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RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information
BACKGROUND: The interactions between non-coding RNAs (ncRNA) and proteins play an essential role in many biological processes. Several high-throughput experimental methods have been applied to detect ncRNA-protein interactions. However, these methods are time-consuming and expensive. Accurate and ef...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029608/ https://www.ncbi.nlm.nih.gov/pubmed/32070279 http://dx.doi.org/10.1186/s12859-020-3406-0 |
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author | Yi, Hai-Cheng You, Zhu-Hong Wang, Mei-Neng Guo, Zhen-Hao Wang, Yan-Bin Zhou, Ji-Ren |
author_facet | Yi, Hai-Cheng You, Zhu-Hong Wang, Mei-Neng Guo, Zhen-Hao Wang, Yan-Bin Zhou, Ji-Ren |
author_sort | Yi, Hai-Cheng |
collection | PubMed |
description | BACKGROUND: The interactions between non-coding RNAs (ncRNA) and proteins play an essential role in many biological processes. Several high-throughput experimental methods have been applied to detect ncRNA-protein interactions. However, these methods are time-consuming and expensive. Accurate and efficient computational methods can assist and accelerate the study of ncRNA-protein interactions. RESULTS: In this work, we develop a stacking ensemble computational framework, RPI-SE, for effectively predicting ncRNA-protein interactions. More specifically, to fully exploit protein and RNA sequence feature, Position Weight Matrix combined with Legendre Moments is applied to obtain protein evolutionary information. Meanwhile, k-mer sparse matrix is employed to extract efficient feature of ncRNA sequences. Finally, an ensemble learning framework integrated different types of base classifier is developed to predict ncRNA-protein interactions using these discriminative features. The accuracy and robustness of RPI-SE was evaluated on three benchmark data sets under five-fold cross-validation and compared with other state-of-the-art methods. CONCLUSIONS: The results demonstrate that RPI-SE is competent for ncRNA-protein interactions prediction task with high accuracy and robustness. It’s anticipated that this work can provide a computational prediction tool to advance ncRNA-protein interactions related biomedical research. |
format | Online Article Text |
id | pubmed-7029608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-70296082020-02-25 RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information Yi, Hai-Cheng You, Zhu-Hong Wang, Mei-Neng Guo, Zhen-Hao Wang, Yan-Bin Zhou, Ji-Ren BMC Bioinformatics Methodology Article BACKGROUND: The interactions between non-coding RNAs (ncRNA) and proteins play an essential role in many biological processes. Several high-throughput experimental methods have been applied to detect ncRNA-protein interactions. However, these methods are time-consuming and expensive. Accurate and efficient computational methods can assist and accelerate the study of ncRNA-protein interactions. RESULTS: In this work, we develop a stacking ensemble computational framework, RPI-SE, for effectively predicting ncRNA-protein interactions. More specifically, to fully exploit protein and RNA sequence feature, Position Weight Matrix combined with Legendre Moments is applied to obtain protein evolutionary information. Meanwhile, k-mer sparse matrix is employed to extract efficient feature of ncRNA sequences. Finally, an ensemble learning framework integrated different types of base classifier is developed to predict ncRNA-protein interactions using these discriminative features. The accuracy and robustness of RPI-SE was evaluated on three benchmark data sets under five-fold cross-validation and compared with other state-of-the-art methods. CONCLUSIONS: The results demonstrate that RPI-SE is competent for ncRNA-protein interactions prediction task with high accuracy and robustness. It’s anticipated that this work can provide a computational prediction tool to advance ncRNA-protein interactions related biomedical research. BioMed Central 2020-02-18 /pmc/articles/PMC7029608/ /pubmed/32070279 http://dx.doi.org/10.1186/s12859-020-3406-0 Text en © The Author(s). 2020 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 | Methodology Article Yi, Hai-Cheng You, Zhu-Hong Wang, Mei-Neng Guo, Zhen-Hao Wang, Yan-Bin Zhou, Ji-Ren RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information |
title | RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information |
title_full | RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information |
title_fullStr | RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information |
title_full_unstemmed | RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information |
title_short | RPI-SE: a stacking ensemble learning framework for ncRNA-protein interactions prediction using sequence information |
title_sort | rpi-se: a stacking ensemble learning framework for ncrna-protein interactions prediction using sequence information |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029608/ https://www.ncbi.nlm.nih.gov/pubmed/32070279 http://dx.doi.org/10.1186/s12859-020-3406-0 |
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