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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 Bioinformatics</journal-id><journal-title-group><journal-title xml:lang="en">Current Bioinformatics</journal-title><trans-title-group xml:lang="ru"><trans-title>Current Bioinformatics</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1574-8936</issn><issn publication-format="electronic">2212-392X</issn><publisher><publisher-name xml:lang="en">Bentham Science</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">643748</article-id><article-id pub-id-type="doi">10.2174/0115748936272939231212102627</article-id><article-categories><subj-group subj-group-type="toc-heading"><subject>Life Sciences</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">STNMDA: A Novel Model for Predicting Potential Microbe-Drug Associations with Structure-Aware Transformer</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Fan</surname><given-names>Liu</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name><surname>Yang</surname><given-names>Xiaoyu</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Lei</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name><surname>Zhu</surname><given-names>Xianyou</given-names></name><email>info@benthamscience.net</email><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff id="aff1"><institution>College of Computer Science and Technology, Hengyang Normal University</institution></aff><aff id="aff2"><institution>, Changsha University, Big Data Innovation and Entrepreneurship Education Center of Hunan Province</institution></aff><aff id="aff3"><institution>, College of Computer Science and Technology, Hengyang Normal University</institution></aff><pub-date date-type="pub" iso-8601-date="2024-10-01" publication-format="electronic"><day>01</day><month>10</month><year>2024</year></pub-date><volume>19</volume><issue>10</issue><issue-title xml:lang="ru"/><fpage>919</fpage><lpage>932</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://journals.eco-vector.com/1574-8936/article/view/643748">https://journals.eco-vector.com/1574-8936/article/view/643748</self-uri><abstract xml:lang="en"><p id="idm46041443744736">Introduction:Microbes are intimately involved in the physiological and pathological processes of numerous diseases. There is a critical need for new drugs to combat microbe-induced diseases in clinical settings. Predicting potential microbe-drug associations is, therefore, essential for both disease treatment and novel drug discovery. However, it is costly and time-consuming to verify these relationships through traditional wet lab approaches.</p><p id="idm46041443748736">Methods:We proposed an efficient computational model, STNMDA, that integrated a StructureAware Transformer (SAT) with a Deep Neural Network (DNN) classifier to infer latent microbedrug associations. The STNMDA began with a "random walk with a restart" approach to construct a heterogeneous network using Gaussian kernel similarity and functional similarity measures for microorganisms and drugs. This heterogeneous network was then fed into the SAT to extract attribute features and graph structures for each drug and microbe node. Finally, the DNN classifier calculated the probability of associations between microbes and drugs.</p><p id="idm46041443752704">Results:Extensive experimental results showed that STNMDA surpassed existing state-of-the-art models in performance on the MDAD and aBiofilm databases. In addition, the feasibility of STNMDA in confirming associations between microbes and drugs was demonstrated through case validations.</p><p id="idm46041443757760">Conclusion:Hence, STNMDA showed promise as a valuable tool for future prediction of microbedrug associations.</p></abstract><kwd-group xml:lang="en"><kwd>Microbe-drug association</kwd><kwd>microbe-disease-drug association</kwd><kwd>structure-aware transformer</kwd><kwd>deep neural network</kwd><kwd>biomarkers</kwd><kwd>bile acids.</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Ma P, Li C, Rahaman MM, et al. 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