Evidence map›Paper›PMID 38898151›Full record

ArticleCommunications biology2024

GOAT: efficient and robust identification of gene set enrichment.

Frank Koopmans

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

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  8. Proinflammatory and cytotoxic CD38American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
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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

1 author.

Frank KoopmansDepartment of Molecular and Cellular Neurobiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University, 1081 HV, Amsterdam, The Netherlands. frank.koopmans@vu.nl.ORCID 0000-0002-4973-5732

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene set enrichment analysis is foundational to the interpretation of high throughput biology. Identifying enriched Gene Ontology (GO) terms or disease-associated gene sets within a list of gene effect sizes that represent experimental outcomes is an everyday task in life science that crucially depends on robust and sensitive statistical tools. We here present GOAT, a parameter-free algorithm for gene set enrichment analysis of preranked gene lists. The algorithm can precompute null distributions from standardized gene scores, enabling enrichment testing of the GO database in one second. Validations using synthetic data show that estimated gene set p-values are well calibrated under the null hypothesis and invariant to gene list length and gene set size. Application to various real-world proteomics and gene expression studies demonstrates that GOAT identifies more significant GO terms as compared to current methods. GOAT is freely available as an R package and user-friendly online tool for gene set enrichment analyses that includes interactive data visualizations: https://ftwkoopmans.github.io/goat .

Indexed as

AlgorithmsAnimalsComputational BiologyDatabases, GeneticGene Expression ProfilingGene OntologyHumansProteomicsSoftware

Identifiers

PMID38898151
PMCPMC11187187

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.