ArticleeLife2026
Prediction of SARS-CoV-2 transmission dynamics based on population-level cycle threshold values: An epidemic transmission and machine learning modeling study.
Article in eLife, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Integrating mathematical modelling and artificial intelligence to combat emerging viral syndemics: A systematic review.New microbes and new infections · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
20 authors.
Funding
Abstract
Polymerase chain reaction (PCR) cycle threshold (Ct) values can be used to estimate the viral burden of Severe Acute Respiratory Syndrome Coronavirus type 2 (SARS-CoV-2) and predict population-level epidemic trends. We investigated the use of epidemic transmission modeling and machine learning (ML) based on Ct value distribution for SARS-CoV-2 incidence prediction in British Columbia, Canada, during an Omicron subvariant BA.1-predominant period from November 2021 to January 2022. Using real-world data, we developed an epidemic transmission model that was first validated on outbreak data and subsequently fitted to province-level data to predict incidence. Using simulated data, we developed a ML pipeline including five models to predict the reproductive number as a measure of transmission potential based on Ct value distribution and validated it on out-of-sample province-level data. The epidemic transmission model demonstrated accurate prediction with the real incidence falling within the 95% credible interval of the predicted MCMC chains for both the long-term care facility outbreak and province-level data. The ML models demonstrated good performance with a mean squared error (MSE) lower than 0.17 across all models and improved performance with increasing sample size. The variability of the Ct distribution around the mean was the strongest predictor of the reproductive number. These modeling approaches demonstrated utility for incidence and reproductive number prediction and have potential to complement traditional surveillance in real time to guide public health interventions.
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Registered trials
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