Map of Participants
The map above shows the locations of the laboratories participating in the Canadian Open Genetics Repository.
The map above shows the locations of the laboratories participating in the Canadian Open Genetics Repository.
Ron Agatep; Peter Ainsworth; Mohammad R Akbari; Melyssa Aronson; Gary Bader; Raveen Basran; Andre Blavier; Andrea Blumenthal; Ian Bosdet; Kym Boycott; Michael Brudno; Kathleen Buckley; Jodi Campbell; Philippe M Campeau; Melanie Care; Nancy Carson; Ronald Carter; George Charames; David Chitayat; George Chong; Edmond Chouinard; Kathy Chun; Kenneth J Craddock; Rod Docking; Andrea Eisen; Zaki El Haffaf; Hanna Faghfoury; Sandra Farrell; Harriet Feilotter; Bridget Fernandez; Marc Fiume; Cynthia Forster-Gibson; Jan Friedman; William D Foulkes; Peter Goodhand; Jessica Gu; Robert Hegele; Spring Holter; Sheri Horsburgh; Lauren Hughes; Stacey Hume; Olga Jarinova; Franny Jewett; Anne Junker; Aly Karsan; Sam Khalouei; Joan Knoll; Elena Kolomietz; Bartha Knoppers; Ryan Lamont; Matthew Lebo; Jordan Lerner-Ellis; Georges Maire; Christian Marshall; Elizabeth McCready; Grant Mitchell; Michael J Moorhouse; Chantal Morel; Tanya Nelson; Abdul Noor; Brian O’Connor; Darren O’Rielly; Francis Ouellette; Jillian Parboosingh; Hilary Racher; Peter Ray; Heidi Rehm; Christie Riddell; Jean-Baptiste Riviere; David S Rosenblatt; Guy Rouleau; Andrea Ruchon; Peter Sabatini; Bekim Sadikovic; Kara Semotiuk; Stephen W Scherer; Cheryl Shuman; Josh Silver; Katherine Siminovitch; Lesley Solomon-Izsak; Jean-Francois Soucy; Marsha Speevak; James Stavropoulos; Lincoln Stein; Rhonda Tannenbaum; Sherryl Taylor; Deborah Terespolsky; Robert Tomaszewski; Tracy Tucker; Richard F Wintle; Beatrix Wong; Nora Wong; Marina Wang; Nicholas Watkins, John S Waye; Shana White; Michael O Woods; Philip Wyatt; Sean Young; Kathleen-Rose Zakoor
The Executive Committee is charged with overall supervision of the project, and is responsible for budget, scheduling and workgroup coordination.
The Bioinformatics and IT Workgroup is responsible for sourcing and developing software and other tools to interpret genetic variation; extracting data from participating labs; and making all project information available to the community at large. This workgroup will be developing, refining, and disseminating the novel variants assessment and phenotype cataloguing tools. They will also be responsible for creating the bioinformatic processes for extracting variant level knowledge data from the various external databases, standardizing the data, and importing it into the unified database. The Bioinformatics and IT Workgroup will also develop and maintain the website with direct input from the other two working groups.
The Data Collection and Standards Workgroup is responsible for defining and monitoring the operational goals of the project, including the scope of data collection, data sources and requirements for shared resources. This group is made up of representatives from each clinical or research laboratory contributing data to the project. This workgroup will be responsible for collecting and synthesizing data from the various stakeholders, communicating these analyses and equivalencies to the Bioinformatics workgroup, and producing the SOPs, guidelines, and policies surrounding the use of the novel variant assessment tool, phenotype cataloguing system, and unified database.
The Outreach and Patient Advocacy Workgroup is responsible for creating awareness of and interest in the long-term benefits of the project, by developing relationships and interactive communications vehicles that will allow the project team to keep all stakeholders up-to-date on our progress, as well as to stay abreast of developments affecting end-users, including patients and groups advocating for the identification and management of both rare and common diseases.
Organizations, Projects, and Consortia with Related Missions
Canadian College of Medical Geneticists
Clinical Sequencing Exploratory Research Consortium
Electronic Medical Records and Genomics (eMERGE) Network
Exome Sequencing Project (ESP)
International Collaboration for Clinical Genomics
International Rare Diseases Research Consortium (IRDiRC)
Leiden Open Variation Database (LOVD)
National Center for Biotechnology Information
Online Mendelian Inheritance in Man (OMIM)
Pharmacogenetics Knowledge Base (PharmGKB)
Pharmacogenetics Research Network
Sharing Clinical Reports Project (SCRP)
Professional Societies
American College of Medical Genetics
American Society of Human Genetics
Association for Molecular Pathology
College of American Pathologists
Government Agencies
Centers for Disease Control and Prevention
National Human Genome Research Institute
National Institute of Child Health and Human Development
Patient Advocacy