Evidence map›Paper›PMID 42018564›Full record

ArticlePLoS computational biology2026

Enhancing generalizability of model discovery across parameter space with multi-experiment equation learning for biological systems.

Maria-Veronica Ciocanel, John T Nardini, Kevin B Flores, Erica M Rutter, Suzanne S Sindi, Alexandria Volkening

Abstract read
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Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Maria-Veronica CiocanelDepartments of Mathematics and Biology, Duke University, Durham, North Carolin, United States of America.ORCID https://orcid.org/0000-0001-6859-4659
John T NardiniDepartment of Mathematics and Statistics, The College of New Jersey, Ewing, New Jersey, United States of America.ORCID https://orcid.org/0000-0002-5503-1934
Kevin B FloresDepartment of Mathematics, Center for Research in Scientific Computation, North Carolina State University, Raleigh, North Carolina, United States of America.ORCID https://orcid.org/0000-0002-4000-6971
Erica M RutterDepartment of Applied Mathematics, University of California Merced, Merced, California, United States of America.
Suzanne S SindiDepartment of Applied Mathematics, University of California Merced, Merced, California, United States of America.
Alexandria VolkeningDepartment of Mathematics, Purdue University, West Lafayette, Indiana, United States of America.ORCID https://orcid.org/0000-0003-3401-5094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Agent-based modeling (ABM) is a powerful tool for understanding self-organizing biological systems, but it is computationally intensive and often not analytically tractable. Equation learning (EQL) methods can derive continuum models from ABM data, but they typically require extensive simulations for each parameter set, raising concerns about generalizability. In this work, we extend EQL to Multi-experiment equation learning (ME-EQL) by introducing two methods: (i) one-at-a-time ME-EQL (OAT ME-EQL), which learns individual models for each parameter set and connects them via interpolation, and (ii) embedded structure ME-EQL (ES ME-EQL), which builds a unified model library across parameters. We demonstrate these methods by learning continuum models from a noisy birth-death mean-field model and from an on-lattice agent-based model of birth, death, and migration with spatial structure, often used to investigate cell biology experiments. We show that both methods significantly reduce the relative error in recovering parameters from agent-based simulations, with OAT ME-EQL offering better generalizability across parameter space. Our findings highlight the potential of equation learning from multiple experiments to enhance the generalizability and interpretability of learned models for complex biological systems.

Indexed as

Machine LearningModels, BiologicalSystems BiologyAnimalsCell BiologyComputational BiologyComputer SimulationPopulation Dynamics

Identifiers

PMID42018564
PMCPMC13132452

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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 Socratic graph.