Evidence map›Paper›PMID 24320951›Full record

ArticleBiometrics2014

A Bayesian extension of the hypergeometric test for functional enrichment analysis.

Jing Cao, Song Zhang

Abstract read
In one paragraph

Article in Biometrics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

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

  1. Pooled it
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  7. Global hinge sites of proteins as target sites for drug binding.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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

2 authors.

Jing CaoDepartment of Statistical Science, Southern Methodist University, Dallas, Texas 75275, U.S.A.
Song Zhang

Funding

UT Southwestern Center for Translational Medicine (UL1/KL2/TL1)UL1TR001105 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2013 to 2017
$24.5M
UT-Southwestern Clinical and Translational Alliance for Research (UT-STAR) (TL1)UL1TR000451 · NCATS · UT SOUTHWESTERN MEDICAL CENTER · PI TOTO, ROBERT DANIEL · 2012 to 2012
$6.3M
Incorporating Gene Ontology and Pathway Knowledge into Over Representation AnalysR15HG006365 · NHGRI · SOUTHERN METHODIST UNIVERSITY · PI CAO, JING · 2011 to 2011
$277k
NCATS NIH HHS UL1 TR000451NCATS NIH HHS UL1TR000451NCATS NIH HHS UL1 TR001105NHGRI NIH HHS 1R15HG006365-01NHGRI NIH HHS R15 HG006365
6 · The paper itself

Abstract

Functional enrichment analysis is conducted on high-throughput data to provide functional interpretation for a list of genes or proteins that share a common property, such as being differentially expressed (DE). The hypergeometric P-value has been widely used to investigate whether genes from pre-defined functional terms, for example, Gene Ontology (GO), are enriched in the DE genes. The hypergeometric P-value has three limitations: (1) computed independently for each term, thus neglecting biological dependence; (2) subject to a size constraint that leads to the tendency of selecting less-specific terms; (3) repeated use of information due to overlapping annotations by the true-path rule. We propose a Bayesian approach based on the non-central hypergeometric model. The GO dependence structure is incorporated through a prior on non-centrality parameters. The likelihood function does not include overlapping information. The inference about enrichment is based on posterior probabilities that do not have a size constraint. This method can detect moderate but consistent enrichment signals and identify sets of closely related and biologically meaningful functional terms rather than isolated terms. We also describe the basic ideas of assumption and implementation of different methods to provide some theoretical insights, which are demonstrated via a simulation study. A real application is presented.

Indexed as

Bayes TheoremData Interpretation, StatisticalGene OntologyCD40 AntigensCell Line, TumorComputational BiologyComputer SimulationGene Expression ProfilingHumansLymphoma, B-CellOligonucleotide Array Sequence AnalysisReceptors, Antigen, B-CellUp-RegulationCD40 AntigensReceptors, Antigen, B-CellFunctional enrichment analysisGene ontologyHypergeometric P-valueModular enrichment analysisNon-central hypergeometric distribution

Identifiers

PMID24320951
PMCPMC3954234

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Registered trials

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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.