iACP-MultiCNN: Multi-channel CNN based anticancer peptides identification

Cancer is one of the most dangerous diseases in the world that often leads to misery and death. Current treatments include different kinds of anticancer therapy which exhibit different types of side effects. Because of certain physicochemical properties, anticancer peptides (ACPs) have opened a new...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Analytical biochemistry 2022-08, Vol.650, p.114707-114707, Article 114707
Hauptverfasser: Aziz, Abu Zahid Bin, Hasan, Md. Al Mehedi, Ahmad, Shamim, Mamun, Md. Al, Shin, Jungpil, Hossain, Md Rahat
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 114707
container_issue
container_start_page 114707
container_title Analytical biochemistry
container_volume 650
creator Aziz, Abu Zahid Bin
Hasan, Md. Al Mehedi
Ahmad, Shamim
Mamun, Md. Al
Shin, Jungpil
Hossain, Md Rahat
description Cancer is one of the most dangerous diseases in the world that often leads to misery and death. Current treatments include different kinds of anticancer therapy which exhibit different types of side effects. Because of certain physicochemical properties, anticancer peptides (ACPs) have opened a new path of treatments for this deadly disease. That is why a well-performed methodology for identifying novel anticancer peptides has great importance in the fight against cancer. In addition to the laboratory techniques, various machine learning and deep learning methodologies have developed in recent years for this task. Although these models have shown reasonable predictive ability, there's still room for improvement in terms of performance and exploring new types of algorithms. In this work, we have proposed a novel multi-channel convolutional neural network (CNN) for identifying anticancer peptides from protein sequences. We have collected data from the existing state-of-the-art methodologies and applied binary encoding for data preprocessing. We have also employed k-fold cross-validation to train our models on benchmark datasets and compared our models' performance on the independent datasets. The comparison has indicated our models' superiority on various evaluation metrics. We think our work can be a valuable asset in finding novel anticancer peptides. We have provided a user-friendly web server for academic purposes and it is publicly available at: http://103.99.176.239/iacp-cnn/. [Display omitted] •Anticancer peptides (ACP) have opened a new pathway for cancer treatments.•We have proposed a multi-channel CNN for identifying ACPs from protein sequence.•This is the first deep learning based methodology for this size of dataset.•Our models' have out-performed the existing works in almost every evaluation metric.•We have also provided a web server to facilitate users for academic purposes.
doi_str_mv 10.1016/j.ab.2022.114707
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2664790684</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0003269722001634</els_id><sourcerecordid>2664790684</sourcerecordid><originalsourceid>FETCH-LOGICAL-c350t-260ddc16aa1cc4a6f92236ff715784a82374a7bcdf0fe68b0fa46c78e9eacd143</originalsourceid><addsrcrecordid>eNp1kDtPwzAURi0EoqWwM6GMLAnXedhJtyriUQkKA8yWY18LV2kS4gSJf49LChuLbX0699P1IeSSQkSBspttJKsohjiOKE058CMyp1CwEBIojskcAJIwZgWfkTPntgCeytgpmSVZxnKaFXOytqvyJXwa68GWm80y-HmF6l02DdaBj4JKOtSBbAarZKOwDzrsBqvRBf7wqfH5YNvmnJwYWTu8ONwL8nZ3-1o-hI_P9-ty9RiqJIPBrwNaK8qkpEqlkpkijhNmDKcZz1OZxwlPJa-UNmCQ5RUYmTLFcyxQKk3TZEGup96ubz9GdIPYWaewrmWD7ehEzFjKC2D5HoUJVX3rXI9GdL3dyf5LUBB7gWIrZCX2AsUk0I9cHdrHaof6b-DXmAeWE4D-j58We-GURS9G2x7VIHRr_2__BtlefvE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2664790684</pqid></control><display><type>article</type><title>iACP-MultiCNN: Multi-channel CNN based anticancer peptides identification</title><source>Elsevier ScienceDirect Journals</source><creator>Aziz, Abu Zahid Bin ; Hasan, Md. Al Mehedi ; Ahmad, Shamim ; Mamun, Md. Al ; Shin, Jungpil ; Hossain, Md Rahat</creator><creatorcontrib>Aziz, Abu Zahid Bin ; Hasan, Md. Al Mehedi ; Ahmad, Shamim ; Mamun, Md. Al ; Shin, Jungpil ; Hossain, Md Rahat</creatorcontrib><description>Cancer is one of the most dangerous diseases in the world that often leads to misery and death. Current treatments include different kinds of anticancer therapy which exhibit different types of side effects. Because of certain physicochemical properties, anticancer peptides (ACPs) have opened a new path of treatments for this deadly disease. That is why a well-performed methodology for identifying novel anticancer peptides has great importance in the fight against cancer. In addition to the laboratory techniques, various machine learning and deep learning methodologies have developed in recent years for this task. Although these models have shown reasonable predictive ability, there's still room for improvement in terms of performance and exploring new