Evidence map›Paper›PMID 39649594›Full record

ArticlemedRxiv : the preprint server for health sciences2025

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 readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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, NY 14853, USA.ORCID 0000-0002-6102-8862
Kiran A ChandrasekherDepartment of Computational Biology, Cornell University, Ithaca, NY 14853, USA.
Benjamin C HallerDepartment of Computational Biology, Cornell University, Ithaca, NY 14853, USA.
Samuel E ChamperDepartment of Computational Biology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0002-4559-7627
Courtney C MurdockDepartment of Entomology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0001-5966-1514
Philipp W MesserDepartment of Computational Biology, Cornell University, Ithaca, NY 14853, USA.ORCID 0000-0001-8453-9377

Funding

Scaling up computational genomics with tree sequencesR01HG012473 · NHGRI · UNIVERSITY OF OREGON · PI PETER Lochhead RALPH · 2023 to 2026
$2.3M
Population genetics of rapid evolutionary processesR35GM152242 · NIGMS · CORNELL UNIVERSITY · PI Philipp W Messer · 2024 to 2026
$1.2M
NHGRI NIH HHS R01 HG012473NIGMS 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. This study investigates the potential of Gaussian Process emulation to overcome this obstacle. 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 trained three Gaussian Process surrogate models on three outcomes: outbreak probability, maximum incidence, and epidemic duration. These surrogate models enable the rapid prediction of outcomes 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 use a dataset comprising more than 1,000 dengue epidemics observed over 12 years in Colombia to calibrate our Gaussian Process model and evaluate its predictive power. The calibrated Gaussian Process model identifies a subset of municipalities with consistently higher average infectivity estimates, which show notable overlap with previously reported dengue disease clusters, suggesting 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

epidemiological modelingGaussian Processesindividual-based modelingstatistical emulationvariance-based sensitivity analysis

Identifiers

PMID39649594
PMCPMC11623728

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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.