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grant RFA-HG-24-023

Population Genomic Screening in Primary Care Sequencing Center (U01 - Clinical Trial Optional)

A grant opportunity is available for a Sequencing Center to support a population screening network. The center will provide sequencing services for 20,000 participants, including variant calling, annotation, confirmation, interpretation, and reporting. This grant is linked with others for Clinical Groups and a Coordinating Center.

This Notice of Funding Opportunity (NOFO) solicits applications for a Sequencing Center to support the new forming population screening network by providing sequencing service for 20,000 study participants, variant calling, annotation and confirmation, interpretation and reporting. This NOFO run…

Funding Source

Agency: National Institutes of Health
Sub-agency: National Human Genome Research Institute
Program: SBIR

Dates

Opportunity Released: August 14, 2024
Open for Submission: August 14, 2024
Submission Deadline: December 2, 2024
Application Window Closes: December 2, 2024

Supporting links

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