The purpose of the Canadian Open Genetics Repository (COGR) is to design technologies that will help medical researchers and physicians diagnose, treat and cure both rare and common diseases. This work belongs to genomic medicine, a healthcare field built on our growing knowledge of the DNA comprising the human genome. This repository contains a single table containing 4933 variants. The data in the table represents a unified, open-access, clinical-grade genetic database, i.e., a large repository based on a commonly shared platform and designed to hold all types of information related to human gene DNA variants and their relationship to disease. This database draws from the genetic holdings in place at clinical labs and hospitals across Canada. Data source: https://opengenetics.ca/ Citations: Lebo, M., Zakoor, KR., Chun, K. et al. Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR). Genet Med 20, 294–302 (2018). https://doi.org/10.1038/gim.2017.80 Lerner-Ellis J, Wang M, White S, et al. Canadian Open Genetics Repository (COGR): a unified clinical genomics...
This collection is openly accessible.
Canadian Open Genetics Repository (COGR) is published on Biomedical AI.