Screening and Functional Validation of Genomic Variants Associated with Human Congenital Anomalies (R01 Clinical Trial Not Allowed)
Department of Health and Human Services
Rapid advances in genotyping and next generation sequencing technologies have led to the identification of genetic variants that are associated with a wide variety of congenital defects including human congenital anomalies (HCAs), intellectual developmental disabilities (IDDs) and inborn errors of metabolism (IEMs). Large quantities of genomic data collected from pediatric congenital anomalies cohorts are available to the research community through several databases such as the Database of Genotypes and Phenotypes (dbGaP), the Gabriella Miller Kids First Data Resource Portal, the European Genome-Phenome Archive and Clinical Genome Resource (ClinGen). The purpose of this initiative is to prom
Funding
Award size
Not specified
Type
Grant
Dates
Deadline
Later
Posted
10/30/2024
Closes
2028-01-07
Eligibility
Eligibility
Native American tribal governments (Federally recognized)Special district governmentsIndependent school districtsPrivate institutions of higher educationNonprofits having a 501(c)(3) status with the IRS, other than institutions of higher educationSmall businessesPublic and State controlled institutions of higher educationCounty governmentsNative American tribal organizations (other than Federally recognized tribal governments)For profit organizations other than small businessesOthers (see text field entitled "Additional Information on Eligibility" for clarification)Public housing authorities/Indian housing authoritiesState governmentsNonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher educationCity or township governments
Program
Funding area
Health - HLIncome Security and Social Services - ISS
Opportunity #
PAR-25-185
Source
Status
Open
Market
Government
Level
Federal
Source
Grants.gov