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dc.contributor.authorHuang, Wen-Linen_US
dc.contributor.authorTung, Chun-Weien_US
dc.contributor.authorHo, Shih-Wenen_US
dc.contributor.authorHwang, Shiow-Fenen_US
dc.contributor.authorHo, Shinn-Yingen_US
dc.date.accessioned2014-12-08T15:12:36Z-
dc.date.available2014-12-08T15:12:36Z-
dc.date.issued2008-02-01en_US
dc.identifier.issn1471-2105en_US
dc.identifier.urihttp://dx.doi.org/10.1186/1471-2105-9-80en_US
dc.identifier.urihttp://hdl.handle.net/11536/9687-
dc.description.abstractBackground: Gene Ontology (GO) annotation, which describes the function of genes and gene products across species, has recently been used to predict protein subcellular and subnuclear localization. Existing GO-based prediction methods for protein subcellular localization use the known accession numbers of query proteins to obtain their annotated GO terms. An accurate prediction method for predicting subcellular localization of novel proteins without known accession numbers, using only the input sequence, is worth developing. Results: This study proposes an efficient sequence-based method (named ProLoc-GO) by mining informative GO terms for predicting protein subcellular localization. For each protein, BLAST is used to obtain a homology with a known accession number to the protein for retrieving the GO annotation. A large number n of all annotated GO terms that have ever appeared are then obtained from a large set of training proteins. A novel genetic algorithm based method (named GOmining) combined with a classifier of support vector machine (SVM) is proposed to simultaneously identify a small number m out of the n GO terms as input features to SVM, where m << n. The m informative GO terms contain the essential GO terms annotating subcellular compartments such as GO: 0005634 (Nucleus), GO: 0005737 (Cytoplasm) and GO: 0005856 (Cytoskeleton). Two existing data sets SCL12 (human protein with 12 locations) and SCL16 (Eukaryotic proteins with 16 locations) with < 25% sequence identity are used to evaluate ProLoc-GO which has been implemented by using a single SVM classifier with the m = 44 and m = 60 informative GO terms, respectively. ProLoc-GO using input sequences yields test accuracies of 88.1% and 83.3% for SCL12 and SCL16, respectively, which are significantly better than the SVM-based methods, which achieve < 35% test accuracies using amino acid composition (AAC) with acid pairs and AAC with dipedtide composition. For comparison, ProLoc-GO using known accession numbers of query proteins yields test accuracies of 90.6% and 85.7%, which is also better than Hum-PLoc (85.0%) and Euk-OET-PLoc (83.7%) using ensemble classifiers with hybridization of GO terms and amphiphilic pseudo amino acid composition for SCL12 and SCL16, respectively. Conclusion: The growth of Gene Ontology in size and popularity has increased the effectiveness of GO-based features. GOmining can serve as a tool for selecting informative GO terms in solving sequence-based prediction problems. The prediction system using ProLoc-GO with input sequences of query proteins for protein subcellular localization has been implemented (see Availability).en_US
dc.language.isoen_USen_US
dc.titleProLoc-GO: Utilizing informative Gene Ontology terms for sequence-based prediction of protein subcellular localizationen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/1471-2105-9-80en_US
dc.identifier.journalBMC BIOINFORMATICSen_US
dc.citation.volume9en_US
dc.citation.issueen_US
dc.citation.epageen_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000253687400001-
dc.citation.woscount53-
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