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Updated: May 29, 2026

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
Published on: December 9, 2022
A deep mutational scanning-informed protein language model predicts SARS-CoV-2 evolution dynamics with spatiotemporal
Sijie Yang1,2,3, Xiaowei Luo2, Jiejian Luo2
1Biomedical Pioneering Innovation Center (BIOPIC), Peking University, Beijing, P. R. China.
Abstract:
Early identification of emerging dominant variants of pathogens such as SARS-CoV-2 is important for effective public health responses, yet existing approaches are not feasible for real-time surveillance. Here we introduce DeepCoV (DMS-Empowered Evolution Prediction of CoronaVirus), a deep-learning framework for the dynamic identification of emerging variants with high potential to become prevalent at spatiotemporal resolution. It integrates deep mutational scanning (DMS)-derived mutation phenotypes, evolutionary sequence data and epidemiological surveillance data reflecting human immune pressures. Benchmarked against logistic regression-based methods and representative deep-learning approaches in simulated retrospective surveillance scenarios, DeepCoV accurately forecasts the dominance of recently circulating lineages a month in advance, achieving a 90% reduction in false discovery rate while capturing temporal and geographic dynamics of variant spread and reconstructing their regional prevalence trajectories. It also identified mutational hotspots of Omicron-derived backbones in silico, revealing convergent evolution trends. This provides a scalable framework for timely identification of immune-evasive variants and critical mutations, providing actionable insights.
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