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 upcoming grant will fund projects to develop, curate, and share valuable genomic resources for the research community, supporting both basic and clinical genomics.
NHGRI seeks applications to study how genomic variations affect genome function and phenotypes using high-throughput methods, as part of the IGVF Consortium.
This grant funds research centers to develop and test computational models analyzing how genomic variations affect genome function, as part of the IGVF Consortium.
This grant will fund a center to coordinate data, tools, and outreach for the GREGoRi program, advancing rare disease genetics research by sharing resources with the research community.