Evidence map›Paper›PMID 41460880›Full record

ArticlePLoS computational biology2025

Gaussian process emulation for exploring complex infectious disease models.

Anna M Langmüller, Kiran A Chandrasekher, Benjamin C Haller, Samuel E Champer, Courtney C Murdock, Philipp W Messer

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Anna M LangmüllerDepartment of Computational Biology, Cornell University, Ithaca, New York, United States of America.ORCID 0000-0002-6102-8862
Kiran A ChandrasekherDepartment of Computational Biology, Cornell University, Ithaca, New York, United States of America.
Benjamin C HallerDepartment of Computational Biology, Cornell University, Ithaca, New York, United States of America.ORCID 0000-0003-1874-8327
Samuel E ChamperDepartment of Computational Biology, Cornell University, Ithaca, New York, United States of America.ORCID 0000-0002-4559-7627
Courtney C MurdockDepartment of Entomology, Cornell University, Ithaca, New York, United States of America.
Philipp W MesserDepartment of Computational Biology, Cornell University, Ithaca, New York, United States of America.

Funding

Population genetics of rapid evolutionary processesR35GM152242 · NIGMS · CORNELL UNIVERSITY · PI Philipp W Messer · 2024 to 2026
$1.2M
NIGMS NIH HHS R35 GM152242
6 · The paper itself

Abstract

Epidemiological models that aim for a high degree of biological realism by simulating every individual in a population are unavoidably complex, with many free parameters, which makes systematic explorations of their dynamics computationally challenging. In this study, we demonstrate how Gaussian Process emulation can overcome this challenge. To simulate disease dynamics, we developed an abstract individual-based model that is loosely inspired by dengue, incorporating some key features shaping dengue epidemics such as social structure, human movement, and seasonality. We focused on three epidemiological metrics derived from the individual-based model outcomes - outbreak probability, maximum incidence, and epidemic duration - and trained three Gaussian Process surrogate models to approximate these metrics. The GP surrogate models enabled the rapid prediction of these epidemiological metrics at any point in the eight-dimensional parameter space of the original model. Our analysis revealed that average infectivity and average human mobility are key drivers of these epidemiological metrics, while the seasonal timing of the first infection can influence the course of the epidemic outbreak. We used a dataset comprising more than 1,000 dengue epidemics observed over 12 years in Colombia to calibrate our Gaussian Process model and evaluated its predictive power. The calibrated Gaussian Process model identified a subset of municipalities with consistently higher average infectivity estimates; the notable overlap between these municipalities and previously reported dengue disease clusters suggests that statistical emulation can facilitate empirical data analysis. Overall, this work underscores the potential of Gaussian Process emulation to enable the use of more complex individual-based models in epidemiology, allowing a higher degree of realism and accuracy that should increase our ability to control diseases of public health concern.

Indexed as

Communicable DiseasesEpidemiological ModelsColombiaComputational BiologyComputer SimulationDengueDisease OutbreaksEpidemicsHumansModels, StatisticalNormal DistributionSeasons

Identifiers

PMID41460880
PMCPMC12774377

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.