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dc.rights.licenseopenen_US
dc.contributor.authorMEGY, Karyn
dc.contributor.authorDOWNES, Kate
dc.contributor.authorMOREL-KOPP, Marie-Christine
dc.contributor.authorBASTIDA, Jose M.
dc.contributor.authorBROOKS, Shannon
dc.contributor.authorBURY, Loredana
dc.contributor.authorLEINOE, Eva
dc.contributor.authorGOMEZ, Keith
dc.contributor.authorMORGAN, Neil V.
dc.contributor.authorOTHMAN, Maha
dc.contributor.authorOUWEHAND, Willem H.
dc.contributor.authorPEREZ BOTERO, Juliana
dc.contributor.authorRIVERA, Jose
dc.contributor.authorSCHULZE, Harald
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorTREGOUET, David-Alexandre
dc.contributor.authorFRESON, Kathleen
dc.date.accessioned2021-10-11T10:14:51Z
dc.date.available2021-10-11T10:14:51Z
dc.date.issued2021-07-13
dc.identifier.issn1538-7836en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/112718
dc.description.abstractEnThe implementation of high-throughput sequencing (HTS) technologies in research and diagnostic laboratories has linked many new genes to rare bleeding, thrombotic, and platelet disorders (BTPD), and revealed multiple genetic variants linked to those disorders, many of them being of uncertain pathogenicity when considering the accepted evidence (variant consequence, frequency in control datasets, number of reported patients, prediction models, and functional assays). The sequencing effort has also resulted in resources for gathering disease-causing variants associated with specific genes, but for BTPD, such well-curated databases exist only for a few genes. On the other hand, submissions by individuals or diagnostic laboratories to the variant database ClinVar are hampered by the lack of a submission process tailored to capture the specific features of hemostatic diseases. As we move toward the implementation of HTS in the diagnosis of BTPD, the Scientific and Standardization Committee for Genetics in Thrombosis and Haemostasis has developed and tested a REDCap-based interface, aimed at the community, to submit curated genetic variants for diagnostic-grade BTPD genes. Here, we describe the use of the interface and the initial submission of 821 variants from 30 different centers covering 14 countries. This open-access variant resource will be shared with the community to improve variant classification and regular bulk data transfer to ClinVar.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enBlood
dc.subject.enGenes
dc.subject.enHemorrhage
dc.subject.enMutation
dc.subject.enPlatelets
dc.subject.enThrombosis
dc.title.enGoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
dc.typeArticle de revueen_US
dc.identifier.doi10.1111/jth.15459en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed34355501en_US
bordeaux.journalJournal of Thrombosis and Haemostasisen_US
bordeaux.page2612-2617en_US
bordeaux.volume19en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue10en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamVINTAGEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03373078
hal.version1
hal.date.transferred2021-10-11T10:14:55Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Thrombosis%20and%20Haemostasis&rft.date=2021-07-13&rft.volume=19&rft.issue=10&rft.spage=2612-2617&rft.epage=2612-2617&rft.eissn=1538-7836&rft.issn=1538-7836&rft.au=MEGY,%20Karyn&DOWNES,%20Kate&MOREL-KOPP,%20Marie-Christine&BASTIDA,%20Jose%20M.&BROOKS,%20Shannon&rft.genre=article


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