Evidence map›Paper›PMID 42773410›Full record

ArticleBMC bioinformatics2026

Systematic detection of predictive gene sets by semantics-based selection.

Peter Eckhardt-Bellmann, Nahla A Taha, Silke D Werle, Johann M Kraus, Nensi Ikonomi, Hans A Kestler

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Article in BMC bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Peter Eckhardt-Bellmann *Institute of Medical Systems Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Baden-Württemberg, Germany.
Nahla A Taha *Institute of Medical Systems Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Baden-Württemberg, Germany.
Silke D WerleInstitute of Medical Systems Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Baden-Württemberg, Germany.
Johann M KrausInstitute of Medical Systems Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Baden-Württemberg, Germany.
Nensi IkonomiInstitute of Medical Systems Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Baden-Württemberg, Germany.
Hans A KestlerInstitute of Medical Systems Biology, Ulm University, Albert-Einstein-Allee 11, 89081, Ulm, Baden-Württemberg, Germany. hans.kestler@uni-ulm.de.ORCID https://orcid.org/0000-0002-4759-5254

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Gene Ontology (GO) is a public resource that describes gene functions and characteristics through a structured vocabulary of standardised terms. It currently contains annotations for over 1.5 million gene products, each linked to one or more GO terms. In this study, we propose integrating this GO-based semantic structure into machine learning systems for medical diagnostics. This approach serves a dual purpose: first, to prioritise genes that are semantically relevant to a given clinical task, thereby refining model input; and second, to enable the analysis of biologically predefined gene sets, which may reveal novel mechanisms underlying disease.

resultsEvaluated across 16 benchmark data sets spanning diverse medical domains, our GO term-informed gene selection method generally outperformed models trained on full gene sets. Further analysis of individual GO terms not only enhanced classification performance but also identified high-performing, task-specific gene subsets that were overlooked during initial gene selection.

conclusionOur findings demonstrate that Gene Ontology can be effectively leveraged for semantics-aware gene selection in clinical machine learning. Moreover, systematically evaluating individual GO terms offers a scalable strategy to uncover new, testable biological hypotheses-revealing gene functions that might otherwise remain hidden when examining only broadly selected gene combinations.

Indexed as

Computational BiologyGene OntologySemanticsDatabases, GeneticHumansMachine LearningGene functionsGene ontologyGene selectionGO terms

Identifiers

PMID42773410
PMCPMC13599332

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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.