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dc.contributor.authorPhasit Charoenkwanen_US
dc.contributor.authorSaeed Ahmeden_US
dc.contributor.authorChanin Nantasenamaten_US
dc.contributor.authorJulian M.W. Quinnen_US
dc.contributor.authorMohammad Ali Monien_US
dc.contributor.authorPietro Lio’en_US
dc.contributor.authorWatshara Shoombuatongen_US
dc.date.accessioned2022-05-27T08:40:42Z-
dc.date.available2022-05-27T08:40:42Z-
dc.date.issued2022-12-01en_US
dc.identifier.issn20452322en_US
dc.identifier.other2-s2.0-85129950097en_US
dc.identifier.other10.1038/s41598-022-11897-zen_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85129950097&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/73378-
dc.description.abstractAmyloid proteins have the ability to form insoluble fibril aggregates that have important pathogenic effects in many tissues. Such amyloidoses are prominently associated with common diseases such as type 2 diabetes, Alzheimer's disease, and Parkinson's disease. There are many types of amyloid proteins, and some proteins that form amyloid aggregates when in a misfolded state. It is difficult to identify such amyloid proteins and their pathogenic properties, but a new and effective approach is by developing effective bioinformatics tools. While several machine learning (ML)-based models for in silico identification of amyloid proteins have been proposed, their predictive performance is limited. In this study, we present AMYPred-FRL, a novel meta-predictor that uses a feature representation learning approach to achieve more accurate amyloid protein identification. AMYPred-FRL combined six well-known ML algorithms (extremely randomized tree, extreme gradient boosting, k-nearest neighbor, logistic regression, random forest, and support vector machine) with ten different sequence-based feature descriptors to generate 60 probabilistic features (PFs), as opposed to state-of-the-art methods developed by a single feature-based approach. A logistic regression recursive feature elimination (LR-RFE) method was used to find the optimal m number of 60 PFs in order to improve the predictive performance. Finally, using the meta-predictor approach, the 20 selected PFs were fed into a logistic regression method to create the final hybrid model (AMYPred-FRL). Both cross-validation and independent tests showed that AMYPred-FRL achieved superior predictive performance than its constituent baseline models. In an extensive independent test, AMYPred-FRL outperformed the existing methods by 5.5% and 16.1%, respectively, with accuracy and MCC of 0.873 and 0.710. To expedite high-throughput prediction, a user-friendly web server of AMYPred-FRL is freely available at http://pmlabstack.pythonanywhere.com/AMYPred-FRL. It is anticipated that AMYPred-FRL will be a useful tool in helping researchers to identify new amyloid proteins.en_US
dc.subjectMultidisciplinaryen_US
dc.titleAMYPred-FRL is a novel approach for accurate prediction of amyloid proteins by using feature representation learningen_US
dc.typeJournalen_US
article.title.sourcetitleScientific Reportsen_US
article.volume12en_US
article.stream.affiliationsDepartment of Computer Science and Technologyen_US
article.stream.affiliationsThe University of Queenslanden_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsGarvan Institute of Medical Researchen_US
article.stream.affiliationsChiang Mai Universityen_US
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