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Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs

BACKGROUND: N(6)-methyladenosine (m(6)A) is an important epigenetic modification which plays various roles in mRNA metabolism and embryogenesis directly related to human diseases. To identify m(6)A in a large scale, machine learning methods have been developed to make predictions on m(6)A sites. How...

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Autores principales: Zhao, Zhixun, Peng, Hui, Lan, Chaowang, Zheng, Yi, Fang, Liang, Li, Jinyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090857/
https://www.ncbi.nlm.nih.gov/pubmed/30068294
http://dx.doi.org/10.1186/s12864-018-4928-y
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author Zhao, Zhixun
Peng, Hui
Lan, Chaowang
Zheng, Yi
Fang, Liang
Li, Jinyan
author_facet Zhao, Zhixun
Peng, Hui
Lan, Chaowang
Zheng, Yi
Fang, Liang
Li, Jinyan
author_sort Zhao, Zhixun
collection PubMed
description BACKGROUND: N(6)-methyladenosine (m(6)A) is an important epigenetic modification which plays various roles in mRNA metabolism and embryogenesis directly related to human diseases. To identify m(6)A in a large scale, machine learning methods have been developed to make predictions on m(6)A sites. However, there are two main drawbacks of these methods. The first is the inadequate learning of the imbalanced m(6)A samples which are much less than the non-m(6)A samples, by their balanced learning approaches. Second, the features used by these methods are not outstanding to represent m(6)A sequence characteristics. RESULTS: We propose to use cost-sensitive learning ideas to resolve the imbalance data issues in the human mRNA m(6)A prediction problem. This cost-sensitive approach applies to the entire imbalanced dataset, without random equal-size selection of negative samples, for an adequate learning. Along with site location and entropy features, top-ranked positions with the highest single nucleotide polymorphism specificity in the window sequences are taken as new features in our imbalance learning. On an independent dataset, our overall prediction performance is much superior to the existing predictors. Our method shows stronger robustness against the imbalance changes in the tests on 9 datasets whose imbalance ratios range from 1:1 to 9:1. Our method also outperforms the existing predictors on 1226 individual transcripts. It is found that the new types of features are indeed of high significance in the m(6)A prediction. The case studies on gene c-Jun and CBFB demonstrate the detailed prediction capacity to improve the prediction performance. CONCLUSION: The proposed cost-sensitive model and the new features are useful in human mRNA m(6)A prediction. Our method achieves better correctness and robustness than the existing predictors in independent test and case studies. The results suggest that imbalance learning is promising to improve the performance of m(6)A prediction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4928-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-60908572018-08-17 Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs Zhao, Zhixun Peng, Hui Lan, Chaowang Zheng, Yi Fang, Liang Li, Jinyan BMC Genomics Research Article BACKGROUND: N(6)-methyladenosine (m(6)A) is an important epigenetic modification which plays various roles in mRNA metabolism and embryogenesis directly related to human diseases. To identify m(6)A in a large scale, machine learning methods have been developed to make predictions on m(6)A sites. However, there are two main drawbacks of these methods. The first is the inadequate learning of the imbalanced m(6)A samples which are much less than the non-m(6)A samples, by their balanced learning approaches. Second, the features used by these methods are not outstanding to represent m(6)A sequence characteristics. RESULTS: We propose to use cost-sensitive learning ideas to resolve the imbalance data issues in the human mRNA m(6)A prediction problem. This cost-sensitive approach applies to the entire imbalanced dataset, without random equal-size selection of negative samples, for an adequate learning. Along with site location and entropy features, top-ranked positions with the highest single nucleotide polymorphism specificity in the window sequences are taken as new features in our imbalance learning. On an independent dataset, our overall prediction performance is much superior to the existing predictors. Our method shows stronger robustness against the imbalance changes in the tests on 9 datasets whose imbalance ratios range from 1:1 to 9:1. Our method also outperforms the existing predictors on 1226 individual transcripts. It is found that the new types of features are indeed of high significance in the m(6)A prediction. The case studies on gene c-Jun and CBFB demonstrate the detailed prediction capacity to improve the prediction performance. CONCLUSION: The proposed cost-sensitive model and the new features are useful in human mRNA m(6)A prediction. Our method achieves better correctness and robustness than the existing predictors in independent test and case studies. The results suggest that imbalance learning is promising to improve the performance of m(6)A prediction. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-4928-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-01 /pmc/articles/PMC6090857/ /pubmed/30068294 http://dx.doi.org/10.1186/s12864-018-4928-y Text en © The Author(s) 2018 Open Access This 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 Article
Zhao, Zhixun
Peng, Hui
Lan, Chaowang
Zheng, Yi
Fang, Liang
Li, Jinyan
Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs
title Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs
title_full Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs
title_fullStr Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs
title_full_unstemmed Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs
title_short Imbalance learning for the prediction of N(6)-Methylation sites in mRNAs
title_sort imbalance learning for the prediction of n(6)-methylation sites in mrnas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090857/
https://www.ncbi.nlm.nih.gov/pubmed/30068294
http://dx.doi.org/10.1186/s12864-018-4928-y
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