Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/75589
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dc.contributor.authorPhasit Charoenkwanen_US
dc.contributor.authorChanin Nantasenamaten_US
dc.contributor.authorMd Mehedi Hasanen_US
dc.contributor.authorMohammad Ali Monien_US
dc.contributor.authorPietro Lioen_US
dc.contributor.authorWatshara Shoombuatongen_US
dc.date.accessioned2022-10-16T07:01:01Z-
dc.date.available2022-10-16T07:01:01Z-
dc.date.issued2021-08-02en_US
dc.identifier.issn14220067en_US
dc.identifier.issn16616596en_US
dc.identifier.other2-s2.0-85112748133en_US
dc.identifier.other10.3390/ijms22168958en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85112748133&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/75589-
dc.description.abstractAccurate identification of bitter peptides is of great importance for better understanding their biochemical and biophysical properties. To date, machine learning‐based methods have be-come effective approaches for providing a good avenue for identifying potential bitter peptides from large‐scale protein datasets. Although few machine learning‐based predictors have been developed for identifying the bitterness of peptides, their prediction performances could be improved. In this study, we developed a new predictor (named iBitter‐Fuse) for achieving more accurate identification of bitter peptides. In the proposed iBitter‐Fuse, we have integrated a variety of feature encoding schemes for providing sufficient information from different aspects, namely consisting of compositional information and physicochemical properties. To enhance the predictive perfor-mance, the customized genetic algorithm utilizing self‐assessment‐report (GA‐SAR) was employed for identifying informative features followed by inputting optimal ones into a support vector machine (SVM)‐based classifier for developing the final model (iBitter‐Fuse). Benchmarking experi-ments based on both 10‐fold cross‐validation and independent tests indicated that the iBitter‐Fuse was able to achieve more accurate performance as compared to state‐of‐the‐art methods. To facili-tate the high‐throughput identification of bitter peptides, the iBitter‐Fuse web server was established and made freely available online. It is anticipated that the iBitter‐Fuse will be a useful tool for aiding the discovery and de novo design of bitter peptides.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemical Engineeringen_US
dc.subjectChemistryen_US
dc.subjectComputer Scienceen_US
dc.titleIbitter‐fuse: A novel sequence‐based bitter peptide predictor by fusing multi‐view featuresen_US
dc.typeJournalen_US
article.title.sourcetitleInternational Journal of Molecular Sciencesen_US
article.volume22en_US
article.stream.affiliationsDepartment of Computer Science and Technologyen_US
article.stream.affiliationsThe University of Queenslanden_US
article.stream.affiliationsTulane University School of Medicineen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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