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Antimicrobial peptide identification using multi-scale convolutional network
BACKGROUND: Antibiotic resistance has become an increasingly serious problem in the past decades. As an alternative choice, antimicrobial peptides (AMPs) have attracted lots of attention. To identify new AMPs, machine learning methods have been commonly used. More recently, some deep learning method...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929291/ https://www.ncbi.nlm.nih.gov/pubmed/31870282 http://dx.doi.org/10.1186/s12859-019-3327-y |
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author | Su, Xin Xu, Jing Yin, Yanbin Quan, Xiongwen Zhang, Han |
author_facet | Su, Xin Xu, Jing Yin, Yanbin Quan, Xiongwen Zhang, Han |
author_sort | Su, Xin |
collection | PubMed |
description | BACKGROUND: Antibiotic resistance has become an increasingly serious problem in the past decades. As an alternative choice, antimicrobial peptides (AMPs) have attracted lots of attention. To identify new AMPs, machine learning methods have been commonly used. More recently, some deep learning methods have also been applied to this problem. RESULTS: In this paper, we designed a deep learning model to identify AMP sequences. We employed the embedding layer and the multi-scale convolutional network in our model. The multi-scale convolutional network, which contains multiple convolutional layers of varying filter lengths, could utilize all latent features captured by the multiple convolutional layers. To further improve the performance, we also incorporated additional information into the designed model and proposed a fusion model. Results showed that our model outperforms the state-of-the-art models on two AMP datasets and the Antimicrobial Peptide Database (APD)3 benchmark dataset. The fusion model also outperforms the state-of-the-art model on an anti-inflammatory peptides (AIPs) dataset at the accuracy. CONCLUSIONS: Multi-scale convolutional network is a novel addition to existing deep neural network (DNN) models. The proposed DNN model and the modified fusion model outperform the state-of-the-art models for new AMP discovery. The source code and data are available at https://github.com/zhanglabNKU/APIN. |
format | Online Article Text |
id | pubmed-6929291 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-69292912019-12-30 Antimicrobial peptide identification using multi-scale convolutional network Su, Xin Xu, Jing Yin, Yanbin Quan, Xiongwen Zhang, Han BMC Bioinformatics Research Article BACKGROUND: Antibiotic resistance has become an increasingly serious problem in the past decades. As an alternative choice, antimicrobial peptides (AMPs) have attracted lots of attention. To identify new AMPs, machine learning methods have been commonly used. More recently, some deep learning methods have also been applied to this problem. RESULTS: In this paper, we designed a deep learning model to identify AMP sequences. We employed the embedding layer and the multi-scale convolutional network in our model. The multi-scale convolutional network, which contains multiple convolutional layers of varying filter lengths, could utilize all latent features captured by the multiple convolutional layers. To further improve the performance, we also incorporated additional information into the designed model and proposed a fusion model. Results showed that our model outperforms the state-of-the-art models on two AMP datasets and the Antimicrobial Peptide Database (APD)3 benchmark dataset. The fusion model also outperforms the state-of-the-art model on an anti-inflammatory peptides (AIPs) dataset at the accuracy. CONCLUSIONS: Multi-scale convolutional network is a novel addition to existing deep neural network (DNN) models. The proposed DNN model and the modified fusion model outperform the state-of-the-art models for new AMP discovery. The source code and data are available at https://github.com/zhanglabNKU/APIN. BioMed Central 2019-12-23 /pmc/articles/PMC6929291/ /pubmed/31870282 http://dx.doi.org/10.1186/s12859-019-3327-y Text en © The Author(s). 2019 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 | Research Article Su, Xin Xu, Jing Yin, Yanbin Quan, Xiongwen Zhang, Han Antimicrobial peptide identification using multi-scale convolutional network |
title | Antimicrobial peptide identification using multi-scale convolutional network |
title_full | Antimicrobial peptide identification using multi-scale convolutional network |
title_fullStr | Antimicrobial peptide identification using multi-scale convolutional network |
title_full_unstemmed | Antimicrobial peptide identification using multi-scale convolutional network |
title_short | Antimicrobial peptide identification using multi-scale convolutional network |
title_sort | antimicrobial peptide identification using multi-scale convolutional network |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929291/ https://www.ncbi.nlm.nih.gov/pubmed/31870282 http://dx.doi.org/10.1186/s12859-019-3327-y |
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