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    § Federal grant opportunity · RFA-RM-27-009

    Single Source: Continued Development of the Gabriella Miller Kids First Pediatric Data Resource Center (U2C Clinical Trial Not Allowed)

    National Institutes of Health is accepting applications for Single Source: Continued Development of the Gabriella Miller Kids First Pediatric Data Resource Center (U2C Clinical Trial Not Allowed). The deadline is January 8, 2027 and the published award range is $3.2M.

    Key facts

    Funder
    National Institutes of Health
    Application deadline
    January 8, 2027
    Award range
    $3.2M
    Eligibility
    private institutions of higher education, state governments, public and indian housing authorities, small businesses, city or township governments, special district governments, other native american tribal organizations, other, federally recognized native american tribal governments, county governments, nonprofits non higher education without 501c3, for profit organizations other than small businesses, independent school districts, nonprofits non higher education with 501c3, public and state institutions of higher education
    Geography
    United States
    Focus areas
    Health
    Opportunity number
    RFA-RM-27-009

    Program overview

    This is a Notice of Funding Opportunity (NOFO) for a Single Source that will invite application(s) from the eligible organization(s) to apply. Please see Section III. Eligibility for additional information. In accordance with NIH standard peer-review processes, the application(s) will be peer-reviewed, and only meritorious application(s) will be considered. This NOFO solicits applications for the continued development of the Gabriella Miller Kids First Pediatric Data Resource Center (DRC), which consists of the following components: a Data Resource Core, a Data Coordination Core, and an Administrative Core. The goal of the cloud-based Data Resource is to accelerate discovery of genetic etiology and shared biologic pathways within and across childhood cancers and congenital anomalies by facilitating access to and querying of annotated genomic sequence and phenotypic data from cohorts of patients with these conditions. The Data Resource Core serves as a research resource where genomic and phenotypic data can be aggregated, accessed, analyzed, and shared within and across the childhood cancer and congenital anomalies research communities as well as the broader scientific community. The Data Coordination Core will work with Kids First investigators and KF Genomic Data Generation Centers to facilitate data collection, harmonization, and sharing. The Administrative Core will oversee administrative activities, work closely with the NIH Kids First Working Group, and with the Kids First Training and Outreach Core, to provide resources to the research community.

    How to apply

    1. Confirm your organization meets the eligibility criteria above.
    2. Read the full funding opportunity announcement from National Institutes of Health.
    3. Draft your narrative against the funder's stated priorities and review criteria.
    4. Submit before January 8, 2027, allowing time for registration and validation.

    View the official funding announcement

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