Data Resource Portal Now Available to the Public!
Data from approximately 8,000 DNA and RNA samples from children affected with cancer or structural birth defects and their families is ready for analysis. This number is expected to grow to more than 30,000 over the next few years. This will enable researchers, clinicians, and patients to work together to accelerate research and promote new discoveries. To learn how to get started using the Data Resource Portal, CLICK HERE TO GET STARTED!
Available Data
MORE ABOUT THE DATASETSOur 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
foundation spotlight
Ear Community Foundation Spotlight
"The [Gabriella Miller] Kids First Data Resource Center is important to Ear Community..."
Read More
“Adolescent Idiopathic Scoliosis (AIS)” Data Available for Access
The NIH Common Fund’s Gabriella Miller Kids First Pediatric Research Program (Kids First) is proud to announce that whole genome sequence (WGS) data for the AIS project...
Read Moreinvestigator spotlight
Azeez Butali, DDS, PhD
University of Iowa
"Kids First is a valuable program because it allows us to identify specific genomic variants that will drive future research on Orofacial Clefts (OFC)..."
Read MoreFunding & Support
The Kids First Data Resource Center is funded by the NIH Common Fund and collaborates with member institutions.
