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DC Field | Value | Language |
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dc.contributor.author | Phasit Charoenkwan | en_US |
dc.contributor.author | Saeed Ahmed | en_US |
dc.contributor.author | Chanin Nantasenamat | en_US |
dc.contributor.author | Julian M.W. Quinn | en_US |
dc.contributor.author | Mohammad Ali Moni | en_US |
dc.contributor.author | Pietro Lio’ | en_US |
dc.contributor.author | Watshara Shoombuatong | en_US |
dc.date.accessioned | 2022-05-27T08:40:42Z | - |
dc.date.available | 2022-05-27T08:40:42Z | - |
dc.date.issued | 2022-12-01 | en_US |
dc.identifier.issn | 20452322 | en_US |
dc.identifier.other | 2-s2.0-85129950097 | en_US |
dc.identifier.other | 10.1038/s41598-022-11897-z | en_US |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85129950097&origin=inward | en_US |
dc.identifier.uri | http://cmuir.cmu.ac.th/jspui/handle/6653943832/73378 | - |
dc.description.abstract | Amyloid 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.subject | Multidisciplinary | en_US |
dc.title | AMYPred-FRL is a novel approach for accurate prediction of amyloid proteins by using feature representation learning | en_US |
dc.type | Journal | en_US |
article.title.sourcetitle | Scientific Reports | en_US |
article.volume | 12 | en_US |
article.stream.affiliations | Department of Computer Science and Technology | en_US |
article.stream.affiliations | The University of Queensland | en_US |
article.stream.affiliations | Mahidol University | en_US |
article.stream.affiliations | Garvan Institute of Medical Research | en_US |
article.stream.affiliations | Chiang Mai University | en_US |
Appears in Collections: | CMUL: Journal Articles |
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