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dc.contributor.authorHuang, Hui-Lingen_US
dc.contributor.authorCharoenkwan, Phasiten_US
dc.contributor.authorKao, Te-Fenen_US
dc.contributor.authorLee, Hua-Chinen_US
dc.contributor.authorChang, Fang-Linen_US
dc.contributor.authorHuang, Wen-Linen_US
dc.contributor.authorHo, Shinn-Jangen_US
dc.contributor.authorShu, Li-Sunen_US
dc.contributor.authorChen, Wen-Liangen_US
dc.contributor.authorHo, Shinn-Yingen_US
dc.date.accessioned2014-12-08T15:28:48Z-
dc.date.available2014-12-08T15:28:48Z-
dc.date.issued2012-12-13en_US
dc.identifier.issn1471-2105en_US
dc.identifier.urihttp://dx.doi.org/10.1186/1471-2105-13-S17-S3en_US
dc.identifier.urihttp://hdl.handle.net/11536/20829-
dc.description.abstractBackground: Existing methods for predicting protein solubility on overexpression in Escherichia coli advance performance by using ensemble classifiers such as two-stage support vector machine (SVM) based classifiers and a number of feature types such as physicochemical properties, amino acid and dipeptide composition, accompanied with feature selection. It is desirable to develop a simple and easily interpretable method for predicting protein solubility, compared to existing complex SVM-based methods. Results: This study proposes a novel scoring card method (SCM) by using dipeptide composition only to estimate solubility scores of sequences for predicting protein solubility. SCM calculates the propensities of 400 individual dipeptides to be soluble using statistic discrimination between soluble and insoluble proteins of a training data set. Consequently, the propensity scores of all dipeptides are further optimized using an intelligent genetic algorithm. The solubility score of a sequence is determined by the weighted sum of all propensity scores and dipeptide composition. To evaluate SCM by performance comparisons, four data sets with different sizes and variation degrees of experimental conditions were used. The results show that the simple method SCM with interpretable propensities of dipeptides has promising performance, compared with existing SVM-based ensemble methods with a number of feature types. Furthermore, the propensities of dipeptides and solubility scores of sequences can provide insights to protein solubility. For example, the analysis of dipeptide scores shows high propensity of a-helix structure and thermophilic proteins to be soluble. Conclusions: The propensities of individual dipeptides to be soluble are varied for proteins under altered experimental conditions. For accurately predicting protein solubility using SCM, it is better to customize the score card of dipeptide propensities by using a training data set under the same specified experimental conditions. The proposed method SCM with solubility scores and dipeptide propensities can be easily applied to the protein function prediction problems that dipeptide composition features play an important role. Availability: The used datasets, source codes of SCM, and supplementary files are available at http://iclab.life.nctu.edu.tw/SCM/.en_US
dc.language.isoen_USen_US
dc.titlePrediction and analysis of protein solubility using a novel scoring card method with dipeptide compositionen_US
dc.typeArticle; Proceedings Paperen_US
dc.identifier.doi10.1186/1471-2105-13-S17-S3en_US
dc.identifier.journalBMC BIOINFORMATICSen_US
dc.citation.volume13en_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:000312985100003-
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