Trajectory-matching ABC-MCMC for simulating heterogeneous dynamics in mechanistic models

preprint OA: closed
📄 Open PDF Full text JSON View at publisher
Full text 1,967 characters · extracted from oa-doi-fallback · click to expand
Abstract The inherent heterogeneity of complex biological systems makes it difficult to experimentally and clinically explore individual outcomes within them. Mechanistic mathematical models are essential tools for studying such heterogeneity. Thus, there is increasing interest in integrating newer mechanistic model-based techniques, like virtual patient cohorts and virtual clinical trials, within experimental and regulatory pipelines to probe relationships that may be difficult or impossible to ascertain through traditional wetlab or clinical experimentation alone. Computational approaches like Approximate Bayesian Computation (ABC) are attractive methods for generating virtual patient cohorts and running virtual clinical trials. Among the various ABC approaches, ABC combined with Markov chain Monte Carlo (ABC-MCMC) is widely used to improve sampling efficiency and guarantee convergence to the approximate posterior. However, ABC-MCMC must meet the acceptance criteria of both approaches, which results in a high rejection rate. In response, we developed a model-based technique called trajectory-matching ABC-MCMC (TM-ABC-MCMC). TM-ABC-MCMC captures the variability of complex biological systems by constraining model trajectories between the upper and lower bounds of available data to generate heterogeneity in model parameters. By testing the method’s performance on existing mechanistic models and comparing to existing ABC-MCMC algorithms, we show that TM-ABC-MCMC accurately reproduces the observed noise in biological systems of varying complexity, all while maintaining computational efficiency. Thus, TM-ABC-MCMC is a new approach for generating heterogeneity in mechanistic mathematical models with implications for model-based experimental design, virtual patient cohorts, and virtual clinical trials. Competing Interest Statement The authors have declared no competing interest. Footnotes Display issue in Figure 1 corrected with revisions.

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.

Source provenance

europepmc
last seen: 2026-05-20T01:45:00.602351+00:00