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VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants
With the progression of the COVID-19 pandemic, large datasets of SARS-CoV-2 genome sequences were collected to closely monitor the evolution of the virus and identify the novel variants/strains. By analyzing genome sequencing data, health authorities can ‘hunt’ novel emerging variants of SARS-CoV-2...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325486/ https://www.ncbi.nlm.nih.gov/pubmed/37410916 http://dx.doi.org/10.1093/database/baad044 |
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author | Pinoli, Pietro Canakoglu, Arif Ceri, Stefano Chiara, Matteo Ferrandi, Erika Minotti, Luca Bernasconi, Anna |
author_facet | Pinoli, Pietro Canakoglu, Arif Ceri, Stefano Chiara, Matteo Ferrandi, Erika Minotti, Luca Bernasconi, Anna |
author_sort | Pinoli, Pietro |
collection | PubMed |
description | With the progression of the COVID-19 pandemic, large datasets of SARS-CoV-2 genome sequences were collected to closely monitor the evolution of the virus and identify the novel variants/strains. By analyzing genome sequencing data, health authorities can ‘hunt’ novel emerging variants of SARS-CoV-2 as early as possible, and then monitor their evolution and spread. We designed VariantHunter, a highly flexible and user-friendly tool for systematically monitoring the evolution of SARS-CoV-2 at global and regional levels. In VariantHunter, amino acid changes are analyzed over an interval of 4 weeks in an arbitrary geographical area (continent, country, or region); for every week in the interval, the prevalence is computed and changes are ranked based on their increase or decrease in prevalence. VariantHunter supports two main types of analysis: lineage-independent and lineage-specific. The former considers all the available data and aims to discover new viral variants. The latter evaluates specific lineages/viral variants to identify novel candidate designations (sub-lineages and sub-variants). Both analyses use simple statistics and visual representations (diffusion charts and heatmaps) to track viral evolution. A dataset explorer allows users to visualize available data and refine their selection. VariantHunter is a web application free to all users. The two types of supported analysis (lineage-independent and lineage-specific) allow user-friendly monitoring of the viral evolution, empowering genomic surveillance without requiring any computational background. Database URL http://gmql.eu/variant_hunter/ |
format | Online Article Text |
id | pubmed-10325486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103254862023-07-07 VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants Pinoli, Pietro Canakoglu, Arif Ceri, Stefano Chiara, Matteo Ferrandi, Erika Minotti, Luca Bernasconi, Anna Database (Oxford) Original Article With the progression of the COVID-19 pandemic, large datasets of SARS-CoV-2 genome sequences were collected to closely monitor the evolution of the virus and identify the novel variants/strains. By analyzing genome sequencing data, health authorities can ‘hunt’ novel emerging variants of SARS-CoV-2 as early as possible, and then monitor their evolution and spread. We designed VariantHunter, a highly flexible and user-friendly tool for systematically monitoring the evolution of SARS-CoV-2 at global and regional levels. In VariantHunter, amino acid changes are analyzed over an interval of 4 weeks in an arbitrary geographical area (continent, country, or region); for every week in the interval, the prevalence is computed and changes are ranked based on their increase or decrease in prevalence. VariantHunter supports two main types of analysis: lineage-independent and lineage-specific. The former considers all the available data and aims to discover new viral variants. The latter evaluates specific lineages/viral variants to identify novel candidate designations (sub-lineages and sub-variants). Both analyses use simple statistics and visual representations (diffusion charts and heatmaps) to track viral evolution. A dataset explorer allows users to visualize available data and refine their selection. VariantHunter is a web application free to all users. The two types of supported analysis (lineage-independent and lineage-specific) allow user-friendly monitoring of the viral evolution, empowering genomic surveillance without requiring any computational background. Database URL http://gmql.eu/variant_hunter/ Oxford University Press 2023-07-06 /pmc/articles/PMC10325486/ /pubmed/37410916 http://dx.doi.org/10.1093/database/baad044 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Pinoli, Pietro Canakoglu, Arif Ceri, Stefano Chiara, Matteo Ferrandi, Erika Minotti, Luca Bernasconi, Anna VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants |
title | VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants |
title_full | VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants |
title_fullStr | VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants |
title_full_unstemmed | VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants |
title_short | VariantHunter: a method and tool for fast detection of emerging SARS-CoV-2 variants |
title_sort | varianthunter: a method and tool for fast detection of emerging sars-cov-2 variants |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10325486/ https://www.ncbi.nlm.nih.gov/pubmed/37410916 http://dx.doi.org/10.1093/database/baad044 |
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