This upcoming grant will fund projects to develop, curate, and share valuable genomic resources for the research community, supporting both basic and clinical genomics.
NHGRI will fund pilot studies using innovative molecular technologies, beyond standard DNA sequencing, to identify genes or variants causing rare genetic disorders, with applications opening in 2026.
This grant will fund research centers to study how genetic variants interact with each other or the environment to influence health, aiming to improve variant testing and genomic predictions.
This grant funds research centers to develop and test computational models analyzing how genomic variations affect genome function, as part of the IGVF Consortium.
NHGRI seeks applications to study how genomic variations affect genome function and phenotypes using high-throughput methods, as part of the IGVF Consortium.