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An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus
Advances in Next Generation Sequencing technologies have enabled the generation of millions of sequences from microorganisms. However, distinguishing the sequence of a novel species from sequencing errors remains a technical challenge when the novel species is highly divergent from the closest known...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223137/ https://www.ncbi.nlm.nih.gov/pubmed/28071766 http://dx.doi.org/10.1038/srep40447 |
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author | Gonzalez, Gabriel Sasaki, Michihito Burkitt-Gray, Lucy Kamiya, Tomonori Tsuji, Noriko M. Sawa, Hirofumi Ito, Kimihito |
author_facet | Gonzalez, Gabriel Sasaki, Michihito Burkitt-Gray, Lucy Kamiya, Tomonori Tsuji, Noriko M. Sawa, Hirofumi Ito, Kimihito |
author_sort | Gonzalez, Gabriel |
collection | PubMed |
description | Advances in Next Generation Sequencing technologies have enabled the generation of millions of sequences from microorganisms. However, distinguishing the sequence of a novel species from sequencing errors remains a technical challenge when the novel species is highly divergent from the closest known species. To solve such a problem, we developed a new method called Optimistic Protein Assembly from Reads (OPAR). This method is based on the assumption that protein sequences could be more conserved than the nucleotide sequences encoding them. By taking advantage of metagenomics, bioinformatics and conventional Sanger sequencing, our method successfully identified all coding regions of the mouse picobirnavirus for the first time. The salvaged sequences indicated that segment 1 of this virus was more divergent from its homologues in other Picobirnaviridae species than segment 2. For this reason, only segment 2 of mouse picobirnavirus has been detected in previous studies. OPAR web tool is available at http://bioinformatics.czc.hokudai.ac.jp/opar/. |
format | Online Article Text |
id | pubmed-5223137 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52231372017-01-11 An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus Gonzalez, Gabriel Sasaki, Michihito Burkitt-Gray, Lucy Kamiya, Tomonori Tsuji, Noriko M. Sawa, Hirofumi Ito, Kimihito Sci Rep Article Advances in Next Generation Sequencing technologies have enabled the generation of millions of sequences from microorganisms. However, distinguishing the sequence of a novel species from sequencing errors remains a technical challenge when the novel species is highly divergent from the closest known species. To solve such a problem, we developed a new method called Optimistic Protein Assembly from Reads (OPAR). This method is based on the assumption that protein sequences could be more conserved than the nucleotide sequences encoding them. By taking advantage of metagenomics, bioinformatics and conventional Sanger sequencing, our method successfully identified all coding regions of the mouse picobirnavirus for the first time. The salvaged sequences indicated that segment 1 of this virus was more divergent from its homologues in other Picobirnaviridae species than segment 2. For this reason, only segment 2 of mouse picobirnavirus has been detected in previous studies. OPAR web tool is available at http://bioinformatics.czc.hokudai.ac.jp/opar/. Nature Publishing Group 2017-01-10 /pmc/articles/PMC5223137/ /pubmed/28071766 http://dx.doi.org/10.1038/srep40447 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Gonzalez, Gabriel Sasaki, Michihito Burkitt-Gray, Lucy Kamiya, Tomonori Tsuji, Noriko M. Sawa, Hirofumi Ito, Kimihito An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
title | An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
title_full | An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
title_fullStr | An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
title_full_unstemmed | An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
title_short | An optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
title_sort | optimistic protein assembly from sequence reads salvaged an uncharacterized segment of mouse picobirnavirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5223137/ https://www.ncbi.nlm.nih.gov/pubmed/28071766 http://dx.doi.org/10.1038/srep40447 |
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