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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Current Computer-Aided Drug Design</journal-id><journal-title-group><journal-title xml:lang="en">Current Computer-Aided Drug Design</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Computer-Aided Drug Design</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1573-4099</issn><issn publication-format="electronic">1875-6697</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">644530</article-id><article-id pub-id-type="doi">10.2174/0115734099258183230929173855</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Chemistry</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Identify Diabetes-related Targets based on ForgeNet_GPC</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Yang</surname><given-names>Bin</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Linlin</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Bao</surname><given-names>Wenzheng</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff id="aff1"><institution>School of Information Science and Engineering, Zaozhuang University</institution></aff><aff id="aff2"><institution>School of Information science and Engineering, Zaozhuang University</institution></aff><aff id="aff3"><institution>School of Information and Electrical Engineering, Xuzhou University of Technology</institution></aff><pub-date date-type="pub" iso-8601-date="2024-07-01" publication-format="electronic"><day>01</day><month>07</month><year>2024</year></pub-date><volume>20</volume><issue>7</issue><issue-title xml:lang="ru"/><fpage>1042</fpage><lpage>1054</lpage><history><date date-type="received" iso-8601-date="2025-01-07"><day>07</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Bentham Science Publishers</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Bentham Science Publishers</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://rjeid.com/1573-4099/article/view/644530">https://rjeid.com/1573-4099/article/view/644530</self-uri><abstract xml:lang="en"><p id="idm46041443762352">Background:Research on potential therapeutic targets and new mechanisms of action can greatly improve the efficiency of new drug development.</p><p id="idm46041443766352">Aims:Polygenic genetic diseases, such as diabetes, are caused by the interaction of multiple gene loci and environmental factors.</p><p id="idm46041443770320">Objective:In this study, a disease target identification algorithm based on protein recognition is proposed.</p><p id="idm46041443777120">Materials and Methods:In this method, the related and unrelated targets are collected from literature databases for treating diabetes. The transcribed proteins corresponding to each target are queried in order to construct a protein dataset. Six protein feature extraction algorithms (AAC, CKSAAGP, DDE, DPC, GAAP, and TPC) are utilized to obtain the feature vectors of each protein, which are merged into the full feature vectors.</p><p id="idm46041443785856">Results:A novel classifier (forgeNet_GPC) based on forgeNet and Gaussian process classifier (GPC) is proposed to classify the proteins.</p><p id="idm46041443793984">Conclusion:In forgeNet_GPC, forgeNet is utilized to select the important features, and GPC is utilized to solve the classification problem. The experimental results reveal that forgeNet_GPC performs better than 22 classifiers in terms of ROC-AUC, PR-AUC, MCC, Youden Index, and Kappa.</p></abstract><kwd-group xml:lang="en"><kwd>Protein</kwd><kwd>target</kwd><kwd>feature extraction</kwd><kwd>classification</kwd><kwd>diabetes</kwd><kwd>polygenic genetic diseases.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Sacks, D.A.; Greenspoon, J.S.; Abu-Fadil, S.; Henry, H.M.; Wolde-Tsadik, G.; Yao, J.F.F. Toward universal criteria for gestational diabetes: The 75-gram glucose tolerance test in pregnancy. Am. J. Obstet. Gynecol., 1995, 172(2), 607-614. doi: 10.1016/0002-9378(95)90580-4 PMID: 7856693</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Alberti, K.G.M.M.; Zimmet, P.; Shaw, J. Metabolic syndrome-a new world-wide definition. A Consensus Statement from the International Diabetes Federation. Diabet. 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