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


Our Partners


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

Get Involved!

Join now and start exploring this useful portal.

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Kids First News & Events

foundation spotlight

November 05, 2018

Ear Community Foundation Spotlight

"The [Gabriella Miller] Kids First Data Resource Center is important to Ear Community..."

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Study Updates
November 02, 2018

“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...

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foundation spotlight

August 16, 2018

The Moebius Syndrome Foundation

“The Moebius Syndrome Foundation is happy to support the Kids First Data Resource Center. We are thrilled to do anything we can..."

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Funding & Support

The Kids First Data Resource Center is funded by the NIH Common Fund and collaborates with member institutions.