This grant is for the continued development of the Gabriella Miller Kids First Pediatric Data Resource Center. It aims to support research into childhood cancers and congenital anomalies by enhancing a cloud-based data resource that helps researchers access and analyze genetic and phenotypic data. The grant will fund three main components: a Data Resource Core, a Data Coordination Core, and an Administrative Core.
Who it's for: This grant is for organizations that can contribute to the development and management of a pediatric data resource center focused on childhood cancers and congenital anomalies. Eligible applicants include various types of educational institutions, government entities, small businesses, nonprofits, and tribal organizations.
More details
Likely Disqualifiers
- Not being a single source as specified
- Proposing a clinical trial
- Not meeting NIH peer-review standards
- Ineligibility based on entity type
- Incomplete application submission
What You May Need
- Detailed project proposal
- Organizational eligibility documentation
- Budget plan
- NIH peer-review compliance
- Data management plan
- Partnership agreements (if applicable)
- Proof of capability to manage a data resource center
Cautions
- This is a single source opportunity, limiting eligibility
- Clinical trials are not allowed
- Strict NIH peer-review process
- Specific focus on childhood cancers and congenital anomalies
Generated from official source details for readability
Eligibility
Eligible Applicant Types
Additional Criteria
Eligible applicants include private institutions of higher education, state governments, public and state institutions of higher education, small businesses, city or township governments, special district governments, other Native American tribal organizations, federally recognized Indian tribal governments, county governments, nonprofits without 501(c)(3) status, for-profit organizations, independent school districts, and nonprofits with 501(c)(3) status. Public and state institutions of higher education are also eligible.
Overview
This grant is for organizations that can contribute to the development and management of a pediatric data resource center focused on childhood cancers and congenital anomalies. Eligible applicants include various types of educational institutions, government entities, small businesses, nonprofits, and tribal organizations.
Likely Disqualifiers
- Not being a single source as specified
- Proposing a clinical trial
- Not meeting NIH peer-review standards
- Ineligibility based on entity type
- Incomplete application submission
Use of Funds
Funds can be used to develop and manage the Data Resource Core, Data Coordination Core, and Administrative Core of the Gabriella Miller Kids First Pediatric Data Resource Center. This includes facilitating data access, collection, harmonization, sharing, and administrative oversight.
Total Program Funding
$5,000,000
Cost Sharing
Not Required
Important Dates
- Posted
- Oct 29, 2026
- Deadline
- Jan 8, 2027(68 days)
- Archive Date
- Mar 8, 2027
- Last Updated
- Oct 29, 2026
Application Checklist
- Verify single source eligibility
- Prepare a comprehensive project proposal
- Ensure compliance with NIH peer-review standards
- Compile necessary organizational documents
- Develop a detailed budget plan
- Draft a data management and sharing plan
- Submit application by the deadline