Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/65764
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dc.contributorDepartment of Computing-
dc.creatorHuang, YA-
dc.creatorYou, ZH-
dc.creatorChen, X-
dc.creatorYan, GY-
dc.date.accessioned2017-05-22T02:09:11Z-
dc.date.available2017-05-22T02:09:11Z-
dc.identifier.urihttp://hdl.handle.net/10397/65764-
dc.language.isoenen_US
dc.publisherBioMed Centralen_US
dc.rights© The Author(s). 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_US
dc.rightsThe following publication Huang, Y. A., You, Z. H., Chen, X., & Yan, G. Y. (2016). Improved protein-protein interactions prediction via weighted sparse representation model combining continuous wavelet descriptor and PseAA composition. BMC Systems Biology, 10(Suppl. 4), 120, 485-548 is available at https://dx.doi.org/10.1186/s12918-016-0360-6en_US
dc.subjectContinuous wavelet transformen_US
dc.subjectProtein sequenceen_US
dc.subjectProtein-protein interactionsen_US
dc.subjectSparse representation based classifieren_US
dc.titleImproved protein-protein interactions prediction via weighted sparse representation model combining continuous wavelet descriptor and PseAA compositionen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage485en_US
dc.identifier.epage548-
dc.identifier.volume10en_US
dc.identifier.doi10.1186/s12918-016-0360-6en_US
dcterms.abstractBackground: Protein-protein interactions (PPIs) are essential to most biological processes. Since bioscience has entered into the era of genome and proteome, there is a growing demand for the knowledge about PPI network. High-throughput biological technologies can be used to identify new PPIs, but they are expensive, time-consuming, and tedious. Therefore, computational methods for predicting PPIs have an important role. For the past years, an increasing number of computational methods such as protein structure-based approaches have been proposed for predicting PPIs. The major limitation in principle of these methods lies in the prior information of the protein to infer PPIs. Therefore, it is of much significance to develop computational methods which only use the information of protein amino acids sequence.-
dcterms.abstractResults: Here, we report a highly efficient approach for predicting PPIs. The main improvements come from the use of a novel protein sequence representation by combining continuous wavelet descriptor and Chou's pseudo amino acid composition (PseAAC), and from adopting weighted sparse representation based classifier (WSRC). This method, cross-validated on the PPIs datasets of Saccharomyces cerevisiae, Human and H. pylori, achieves an excellent results with accuracies as high as 92.50%, 95.54% and 84.28% respectively, significantly better than previously proposed methods. Extensive experiments are performed to compare the proposed method with state-of-the-art Support Vector Machine (SVM) classifier.-
dcterms.abstractConclusions: The outstanding results yield by our model that the proposed feature extraction method combing two kinds of descriptors have strong expression ability and are expected to provide comprehensive and effective information for machine learning-based classification models. In addition, the prediction performance in the comparison experiments shows the well cooperation between the combined feature and WSRC. Thus, the proposed method is a very efficient method to predict PPIs and may be a useful supplementary tool for future proteomics studies.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBMC systems biology, 2016 , v. 10, suppl. 4, 120, p. 485-548-
dcterms.isPartOfBMC systems biology-
dcterms.issued2016-
dc.identifier.isiWOS:000392598000010-
dc.identifier.scopus2-s2.0-85006842031-
dc.identifier.eissn1752-0509en_US
dc.identifier.artn120en_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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