Simulation and inference methods for non-Markovian stochastic reaction networks

Stochastic models of reaction networks are widely used to capture intrinsic noise in complex systems in the life sciences. Typical formulations of these models are based on Markov processes for which there is extensive research on efficient simulation and inference. However, there are complex processes in biology, such as gene transcription and translation, that introduce history dependent dynamics requiring non-Markovian processes to accurately capture the stochastic dynamics of the system. This greater realism comes with additional computational challenges for simulation and parameter inference. We develop efficient stochastic simulation algorithms for well-mixed non-Markovian stochastic reaction networks with stochastic delays that depend on system state and time. Our methods generalize the next reaction method and τ-leaping method to support arbitrary inter-event time distributions while preserving computational scalability. We also introduce a coupling scheme to generate exact non-Markovian sample paths that are positively correlated to an approximate non-Markovian τ-leaping sample path. This enables substantial computational gains for simulation and Bayesian inference through multilevel Monte Carlo and multifidelity schemes. We demonstrate the effectiveness of our approach using several non-Markovian examples, showing substantial gains in both simulation accuracy and inference efficiency. These results extend the practical applicability of non-Markovian models in systems biology and beyond.

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Publication Details

Journal
PLoS Computational Biology
Published
2026-08-26
DOI
https://doi.org/10.1371/journal.pcbi.1014687
Primary Topic
Gene Regulatory Network Analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Simulation and inference methods for non-Markovian stochastic reaction networks

David J. Warne, Thomas P. Steele
PLoS Computational Biology
Gene Regulatory Network Analysis
article

Simulation and inference methods for non-Markovian stochastic reaction networks

David J. Warne, Thomas P. Steele
article en

Abstract

Stochastic models of reaction networks are widely used to capture intrinsic noise in complex systems in the life sciences. Typical formulations of these models are based on Markov processes for which there is extensive research on efficient simulation and inference. However, there are complex processes in biology, such as gene transcription and translation, that introduce history dependent dynamics requiring non-Markovian processes to accurately capture the stochastic dynamics of the system. This greater realism comes with additional computational challenges for simulation and parameter inference. We develop efficient stochastic simulation algorithms for well-mixed non-Markovian stochastic reaction networks with stochastic delays that depend on system state and time. Our methods generalize the next reaction method and τ-leaping method to support arbitrary inter-event time distributions while preserving computational scalability. We also introduce a coupling scheme to generate exact non-Markovian sample paths that are positively correlated to an approximate non-Markovian τ-leaping sample path. This enables substantial computational gains for simulation and Bayesian inference through multilevel Monte Carlo and multifidelity schemes. We demonstrate the effectiveness of our approach using several non-Markovian examples, showing substantial gains in both simulation accuracy and inference efficiency. These results extend the practical applicability of non-Markovian models in systems biology and beyond.

PLoS Computational BiologyVol. 22(8)
Queensland University of Technology (AU)
Queensland University of Technology, Australian Research Council
Responsible consumption and production
Openalex Percentile: Top 17%
Gene Regulatory Network Analysis
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