Opportunity Information: Apply for RFA MH 19 148
This opportunity, titled "BRAIN Initiative Cell Census Network (BICCN) Scalable Technologies and Tools for Brain Cell Census (R01 Clinical Trial Not Allowed)" (Funding Opportunity Number RFA-MH-19-148), is a National Institutes of Health (NIH) discretionary grant program that supports research aimed at speeding up and strengthening the technologies and tools used to identify, classify, and map brain cell types and the circuits they form. The central goal is to push brain cell census work beyond current constraints by encouraging platforms, workflows, and resources that can operate at scale, so researchers can conduct faster and more comprehensive surveys of brain cellular diversity across space and time. Because it is an R01 mechanism, projects are expected to be substantial, well-justified, and capable of delivering impactful advances or resources for the broader neuroscience community. Clinical trials are explicitly not allowed under this announcement.
A major emphasis of the announcement is removing bottlenecks in the existing brain cell census pipeline. In practical terms, NIH is looking for improvements that make it easier to generate high-quality cell census datasets, whether the bottleneck is tissue handling, molecular profiling throughput, spatial mapping, anatomical registration, circuit tracing, data processing, or another limiting step that slows progress or reduces data quality. Proposals are expected to focus on scalable approaches, meaning the methods should be suited to large studies rather than one-off demonstrations, and should be engineered with robustness and reproducibility in mind so they can be adopted widely and not just used in a single lab.
Another strong priority is tighter integration of experimental and computational components. The FOA encourages projects that combine lab-based methods (for example, sampling strategies, tissue processing, labeling, imaging, sequencing, or electrophysiology workflows) with computational approaches (such as pipelines for data processing, cell-type classification, multimodal integration, spatial registration, and visualization). The intent is to reduce barriers to hypothesis-driven research by making cell census generation and analysis more accessible, more standardized, and more directly usable by neuroscientists who want to ask biological questions rather than spend years building infrastructure.
The announcement also signals that technology development alone is not the end point; applicants are expected to demonstrate real utility. To do that, projects should generate a substantial amount of spatiotemporal cell census data and/or community resources using the improved platforms. "Spatiotemporal" reflects the interest in not only what cell types exist, but where they are located in brain structures, how they connect in circuits, and how these features may vary across developmental stages, brain regions, or other relevant dimensions. The data and resources produced are meant to help validate the approach at meaningful scale and to accelerate downstream science by others.
In addition, the FOA explicitly calls for comparative and benchmarking studies. NIH is seeking efforts that use appropriate criteria to evaluate and compare biospecimen quality, tool or technology performance, and the effectiveness of computational approaches. This suggests an expectation for rigorous metrics, reference standards where feasible, and clear evaluation frameworks so the field can identify which methods work best for specific use cases. Benchmarking can include head-to-head comparisons, cross-site reproducibility checks, or systematic assessments of sensitivity, accuracy, throughput, cost, and failure modes, provided the criteria are well-justified and informative for the broader community.
All funded projects are expected to align with the broader goals of the BRAIN Initiative Cell Census Network (BICCN). That alignment includes generating substantial cell census data either directly through the proposed work or through collaboration with BICCN efforts, and contributing in ways that improve the overall ecosystem of tools, data, and standards that the network depends on. In other words, this is not just about producing a single dataset or a single tool, but about strengthening the overall capacity of the field to map and understand brain cell types and circuits in a systematic, scalable way.
From an administrative standpoint, the program is issued by NIH as a grant (Funding Instrument: Grant) within activity areas that span education, health, and social services-related categories in federal classification systems, and it lists multiple CFDA numbers associated with NIH programs (93.173, 93.213, 93.242, 93.273, 93.279, 93.286, 93.853, 93.865, 93.866, 93.867). The original closing date shown in the source data is 2020-01-24, and the FOA record creation date is 2018-09-21. The award ceiling and expected number of awards are not specified in the provided text, which typically means applicants should rely on the full FOA details and NIH budget guidance for expectations about scale and scope.