types of algorithms. In this work, we have proposed a novel multi-channel convolutional neural network (CNN) for identifying anticancer peptides from protein sequences. We have collected data from the existing state-of-the-art methodologies and applied binary encoding for data preprocessing. We have also employed k-fold cross-validation to train our models on benchmark datasets and compared our models' performance on the independent datasets. The comparison has indicated our models' superiority on various evaluation metrics. We think our work can be a valuable asset in finding novel anticancer peptides. We have provided a user-friendly web server for academic purposes and it is publicly available at: http://103.99.176.239/iacp-cnn/. [Display omitted] •Anticancer peptides (ACP) have opened a new pathway for cancer treatments.•We have proposed a multi-channel CNN for identifying ACPs from protein sequence.•This is the first deep learning based methodology for this size of dataset.•Our models' have out-performed the existing works in almost every evaluation metric.•We have also provided a web server to facilitate users for academic purposes.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2022.114707</identifier><identifier>PMID: 35568159</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><ispartof>Analytical biochemistry, 2022-08, Vol.650, p.114707-114707, Article 114707</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-260ddc16aa1cc4a6f92236ff715784a82374a7bcdf0fe68b0fa46c78e9eacd143</citedby><cites>FETCH-LOGICAL-c350t-260ddc16aa1cc4a6f92236ff715784a82374a7bcdf0fe68b0fa46c78e9eacd143</cites><orcidid>0000-0002-7757-8551 ; 0000-0003-1546-3959 ; 0000-0002-6835-8274 ; 0000-0001-8995-8052 ; 0000-0002-7476-2468</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0003269722001634$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35568159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aziz, Abu Zahid Bin</creatorcontrib><creatorcontrib>Hasan, Md. Al Mehedi</creatorcontrib><creatorcontrib>Ahmad, Shamim</creatorcontrib><creatorcontrib>Mamun, Md. Al</creatorcontrib><creatorcontrib>Shin, Jungpil</creatorcontrib><creatorcontrib>Hossain, Md Rahat</creatorcontrib><title>iACP-MultiCNN: Multi-channel CNN based anticancer peptides identification</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>Cancer is one of the most dangerous diseases in the world that often leads to misery and death. Current treatments include different kinds of anticancer therapy which exhibit different types of side effects. Because of certain physicochemical properties, anticancer peptides (ACPs) have opened a new path of treatments for this deadly disease. That is why a well-performed methodology for identifying novel anticancer peptides has great importance in the fight against cancer. In addition to the laboratory techniques, various machine learning and deep learning methodologies have developed in recent years for this task. Although these models have shown reasonable predictive ability, there's still room for improvement in terms of performance and exploring new types of algorithms. In this work, we have proposed a novel multi-channel convolutional neural network (CNN) for identifying anticancer peptides from protein sequences. We have collected data from the existing state-of-the-art methodologies and applied binary encoding for data preprocessing. We have also employed k-fold cross-validation to train our models on benchmark datasets and compared our models' performance on the independent datasets. The comparison has indicated our models' superiority on various evaluation metrics. We think our work can be a valuable asset in finding novel anticancer peptides. We have provided a user-friendly web server for academic purposes and it is publicly available at: http://103.99.176.239/iacp-cnn/. [Display omitted] •Anticancer peptides (ACP) have opened a new pathway for cancer treatments.•We have proposed a multi-channel CNN for identifying ACPs from protein sequence.•This is the first deep learning based methodology for this size of dataset.•Our models' have out-performed the existing works in almost every evaluation metric.•We have also provided a web server to facilitate users for academic purposes.