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NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination

BACKGROUND: 2′-O-methylation (2′-O-me or Nm) is a post-transcriptional RNA methylation modified at 2′-hydroxy, which is common in mRNAs and various non-coding RNAs. Previous studies revealed the significance of Nm in multiple biological processes. With Nm getting more and more attention, a revolutio...

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Autores principales: Zhou, Yiran, Cui, Qinghua, Zhou, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929462/
https://www.ncbi.nlm.nih.gov/pubmed/31874624
http://dx.doi.org/10.1186/s12859-019-3265-8
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author Zhou, Yiran
Cui, Qinghua
Zhou, Yuan
author_facet Zhou, Yiran
Cui, Qinghua
Zhou, Yuan
author_sort Zhou, Yiran
collection PubMed
description BACKGROUND: 2′-O-methylation (2′-O-me or Nm) is a post-transcriptional RNA methylation modified at 2′-hydroxy, which is common in mRNAs and various non-coding RNAs. Previous studies revealed the significance of Nm in multiple biological processes. With Nm getting more and more attention, a revolutionary technique termed Nm-seq, was developed to profile Nm sites mainly in mRNA with single nucleotide resolution and high sensitivity. In a recent work, supported by the Nm-seq data, we have reported a method in silico for predicting Nm sites, which relies on nucleotide sequence information, and established an online server named NmSEER. More recently, a more confident dataset produced by refined Nm-seq was available. Therefore, in this work, we redesigned the prediction model to achieve a more robust performance on the new data. RESULTS: We redesigned the prediction model from two perspectives, including machine learning algorithm and multi-encoding scheme combination. With optimization by 5-fold cross-validation tests and evaluation by independent test respectively, random forest was selected as the most robust algorithm. Meanwhile, one-hot encoding, together with position-specific dinucleotide sequence profile and K-nucleotide frequency encoding were collectively applied to build the final predictor. CONCLUSIONS: The predictor of updated version, named NmSEER V2.0, achieves an accurate prediction performance (AUROC = 0.862) and has been settled into a brand-new server, which is available at http://www.rnanut.net/nmseer-v2/ for free.
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spelling pubmed-69294622019-12-30 NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination Zhou, Yiran Cui, Qinghua Zhou, Yuan BMC Bioinformatics Research BACKGROUND: 2′-O-methylation (2′-O-me or Nm) is a post-transcriptional RNA methylation modified at 2′-hydroxy, which is common in mRNAs and various non-coding RNAs. Previous studies revealed the significance of Nm in multiple biological processes. With Nm getting more and more attention, a revolutionary technique termed Nm-seq, was developed to profile Nm sites mainly in mRNA with single nucleotide resolution and high sensitivity. In a recent work, supported by the Nm-seq data, we have reported a method in silico for predicting Nm sites, which relies on nucleotide sequence information, and established an online server named NmSEER. More recently, a more confident dataset produced by refined Nm-seq was available. Therefore, in this work, we redesigned the prediction model to achieve a more robust performance on the new data. RESULTS: We redesigned the prediction model from two perspectives, including machine learning algorithm and multi-encoding scheme combination. With optimization by 5-fold cross-validation tests and evaluation by independent test respectively, random forest was selected as the most robust algorithm. Meanwhile, one-hot encoding, together with position-specific dinucleotide sequence profile and K-nucleotide frequency encoding were collectively applied to build the final predictor. CONCLUSIONS: The predictor of updated version, named NmSEER V2.0, achieves an accurate prediction performance (AUROC = 0.862) and has been settled into a brand-new server, which is available at http://www.rnanut.net/nmseer-v2/ for free. BioMed Central 2019-12-24 /pmc/articles/PMC6929462/ /pubmed/31874624 http://dx.doi.org/10.1186/s12859-019-3265-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Zhou, Yiran
Cui, Qinghua
Zhou, Yuan
NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination
title NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination
title_full NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination
title_fullStr NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination
title_full_unstemmed NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination
title_short NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination
title_sort nmseer v2.0: a prediction tool for 2′-o-methylation sites based on random forest and multi-encoding combination
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929462/
https://www.ncbi.nlm.nih.gov/pubmed/31874624
http://dx.doi.org/10.1186/s12859-019-3265-8
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