The Common Fund’s Gabriella Miller Kids First Pediatric Research Program (Kids First) is pleased to announce that whole genome sequence data for the “Genomic Studies of Orofacial Cleft Birth Defects” project (Accession Number:phs001168.v1.p1) are now available for access through NIH’s Database of Genotypes and Phenotypes (dbGaP)https://www.ncbi.nlm.nih.gov/p
This Kids First cohort was selected for sequencing in 2015. Additional datasets from childhood cancer and other structural birth defects patient cohorts, selected through our X01 projects are forthcoming.
To view abstracts for additional Kids First X01 projects and estimated data release dates, visit: https://commonfund.nih.gov/kid
sfirst/X01Projects and the Frequently Asked Questions page for guidance on how to access the data.
For questions, please email: KidsFirst@od.nih.gov.