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A framework for improving microRNA prediction in non-human genomes
The prediction of novel pre-microRNA (miRNA) from genomic sequence has received considerable attention recently. However, the majority of studies have focused on the human genome. Previous studies have demonstrated that sensitivity (correctly detecting true miRNA) is sustained when human-trained met...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787757/ https://www.ncbi.nlm.nih.gov/pubmed/26163062 http://dx.doi.org/10.1093/nar/gkv698 |
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author | Peace, Robert J. Biggar, Kyle K. Storey, Kenneth B. Green, James R. |
author_facet | Peace, Robert J. Biggar, Kyle K. Storey, Kenneth B. Green, James R. |
author_sort | Peace, Robert J. |
collection | PubMed |
description | The prediction of novel pre-microRNA (miRNA) from genomic sequence has received considerable attention recently. However, the majority of studies have focused on the human genome. Previous studies have demonstrated that sensitivity (correctly detecting true miRNA) is sustained when human-trained methods are applied to other species, however they have failed to report the dramatic drop in specificity (the ability to correctly reject non-miRNA sequences) in non-human genomes. Considering the ratio of true miRNA sequences to pseudo-miRNA sequences is on the order of 1:1000, such low specificity prevents the application of most existing tools to non-human genomes, as the number of false positives overwhelms the true predictions. We here introduce a framework (SMIRP) for creating species-specific miRNA prediction systems, leveraging sequence conservation and phylogenetic distance information. Substantial improvements in specificity and precision are obtained for four non-human test species when our framework is applied to three different prediction systems representing two types of classifiers (support vector machine and Random Forest), based on three different feature sets, with both human-specific and taxon-wide training data. The SMIRP framework is potentially applicable to all miRNA prediction systems and we expect substantial improvement in precision and specificity, while sustaining sensitivity, independent of the machine learning technique chosen. |
format | Online Article Text |
id | pubmed-4787757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47877572016-03-14 A framework for improving microRNA prediction in non-human genomes Peace, Robert J. Biggar, Kyle K. Storey, Kenneth B. Green, James R. Nucleic Acids Res Methods Online The prediction of novel pre-microRNA (miRNA) from genomic sequence has received considerable attention recently. However, the majority of studies have focused on the human genome. Previous studies have demonstrated that sensitivity (correctly detecting true miRNA) is sustained when human-trained methods are applied to other species, however they have failed to report the dramatic drop in specificity (the ability to correctly reject non-miRNA sequences) in non-human genomes. Considering the ratio of true miRNA sequences to pseudo-miRNA sequences is on the order of 1:1000, such low specificity prevents the application of most existing tools to non-human genomes, as the number of false positives overwhelms the true predictions. We here introduce a framework (SMIRP) for creating species-specific miRNA prediction systems, leveraging sequence conservation and phylogenetic distance information. Substantial improvements in specificity and precision are obtained for four non-human test species when our framework is applied to three different prediction systems representing two types of classifiers (support vector machine and Random Forest), based on three different feature sets, with both human-specific and taxon-wide training data. The SMIRP framework is potentially applicable to all miRNA prediction systems and we expect substantial improvement in precision and specificity, while sustaining sensitivity, independent of the machine learning technique chosen. Oxford University Press 2015-11-16 2015-07-10 /pmc/articles/PMC4787757/ /pubmed/26163062 http://dx.doi.org/10.1093/nar/gkv698 Text en © The Author(s) 2015. 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 | Methods Online Peace, Robert J. Biggar, Kyle K. Storey, Kenneth B. Green, James R. A framework for improving microRNA prediction in non-human genomes |
title | A framework for improving microRNA prediction in non-human genomes |
title_full | A framework for improving microRNA prediction in non-human genomes |
title_fullStr | A framework for improving microRNA prediction in non-human genomes |
title_full_unstemmed | A framework for improving microRNA prediction in non-human genomes |
title_short | A framework for improving microRNA prediction in non-human genomes |
title_sort | framework for improving microrna prediction in non-human genomes |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787757/ https://www.ncbi.nlm.nih.gov/pubmed/26163062 http://dx.doi.org/10.1093/nar/gkv698 |
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