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ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites
BACKGROUND: Human dicer is an enzyme that cleaves pre-miRNAs into miRNAs. Several models have been developed to predict human dicer cleavage sites, including PHDCleav and LBSizeCleav. Given an input sequence, these models can predict whether the sequence contains a cleavage site. However, these mode...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7877110/ https://www.ncbi.nlm.nih.gov/pubmed/33568063 http://dx.doi.org/10.1186/s12859-021-03993-0 |
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author | Liu, Pengyu Song, Jiangning Lin, Chun-Yu Akutsu, Tatsuya |
author_facet | Liu, Pengyu Song, Jiangning Lin, Chun-Yu Akutsu, Tatsuya |
author_sort | Liu, Pengyu |
collection | PubMed |
description | BACKGROUND: Human dicer is an enzyme that cleaves pre-miRNAs into miRNAs. Several models have been developed to predict human dicer cleavage sites, including PHDCleav and LBSizeCleav. Given an input sequence, these models can predict whether the sequence contains a cleavage site. However, these models only consider each sequence independently and lack interpretability. Therefore, it is necessary to develop an accurate and explainable predictor, which employs relations between different sequences, to enhance the understanding of the mechanism by which human dicer cleaves pre-miRNA. RESULTS: In this study, we develop an accurate and explainable predictor for human dicer cleavage site – ReCGBM. We design relational features and class features as inputs to a lightGBM model. Computational experiments show that ReCGBM achieves the best performance compared to the existing methods. Further, we find that features in close proximity to the center of pre-miRNA are more important and make a significant contribution to the performance improvement of the developed method. CONCLUSIONS: The results of this study show that ReCGBM is an interpretable and accurate predictor. Besides, the analyses of feature importance show that it might be of particular interest to consider more informative features close to the center of the pre-miRNA in future predictors. |
format | Online Article Text |
id | pubmed-7877110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78771102021-02-11 ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites Liu, Pengyu Song, Jiangning Lin, Chun-Yu Akutsu, Tatsuya BMC Bioinformatics Methodology Article BACKGROUND: Human dicer is an enzyme that cleaves pre-miRNAs into miRNAs. Several models have been developed to predict human dicer cleavage sites, including PHDCleav and LBSizeCleav. Given an input sequence, these models can predict whether the sequence contains a cleavage site. However, these models only consider each sequence independently and lack interpretability. Therefore, it is necessary to develop an accurate and explainable predictor, which employs relations between different sequences, to enhance the understanding of the mechanism by which human dicer cleaves pre-miRNA. RESULTS: In this study, we develop an accurate and explainable predictor for human dicer cleavage site – ReCGBM. We design relational features and class features as inputs to a lightGBM model. Computational experiments show that ReCGBM achieves the best performance compared to the existing methods. Further, we find that features in close proximity to the center of pre-miRNA are more important and make a significant contribution to the performance improvement of the developed method. CONCLUSIONS: The results of this study show that ReCGBM is an interpretable and accurate predictor. Besides, the analyses of feature importance show that it might be of particular interest to consider more informative features close to the center of the pre-miRNA in future predictors. BioMed Central 2021-02-10 /pmc/articles/PMC7877110/ /pubmed/33568063 http://dx.doi.org/10.1186/s12859-021-03993-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Methodology Article Liu, Pengyu Song, Jiangning Lin, Chun-Yu Akutsu, Tatsuya ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites |
title | ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites |
title_full | ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites |
title_fullStr | ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites |
title_full_unstemmed | ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites |
title_short | ReCGBM: a gradient boosting-based method for predicting human dicer cleavage sites |
title_sort | recgbm: a gradient boosting-based method for predicting human dicer cleavage sites |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7877110/ https://www.ncbi.nlm.nih.gov/pubmed/33568063 http://dx.doi.org/10.1186/s12859-021-03993-0 |
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