Eligibility is broad and includes many types of domestic U.S. applicants such as state, county, and local governments; special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments; public housing authorities/Indian housing authorities; tribal organizations that are not federally recognized governments; nonprofit organizations with or without 501(c)(3) status (outside higher education); for-profit organizations other than small businesses; and small businesses. The announcement also explicitly calls out additional eligible applicant categories including Alaska Native and Native Hawaiian Serving Institutions, Asian American Native American Pacific Islander Serving Institutions (AANAPISIs), Hispanic-serving Institutions, Historically Black Colleges and Universities (HBCUs), Tribally Controlled Colleges and Universities (TCCUs), faith-based or community-based organizations, eligible federal agencies, regional organizations, U.S. territories or possessions, and even non-domestic (non-U.S.) entities (foreign organizations), as well as Indian/Native American tribal governments other than federally recognized ones.
Taken together, the opportunity is aimed at accelerating brain cell census progress by funding scalable, high-impact technology and resource development that is validated through real data production, strengthened through tight experimental-computational integration, and made credible through careful benchmarking. The end product NIH is trying to drive is a faster, more standardized, and more powerful set of platforms and datasets that help the BICCN and the broader neuroscience community more completely define brain cell types and the circuits they form.Apply for RFA MH 19 148
- The National Institutes of Health in the education, health, income security and social services sector is offering a public funding opportunity titled "BRAIN Initiative Cell Census Network (BICCN) Scalable Technologies and Tools for Brain Cell Census (R01 Clinical Trial Not Allowed)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 93.173, 93.213, 93.242, 93.273, 93.279, 93.286, 93.853, 93.865, 93.866, 93.867.
- This funding opportunity was created on 2018-09-21.
- Applicants must submit their applications by 2020-01-24. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Eligible applicants include: State governments, County governments, City or township governments, Special district governments, Independent school districts, Public and State controlled institutions of higher education, Native American tribal governments (Federally recognized), Public housing authorities/Indian housing authorities, Native American tribal organizations (other than Federally recognized tribal governments), Nonprofits having a 501 (c) (3) status with the IRS, other than institutions of higher education, Nonprofits that do not have a 501 (c) (3) status with the IRS, other than institutions of higher education, Private institutions of higher education, For-profit organizations other than small businesses, Small businesses, Others.
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Frequently Asked Questions (FAQs)
What is the official title of this funding opportunity?
The opportunity is titled "BRAIN Initiative Cell Census Network (BICCN) Scalable Technologies and Tools for Brain Cell Census (R01 Clinical Trial Not Allowed)."
What is the Funding Opportunity Number (FOA number)?
The Funding Opportunity Number is RFA-MH-19-148.
Which federal agency is offering this grant?
This is a National Institutes of Health (NIH) discretionary grant program.
What type of funding instrument is being used?
The funding instrument is a grant.
What activity mechanism does this opportunity use?
This opportunity uses the NIH R01 mechanism, which typically supports substantial, well-justified projects expected to deliver impactful advances or widely usable resources.
Are clinical trials allowed under this FOA?
No. Clinical trials are explicitly not allowed under this announcement.
What is the overall purpose of this opportunity?
The purpose is to speed up and strengthen technologies and tools used to identify, classify, and map brain cell types and the circuits they form, with an emphasis on approaches that can operate at scale.
What does "brain cell census" mean in the context of this FOA?
In this context, brain cell census work refers to identifying, classifying, and mapping brain cell types, including where they are located and how they participate in circuits, using scalable experimental and computational methods.
What does NIH mean by "scalable" approaches here?
"Scalable" means platforms, workflows, and resources that are suited to large studies rather than one-off demonstrations, and that are engineered for robustness and reproducibility so they can be broadly adopted beyond a single lab.
What kinds of bottlenecks is NIH trying to remove?
The FOA emphasizes removing bottlenecks anywhere in the brain cell census pipeline, including (but not limited to) tissue handling, molecular profiling throughput, spatial mapping, anatomical registration, circuit tracing, and data processing, as well as other limiting steps that slow progress or reduce data quality.
Is this opportunity focused only on technology development?
No. The announcement signals that technology development alone is not the end point. Applicants are expected to demonstrate real utility by generating a substantial amount of spatiotemporal cell census data and/or community resources using the improved platforms.
What does "spatiotemporal" cell census data refer to?
"Spatiotemporal" reflects interest in what cell types exist, where they are located in brain structures, how they connect in circuits, and how these features may vary across developmental stages, brain regions, or other relevant dimensions.
