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MRPrimerV: a database of PCR primers for RNA virus detection
Many infectious diseases are caused by viral infections, and in particular by RNA viruses such as MERS, Ebola and Zika. To understand viral disease, detection and identification of these viruses are essential. Although PCR is widely used for rapid virus identification due to its low cost and high se...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210568/ https://www.ncbi.nlm.nih.gov/pubmed/27899620 http://dx.doi.org/10.1093/nar/gkw1095 |
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author | Kim, Hyerin Kang, NaNa An, KyuHyeon Kim, Doyun Koo, JaeHyung Kim, Min-Soo |
author_facet | Kim, Hyerin Kang, NaNa An, KyuHyeon Kim, Doyun Koo, JaeHyung Kim, Min-Soo |
author_sort | Kim, Hyerin |
collection | PubMed |
description | Many infectious diseases are caused by viral infections, and in particular by RNA viruses such as MERS, Ebola and Zika. To understand viral disease, detection and identification of these viruses are essential. Although PCR is widely used for rapid virus identification due to its low cost and high sensitivity and specificity, very few online database resources have compiled PCR primers for RNA viruses. To effectively detect viruses, the MRPrimerV database (http://MRPrimerV.com) contains 152 380 247 PCR primer pairs for detection of 1818 viruses, covering 7144 coding sequences (CDSs), representing 100% of the RNA viruses in the most up-to-date NCBI RefSeq database. Due to rigorous similarity testing against all human and viral sequences, every primer in MRPrimerV is highly target-specific. Because MRPrimerV ranks CDSs by the penalty scores of their best primer, users need only use the first primer pair for a single-phase PCR or the first two primer pairs for two-phase PCR. Moreover, MRPrimerV provides the list of genome neighbors that can be detected using each primer pair, covering 22 192 variants of 532 RefSeq RNA viruses. We believe that the public availability of MRPrimerV will facilitate viral metagenomics studies aimed at evaluating the variability of viruses, as well as other scientific tasks. |
format | Online Article Text |
id | pubmed-5210568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-52105682017-01-05 MRPrimerV: a database of PCR primers for RNA virus detection Kim, Hyerin Kang, NaNa An, KyuHyeon Kim, Doyun Koo, JaeHyung Kim, Min-Soo Nucleic Acids Res Database Issue Many infectious diseases are caused by viral infections, and in particular by RNA viruses such as MERS, Ebola and Zika. To understand viral disease, detection and identification of these viruses are essential. Although PCR is widely used for rapid virus identification due to its low cost and high sensitivity and specificity, very few online database resources have compiled PCR primers for RNA viruses. To effectively detect viruses, the MRPrimerV database (http://MRPrimerV.com) contains 152 380 247 PCR primer pairs for detection of 1818 viruses, covering 7144 coding sequences (CDSs), representing 100% of the RNA viruses in the most up-to-date NCBI RefSeq database. Due to rigorous similarity testing against all human and viral sequences, every primer in MRPrimerV is highly target-specific. Because MRPrimerV ranks CDSs by the penalty scores of their best primer, users need only use the first primer pair for a single-phase PCR or the first two primer pairs for two-phase PCR. Moreover, MRPrimerV provides the list of genome neighbors that can be detected using each primer pair, covering 22 192 variants of 532 RefSeq RNA viruses. We believe that the public availability of MRPrimerV will facilitate viral metagenomics studies aimed at evaluating the variability of viruses, as well as other scientific tasks. Oxford University Press 2017-01-04 2016-11-28 /pmc/articles/PMC5210568/ /pubmed/27899620 http://dx.doi.org/10.1093/nar/gkw1095 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Database Issue Kim, Hyerin Kang, NaNa An, KyuHyeon Kim, Doyun Koo, JaeHyung Kim, Min-Soo MRPrimerV: a database of PCR primers for RNA virus detection |
title | MRPrimerV: a database of PCR primers for RNA virus detection |
title_full | MRPrimerV: a database of PCR primers for RNA virus detection |
title_fullStr | MRPrimerV: a database of PCR primers for RNA virus detection |
title_full_unstemmed | MRPrimerV: a database of PCR primers for RNA virus detection |
title_short | MRPrimerV: a database of PCR primers for RNA virus detection |
title_sort | mrprimerv: a database of pcr primers for rna virus detection |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210568/ https://www.ncbi.nlm.nih.gov/pubmed/27899620 http://dx.doi.org/10.1093/nar/gkw1095 |
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