Evidence map›Paper›PMID 42178383›Full record

ArticleBioinformatics (Oxford, England)2026

Control-guided refinement of partially specified Boolean networks: applications to RTK signaling.

Eva Šmijáková, Luboš Brim, Samuel Pastva, David Šafránek

Erratum issuedAbstract read
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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. An erratum has been issued. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Eva ŠmijákováFaculty of Informatics, Masaryk University, Brno 60200, Czech Republic.
Luboš BrimFaculty of Informatics, Masaryk University, Brno 60200, Czech Republic.
Samuel PastvaFaculty of Informatics, Masaryk University, Brno 60200, Czech Republic.ORCID 0000-0003-1993-0331
David ŠafránekFaculty of Informatics, Masaryk University, Brno 60200, Czech Republic.ORCID 0000-0002-0713-2431

Funding

Masaryk University Grant Agency
6 · The paper itself

Abstract

motivationSystem control can be used to provide new insights into the dynamics of biological systems. A key application is the identification of therapeutic targets in silico, which requires an executable model of the system's dynamics. However, such models are typically underspecified due to incomplete mechanistic knowledge.

resultsWe introduce a novel computational framework that employs control-guided model refinement, predicting informative perturbation experiments to reduce knowledge gaps. The approach is based on partially specified Boolean networks (PSBNs), which enable direct integration of uncertain or incomplete information into executable models. We further extend the framework to handle oscillatory phenotypes as explicit control targets. The applicability of the method is demonstrated on receptor-tyrosine kinase (RTK) signaling, with a focus on fibroblast growth factor signaling in the context of skeletal dysplasias and cancer. We obtain several new insights into modelling of the FGFR3-MAPK pathway. AVAILABILITY AND IMPLEMENTATION: Code and datasets are available at https://doi.org/10.5281/zenodo.16886813.

Indexed as

Computational BiologyModels, BiologicalReceptor Protein-Tyrosine KinasesSignal TransductionAlgorithmsFibroblast Growth FactorsHumansFibroblast Growth FactorsReceptor Protein-Tyrosine Kinases

Identifiers

PMID42178383
PMCPMC13303288

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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.