Predictive Modeling of COVID-19 Variant Peak Prevalence and Duration Using GISAID Data Across 15 Countries
Zhang, Y.; Rob, P.; Chen, K.; Overton, C. E.; Jung, J.; Jo, Y.
Show abstract
BackgroundRapid emergence and replacement of SARS-CoV-2 variants underscore the need for early and reliable indicators of variant dominance to guide timely public health response. However, early genomic trajectories are typically short, sparse, and noisy, with strong fluctuations and substantial cross-country heterogeneity in sequencing intensity and reporting. MethodsWe develop a scalable forecasting framework that predicts whether new variants will reach high prevalence and how long they will persist based on their initial genomic growth patterns. Using more than nine million sequences from 15 countries (GISAID, 2020-2024), we characterize dominance through peak prevalence and duration above 10% and extract early growth descriptors from the first 2-4 weeks after a lineage surpasses 1% frequency. Outcomes were classified using multiple models (GLM, GAM, SVM, CART, Elastic Net, and SuperLearner). We evaluated performance based on accuracy and utilized SHAP analysis to interpret feature importance. ResultsThe Super Learner ensemble model achieved the best performance, achieving up to 0.76 accuracy for peak-share prediction, and up to 0.70 accuracy for duration classification--substantially outperforming all individual models. SHAP analysis showed that variants achieving high peaks exhibit strong but structurally coherent early growth, whereas prolonged dominance is associated not with early surges but with sustained, moderate short-term fluctuations embedded within a stable trajectory. ConclusionThis framework defines minimum surveillance thresholds ([≥]100 sequences in 30 days, [≥]1% detection share), variant grouping rules, and noise-filtering protocols, enabling cross-country comparison and country-specific forecasting. It provides a lightweight, reproducible early-warning tool for genomic surveillance and real-time epidemic intelligence. SignificanceIdentifying emerging SARS-CoV-2 variants capable of driving new surges is critical for global preparedness but remains challenging due to sparse early data. We present a machine learning framework that forecasts variant dominance using only the first 2-4 weeks of genomic growth. Analyzing nine million sequences across 15 countries, we reveal two distinct epidemiological signatures: high peak prevalence is driven by explosive, coherent early expansion, while long-term persistence is predicted by sustained, moderate fluctuations rather than initial speed. By establishing minimum surveillance thresholds, this work delivers a scalable, data-efficient early-warning tool that links early genomic signatures of viral fitness to downstream population-level dominance, achieving high predictive accuracy with a minimal number of sequences.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Fitness models provide accurate short-term forecasts of SARS-CoV-2 variant frequency 97%
- Sensible Long-lead Forecast of COVID-19 Epidemic Outcomes 95%
- Generalizing population RT-qPCR cycle threshold values-informed estimation of epidemiological dynamics: Impact of surveillance practices and pathogen variability 94%
Similar papers in this journal
- Characterizing Spatial Epidemiology in a Heterogeneous Transmission Landscape Using a Novel Spatial Transmission Count Statistic 94%
- COVID-19 in Italy: targeted testing as a proxy of limited health care facilities and a key to reducing hospitalization rate and the death toll 93%
- SARS-CoV-2 transmission dynamics in Belarus revealed by genomic and incidence data analysis 93%
Similar papers in this journal
Similar papers in this journal
- SARS-CoV-2 introductions to the island of Ireland 92%
- Profiling SARS-CoV-2 mutation fingerprints that range from the viral pangenome to individual infection quasispecies 92%
- Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex Lipoprotein(a) KIV-2 VNTR 91%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.