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DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion
An emerging type of therapeutic agent, anticancer peptides (ACPs), has attracted attention because of its lower risk of toxic side effects. However process of identifying ACPs using experimental methods is both time-consuming and laborious. In this study, we developed a new and efficient algorithm t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344685/ https://www.ncbi.nlm.nih.gov/pubmed/34414035 http://dx.doi.org/10.7717/peerj.11906 |
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author | Cao, Ruifen Wang, Meng Bin, Yannan Zheng, Chunhou |
author_facet | Cao, Ruifen Wang, Meng Bin, Yannan Zheng, Chunhou |
author_sort | Cao, Ruifen |
collection | PubMed |
description | An emerging type of therapeutic agent, anticancer peptides (ACPs), has attracted attention because of its lower risk of toxic side effects. However process of identifying ACPs using experimental methods is both time-consuming and laborious. In this study, we developed a new and efficient algorithm that predicts ACPs by fusing multi-view features based on dual-channel deep neural network ensemble model. In the model, one channel used the convolutional neural network CNN to automatically extract the potential spatial features of a sequence. Another channel was used to process and extract more effective features from handcrafted features. Additionally, an effective feature fusion method was explored for the mutual fusion of different features. Finally, we adopted the neural network to predict ACPs based on the fusion features. The performance comparisons across the single and fusion features showed that the fusion of multi-view features could effectively improve the model’s predictive ability. Among these, the fusion of the features extracted by the CNN and composition of k-spaced amino acid group pairs achieved the best performance. To further validate the performance of our model, we compared it with other existing methods using two independent test sets. The results showed that our model’s area under curve was 0.90, which was higher than that of the other existing methods on the first test set and higher than most of the other existing methods on the second test set. The source code and datasets are available at https://github.com/wame-ng/DLFF-ACP. |
format | Online Article Text |
id | pubmed-8344685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83446852021-08-18 DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion Cao, Ruifen Wang, Meng Bin, Yannan Zheng, Chunhou PeerJ Bioinformatics An emerging type of therapeutic agent, anticancer peptides (ACPs), has attracted attention because of its lower risk of toxic side effects. However process of identifying ACPs using experimental methods is both time-consuming and laborious. In this study, we developed a new and efficient algorithm that predicts ACPs by fusing multi-view features based on dual-channel deep neural network ensemble model. In the model, one channel used the convolutional neural network CNN to automatically extract the potential spatial features of a sequence. Another channel was used to process and extract more effective features from handcrafted features. Additionally, an effective feature fusion method was explored for the mutual fusion of different features. Finally, we adopted the neural network to predict ACPs based on the fusion features. The performance comparisons across the single and fusion features showed that the fusion of multi-view features could effectively improve the model’s predictive ability. Among these, the fusion of the features extracted by the CNN and composition of k-spaced amino acid group pairs achieved the best performance. To further validate the performance of our model, we compared it with other existing methods using two independent test sets. The results showed that our model’s area under curve was 0.90, which was higher than that of the other existing methods on the first test set and higher than most of the other existing methods on the second test set. The source code and datasets are available at https://github.com/wame-ng/DLFF-ACP. PeerJ Inc. 2021-08-03 /pmc/articles/PMC8344685/ /pubmed/34414035 http://dx.doi.org/10.7717/peerj.11906 Text en ©2021 Cao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Bioinformatics Cao, Ruifen Wang, Meng Bin, Yannan Zheng, Chunhou DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion |
title | DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion |
title_full | DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion |
title_fullStr | DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion |
title_full_unstemmed | DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion |
title_short | DLFF-ACP: prediction of ACPs based on deep learning and multi-view features fusion |
title_sort | dlff-acp: prediction of acps based on deep learning and multi-view features fusion |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344685/ https://www.ncbi.nlm.nih.gov/pubmed/34414035 http://dx.doi.org/10.7717/peerj.11906 |
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