Discovery of the Genetic Basis of Childhood Cancers and of Congenital Anomalies: Gabriella Miller Kids First Pediatric Research Program (X01 Clinical Trial Not Allowed)
Department of Health and Human Services
As part of the Gabriella Miller Kids First Pediatric Research Program (Kids First Program), the NIH invites applications to submit samples from pediatric cohorts for whole genome sequencing at a Kids First Program supported genomic data generating centers. Applicants are encouraged to propose sequencing of existing pediatric cancer or congenital anomaly cohorts to elucidate the genetic contribution (somatic and/or germline) to childhood cancers, to investigate the genetic etiology of congenital anomalies, to study the molecular basis of the associations between congenital anomalies and increased cancer risk, or to expand the range of pediatric disorders included within the Kids First Data Re
Funding
Award size
Not specified
Type
Other
Dates
Deadline
Later
Posted
06/18/2026
Closes
2027-01-11
Eligibility
Eligibility
Public and State controlled institutions of higher educationPrivate institutions of higher educationSpecial district governmentsNonprofits having a 501(c)(3) status with the IRS, other than institutions of higher educationIndependent school districtsSmall businessesPublic housing authorities/Indian housing authoritiesFor profit organizations other than small businessesOthers (see text field entitled "Additional Information on Eligibility" for clarification)County governmentsNative American tribal organizations (other than Federally recognized tribal governments)State governmentsCity or township governmentsNative American tribal governments (Federally recognized)Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education
Program
Funding area
Health - HL
Opportunity #
PAR-27-071
Source
Status
Open
Market
Government
Level
Federal
Source
Grants.gov