PMut: A web-based tool for the annotation of pathological variants on proteins, 2017 update

dc.contributor.authorLópez Ferrando, Víctorca
dc.contributor.authorGazzo, Andrea M.ca
dc.contributor.authorCruz, Xavier de laca
dc.contributor.authorOrozco, Modestoca
dc.contributor.authorGelpí, Josep Lluísca
dc.date.accessioned2018-07-02T07:45:45Z
dc.date.available2018-07-02T07:45:45Z
dc.date.issued2017
dc.description.abstractWe present here a full update of the PMut predictor, active since 2005 and with a large acceptance in the field of predicting Mendelian pathological mutations. PMut internal engine has been renewed, and converted into a fully featured standalone training and prediction engine that not only powers PMut web portal, but that can generate custom predictors with alternative training sets or validation schemas. PMut Web portal allows the user to perform pathology predictions, to access a complete repository of pre-calculated predictions, and to generate and validate new predictors. The default predictor performs with good quality scores (MCC values of 0.61 on 10-fold cross validation, and 0.42 on a blind test with SwissVar 2016 mutations). The PMut portal is freely accessible at http://mmb.irbbarcelona.org/PMut. A complete help and tutorial is available at http://mmb.irbbarcelona.org/PMut/help.
dc.description.sponsorshipSpanish Ministry of Science [BIO2015-64802-R-32868, SEV-2015-0493, TIN2012-34557, TEC2015-67774-C2-2-R, SAF2016-80255-R]; Catalan Government [2014-SGR-134, 2014-SGR-1051]; Instituto de Salud Carlos III-Instituto Nacional de Bioinformática [INB; PT13/0001/0019, PT13/0001/0028]; European Union, H2020 programme [Elixir-Excelerate: 676559; BioExcel: 674728 and MuG: 676566]; La Caixa Foundation fellowship [to V.L.F.]. Funding for open access charge: European Union and Spanish Ministry of Science.
dc.format.mimetypeapplication/pdf
dc.identifier.citationLópez-Ferrando V, Gazzo A, de la Cruz X, Orozco M, Gelpí JL. PMut: a web-based tool for the annotation of pathological variants on proteins, 2017 update. Nucleic Acids Res. 2017 Jul 3;45(W1):W222-W228. DOI: 10.1093/nar/gkx313
dc.identifier.doihttp://dx.doi.org/10.1093/nar/gkx313
dc.identifier.issn0305-1048
dc.identifier.urihttp://hdl.handle.net/10230/35009
dc.language.isoeng
dc.publisherOxford University Pressca
dc.relation.ispartofNucleic Acids Res. 2017 Jul 3;45(W1):W222-W228
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/676559
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/1PE/BIO2015-64802-R
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/1PE/SAF2016-80255-R
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/674728
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/676566
dc.rights© The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.titlePMut: A web-based tool for the annotation of pathological variants on proteins, 2017 updateca
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion

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