Explore and Connect with Research Data Today!
The NIH Common Fund-supported Gabriella Miller Kids First Data Resource Center enables researchers, clinicians, and patients to work together to accelerate research and promote new discoveries for children affected with cancer and structural birth defects. Data from over 11,000 samples, including DNA and RNA, is available to empower your research today. Data collected from more than 30,000 samples are expected to be available in the next few years. Learn how to get started using the Data Resource Portal today!
Available Data
Note: Due to technical limitations, these counts currently include TARGET AML & Neuroblastoma, whose meta data are only indexed on the portal. The genomic data does not reside at the DRC.
MORE ABOUT THE DATASETS
Our Partners
Researchers
Search, view, analyze, and identify currently accessible data along with your own to support your research
Healthcare Professionals
Map patients in your disease of interest by disease characteristics and view molecular profiling
Patients/Family Members
Learn about disease-specific research, become a Kids First partner, and support data sharing
Community Members
Learn about scientific discoveries in pediatric cancer and structural birth defects
Kids First News & Events
investigator spotlight
Adam Resnick, PhD
Children's Hospital of Philadelphia
“Pediatric cancers, structural birth defects, and other diseases of development likely share mechanisms that..."
Read Morefoundation spotlight
PHACE Syndrome Community
“The PHACE Syndrome Community is honored to partner with [the Kids First DRC]..."
Read Moreinvestigator spotlight
Dawn Siegel, MD
Medical College of Wisconsin
"Dr. Siegel has a particular interest in general pediatric dermatology..."
Read MoreFunding & Support
The Gabriella Miller Kids First Data Resource Center is funded by the NIH Common Fund and collaborates with member institutions.
