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CPPred: coding potential prediction based on the global description of RNA sequence
The rapid and accurate approach to distinguish between coding RNAs and ncRNAs has been playing a critical role in analyzing thousands of novel transcripts, which have been generated in recent years by next-generation sequencing technology. Previously developed methods CPAT, CPC2 and PLEK can disting...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486542/ https://www.ncbi.nlm.nih.gov/pubmed/30753596 http://dx.doi.org/10.1093/nar/gkz087 |
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author | Tong, Xiaoxue Liu, Shiyong |
author_facet | Tong, Xiaoxue Liu, Shiyong |
author_sort | Tong, Xiaoxue |
collection | PubMed |
description | The rapid and accurate approach to distinguish between coding RNAs and ncRNAs has been playing a critical role in analyzing thousands of novel transcripts, which have been generated in recent years by next-generation sequencing technology. Previously developed methods CPAT, CPC2 and PLEK can distinguish coding RNAs and ncRNAs very well, but poorly distinguish between small coding RNAs and small ncRNAs. Herein, we report an approach, CPPred (coding potential prediction), which is based on SVM classifier and multiple sequence features including novel RNA features encoded by the global description. The CPPred can better distinguish not only between coding RNAs and ncRNAs, but also between small coding RNAs and small ncRNAs than the state-of-the-art methods due to the addition of the novel RNA features. A recent study proposes 1335 novel human coding RNAs from a large number of RNA-seq datasets. However, only 119 transcripts are predicted as coding RNAs by the CPPred. In fact, almost all proposed novel coding RNAs are ncRNAs (91.1%), which is consistent with previous reports. Remarkably, we also reveal that the global description of encoding features (T2, C0 and GC) plays an important role in the prediction of coding potential. |
format | Online Article Text |
id | pubmed-6486542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64865422019-05-01 CPPred: coding potential prediction based on the global description of RNA sequence Tong, Xiaoxue Liu, Shiyong Nucleic Acids Res Methods Online The rapid and accurate approach to distinguish between coding RNAs and ncRNAs has been playing a critical role in analyzing thousands of novel transcripts, which have been generated in recent years by next-generation sequencing technology. Previously developed methods CPAT, CPC2 and PLEK can distinguish coding RNAs and ncRNAs very well, but poorly distinguish between small coding RNAs and small ncRNAs. Herein, we report an approach, CPPred (coding potential prediction), which is based on SVM classifier and multiple sequence features including novel RNA features encoded by the global description. The CPPred can better distinguish not only between coding RNAs and ncRNAs, but also between small coding RNAs and small ncRNAs than the state-of-the-art methods due to the addition of the novel RNA features. A recent study proposes 1335 novel human coding RNAs from a large number of RNA-seq datasets. However, only 119 transcripts are predicted as coding RNAs by the CPPred. In fact, almost all proposed novel coding RNAs are ncRNAs (91.1%), which is consistent with previous reports. Remarkably, we also reveal that the global description of encoding features (T2, C0 and GC) plays an important role in the prediction of coding potential. Oxford University Press 2019-05-07 2019-02-11 /pmc/articles/PMC6486542/ /pubmed/30753596 http://dx.doi.org/10.1093/nar/gkz087 Text en © The Author(s) 2019. 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 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 | Methods Online Tong, Xiaoxue Liu, Shiyong CPPred: coding potential prediction based on the global description of RNA sequence |
title | CPPred: coding potential prediction based on the global description of RNA sequence |
title_full | CPPred: coding potential prediction based on the global description of RNA sequence |
title_fullStr | CPPred: coding potential prediction based on the global description of RNA sequence |
title_full_unstemmed | CPPred: coding potential prediction based on the global description of RNA sequence |
title_short | CPPred: coding potential prediction based on the global description of RNA sequence |
title_sort | cppred: coding potential prediction based on the global description of rna sequence |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486542/ https://www.ncbi.nlm.nih.gov/pubmed/30753596 http://dx.doi.org/10.1093/nar/gkz087 |
work_keys_str_mv | AT tongxiaoxue cppredcodingpotentialpredictionbasedontheglobaldescriptionofrnasequence AT liushiyong cppredcodingpotentialpredictionbasedontheglobaldescriptionofrnasequence |