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AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution

With the global epidemic of SARS-CoV-2, it is important to effectively monitor the variation, haplotype subgroup epidemic trends and key mutations of SARS-CoV-2 over time. This is of great significance to the development of new vaccines, the update of therapeutic drugs, and the improvement of detect...

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Autores principales: Xi, Binbin, Jiang, Dawei, Li, Shuhua, Lon, Jerome R., Bai, Yunmeng, Lin, Shudai, Hu, Meiling, Meng, Yuhuan, Qu, Yimo, Huang, Yuting, Liu, Wei, Huang, Lizhen, Du, Hongli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020629/
https://www.ncbi.nlm.nih.gov/pubmed/33841748
http://dx.doi.org/10.1016/j.csbj.2021.04.002
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author Xi, Binbin
Jiang, Dawei
Li, Shuhua
Lon, Jerome R.
Bai, Yunmeng
Lin, Shudai
Hu, Meiling
Meng, Yuhuan
Qu, Yimo
Huang, Yuting
Liu, Wei
Huang, Lizhen
Du, Hongli
author_facet Xi, Binbin
Jiang, Dawei
Li, Shuhua
Lon, Jerome R.
Bai, Yunmeng
Lin, Shudai
Hu, Meiling
Meng, Yuhuan
Qu, Yimo
Huang, Yuting
Liu, Wei
Huang, Lizhen
Du, Hongli
author_sort Xi, Binbin
collection PubMed
description With the global epidemic of SARS-CoV-2, it is important to effectively monitor the variation, haplotype subgroup epidemic trends and key mutations of SARS-CoV-2 over time. This is of great significance to the development of new vaccines, the update of therapeutic drugs, and the improvement of detection methods. The AutoVEM tool developed in the present study could complete all mutations detections, haplotypes classification, haplotype subgroup epidemic trends and candidate key mutations analysis for 131,576 SARS-CoV-2 genome sequences in 18 h on a 1 core CPU and 2 GB RAM computer. Through haplotype subgroup epidemic trends analysis of 131,576 genome sequences, the great significance of the previous 4 specific sites (C241T, C3037T, C14408T and A23403G) was further revealed, and 6 new mutation sites of highly linked (T445C, C6286T, C22227T, G25563T, C26801G and G29645T) were discovered for the first time that might be related to the infectivity, pathogenicity or host adaptability of SARS-CoV-2. In brief, we proposed an integrative method and developed an efficient automated tool to monitor haplotype subgroup epidemic trends and screen for the candidate key mutations in the evolution of SARS-CoV-2 over time for the first time, and all data could be updated quickly to track the prevalence of previous key mutations and new candidate key mutations because of high efficiency of the tool. In addition, the idea of combinatorial analysis in the present study can also provide a reference for the mutation monitoring of other viruses.
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spelling pubmed-80206292021-04-06 AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution Xi, Binbin Jiang, Dawei Li, Shuhua Lon, Jerome R. Bai, Yunmeng Lin, Shudai Hu, Meiling Meng, Yuhuan Qu, Yimo Huang, Yuting Liu, Wei Huang, Lizhen Du, Hongli Comput Struct Biotechnol J Research Article With the global epidemic of SARS-CoV-2, it is important to effectively monitor the variation, haplotype subgroup epidemic trends and key mutations of SARS-CoV-2 over time. This is of great significance to the development of new vaccines, the update of therapeutic drugs, and the improvement of detection methods. The AutoVEM tool developed in the present study could complete all mutations detections, haplotypes classification, haplotype subgroup epidemic trends and candidate key mutations analysis for 131,576 SARS-CoV-2 genome sequences in 18 h on a 1 core CPU and 2 GB RAM computer. Through haplotype subgroup epidemic trends analysis of 131,576 genome sequences, the great significance of the previous 4 specific sites (C241T, C3037T, C14408T and A23403G) was further revealed, and 6 new mutation sites of highly linked (T445C, C6286T, C22227T, G25563T, C26801G and G29645T) were discovered for the first time that might be related to the infectivity, pathogenicity or host adaptability of SARS-CoV-2. In brief, we proposed an integrative method and developed an efficient automated tool to monitor haplotype subgroup epidemic trends and screen for the candidate key mutations in the evolution of SARS-CoV-2 over time for the first time, and all data could be updated quickly to track the prevalence of previous key mutations and new candidate key mutations because of high efficiency of the tool. In addition, the idea of combinatorial analysis in the present study can also provide a reference for the mutation monitoring of other viruses. Research Network of Computational and Structural Biotechnology 2021-04-05 /pmc/articles/PMC8020629/ /pubmed/33841748 http://dx.doi.org/10.1016/j.csbj.2021.04.002 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Xi, Binbin
Jiang, Dawei
Li, Shuhua
Lon, Jerome R.
Bai, Yunmeng
Lin, Shudai
Hu, Meiling
Meng, Yuhuan
Qu, Yimo
Huang, Yuting
Liu, Wei
Huang, Lizhen
Du, Hongli
AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution
title AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution
title_full AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution
title_fullStr AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution
title_full_unstemmed AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution
title_short AutoVEM: An automated tool to real-time monitor epidemic trends and key mutations in SARS-CoV-2 evolution
title_sort autovem: an automated tool to real-time monitor epidemic trends and key mutations in sars-cov-2 evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020629/
https://www.ncbi.nlm.nih.gov/pubmed/33841748
http://dx.doi.org/10.1016/j.csbj.2021.04.002
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