Screening and Functional Validation of Genomic Variants Associated with Human Congenital Anomalies (R01 Clinical Trial Not Allowed)
Screening and Functional Validation of Genomic Variants Associated with Human Congenital Anomalies (R01 Clinical Trial Not Allowed) is offered by National Institutes of Health. Max award: Not specified. Applications close on .
National Institutes of Health has 666 open grants in our daily copy of Grants.gov data.
| Opportunity number | PAR-25-185 |
|---|---|
| Agency | National Institutes of Health |
| Status | Posted |
| Posted | |
| Closes | |
| Award ceiling | Not specified |
| Award floor | Not specified |
| Total program funding | Not specified |
| Expected awards | Not specified |
| Who can apply | For profit organizations other than small businesses, Private institutions of higher education, Nonprofits having a 501(c)(3) status with the IRS, other than institutions of higher education, Special district governments, City or township governments, Native American tribal organizations (other than Federally recognized tribal governments), State governments, Small businesses, Independent school districts, Native American tribal governments (Federally recognized), County governments, Public and State controlled institutions of higher education, Public housing authorities/Indian housing authorities, Nonprofits that do not have a 501(c)(3) status with the IRS, other than institutions of higher education, Others (see text field entitled "Additional Information on Eligibility" for clarification) |
| Category | Health, Income Security and Social Services |
Summary (excerpt)
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…
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