NIH Kids First Program: Genomic Research on Childhood Cancers and Congenital Anomalies

NIH Kids First Program: Genomic Research on Childhood Cancers and Congenital Anomalies

Due Date: 01/11/2027

The Discovery of the Genetic Basis of Childhood Cancers and of Congenital Anomalies: Gabriella Miller Kids First Pediatric Research Program (X01 Clinical Trial Not Allowed) provides researchers with access to genomic sequencing and related data-generation resources for pediatric cancer and congenital anomaly cohorts.

The NIH Common Fund initiative invites applications to submit existing pediatric cohort samples for whole-genome sequencing and, when justified, additional approaches such as exome, transcriptome, long-read, clinical-grade, proteomic, and epigenomic analyses. Generated genomic, clinical, and phenotypic data will become part of the Kids First Data Resource Center and will be shared with the research community.

Eligibility Criteria

  • Public and state-controlled institutions of higher education are eligible to apply.
  • Private institutions of higher education are eligible.
  • Nonprofit organizations with or without 501(c)(3) status may apply.
  • Small businesses and other for-profit organizations are eligible.
  • State, county, city or township, and special district governments may apply.
  • Foreign organizations, non-domestic components of U.S. organizations, and foreign components are not eligible. Simpler Grants

Funding Details

  • Funding Mechanism: X01 Resource Access Award
  • Award Amount: No direct funds are associated with this opportunity.
  • The award provides access to Kids First Program research resources, including sequencing and related data-generation services.
  • Maximum Project Period: 1 year.

Deadline

  • Open Date: December 11, 2026
  • Application Deadline: January 11, 2027
  • Application Time: 5:00 PM local time of the applicant organization
  • Earliest Start Date: April 2027
  • Expiration Date: January 12, 2027. Simpler Grants

Further Information