The Gabriella Miller Kids First Data Resource for genomic research in pediatric cancer and congenital anomalies.

The Gabriella Miller Kids First Data Resource has provided genomic data from over 30,000 pediatric participants, enabling breakthroughs in childhood cancer and congenital anomalies research.

• Why it matters: This resource addresses the critical need for comprehensive genomic data to understand and treat pediatric conditions, filling a gap in available research tools and datasets.
• What they did: The program collected and annotated genomic, demographic, and clinical data from more than 30,000 participants, making it accessible for secondary research through web-based platforms.
• The result: The availability of this data has led to significant research breakthroughs and supports future expansion of tools and modalities to advance pediatric life-saving research.