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 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.
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.
NIH funds testing centers to evaluate the safety and efficacy of somatic cell genome editing for human disease therapies using preclinical models; clinical trials are not allowed.