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Identification of DNA-Binding Proteins Using Mixed Feature Representation Methods
DNA-binding proteins play vital roles in cellular processes, such as DNA packaging, replication, transcription, regulation, and other DNA-associated activities. The current main prediction method is based on machine learning, and its accuracy mainly depends on the features extraction method. Therefo...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2017-09, Vol.22 (10), p.1602 |
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description | DNA-binding proteins play vital roles in cellular processes, such as DNA packaging, replication, transcription, regulation, and other DNA-associated activities. The current main prediction method is based on machine learning, and its accuracy mainly depends on the features extraction method. Therefore, using an efficient feature representation method is important to enhance the classification accuracy. However, existing feature representation methods cannot efficiently distinguish DNA-binding proteins from non-DNA-binding proteins. In this paper, a multi-feature representation method, which combines three feature representation methods, namely, K-Skip-N-Grams, Information theory, and Sequential and structural features (SSF), is used to represent the protein sequences and improve feature representation ability. In addition, the classifier is a support vector machine. The mixed-feature representation method is evaluated using 10-fold cross-validation and a test set. Feature vectors, which are obtained from a combination of three feature extractions, show the best performance in 10-fold cross-validation both under non-dimensional reduction and dimensional reduction by max-relevance-max-distance. Moreover, the reduced mixed feature method performs better than the non-reduced mixed feature technique. The feature vectors, which are a combination of SSF and K-Skip-N-Grams, show the best performance in the test set. Among these methods, mixed features exhibit superiority over the single features. |
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The current main prediction method is based on machine learning, and its accuracy mainly depends on the features extraction method. Therefore, using an efficient feature representation method is important to enhance the classification accuracy. However, existing feature representation methods cannot efficiently distinguish DNA-binding proteins from non-DNA-binding proteins. In this paper, a multi-feature representation method, which combines three feature representation methods, namely, K-Skip-N-Grams, Information theory, and Sequential and structural features (SSF), is used to represent the protein sequences and improve feature representation ability. In addition, the classifier is a support vector machine. The mixed-feature representation method is evaluated using 10-fold cross-validation and a test set. Feature vectors, which are obtained from a combination of three feature extractions, show the best performance in 10-fold cross-validation both under non-dimensional reduction and dimensional reduction by max-relevance-max-distance. Moreover, the reduced mixed feature method performs better than the non-reduced mixed feature technique. The feature vectors, which are a combination of SSF and K-Skip-N-Grams, show the best performance in the test set. Among these methods, mixed features exhibit superiority over the single features.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules22101602</identifier><identifier>PMID: 28937647</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Amino Acid Sequence ; Computational Biology - methods ; Deoxyribonucleic acid ; DNA ; DNA - chemistry ; DNA biosynthesis ; DNA-binding protein ; DNA-Binding Proteins - metabolism ; Gene regulation ; Identification methods ; Information theory ; Learning algorithms ; Machine Learning ; Methods ; mixed feature representation methods ; Packaging ; Proteins ; Representations ; Support Vector Machine ; Test procedures ; Transcription</subject><ispartof>Molecules (Basel, Switzerland), 2017-09, Vol.22 (10), p.1602</ispartof><rights>Copyright MDPI AG 2017</rights><rights>2017 by the authors. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-e0d00e190d4bba44557a5f48c9318de1c9f5921fdaf3cd85663a6f59b20fe8f13</citedby><cites>FETCH-LOGICAL-c493t-e0d00e190d4bba44557a5f48c9318de1c9f5921fdaf3cd85663a6f59b20fe8f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1965692921/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1965692921?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28937647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qu, Kaiyang</creatorcontrib><creatorcontrib>Han, Ke</creatorcontrib><creatorcontrib>Wu, Song</creatorcontrib><creatorcontrib>Wang, Guohua</creatorcontrib><creatorcontrib>Wei, Leyi</creatorcontrib><title>Identification of DNA-Binding Proteins Using Mixed Feature Representation Methods</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>DNA-binding proteins play vital roles in cellular processes, such as DNA packaging, replication, transcription, regulation, and other DNA-associated activities. The current main prediction method is based on machine learning, and its accuracy mainly depends on the features extraction method. Therefore, using an efficient feature representation method is important to enhance the classification accuracy. However, existing feature representation methods cannot efficiently distinguish DNA-binding proteins from non-DNA-binding proteins. In this paper, a multi-feature representation method, which combines three feature representation methods, namely, K-Skip-N-Grams, Information theory, and Sequential and structural features (SSF), is used to represent the protein sequences and improve feature representation ability. In addition, the classifier is a support vector machine. The mixed-feature representation method is evaluated using 10-fold cross-validation and a test set. Feature vectors, which are obtained from a combination of three feature extractions, show the best performance in 10-fold cross-validation both under non-dimensional reduction and dimensional reduction by max-relevance-max-distance. Moreover, the reduced mixed feature method performs better than the non-reduced mixed feature technique. The feature vectors, which are a combination of SSF and K-Skip-N-Grams, show the best performance in the test set. Among these methods, mixed features exhibit superiority over the single features.