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DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data
The generation of different types of defective viral genomes (DVG) is an unavoidable consequence of the error-prone replication of RNA viruses. In recent years, a particular class of DVGs, those containing long deletions or genome rearrangements, has gain interest due to their potential therapeutic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144107/ https://www.ncbi.nlm.nih.gov/pubmed/35632855 http://dx.doi.org/10.3390/v14051114 |
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author | Olmo-Uceda, Maria J. Muñoz-Sánchez, Juan C. Lasso-Giraldo, Wilberth Arnau, Vicente Díaz-Villanueva, Wladimiro Elena, Santiago F. |
author_facet | Olmo-Uceda, Maria J. Muñoz-Sánchez, Juan C. Lasso-Giraldo, Wilberth Arnau, Vicente Díaz-Villanueva, Wladimiro Elena, Santiago F. |
author_sort | Olmo-Uceda, Maria J. |
collection | PubMed |
description | The generation of different types of defective viral genomes (DVG) is an unavoidable consequence of the error-prone replication of RNA viruses. In recent years, a particular class of DVGs, those containing long deletions or genome rearrangements, has gain interest due to their potential therapeutic and biotechnological applications. Identifying such DVGs in high-throughput sequencing (HTS) data has become an interesting computational problem. Several algorithms have been proposed to accomplish this goal, though all incur false positives, a problem of practical interest if such DVGs have to be synthetized and tested in the laboratory. We present a metasearch tool, DVGfinder, that wraps the two most commonly used DVG search algorithms in a single workflow for the identification of the DVGs in HTS data. DVGfinder processes the results of ViReMa-a and DI-tector and uses a gradient boosting classifier machine learning algorithm to reduce the number of false-positive events. The program also generates output files in user-friendly HTML format, which can help users to explore the DVGs identified in the sample. We evaluated the performance of DVGfinder compared to the two search algorithms used separately and found that it slightly improves sensitivities for low-coverage synthetic HTS data and DI-tector precision for high-coverage samples. The metasearch program also showed higher sensitivity on a real sample for which a set of copy-backs were previously validated. |
format | Online Article Text |
id | pubmed-9144107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91441072022-05-29 DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data Olmo-Uceda, Maria J. Muñoz-Sánchez, Juan C. Lasso-Giraldo, Wilberth Arnau, Vicente Díaz-Villanueva, Wladimiro Elena, Santiago F. Viruses Article The generation of different types of defective viral genomes (DVG) is an unavoidable consequence of the error-prone replication of RNA viruses. In recent years, a particular class of DVGs, those containing long deletions or genome rearrangements, has gain interest due to their potential therapeutic and biotechnological applications. Identifying such DVGs in high-throughput sequencing (HTS) data has become an interesting computational problem. Several algorithms have been proposed to accomplish this goal, though all incur false positives, a problem of practical interest if such DVGs have to be synthetized and tested in the laboratory. We present a metasearch tool, DVGfinder, that wraps the two most commonly used DVG search algorithms in a single workflow for the identification of the DVGs in HTS data. DVGfinder processes the results of ViReMa-a and DI-tector and uses a gradient boosting classifier machine learning algorithm to reduce the number of false-positive events. The program also generates output files in user-friendly HTML format, which can help users to explore the DVGs identified in the sample. We evaluated the performance of DVGfinder compared to the two search algorithms used separately and found that it slightly improves sensitivities for low-coverage synthetic HTS data and DI-tector precision for high-coverage samples. The metasearch program also showed higher sensitivity on a real sample for which a set of copy-backs were previously validated. MDPI 2022-05-23 /pmc/articles/PMC9144107/ /pubmed/35632855 http://dx.doi.org/10.3390/v14051114 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Olmo-Uceda, Maria J. Muñoz-Sánchez, Juan C. Lasso-Giraldo, Wilberth Arnau, Vicente Díaz-Villanueva, Wladimiro Elena, Santiago F. DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data |
title | DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data |
title_full | DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data |
title_fullStr | DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data |
title_full_unstemmed | DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data |
title_short | DVGfinder: A Metasearch Tool for Identifying Defective Viral Genomes in RNA-Seq Data |
title_sort | dvgfinder: a metasearch tool for identifying defective viral genomes in rna-seq data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9144107/ https://www.ncbi.nlm.nih.gov/pubmed/35632855 http://dx.doi.org/10.3390/v14051114 |
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