This is an NIH program that pays for whole-genome and other sequencing of existing pediatric cancer or congenital anomaly cohorts, with the resulting data going into a shared public research resource. It is for organizations that already hold patient cohorts and biospecimens and want them sequenced, not for businesses looking for general operating funds or product development money. If you have no existing pediatric cohort, sequencing capability, or research program, do not bother.
| Industry | Estimated fit |
|---|---|
| Healthcare & BiotechMatches your industry (clinical) | 72 |
| Social Services & NonprofitMatches your industry (community) | 66 |
| Agriculture & FarmingLimit: Not clearly about your industry or what you need funding for; check the… | 54 |
| Arts & CultureLimit: Not clearly about your industry or what you need funding for; check the… | 54 |
| Education & TrainingLimit: Not clearly about your industry or what you need funding for; check the… | 54 |
| Energy & Clean TechLimit: Nothing in this notice points to energy & clean tech | 54 |
| Industry | Estimated fit |
|---|---|
| Environment & ConservationLimit: Nothing in this notice points to environment & conservation | 54 |
| Finance & BankingLimit: Not clearly about your industry or what you need funding for; check the… | 54 |
| Food & BeverageLimit: Not clearly about your industry or what you need funding for; check the… | 54 |
| Housing & Real EstateLimit: Not clearly about your industry or what you need funding for; check the… | 54 |
| ManufacturingLimit: Nothing in this notice points to manufacturing | 54 |
| Retail & E-CommerceLimit: Nothing in this notice points to retail & e-commerce | 54 |
| Technology & SoftwareLimit: Nothing in this notice points to technology & software | 54 |
| Construction & InfrastructureLimit: Nothing in this notice points to construction & infrastructure | 51 |
| Transportation & LogisticsLimit: Nothing in this notice points to transportation & logistics | 51 |
These are our matcher’s estimates for a typical business in each industry. A real match depends on your size, your state and what you need the money for — check your own fit.
NIH Kids First X01 program: researchers and organizations (including small businesses and for-profits) may submit existing pediatric cancer or congenital anomaly cohorts for free whole-genome and other sequencing at NIH-supported centers; resulting data go to the shared Kids First Data Resource. US-based entities only.
As part of the Gabriella Miller Kids First Pediatric Research Program (Kids First Program), the NIH invites applications to submit samples from pediatric cohorts for whole genome sequencing at a Kids First Program supported genomic data generating centers. Applicants are encouraged to propose sequencing of existing pediatric cancer or congenital anomaly cohorts to elucidate the genetic contribution (somatic and/or germline) to childhood cancers, to investigate the genetic etiology of congenital anomalies, to study the molecular basis of the associations between congenital anomalies and increased cancer risk, or to expand the range of pediatric disorders included within the Kids First Data Resource. The program will accept applications that propose whole genome, exome, and transcriptome sequencing, as well as clinical-grade sequencing, long-read sequencing, proteomics, and epigenomic assays of tumor or affected tissue, when justified. Applicants are encouraged to propose cohorts to increase representation of existing Kids First Program projects. These data, and associated clinical and phenotypic data, will become part of the Kids First Data Resource Center for sharing with the research community.
Refer to Section III. Eligibility Information in the NOFO for additional information on eligibility.Foreign Organizations/Foreign CollaborationsNon-domestic (non-U.S.) Entities (Foreign Organizations) are not eligible to apply.Non-domestic (non-U.S.) components of U.S. Organizations are not eligible to apply.Foreign components, as defined in the NIH Grants Policy Statement, are not allowed.
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