</description><subject>Amino Acid Sequence</subject><subject>Computational Biology - methods</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>DNA biosynthesis</subject><subject>DNA-binding protein</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Gene regulation</subject><subject>Identification methods</subject><subject>Information theory</subject><subject>Learning algorithms</subject><subject>Machine Learning</subject><subject>Methods</subject><subject>mixed feature representation methods</subject><subject>Packaging</subject><subject>Proteins</subject><subject>Representations</subject><subject>Support Vector Machine</subject><subject>Test procedures</subject><subject>Transcription</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkV9vFSEQxYnR2Fr9AL6YTXzxZZUBloUXk1qt3qT1X-wzYWG45WbvcoVdo99e6q1Nq0_AcM4vc2YIeQr0JeeavtqmEd0yYmEMKEjK7pFDEIy2nAp9_9b9gDwqZUMpAwHdQ3LAlOa9FP0h-bLyOM0xRGfnmKYmhebtx-P2TZx8nNbN55xmjFNpLsrV8zz-RN-cop2XjM1X3GUs1b63nuN8mXx5TB4EOxZ8cn0ekYvTd99OPrRnn96vTo7PWic0n1uknlIETb0YBitE1_W2C0I5zUF5BKdDpxkEbwN3XnVScitraWA0oArAj8hqz_XJbswux63Nv0yy0fwppLw2Ns_RjWiUcgMfOkFl8MJTUMAHkEMQVnFFmays13vWbhm26F3NlO14B3r3Z4qXZp1-GAkd1M4r4MU1IKfvC5bZbGNxOI52wrQUA1ow2Qveqyp9_o90k5Y81VFVleykZjV2VcFe5XIqJWO4aQaouVq--W_51fPsdoobx99t89-FLq0D</recordid><startdate>20170922</startdate><enddate>20170922</enddate><creator>Qu, Kaiyang</creator><creator>Han, Ke</creator><creator>Wu, Song</creator><creator>Wang, Guohua</creator><creator>Wei, Leyi</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20170922</creationdate><title>Identification of DNA-Binding Proteins Using Mixed Feature Representation Methods</title><author>Qu, Kaiyang ; Han, Ke ; Wu, Song ; Wang, Guohua ; Wei, Leyi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-e0d00e190d4bba44557a5f48c9318de1c9f5921fdaf3cd85663a6f59b20fe8f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Amino Acid Sequence</topic><topic>Computational Biology - methods</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>DNA biosynthesis</topic><topic>DNA-binding protein</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Gene regulation</topic><topic>Identification methods</topic><topic>Information theory</topic><topic>Learning algorithms</topic><topic>Machine Learning</topic><topic>Methods</topic><topic>mixed feature representation methods</topic><topic>Packaging</topic><topic>Proteins</topic><topic>Representations</topic><topic>Support Vector Machine</topic><topic>Test procedures</topic><topic>Transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qu, Kaiyang</creatorcontrib><creatorcontrib>Han, Ke</creatorcontrib><creatorcontrib>Wu, Song</creatorcontrib><creatorcontrib>Wang, Guohua</creatorcontrib><creatorcontrib>Wei, Leyi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qu, Kaiyang</au><au>Han, Ke</au><au>Wu, Song</au><au>Wang, Guohua</au><au>Wei, Leyi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of DNA-Binding Proteins Using Mixed Feature Representation Methods</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2017-09-22</date><risdate>2017</risdate><volume>22</volume><issue>10</issue><spage>1602</spage><pages>1602-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>DNA-binding proteins play vital roles in cellular processes, such as DNA packaging, replication, transcription, regulation, and other DNA-associated activities. The current main prediction method is based on machine learning, and its accuracy mainly depends on the features extraction method. Therefore, using an efficient feature representation method is important to enhance the classification accuracy. However, existing feature representation methods cannot efficiently distinguish DNA-binding proteins from non-DNA-binding proteins. In this paper, a multi-feature representation method, which combines three feature representation methods, namely, K-Skip-N-Grams, Information theory, and Sequential and structural features (SSF), is used to represent the protein sequences and improve feature representation ability. In addition, the classifier is a support vector machine. The mixed-feature representation method is evaluated using 10-fold cross-validation and a test set. Feature vectors, which are obtained from a combination of three feature extractions, show the best performance in 10-fold cross-validation both under non-dimensional reduction and dimensional reduction by max-relevance-max-distance. Moreover, the reduced mixed feature method performs better than the non-reduced mixed feature technique. The feature vectors, which are a combination of SSF and K-Skip-N-Grams, show the best performance in the test set. Among these methods, mixed features exhibit superiority over the single features.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>28937647</pmid><doi>10.3390/molecules22101602</doi><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Computational Biology - methods Deoxyribonucleic acid DNA DNA - chemistry DNA biosynthesis DNA-binding protein DNA-Binding Proteins - metabolism Gene regulation Identification methods Information theory Learning algorithms Machine Learning Methods mixed feature representation methods Packaging Proteins Representations Support Vector Machine Test procedures Transcription |
title | Identification of DNA-Binding Proteins Using Mixed Feature Representation Methods |
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