Somatic Mosaicism across Human Tissues (SMaHT) Program: National Somatic Mosaicism Commons Data Analysis & Organizational Center (UM1 Clinical Trial Not Allowed)
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The National Institutes of Health is seeking support for Stage 2 of the Somatic Mosaicism across Human Tissues (SMaHT) Network through the establishment of the National Somatic Mosaicism Commons Data Analysis and Organizational Center. This initiative aims to advance the understanding of biological processes and disease mechanisms by leveraging multi-omic somatic mutation datasets from human tissues across all three germ layers. The Center will serve as a central hub for network governance, coordination, and the development of tools and platforms designed for both network members and the broader clinical and research communities. Key responsibilities of the Center include managing network data and creating essential resources such as the SMaHT data portal, a Variant Catalog, a variant browser, and various visualization tools. Additionally, the Center will provide analysis-ready data releases and lead outreach and training efforts to ensure the research community can effectively utilize these complex datasets. This forecasted opportunity is managed by the Department of Health and Human Services and specifically prohibits clinical trials.
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The purpose of the Somatic Mosaicism across Human Tissues (SMaHT) Network is to advance the discovery of biological processes and disease mechanisms mediated by somatic mutations in human tissues. Since 2023, the program has generated multi-omic somatic mutation datasets from a standardized set of human tissues spanning all three germ layers. Building on the Stage 1 foundation, the NIH intends to issue a Notice of Funding Opportunity (NOFO) seeking support for Stage 2 through the National Somatic Mosaicism Commons Data Analysis & Organizational Center. The National Somatic Mosaicism Commons Data Analysis & Organizational Center combines data management and analysis with network governance, coordination, outreach, and training. The Center will develop tools and platforms that allow SMaHT Network members and the wider clinical and research communities to investigate and use these complex datasets.
The center will be responsible for managing network data and providing access to data analysis tools developed in the program. This will include building the SMaHT data portal, Variant Catalog, variant browser, visualization tools, and analysis-ready releases. The center will also conduct outreach to clinical and research communities and provide training in SMaHT resources.
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