differences in the distribution of the effect of some experimental condition between genes in gene sets of interest. We have developed a unifying framework for GSA that first fits effect size distributions, and then tests for differences in these distributions between gene sets. These differences can be in the proportions of genes that are perturbed or in the sign or size of the effects. Inspired by statistical meta-analysis, we take into account the uncertainty in effect size estimates by reducing the influence of genes with greater uncertainty on the estimation of distribution parameters. We demonstrate, using simulation and by application to real data, that this approach provides significant gains in performance over existing methods. Furthermore, the statistical tests carried out are defined in terms of effect sizes, rather than the results of prior statistical tests measuring these changes, which leads to improved interpretability and greater robustness to variation in sample sizes.

Indexed as

GenomeResearch DesignComputer SimulationSample Size

Identifiers

PMID36197939
PMCPMC9576052
OpenAlexW4302275509

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.