AMYPred-FRL is a novel approach for accurate prediction of amyloid proteins by using feature representation learning

dc.contributor.authorCharoenkwan P.
dc.contributor.authorAhmed S.
dc.contributor.authorNantasenamat C.
dc.contributor.authorQuinn J.M.W.
dc.contributor.authorMoni M.A.
dc.contributor.authorLio’ P.
dc.contributor.authorShoombuatong W.
dc.contributor.otherMahidol University
dc.date.accessioned2023-06-18T18:04:26Z
dc.date.available2023-06-18T18:04:26Z
dc.date.issued2022-12-01
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.
dc.identifier.citationScientific Reports Vol.12 No.1 (2022)
dc.identifier.doi10.1038/s41598-022-11897-z
dc.identifier.eissn20452322
dc.identifier.pmid35546347
dc.identifier.scopus2-s2.0-85129950097
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/86421
dc.rights.holderSCOPUS
dc.subjectMultidisciplinary
dc.titleAMYPred-FRL is a novel approach for accurate prediction of amyloid proteins by using feature representation learning
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85129950097&origin=inward
oaire.citation.issue1
oaire.citation.titleScientific Reports
oaire.citation.volume12
oairecerif.author.affiliationDepartment of Computer Science and Technology
oairecerif.author.affiliationThe University of Queensland
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationGarvan Institute of Medical Research
oairecerif.author.affiliationChiang Mai University

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