Please use this identifier to cite or link to this item: http://ir.juit.ac.in:8080/jspui/jspui/handle/123456789/9271
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dc.contributor.authorGupta, Arun-
dc.contributor.authorChandra, Sharat-
dc.contributor.authorSingh, Tiratha Raj-
dc.date.accessioned2023-01-17T10:45:38Z-
dc.date.available2023-01-17T10:45:38Z-
dc.date.issued2014-
dc.identifier.urihttp://ir.juit.ac.in:8080/jspui/jspui/handle/123456789/9271-
dc.description.abstractBinding of Major histocompatibility complex (MHC) peptide is a prerequisite for T cell activation in the immune system. MHC-binding peptides have shown promising results for immunodiagnostics and immunotherapeutic purposes. HLA-B*2705 is found to be associated with the development of variety of autoimmune diseases including Ankylosing spondylitis. Detecting MHC class I allele HLAB* 2705 binding peptides can reduce the number of peptides that need to be tested experimentally. This work describes the implementation of SVM algorithm, developed for the identification of HLA-B*2705 binding peptides in antigenic sequences. The specificity and sensitivity obtained during the development of this server are 85 and 86 %, respectively. Whereas average precision and average recall values were observed to be 85 and 86 %, respectively. Training on widescale data made thismethod more accurate and robust than all available other methods for the HLA-B*2705 allele and would prove its usability in the biomedical domain. A web server HLA-B27pred is available at http://www.nuccore.org/ hlab27pred for academic and research purpose.en_US
dc.language.isoenen_US
dc.publisherJaypee University of Information Technology, Solan, H.P.en_US
dc.subjectAnkylosing spondylitisen_US
dc.subjectMHC-binding peptidesen_US
dc.subjectImmunoinformaticsen_US
dc.titleHLAB27Pred: SVM-based precise method for predicting HLA-B*2705 binding peptides in antigenic sequencesen_US
dc.typeArticleen_US
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