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dc.creatorJurtz, Vanessa-
dc.creatorPaul, Sinu-
dc.creatorAndreatta, Massimo-
dc.creatorMarcatili, Paolo-
dc.creatorPeters, Bjoern-
dc.creatorNielsen, Morten-
dc.date2018-06-14T14:48:34Z-
dc.date2018-06-14T14:48:34Z-
dc.date2017-11-
dc.date2018-06-13T14:57:10Z-
dc.date.accessioned2019-04-29T15:41:49Z-
dc.date.available2019-04-29T15:41:49Z-
dc.date.issued2017-11-
dc.identifierJurtz, Vanessa; Paul, Sinu; Andreatta, Massimo; Marcatili, Paolo; Peters, Bjoern; et al.; Netmhcpan-4.0: Improved peptide-MHC class I interaction predictions integrating eluted ligand and peptide binding affinity data; American Association of Immunologists; Journal of Immunology; 199; 9; 11-2017; 3360-3368-
dc.identifier0022-1767-
dc.identifierhttp://hdl.handle.net/11336/48622-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/299792-
dc.descriptionCytotoxic T cells are of central importance in the immune system's response to disease. They recognize defective cells by binding to peptides presented on the cell surface by MHC class I molecules. Peptide binding to MHC molecules is the single most selective step in the Ag-presentation pathway. Therefore, in the quest for T cell epitopes, the prediction of peptide binding to MHC molecules has attracted widespread attention. In the past, predictors of peptide-MHC interactions have primarily been trained on binding affinity data. Recently, an increasing number of MHC-presented peptides identified by mass spectrometry have been reported containing information about peptide-processing steps in the presentation pathway and the length distribution of naturally presented peptides. In this article, we present NetMHCpan-4.0, a method trained on binding affinity and eluted ligand data leveraging the information from both data types. Large-scale benchmarking of the method demonstrates an increase in predictive performance compared with state-of-the-art methods when it comes to identification of naturally processed ligands, cancer neoantigens, and T cell epitopes.-
dc.descriptionFil: Jurtz, Vanessa. Technical University of Denmark; Dinamarca-
dc.descriptionFil: Paul, Sinu. La Jolla Institute for Allergy and Immunology; Estados Unidos-
dc.descriptionFil: Andreatta, Massimo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentina-
dc.descriptionFil: Marcatili, Paolo. Technical University of Denmark; Dinamarca-
dc.descriptionFil: Peters, Bjoern. La Jolla Institute for Allergy and Immunology; Estados Unidos-
dc.descriptionFil: Nielsen, Morten. Technical University of Denmark; Dinamarca. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Biotecnológicas. Universidad Nacional de San Martín. Instituto de Investigaciones Biotecnológicas; Argentina-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherAmerican Association of Immunologists-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.4049/jimmunol.1700893-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/http://www.jimmunol.org/content/199/9/3360-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.subjectMHC-
dc.subjectligands-
dc.subjectepitopes-
dc.subjectmachine learning-
dc.subjectOtras Ciencias Biológicas-
dc.subjectCiencias Biológicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titleNetmhcpan-4.0: Improved peptide-MHC class I interaction predictions integrating eluted ligand and peptide binding affinity data-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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