Evidence map›Paper›PMID 42549893›Full record

ArticleBioinformatics (Oxford, England)2026

Trans-dimensional Bayesian model averaging for 13C-metabolic flux analysis: evidence-based flux inference under structural model uncertainty.

Johann F Jadebeck, Anton Stratmann, Martin Beyß, Katharina Nöh

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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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4 authors.

Johann F JadebeckInstitute of Bio- and Geosciences, Forschungszentrum Jülich, Wilhelm-Johnen Straße, Jülich 52428, Germany.ORCID 0000-0002-5026-1546
Anton StratmannInstitute of Bio- and Geosciences, Forschungszentrum Jülich, Wilhelm-Johnen Straße, Jülich 52428, Germany.ORCID 0000-0001-8391-3398
Martin BeyßInstitute of Bio- and Geosciences, Forschungszentrum Jülich, Wilhelm-Johnen Straße, Jülich 52428, Germany.ORCID 0000-0002-5383-3415
Katharina NöhInstitute of Bio- and Geosciences, Forschungszentrum Jülich, Wilhelm-Johnen Straße, Jülich 52428, Germany.ORCID 0000-0002-5407-2275

Funding

Helmholtz Association of German Research CentresHelmholtz School for Data Science in Life, Earth, and Energy
6 · The paper itself

Abstract

motivationAccurate quantification of intracellular metabolic fluxes is central to systems biology and biotechnology. Flux estimation relies on biochemical network models, with 13C-metabolic flux analysis (MFA) being the state-of-the-art approach. However, isotope labeling data are often insufficient to uniquely support a single network formulation. In such cases, flux estimates become model-dependent, highlighting the need for methods that explicitly account for structural uncertainty. Bayesian model averaging provides a principled framework for this purpose, but its application to 13C-MFA has so far been restricted to uncertainty in reaction bidirectionality within fixed network topologies.

resultsWe introduce a scalable Bayesian inference framework for 13C-MFA, Bayesian model set averaging, that applies Bayesian model averaging to encompass uncertainty in reactions and pathways. Our approach combines reversible jump Markov chain Monte Carlo for trans-dimensional exploration of structural hypotheses with diffusive nested sampling for robust estimation of model evidences, enabling averaging over large families of metabolic network structures. Using illustrative and application-scale synthetic case studies, we demonstrate that the method yields robust flux estimates, reveals when multiple network configurations are statistically indistinguishable, and recovers the correct data-supported pathway configuration as data informativeness increases. Rather than conditioning inference on a single assumed network structure, the framework quantifies posterior support for alternative reaction and pathway hypotheses and propagates the resulting structural uncertainty into flux estimates. The approach scales to billions of model variants, providing a practical foundation for quantitative Bayesian flux inference under structural model uncertainty in 13C-MFA. AVAILABILITY AND IMPLEMENTATION: Sources and scripts to replicate results are available at https://github.com/JuBiotech/Supplement-to-Jadebeck-et-al.-2026.

Indexed as

Carbon IsotopesMetabolic Flux AnalysisModels, BiologicalBayes TheoremMarkov ChainsMetabolic Networks and PathwaysMonte Carlo MethodSystems BiologyUncertaintyCarbon Isotopes

Identifiers

PMID42549893
PMCPMC13549947

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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.