North America
Children’s Hospital Los Angeles
Los Angeles, California, United States of America
Children’s Hospital of Philadelphia
Philadelphia, Pennsylvania, United States of America
Columbia University Medical Center
New York, New York, United States of America
Duke University Medical Center
Durham, North Carolina, United States of America
Dana-Farber Cancer Institute
Boston, Massachusetts, United States of America
The Louisiana State University Health
Sciences Center
New Orleans, Louisiana, United States of America
Memorial Sloan Kettering Cancer Center
New York, New York, United States of America
Providence Cancer Institute
Portland, Oregon, United States of America
Sidney Kimmel Cancer Center at Johns
Hopkins University; Allegheny Health
Network, Affiliate
Baltimore, Maryland, United States of America
The University of California, San Francisco –
Helen Diller Family Comprehensive Cancer
Center
San Francisco, California, United States of America
The University of Chicago
Chicago, Illinois, United States of America
University Health Network – Princess
Margaret Cancer Centre
Toronto, Ontario, Canada
University of Miami – Sylvester
Comprehensive Cancer Center
Miami, Florida, United States of America
Vanderbilt University Medical Center /
Ingram Cancer Center
Nashville, Tennessee, United States of America
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States of America
Yale University
New Haven, Connecticut, United States of America
Europe
Institut Gustave Roussy
Paris, France
The Netherlands Cancer Institute,
Amsterdam, on behalf of the Center for
Personalized Cancer Treatment
Utrecht, Netherlands
Vall d’Hebron Institute of Oncology
Barcelona, Spain
Asia
Korea University Anam Hospital
Seoul, Korea
Participating Institution Requirements
- Provide 500 genomic records to start (Data must be CLIA- or ISO-certified)
- Provide 500 genomic records each subsequent year of participation (Data must be CLIA- or ISO-certified)
- Limited Data sets as defined by 45 C.F.R. § 164.514(e) will be provided
- If de-identified datasets are provided, the process must adhere to the project’s established protocols
- Maintain IRB approval
- Meet data standards and deadlines
- Participate in meetings
- Participate in committees and subcommittees
- Execute the Main Participation Agreement and agree to all exhibits, including the Data User Agreement