Early-stage Biomedical Data Repositories and Knowledgebases (R24 Clinical Trial Not Allowed)
This funding opportunity supports the creation and enhancement of early-stage biomedical data repositories and knowledgebases that serve the research community by ensuring data is easily findable, accessible, interoperable, and reusable.
Description
The NIH is offering funding through the "Early-stage Biomedical Data Repositories and Knowledgebases (R24 - Clinical Trial Not Allowed)" program, which aims to support the development of new or early-stage data repositories and knowledgebases valuable to the biomedical research community. The initiative focuses on pilot activities that demonstrate the need and impact of these resources, including transitioning existing investigator-initiated efforts into standardized, governed repositories or knowledgebases.
Data repositories are intended to store, manage, and distribute biomedical data following FAIR principles (Findable, Accessible, Interoperable, Reusable), while knowledgebases organize and annotate data, often pulling from multiple repositories. This program seeks to fund projects that meet the needs of specific scientific communities, provide high-quality data management, and engage with users for long-term sustainability and relevance.
Eligible applicants include higher education institutions, nonprofits, and for-profit organizations, both domestic and foreign. Budgets may not exceed $350,000 in direct costs annually, with a maximum project period of four years. Applications are due by January 25, 2024, with subsequent submission dates extending through January 2026. Applicants are encouraged to consult with NIH staff early to ensure alignment with program goals.