</description><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp1kDtPwzAURi0EoqWwM6GMLAnXedhJtyriUQkKA8yWY18LV2kS4gSJf49LChuLbX0699P1IeSSQkSBspttJKsohjiOKE058CMyp1CwEBIojskcAJIwZgWfkTPntgCeytgpmSVZxnKaFXOytqvyJXwa68GWm80y-HmF6l02DdaBj4JKOtSBbAarZKOwDzrsBqvRBf7wqfH5YNvmnJwYWTu8ONwL8nZ3-1o-hI_P9-ty9RiqJIPBrwNaK8qkpEqlkpkijhNmDKcZz1OZxwlPJa-UNmCQ5RUYmTLFcyxQKk3TZEGup96ubz9GdIPYWaewrmWD7ehEzFjKC2D5HoUJVX3rXI9GdL3dyf5LUBB7gWIrZCX2AsUk0I9cHdrHaof6b-DXmAeWE4D-j58We-GURS9G2x7VIHRr_2__BtlefvE</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Aziz, Abu Zahid Bin</creator><creator>Hasan, Md. Al Mehedi</creator><creator>Ahmad, Shamim</creator><creator>Mamun, Md. Al</creator><creator>Shin, Jungpil</creator><creator>Hossain, Md Rahat</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7757-8551</orcidid><orcidid>https://orcid.org/0000-0003-1546-3959</orcidid><orcidid>https://orcid.org/0000-0002-6835-8274</orcidid><orcidid>https://orcid.org/0000-0001-8995-8052</orcidid><orcidid>https://orcid.org/0000-0002-7476-2468</orcidid></search><sort><creationdate>20220801</creationdate><title>iACP-MultiCNN: Multi-channel CNN based anticancer peptides identification</title><author>Aziz, Abu Zahid Bin ; Hasan, Md. Al Mehedi ; Ahmad, Shamim ; Mamun, Md. Al ; Shin, Jungpil ; Hossain, Md Rahat</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-260ddc16aa1cc4a6f92236ff715784a82374a7bcdf0fe68b0fa46c78e9eacd143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aziz, Abu Zahid Bin</creatorcontrib><creatorcontrib>Hasan, Md. Al Mehedi</creatorcontrib><creatorcontrib>Ahmad, Shamim</creatorcontrib><creatorcontrib>Mamun, Md. Al</creatorcontrib><creatorcontrib>Shin, Jungpil</creatorcontrib><creatorcontrib>Hossain, Md Rahat</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aziz, Abu Zahid Bin</au><au>Hasan, Md. Al Mehedi</au><au>Ahmad, Shamim</au><au>Mamun, Md. Al</au><au>Shin, Jungpil</au><au>Hossain, Md Rahat</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>iACP-MultiCNN: Multi-channel CNN based anticancer peptides identification</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>650</volume><spage>114707</spage><epage>114707</epage><pages>114707-114707</pages><artnum>114707</artnum><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>Cancer is one of the most dangerous diseases in the world that often leads to misery and death. Current treatments include different kinds of anticancer therapy which exhibit different types of side effects. Because of certain physicochemical properties, anticancer peptides (ACPs) have opened a new path of treatments for this deadly disease. That is why a well-performed methodology for identifying novel anticancer peptides has great importance in the fight against cancer. In addition to the laboratory techniques, various machine learning and deep learning methodologies have developed in recent years for this task. Although these models have shown reasonable predictive ability, there's still room for improvement in terms of performance and exploring new types of algorithms. In this work, we have proposed a novel multi-channel convolutional neural network (CNN) for identifying anticancer peptides from protein sequences. We have collected data from the existing state-of-the-art methodologies and applied binary encoding for data preprocessing. We have also employed k-fold cross-validation to train our models on benchmark datasets and compared our models' performance on the independent datasets. The comparison has indicated our models' superiority on various evaluation metrics. We think our work can be a valuable asset in finding novel anticancer peptides. We have provided a user-friendly web server for academic purposes and it is publicly available at: http://103.99.176.239/iacp-cnn/. [Display omitted] •Anticancer peptides (ACP) have opened a new pathway for cancer treatments.•We have proposed a multi-channel CNN for identifying ACPs from protein sequence.•This is the first deep learning based methodology for this size of dataset.•Our models' have out-performed the existing works in almost every evaluation metric.•We have also provided a web server to facilitate users for academic purposes.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>35568159</pmid><doi>10.1016/j.ab.2022.114707</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7757-8551</orcidid><orcidid>https://orcid.org/0000-0003-1546-3959</orcidid><orcidid>https://orcid.org/0000-0002-6835-8274</orcidid><orcidid>https://orcid.org/0000-0001-8995-8052</orcidid><orcidid>https://orcid.org/0000-0002-7476-2468</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0003-2697
ispartof Analytical biochemistry, 2022-08, Vol.650, p.114707-114707, Article 114707
issn 0003-2697
1096-0309
language eng
recordid cdi_proquest_miscellaneous_2664790684
source Elsevier ScienceDirect Journals
title iACP-MultiCNN: Multi-channel CNN based anticancer peptides identification
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T15%3A40%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=iACP-MultiCNN:%20Multi-channel%20CNN%20based%20anticancer%20peptides%20identification&rft.jtitle=Analytical%20biochemistry&rft.au=Aziz,%20Abu%20Zahid%20Bin&rft.date=2022-08-01&rft.volume=650&rft.spage=114707&rft.epage=114707&rft.pages=114707-114707&rft.artnum=114707&rft.issn=0003-2697&rft.eissn=1096-0309&rft_id=info:doi/10.1016/j.ab.2022.114707&rft_dat=%3Cproquest_cross%3E2664790684%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2664790684&rft_id=info:pmid/35568159&rft_els_id=S0003269722001634&rfr_iscdi=true