Evidence map›Paper›PMID 42224360›Full record

ArticlePLoS computational biology2026

On real-time calibrated prediction for complex model-based decision support in pandemics: Part 2.

Trevelyan J McKinley, Daniel B Williamson, Xiaoyu Xiong, James M Salter, Robert Challen, Leon Danon, Ben Youngman, Doug McNeall

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Trevelyan J McKinleyUniversity of Exeter Medical School, University of Exeter, Exeter, United Kingdom.ORCID https://orcid.org/0000-0002-9485-3236
Daniel B WilliamsonDepartment of Mathematics and Statistics, University of Exeter, Exeter, United Kingdom.
Xiaoyu XiongDepartment of Mathematics and Statistics, University of Exeter, Exeter, United Kingdom.
James M SalterDepartment of Mathematics and Statistics, University of Exeter, Exeter, United Kingdom.
Robert ChallenSchool of Engineering Mathematics and Technology, University of Bristol, Bristol, United Kingdom.
Leon DanonSchool of Engineering Mathematics and Technology, University of Bristol, Bristol, United Kingdom.
Ben YoungmanDepartment of Mathematics and Statistics, University of Exeter, Exeter, United Kingdom.
Doug McNeallHadley Centre for Climate Science and Services, UK Met Office, Exeter, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calibration of complex stochastic infectious disease models is challenging. These often have high-dimensional input and output spaces, with the models exhibiting complex, non-linear dynamics. Coupled with a paucity of necessary data, this results in a large number of non-ignorable hidden states that must be handled by the inference routine. Likelihood-based approaches to this missing data problem are very flexible, but challenging to scale, due to having to monitor and update these hidden states. Methods based on simulating the hidden states directly from the model-of-interest have an advantage that they are often more straightforward to code, and thus are easier to implement and adapt in real-time. However, these often require evaluating very large numbers of simulations, rendering them infeasible for many large-scale problems. We present a framework for using emulation-based methods to calibrate a large-scale, stochastic, age-structured, spatial meta-population model of COVID-19 transmission in England and Wales. By embedding a model discrepancy process into the simulation model, and combining this with particle filtering, we show that it is possible to calibrate complex models to high-dimensional data by emulating the log-likelihood surface instead of individual data points. The use of embedded model discrepancy also helps to alleviate other key challenges, such as the introduction of infection across space and time. We conclude with a discussion of major challenges remaining and key areas for future work.

Indexed as

COVID-19Decision Support TechniquesPandemicsCalibrationComputational BiologyComputer SimulationEnglandHumansLikelihood FunctionsModels, BiologicalSARS-CoV-2Stochastic ProcessesWales

Identifiers

PMID42224360
PMCPMC13271513

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.