A prediction of mutations in infectious viruses using artificial intelligence

被引:0
|
作者
Won Jong Choi [1 ]
Jongkeun Park [2 ]
Do Young Seong [2 ]
Dae Sun Chung [1 ]
Dongwan Hong [2 ]
机构
[1] Department of Precision Medicine and Big Data, College of Medicine, The Catholic University of Korea, Seoul
[2] Department of Medical Informatics, The Catholic University of Korea, Seoul
[3] Department of Medical Sciences, Graduate Schoolof, College of Medicine, The Catholic University of Korea, Seoul
[4] Precision Medicine Research Center, College of Medicine, The Catholic University of Korea, Seoul
[5] Cancer Evolution Research Center, College of Medicine, The Catholic University of Korea, Seoul
[6] College of Medicine, CMC Institute for Basic Medical Science, The Catholic University of Korea, Seoul
基金
新加坡国家研究基金会;
关键词
Clade; Deep learning; Machine learning; Mutation; Prediction; SARS-CoV-2;
D O I
10.1186/s44342-024-00019-y
中图分类号
学科分类号
摘要
Many subtypes of SARS-CoV-2 have emerged since its early stages, with mutations showing regional and racial differences. These mutations significantly affected the infectivity and severity of the virus. This study aimed to predict the mutations that occur during the evolution of SARS-CoV-2 and identify the key characteristics for making these predictions. We collected and organized data on the lineage, date, clade, and mutations of SARS-CoV-2 from publicly available databases and processed them to predict the mutations. In addition, we utilized various artificial intelligence models to predict newly emerging mutations and created various training sets based on clade information. Using only mutation information resulted in low performance of the learning models, whereas incorporating clade differentiation resulted in high performance in machine learning models, including XGBoost (accuracy: 0.999). However, mutations fixed in the receptor-binding motif (RBM) region of Omicron resulted in decreased predictive performance. Using these models, we predicted potential mutation positions for 24C, following the recently emerged 24A and 24B clades. We identified a mutation at position Q493 in the RBM region. Our study developed effective artificial intelligence models and characteristics for predicting new mutations in continuously evolving infectious viruses. © The Author(s) 2024.
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