Evidence map›Paper›PMID 41340889›Full record

ArticleComputational and structural biotechnology journal2025

Slimformer: An NLP-based web server for semantic categorization of gene sets.

Fionn Daire Keogh, Jonas Marx, Alicia Hiemisch, Rainer Koenig

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. 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
–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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  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.

Fionn Daire KeoghInstitute of Infectious Diseases and Infection Control, Jena University Hospital, Jena, Germany.
Jonas MarxFunctional Proteomics, Jena University Hospital, Jena, Germany.
Alicia HiemischInstitute of Infectious Diseases and Infection Control, Jena University Hospital, Jena, Germany.
Rainer KoenigInstitute of Infectious Diseases and Infection Control, Jena University Hospital, Jena, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Omics data analysis often yields extensive lists of genes or enriched gene sets, making it difficult to interpret the underlying cellular mechanisms. Existing gene set categorization methods typically rely on the Gene Ontology hierarchy, neglecting semantic similarity encoded in textual descriptions. We developed Slimformer, an embedding-based Natural Language Processing model that learns contextual relationships between gene sets based on their names, descriptions, and associated genes. A supervised classifier then assigns these embeddings to process categories, trained on a manually curated gold standard. Applied to 2856 annotated gene sets, Slimformer achieved 82.4 % balanced accuracy and an F1-score of 0.867. Applied to gene expression data from human cells infected with Respiratory Syncytial Virus, Slimformer revealed strong downregulation of major cell cycle processes which is highly relevant for the viral pathomechanism, which was overlooked by other tools we tested. By integrating linguistic and functional information, Slimformer enhances the interpretability of omics data and provides a flexible framework for systematic gene set categorization.

Indexed as

Document embeddingsGene ontologyGene set enrichment analysisNatural language processingRespiratory syncytial virus

Identifiers

PMID41340889
PMCPMC12671349

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.