ArticleThe Journal of chemical physics2013
Adaptively biased sequential importance sampling for rare events in reaction networks with comparison to exact solutions from finite buffer dCME method.
Article in The Journal of chemical physics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.
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Who cites it
14 citing papers in PubMed.
- Truncating the time-evolving discrete chemical master equation for stochastic biological networks.Biophysical journal · 2026Article
- Exact Probability Landscapes of Stochastic Phenotype Switching in Feed-Forward Loops: Phase Diagrams of Multimodality.Frontiers in genetics · 2021Article
- Discrete and continuous models of probability flux of switching dynamics: Uncovering stochastic oscillations in a toggle-switch system.The Journal of chemical physics · 2019Article
- Evolution of Coagulation-Fragmentation Stochastic Processes Using Accurate Chemical Master Equation Approach.Communications in information and systems · 2019Article
- Discrete flux and velocity fields of probability and their global maps in reaction systems.The Journal of chemical physics · 2018Article
- Computational construction of 3D chromatin ensembles and prediction of functional interactions of alpha-globin locus from 5C data.Nucleic acids research · 2017Article
- PRODIGEN: visualizing the probability landscape of stochastic gene regulatory networks in state and time space.BMC bioinformatics · 2017Article
- Distance-Guided Forward and Backward Chain-Growth Monte Carlo Method for Conformational Sampling and Structural Prediction of Antibody CDR-H3 Loops.Journal of chemical theory and computation · 2017Article
- Mechanisms of stochastic focusing and defocusing in biological reaction networks: insight from accurate chemical master equation (ACME) solutions.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference · 2016Article
- Challenges in structural approaches to cell modeling.Journal of molecular biology · 2016Review
- State Space Truncation with Quantified Errors for Accurate Solutions to Discrete Chemical Master Equation.Bulletin of mathematical biology · 2016Article
- ACCURATE CHEMICAL MASTER EQUATION SOLUTION USING MULTI-FINITE BUFFERS.Multiscale modeling & simulation : a SIAM interdisciplinary journal · 2016Article
- Conformational sampling and structure prediction of multiple interacting loops in soluble and β-barrel membrane proteins using multi-loop distance-guided chain-growth Monte Carlo method.Bioinformatics (Oxford, England) · 2015Article
- Multiscale Modeling of Cellular Epigenetic States: Stochasticity in Molecular Networks, Chromatin Folding in Cell Nuclei, and Tissue Pattern Formation of Cells.Critical reviews in biomedical engineering · 2015Article
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2 authors.
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Abstract
Critical events that occur rarely in biological processes are of great importance, but are challenging to study using Monte Carlo simulation. By introducing biases to reaction selection and reaction rates, weighted stochastic simulation algorithms based on importance sampling allow rare events to be sampled more effectively. However, existing methods do not address the important issue of barrier crossing, which often arises from multistable networks and systems with complex probability landscape. In addition, the proliferation of parameters and the associated computing cost pose significant problems. Here we introduce a general theoretical framework for obtaining optimized biases in sampling individual reactions for estimating probabilities of rare events. We further describe a practical algorithm called adaptively biased sequential importance sampling (ABSIS) method for efficient probability estimation. By adopting a look-ahead strategy and by enumerating short paths from the current state, we estimate the reaction-specific and state-specific forward and backward moving probabilities of the system, which are then used to bias reaction selections. The ABSIS algorithm can automatically detect barrier-crossing regions, and can adjust bias adaptively at different steps of the sampling process, with bias determined by the outcome of exhaustively generated short paths. In addition, there are only two bias parameters to be determined, regardless of the number of the reactions and the complexity of the network. We have applied the ABSIS method to four biochemical networks: the birth-death process, the reversible isomerization, the bistable Schlögl model, and the enzymatic futile cycle model. For comparison, we have also applied the finite buffer discrete chemical master equation (dCME) method recently developed to obtain exact numerical solutions of the underlying discrete chemical master equations of these problems. This allows us to assess sampling results objectively by comparing simulation results with true answers. Overall, ABSIS can accurately and efficiently estimate rare event probabilities for all examples, often with smaller variance than other importance sampling algorithms. The ABSIS method is general and can be applied to study rare events of other stochastic networks with complex probability landscape.
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