Evidence map›Paper›PMID 42484158›Full record

ArticleBioinformatics (Oxford, England)2026

SignifiKANTE: efficient P-value computation for gene regulatory networks.

Fabian Woller, Paul Martini, Souptik Sen, David B Blumenthal, Anne Hartebrodt

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Article in Bioinformatics (Oxford, England), 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fabian WollerBiomedical Network Science Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID 0000-0001-5492-6819
Paul MartiniBiomedical Network Science Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID 0009-0004-8853-7351
Souptik SenBiomedical Network Science Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID 0009-0000-7486-2613
David B BlumenthalBiomedical Network Science Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID 0000-0001-8651-750X
Anne HartebrodtBiomedical Network Science Lab, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.ORCID 0000-0002-9172-3137

Funding

German Research Foundation 516188180
6 · The paper itself

Abstract

motivationGene regulatory networks (GRNs) are graph-based representations of regulatory relationships between transcription factors and target genes. Various tools exist to infer GRNs from gene expression data, but since GRN inference itself is already computationally intensive, statistical significance estimates are often omitted. While naïve permutation-based empirical P-value computation methods are relatively straightforward to implement, they are prohibitively expensive when applied to popular regression-based GRN inference methods and realistically sized datasets.

resultsTo address this bottleneck, we developed SignifiKANTE, a tool to efficiently quantify edge significance in GRNs obtained via any regression-based GRN inference method. SignifiKANTE is based on the key insight that the background count distributions of groups of target genes may be highly similar, even if their expression vectors show distinct behavior. Relying on this insight, SignifiKANTE uses gene clustering based on the 1-Wasserstein distance to create a small, constant number of background distributions which enables the simultaneous computation of approximate permutation-based P-values for multiple target genes. This reduces the runtime by orders of magnitudes (for some datasets, from several weeks to few hours), without compromising faithfulness of the obtained P-values. AVAILABILITY AND IMPLEMENTATION: SignifiKANTE's Python source code is available at https://github.com/bionetslab/SignifiKANTE, a packaged version at https://pypi.org/project/signifikante, and scripts to reproduce the results at https://github.com/bionetslab/SignifiKANTE_Results.

Indexed as

Computational BiologyGene Regulatory NetworksSoftwareAlgorithmsGene Expression Profiling

Identifiers

PMID42484158
PMCPMC13549948

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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.