Does the FOA encourage combining experimental and computational work?
Yes. A strong priority is tighter integration of experimental and computational components, such as combining lab-based methods with computational pipelines for processing, cell-type classification, multimodal integration, spatial registration, visualization, and related tasks.
What are examples of experimental components mentioned as relevant?
Examples include sampling strategies, tissue processing, labeling, imaging, sequencing, and electrophysiology workflows.
What are examples of computational components mentioned as relevant?
Examples include pipelines for data processing, cell-type classification, multimodal data integration, spatial registration, and visualization.
Why does the FOA emphasize experimental-computational integration?
The intent is to reduce barriers to hypothesis-driven research by making cell census generation and analysis more accessible, more standardized, and more directly usable by neuroscientists who want to ask biological questions rather than spend years building infrastructure.
Are benchmarking and comparative studies part of what NIH is looking for?
Yes. The FOA explicitly calls for comparative and benchmarking studies to evaluate biospecimen quality, tool or technology performance, and the effectiveness of computational approaches using appropriate, well-justified criteria.
What kinds of benchmarking criteria are suggested by the FOA?
The announcement points toward rigorous metrics and clear evaluation frameworks, potentially including sensitivity, accuracy, throughput, cost, failure modes, head-to-head comparisons, and cross-site reproducibility checks (where appropriate and well-justified).
How should projects relate to the BRAIN Initiative Cell Census Network (BICCN)?
All funded projects are expected to align with broader BICCN goals by generating substantial cell census data directly through the proposed work or through collaboration with BICCN efforts, and by strengthening the ecosystem of tools, data, and standards used by the network and community.
Is this opportunity aimed at producing a single dataset or a single tool?
No. The description emphasizes strengthening overall capacity for systematic, scalable mapping of brain cell types and circuits, rather than only producing a single dataset or one isolated tool.
Is the award ceiling provided in the information shown?
No. The award ceiling is not specified in the provided text.
Is the expected number of awards provided in the information shown?
No. The expected number of awards is not specified in the provided text.
What is the original closing date listed in the source information?
The original closing date shown is 2020-01-24.
What is the FOA record creation date listed in the source information?
The FOA record creation date shown is 2018-09-21.
What general federal activity areas are associated with this opportunity?
The program is described as spanning activity areas that include education, health, and social services-related categories in federal classification systems.
Which CFDA numbers are associated with this opportunity?
The opportunity lists multiple CFDA numbers: 93.173, 93.213, 93.242, 93.273, 93.279, 93.286, 93.853, 93.865, 93.866, and 93.867.
Who is eligible to apply?
Eligibility is broad and includes many types of applicants, including state, county, and local governments; special district governments; independent school districts; public and state-controlled institutions of higher education; private institutions of higher education; federally recognized Native American tribal governments; public housing authorities/Indian housing authorities; tribal organizations that are not federally recognized governments; nonprofit organizations with or without 501(c)(3) status (outside higher education); for-profit organizations other than small businesses; and small businesses.
Are minority-serving institutions and community-based organizations eligible?
Yes. The announcement explicitly includes Alaska Native and Native Hawaiian Serving Institutions, AANAPISIs, Hispanic-serving Institutions, HBCUs, TCCUs, and faith-based or community-based organizations among eligible categories.
Are federal agencies eligible to apply?
Yes. Eligible federal agencies are explicitly listed among eligible applicant categories.
Are U.S. territories or possessions eligible?
Yes. U.S. territories or possessions are explicitly listed as eligible.
Are foreign (non-U.S.) organizations eligible?
Yes. The eligibility list explicitly includes non-domestic (non-U.S.) entities (foreign organizations).
Does the FOA include tribal governments that are not federally recognized?
Yes. It explicitly includes Indian/Native American tribal governments other than federally recognized ones, and also mentions tribal organizations that are not federally recognized governments.
What is NIH ultimately trying to drive with this program?
The program aims to accelerate brain cell census progress by funding scalable, high-impact technology and resource development that is validated through meaningful data production, strengthened through experimental-computational integration, and made credible through careful benchmarking, resulting in more standardized and powerful platforms and datasets for defining brain cell types and circuits.
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