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 DataMORE ABOUT THE DATASETS
Kids First News & Events
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 More