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dc.contributor.authorLerner-Ellis, Jordanen_US
dc.contributor.authorWang, Marinaen_US
dc.contributor.authorWhite, Shanaen_US
dc.contributor.authorLebo, Matthew Sen_US
dc.date.accessioned2015-08-03T14:02:43Z
dc.date.issued2015en_US
dc.identifier.citationLerner-Ellis, Jordan, Marina Wang, Shana White, and Matthew S Lebo. 2015. “Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations.” Journal of Medical Genetics 52 (7): 438-445. doi:10.1136/jmedgenet-2014-102933. http://dx.doi.org/10.1136/jmedgenet-2014-102933.en
dc.identifier.issn0022-2593en
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:17820938
dc.description.abstractBackground: The Canadian Open Genetics Repository is a collaborative effort for the collection, storage, sharing and robust analysis of variants reported by medical diagnostics laboratories across Canada. As clinical laboratories adopt modern genomics technologies, the need for this type of collaborative framework is increasingly important. Methods: A survey to assess existing protocols for variant classification and reporting was delivered to clinical genetics laboratories across Canada. Based on feedback from this survey, a variant assessment tool was made available to all laboratories. Each participating laboratory was provided with an instance of GeneInsight, a software featuring versioning and approval processes for variant assessments and interpretations and allowing for variant data to be shared between instances. Guidelines were established for sharing data among clinical laboratories and in the final outreach phase, data will be made readily available to patient advocacy groups for general use. Results: The survey demonstrated the need for improved standardisation and data sharing across the country. A variant assessment template was made available to the community to aid with standardisation. Instances of the GeneInsight tool were provided to clinical diagnostic laboratories across Canada for the purpose of uploading, transferring, accessing and sharing variant data. Conclusions: As an ongoing endeavour and a permanent resource, the Canadian Open Genetics Repository aims to serve as a focal point for the collaboration of Canadian laboratories with other countries in the development of tools that take full advantage of laboratory data in diagnosing, managing and treating genetic diseases.en
dc.language.isoen_USen
dc.publisherBMJ Publishing Groupen
dc.relation.isversionofdoi:10.1136/jmedgenet-2014-102933en
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501169/pdf/en
dash.licenseLAAen_US
dc.subjectGenetic screening/counsellingen
dc.subjectClinical geneticsen
dc.subjectDiagnostics testsen
dc.subjectEvidence Based Practiceen
dc.subjectGeneticsen
dc.titleCanadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretationsen
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden
dc.relation.journalJournal of Medical Geneticsen
dash.depositing.authorLebo, Matthew Sen_US
dc.date.available2015-08-03T14:02:43Z
dc.identifier.doi10.1136/jmedgenet-2014-102933*
dash.contributor.affiliatedLebo, Matthew


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