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TarPmiR: a new approach for microRNA target site prediction
Motivation: The identification of microRNA (miRNA) target sites is fundamentally important for studying gene regulation. There are dozens of computational methods available for miRNA target site prediction. Despite their existence, we still cannot reliably identify miRNA target sites, partially due...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018371/ https://www.ncbi.nlm.nih.gov/pubmed/27207945 http://dx.doi.org/10.1093/bioinformatics/btw318 |
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author | Ding, Jun Li, Xiaoman Hu, Haiyan |
author_facet | Ding, Jun Li, Xiaoman Hu, Haiyan |
author_sort | Ding, Jun |
collection | PubMed |
description | Motivation: The identification of microRNA (miRNA) target sites is fundamentally important for studying gene regulation. There are dozens of computational methods available for miRNA target site prediction. Despite their existence, we still cannot reliably identify miRNA target sites, partially due to our limited understanding of the characteristics of miRNA target sites. The recently published CLASH (crosslinking ligation and sequencing of hybrids) data provide an unprecedented opportunity to study the characteristics of miRNA target sites and improve miRNA target site prediction methods. Results: Applying four different machine learning approaches to the CLASH data, we identified seven new features of miRNA target sites. Combining these new features with those commonly used by existing miRNA target prediction algorithms, we developed an approach called TarPmiR for miRNA target site prediction. Testing on two human and one mouse non-CLASH datasets, we showed that TarPmiR predicted more than 74.2% of true miRNA target sites in each dataset. Compared with three existing approaches, we demonstrated that TarPmiR is superior to these existing approaches in terms of better recall and better precision. Availability and Implementation: The TarPmiR software is freely available at http://hulab.ucf.edu/research/projects/miRNA/TarPmiR/. Contacts: haihu@cs.ucf.edu or xiaoman@mail.ucf.edu Supplementary information: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-5018371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50183712016-09-12 TarPmiR: a new approach for microRNA target site prediction Ding, Jun Li, Xiaoman Hu, Haiyan Bioinformatics Original Papers Motivation: The identification of microRNA (miRNA) target sites is fundamentally important for studying gene regulation. There are dozens of computational methods available for miRNA target site prediction. Despite their existence, we still cannot reliably identify miRNA target sites, partially due to our limited understanding of the characteristics of miRNA target sites. The recently published CLASH (crosslinking ligation and sequencing of hybrids) data provide an unprecedented opportunity to study the characteristics of miRNA target sites and improve miRNA target site prediction methods. Results: Applying four different machine learning approaches to the CLASH data, we identified seven new features of miRNA target sites. Combining these new features with those commonly used by existing miRNA target prediction algorithms, we developed an approach called TarPmiR for miRNA target site prediction. Testing on two human and one mouse non-CLASH datasets, we showed that TarPmiR predicted more than 74.2% of true miRNA target sites in each dataset. Compared with three existing approaches, we demonstrated that TarPmiR is superior to these existing approaches in terms of better recall and better precision. Availability and Implementation: The TarPmiR software is freely available at http://hulab.ucf.edu/research/projects/miRNA/TarPmiR/. Contacts: haihu@cs.ucf.edu or xiaoman@mail.ucf.edu Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2016-09-15 2016-05-20 /pmc/articles/PMC5018371/ /pubmed/27207945 http://dx.doi.org/10.1093/bioinformatics/btw318 Text en © The Author 2016. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial 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 | Original Papers Ding, Jun Li, Xiaoman Hu, Haiyan TarPmiR: a new approach for microRNA target site prediction |
title | TarPmiR: a new approach for microRNA target site prediction |
title_full | TarPmiR: a new approach for microRNA target site prediction |
title_fullStr | TarPmiR: a new approach for microRNA target site prediction |
title_full_unstemmed | TarPmiR: a new approach for microRNA target site prediction |
title_short | TarPmiR: a new approach for microRNA target site prediction |
title_sort | tarpmir: a new approach for microrna target site prediction |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018371/ https://www.ncbi.nlm.nih.gov/pubmed/27207945 http://dx.doi.org/10.1093/bioinformatics/btw318 |
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