Evidence map›Paper›PMID 40163580›Full record

ArticlePLoS computational biology2025

GeneCOCOA: Detecting context-specific functions of individual genes using co-expression data.

Simonida Zehr, Sebastian Wolf, Thomas Oellerich, Matthias S Leisegang, Ralf P Brandes, Marcel H Schulz, Timothy Warwick

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. 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

7 authors.

Simonida ZehrGoethe University Frankfurt, Institute for Cardiovascular Physiology, Frankfurt am Main, Germany.
Sebastian WolfGoethe University Frankfurt, University Hospital, Department of Medicine II, Haematology/Oncology, Frankfurt am Main, Germany.
Thomas OellerichGoethe University Frankfurt, University Hospital, Department of Medicine II, Haematology/Oncology, Frankfurt am Main, Germany.
Matthias S LeisegangGoethe University Frankfurt, Institute for Cardiovascular Physiology, Frankfurt am Main, Germany.ORCID 0000-0002-6084-6484
Ralf P BrandesGoethe University Frankfurt, Institute for Cardiovascular Physiology, Frankfurt am Main, Germany.
Marcel H SchulzGerman Centre for Cardiovascular Research (DZHK), Partner site Rhine-Main, Frankfurt am Main, Germany.
Timothy WarwickGoethe University Frankfurt, Institute for Cardiovascular Physiology, Frankfurt am Main, Germany.ORCID 0000-0002-6804-2931

Funding

Deutsche Forschungsgemeinschaft (DFG)Goethe University Frankfurt am Main, the German Centre for Cardiovascular ResearchHessian Center for Artificial Intelligence
6 · The paper itself

Abstract

Extraction of meaningful biological insight from gene expression profiling often focuses on the identification of statistically enriched terms or pathways. These methods typically use gene sets as input data, and subsequently return overrepresented terms along with associated statistics describing their enrichment. This approach does not cater to analyses focused on a single gene-of-interest, particularly when the gene lacks prior functional characterization. To address this, we formulated GeneCOCOA, a method which utilizes context-specific gene co-expression and curated functional gene sets, but focuses on a user-supplied gene-of-interest (GOI). The co-expression between the GOI and subsets of genes from functional groups (e.g. pathways, GO terms) is derived using linear regression, and resulting root-mean-square error values are compared against background values obtained from randomly selected genes. The resulting p values provide a statistical ranking of functional gene sets from any collection, along with their associated terms, based on their co-expression with the gene of interest in a manner specific to the context and experiment. GeneCOCOA thereby provides biological insight into both gene function, and putative regulatory mechanisms by which the expression of the GOI is controlled. Despite its relative simplicity, GeneCOCOA outperforms similar methods in the accurate recall of known gene-disease associations. We furthermore include a differential GeneCOCOA mode, thus presenting the first implementation of a gene-focused approach to experiment-specific gene set enrichment analysis. GeneCOCOA is formulated as an R package for ease-of-use, available at https://github.com/si-ze/geneCOCOA.

Indexed as

Computational BiologyGene Expression ProfilingSoftwareAlgorithmsDatabases, GeneticHumans

Identifiers

PMID40163580
PMCPMC11964461

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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.