ArticleThe journal of physical chemistry. B2019
Bayesian Estimation for Stochastic Gene Expression Using Multifidelity Models.
Article in The journal of physical chemistry. B, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Avoiding matrix exponentials for large transition rate matrices.The Journal of chemical physics · 2024Article
- Review
- Monte Carlo samplers for efficient network inference.PLoS computational biology · 2023Article
- Studying stochastic systems biology of the cell with single-cell genomics data.bioRxiv : the preprint server for biology · 2023Article
- Gene expression model inference from snapshot RNA data using Bayesian non-parametrics.Nature computational science · 2023Article
- Systematic comparison of modeling fidelity levels and parameter inference settings applied to negative feedback gene regulation.PLoS computational biology · 2022Article
- BAYESIAN INFERENCE OF STOCHASTIC REACTION NETWORKS USING MULTIFIDELITY SEQUENTIAL TEMPERED MARKOV CHAIN MONTE CARLO.International journal for uncertainty quantification · 2020Article
- The finite state projection based Fisher information matrix approach to estimate information and optimize single-cell experiments.PLoS computational biology · 2019Article
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Authors and funding
4 authors.
Funding
Abstract
The finite state projection (FSP) approach to solving the chemical master equation has enabled successful inference of discrete stochastic models to predict single-cell gene regulation dynamics. Unfortunately, the FSP approach is highly computationally intensive for all but the simplest models, an issue that is highly problematic when parameter inference and uncertainty quantification takes enormous numbers of parameter evaluations. To address this issue, we propose two new computational methods for the Bayesian inference of stochastic gene expression parameters given single-cell experiments. We formulate and verify an adaptive delayed acceptance Metropolis-Hastings (ADAMH) algorithm to utilize with reduced Krylov-basis projections of the FSP. We then introduce an extension of the ADAMH into a hybrid scheme that consists of an initial phase to construct a reduced model and a faster second phase to sample from the approximate posterior distribution determined by the constructed model. We test and compare both algorithms to an adaptive Metropolis algorithm with full FSP-based likelihood evaluations on three example models and simulated data to show that the new ADAMH variants achieve substantial speedup in comparison to the full FSP approach. By reducing the computational costs of parameter estimation, we expect the ADAMH approach to enable efficient data-driven estimation for more complex gene regulation models.
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Registered trials
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.