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A sequence-based multiple kernel model for identifying DNA-binding proteins
BACKGROUND: DNA-Binding Proteins (DBP) plays a pivotal role in biological system. A mounting number of researchers are studying the mechanism and detection methods. To detect DBP, the tradition experimental method is time-consuming and resource-consuming. In recent years, Machine Learning methods ha...
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/PMC8167993/ https://www.ncbi.nlm.nih.gov/pubmed/34058979 http://dx.doi.org/10.1186/s12859-020-03875-x |
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author | Qian, Yuqing Jiang, Limin Ding, Yijie Tang, Jijun Guo, Fei |
author_facet | Qian, Yuqing Jiang, Limin Ding, Yijie Tang, Jijun Guo, Fei |
author_sort | Qian, Yuqing |
collection | PubMed |
description | BACKGROUND: DNA-Binding Proteins (DBP) plays a pivotal role in biological system. A mounting number of researchers are studying the mechanism and detection methods. To detect DBP, the tradition experimental method is time-consuming and resource-consuming. In recent years, Machine Learning methods have been used to detect DBP. However, it is difficult to adequately describe the information of proteins in predicting DNA-binding proteins. In this study, we extract six features from protein sequence and use Multiple Kernel Learning-based on Centered Kernel Alignment to integrate these features. The integrated feature is fed into Support Vector Machine to build predictive model and detect new DBP. RESULTS: In our work, date sets of PDB1075 and PDB186 are employed to test our method. From the results, our model obtains better results (accuracy) than other existing methods on PDB1075 ([Formula: see text] ) and PDB186 ([Formula: see text] ), respectively. CONCLUSION: Multiple kernel learning could fuse the complementary information between different features. Compared with existing methods, our method achieves comparable and best results on benchmark data sets. |
format | Online Article Text |
id | pubmed-8167993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81679932021-06-02 A sequence-based multiple kernel model for identifying DNA-binding proteins Qian, Yuqing Jiang, Limin Ding, Yijie Tang, Jijun Guo, Fei BMC Bioinformatics Research BACKGROUND: DNA-Binding Proteins (DBP) plays a pivotal role in biological system. A mounting number of researchers are studying the mechanism and detection methods. To detect DBP, the tradition experimental method is time-consuming and resource-consuming. In recent years, Machine Learning methods have been used to detect DBP. However, it is difficult to adequately describe the information of proteins in predicting DNA-binding proteins. In this study, we extract six features from protein sequence and use Multiple Kernel Learning-based on Centered Kernel Alignment to integrate these features. The integrated feature is fed into Support Vector Machine to build predictive model and detect new DBP. RESULTS: In our work, date sets of PDB1075 and PDB186 are employed to test our method. From the results, our model obtains better results (accuracy) than other existing methods on PDB1075 ([Formula: see text] ) and PDB186 ([Formula: see text] ), respectively. CONCLUSION: Multiple kernel learning could fuse the complementary information between different features. Compared with existing methods, our method achieves comparable and best results on benchmark data sets. BioMed Central 2021-05-31 /pmc/articles/PMC8167993/ /pubmed/34058979 http://dx.doi.org/10.1186/s12859-020-03875-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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 | Research Qian, Yuqing Jiang, Limin Ding, Yijie Tang, Jijun Guo, Fei A sequence-based multiple kernel model for identifying DNA-binding proteins |
title | A sequence-based multiple kernel model for identifying DNA-binding proteins |
title_full | A sequence-based multiple kernel model for identifying DNA-binding proteins |
title_fullStr | A sequence-based multiple kernel model for identifying DNA-binding proteins |
title_full_unstemmed | A sequence-based multiple kernel model for identifying DNA-binding proteins |
title_short | A sequence-based multiple kernel model for identifying DNA-binding proteins |
title_sort | sequence-based multiple kernel model for identifying dna-binding proteins |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8167993/ https://www.ncbi.nlm.nih.gov/pubmed/34058979 http://dx.doi.org/10.1186/s12859-020-03875-x |
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