ArticlePLoS computational biology2022
Systematic comparison of modeling fidelity levels and parameter inference settings applied to negative feedback gene regulation.
Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Threshold-Filtered Kinetic Monte Carlo Simulation for Real-Time Simulation and Control of Biomass Fractionation.Industrial & engineering chemistry research · 2026Article
- AI-powered simulation-based inference of a genuinely spatial-stochastic gene regulation model of early mouse embryogenesis.PLoS computational biology · 2024Article
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Authors and funding
4 authors.
Funding
Abstract
Quantitative stochastic models of gene regulatory networks are important tools for studying cellular regulation. Such models can be formulated at many different levels of fidelity. A practical challenge is to determine what model fidelity to use in order to get accurate and representative results. The choice is important, because models of successively higher fidelity come at a rapidly increasing computational cost. In some situations, the level of detail is clearly motivated by the question under study. In many situations however, many model options could qualitatively agree with available data, depending on the amount of data and the nature of the observations. Here, an important distinction is whether we are interested in inferring the true (but unknown) physical parameters of the model or if it is sufficient to be able to capture and explain available data. The situation becomes complicated from a computational perspective because inference needs to be approximate. Most often it is based on likelihood-free Approximate Bayesian Computation (ABC) and here determining which summary statistics to use, as well as how much data is needed to reach the desired level of accuracy, are difficult tasks. Ultimately, all of these aspects-the model fidelity, the available data, and the numerical choices for inference-interplay in a complex manner. In this paper we develop a computational pipeline designed to systematically evaluate inference accuracy for a wide range of true known parameters. We then use it to explore inference settings for negative feedback gene regulation. In particular, we compare a detailed spatial stochastic model, a coarse-grained compartment-based multiscale model, and the standard well-mixed model, across several data-scenarios and for multiple numerical options for parameter inference. Practically speaking, this pipeline can be used as a preliminary step to guide modelers prior to gathering experimental data. By training Gaussian processes to approximate the distance function values, we are able to substantially reduce the computational cost of running the pipeline.
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Registered trials
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