Evidence map›Paper›PMID 23460833›Full record

ArticlePloS one2013

An ensemble method for predicting subnuclear localizations from primary protein structures.

Guo Sheng Han, Zu Guo Yu, Vo Anh, Anaththa P D Krishnajith, Yu-Chu Tian

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Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

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18citing papers in PubMed
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3 · Its place in the literature

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18 citing papers in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Guo Sheng HanSchool of Mathematics and Computational Science, Xiangtan University, Xiangtan City, Hunan, China.
Zu Guo Yu
Vo Anh
Anaththa P D Krishnajith
Yu-Chu Tian

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPredicting protein subnuclear localization is a challenging problem. Some previous works based on non-sequence information including Gene Ontology annotations and kernel fusion have respective limitations. The aim of this work is twofold: one is to propose a novel individual feature extraction method; another is to develop an ensemble method to improve prediction performance using comprehensive information represented in the form of high dimensional feature vector obtained by 11 feature extraction methods. METHODOLOGY/PRINCIPAL

findingsA novel two-stage multiclass support vector machine is proposed to predict protein subnuclear localizations. It only considers those feature extraction methods based on amino acid classifications and physicochemical properties. In order to speed up our system, an automatic search method for the kernel parameter is used. The prediction performance of our method is evaluated on four datasets: Lei dataset, multi-localization dataset, SNL9 dataset and a new independent dataset. The overall accuracy of prediction for 6 localizations on Lei dataset is 75.2% and that for 9 localizations on SNL9 dataset is 72.1% in the leave-one-out cross validation, 71.7% for the multi-localization dataset and 69.8% for the new independent dataset, respectively. Comparisons with those existing methods show that our method performs better for both single-localization and multi-localization proteins and achieves more balanced sensitivities and specificities on large-size and small-size subcellular localizations. The overall accuracy improvements are 4.0% and 4.7% for single-localization proteins and 6.5% for multi-localization proteins. The reliability and stability of our classification model are further confirmed by permutation analysis.

conclusionsIt can be concluded that our method is effective and valuable for predicting protein subnuclear localizations. A web server has been designed to implement the proposed method. It is freely available at http://bioinformatics.awowshop.com/snlpred_page.php.

Indexed as

Amino Acid SequenceCell NucleusDatabases, ProteinModels, MolecularProteinsProtein TransportReproducibility of ResultsROC CurveSequence Analysis, ProteinSubcellular FractionsSupport Vector MachineProteins

Identifiers

PMID23460833
PMCPMC3584121

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.