Evidence map›Paper›PMID 32527218›Full record

ArticleBMC bioinformatics2020

Exact solving and sensitivity analysis of stochastic continuous time Boolean models.

Mihály Koltai, Vincent Noel, Andrei Zinovyev, Laurence Calzone, Emmanuel Barillot

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Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Boolean modelling as a logic-based dynamic approach in systems medicine.Computational and structural biotechnology journal · 2022
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Mihály KoltaiInstitut Curie, PSL Research University, Paris, F-75005, France. mihaly.koltai@curie.fr.ORCID http://orcid.org/0000-0002-7341-5114
Vincent NoelInstitut Curie, PSL Research University, Paris, F-75005, France.
Andrei ZinovyevInstitut Curie, PSL Research University, Paris, F-75005, France.
Laurence CalzoneInstitut Curie, PSL Research University, Paris, F-75005, France.
Emmanuel BarillotInstitut Curie, PSL Research University, Paris, F-75005, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSolutions to stochastic Boolean models are usually estimated by Monte Carlo simulations, but as the state space of these models can be enormous, there is an inherent uncertainty about the accuracy of Monte Carlo estimates and whether simulations have reached all attractors. Moreover, these models have timescale parameters (transition rates) that the probability values of stationary solutions depend on in complex ways, raising the necessity of parameter sensitivity analysis. We address these two issues by an exact calculation method for this class of models.

resultsWe show that the stationary probability values of the attractors of stochastic (asynchronous) continuous time Boolean models can be exactly calculated. The calculation does not require Monte Carlo simulations, instead it uses graph theoretical and matrix calculation methods previously applied in the context of chemical kinetics. In this version of the asynchronous updating framework the states of a logical model define a continuous time Markov chain and for a given initial condition the stationary solution is fully defined by the right and left nullspace of the master equation's kinetic matrix. We use topological sorting of the state transition graph and the dependencies between the nullspaces and the kinetic matrix to derive the stationary solution without simulations. We apply this calculation to several published Boolean models to analyze the under-explored question of the effect of transition rates on the stationary solutions and show they can be sensitive to parameter changes. The analysis distinguishes processes robust or, alternatively, sensitive to parameter values, providing both methodological and biological insights.

conclusionUp to an intermediate size (the biggest model analyzed is 23 nodes) stochastic Boolean models can be efficiently solved by an exact matrix method, without using Monte Carlo simulations. Sensitivity analysis with respect to the model's timescale parameters often reveals a small subset of all parameters that primarily determine the stationary probability of attractor states.

Indexed as

Models, BiologicalMonte Carlo MethodStochastic ProcessesAsynchronous updatingBoolean modelingContinuous time Markov chainExact methodSteady state solutionStochastic model

Identifiers

PMID32527218
PMCPMC7291460

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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.