Scout | Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial Not Allowed)

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Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial Not Allowed)

This grant opportunity aims to support research that investigates genetic variants linked to congenital defects, such as structural birth defects, intellectual developmental disabilities, and inborn errors of metabolism. It focuses on using genomic data available from databases like dbGaP and the Gabriella Miller Kids First Data Resource Portal. The goal is to encourage the screening, validati…

Source

Agency: National Institutes of Health

Program: SBIR

Award

Award Ceiling: $499,999

Funding Amount: $499,999

Dates

Application Window Closes: May 7, 2025

Opportunity Released: May 5, 2021

Open for Submission: May 5, 2021

Submission Deadline: May 7, 2025

Keywords

genomic variants

birth defects

genetic screening

functional validation

congenital defects

in-silico tools

pediatric genomics

intellectual developmental disabilities

next generation sequencing

genetic research databases

Supporting Links

Documents

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