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    EcmPred: Prediction of extracellular matrix proteins based on random forest with maximum relevance minimum redundancy feature selection

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    Type
    Article
    Authors
    Kandaswamy, Krishna Kumar Umar
    Ganesan, Pugalenthi
    Kalies, Kai Uwe
    Hartmann, Enno
    Martinetz, Thomas M.
    KAUST Department
    Bioscience Core Lab
    Core Labs
    Date
    2013-01
    Permanent link to this record
    http://hdl.handle.net/10754/562580
    
    Metadata
    Show full item record
    Abstract
    The extracellular matrix (ECM) is a major component of tissues of multicellular organisms. It consists of secreted macromolecules, mainly polysaccharides and glycoproteins. Malfunctions of ECM proteins lead to severe disorders such as marfan syndrome, osteogenesis imperfecta, numerous chondrodysplasias, and skin diseases. In this work, we report a random forest approach, EcmPred, for the prediction of ECM proteins from protein sequences. EcmPred was trained on a dataset containing 300 ECM and 300 non-ECM and tested on a dataset containing 145 ECM and 4187 non-ECM proteins. EcmPred achieved 83% accuracy on the training and 77% on the test dataset. EcmPred predicted 15 out of 20 experimentally verified ECM proteins. By scanning the entire human proteome, we predicted novel ECM proteins validated with gene ontology and InterPro. The dataset and standalone version of the EcmPred software is available at http://www.inb.uni-luebeck.de/tools-demos/Extracellular_matrix_proteins/EcmPred. © 2012 Elsevier Ltd.
    Citation
    Kandaswamy, K. K., Pugalenthi, G., Kalies, K.-U., Hartmann, E., & Martinetz, T. (2013). EcmPred: Prediction of extracellular matrix proteins based on random forest with maximum relevance minimum redundancy feature selection. Journal of Theoretical Biology, 317, 377–383. doi:10.1016/j.jtbi.2012.10.015
    Sponsors
    This work was supported by the Graduate School for Computing in Medicine and Life Sciences funded by Germany's Excellence Initiative [DFG GSC 235/1]. KKK acknowledges Dr. Bianca Habermann, Max Planck Institute for Biology of Ageing, Germany for her support.
    Publisher
    Elsevier BV
    Journal
    Journal of Theoretical Biology
    DOI
    10.1016/j.jtbi.2012.10.015
    PubMed ID
    23123454
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.jtbi.2012.10.015
    Scopus Count
    Collections
    Articles; Bioscience Core Lab

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