NIH Blueprint Initiative: Tools for Germline Gene Editing in the Nervous System
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The NIH Blueprint Initiative aims to support and enhance the development and application of germline and somatic transgenic and gene-editing technologies in experimental models that replicate key aspects of human brain anatomy, circuitry, cognition, behavior, and lifespan. Building upon existing marmoset gene-editing infrastructure, this effort seeks to integrate New Approach Methodologies (NAMs) alongside other models to deepen the understanding of human brain function and neurological diseases. A particular focus is placed on developing and validating human-derived NAMs that allow cross-species developmental comparisons, which are crucial for studying complex neurodevelopmental and behavioral disorders such as autism spectrum disorders and schizophrenia that current models struggle to fully capture. The initiative emphasizes the importance of selecting and justifying appropriate experimental models, especially when addressing neuroanatomical and functional questions related to brain disease and cognition. It aims to accelerate research advances by prioritizing investment in human-derived NAMs for conditions that remain inadequately modeled. The contract is managed under the authority of the Department of Health and Human Services through the National Institutes of Health and specifically targets projects that contribute to tools for germline gene editing within the nervous system. Interested parties can seek further information or contact the program directly via the provided email for collaboration or grant opportunities.
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The NIH Blueprint (a consortium of NIH Institutes that support neuroscience research) seeks to advance its mission by supporting the development, optimization, validation, and application of germline and somatic transgenic and gene-editing approaches in experimental systems modeling key features of human brain anatomy, circuitry, cognition, behavior, and lifespan. This initiative will build on the previously supported marmoset gene-editing infrastructure, by integrating New Approach Methodologies (NAMs) with other models, to advance understanding of human brain function and disease, including human-derived NAMs for cross-species comparisons across development. Many mechanisms of complex conditions, such as autism spectrum disorders, schizophrenia, and other behavioral/developmental disorders, cannot yet be captured in NAMs and are therefore high priorities for research investment to accelerate development and validation of human-derived NAMs. Appropriate models should be used and clearly justified as necessary for questions involving neuroanatomy, circuit function, cognition, behavior, or lifespan phenotyping related to human brain disease and function. Grant authorities are as follows: 42 U.S.C 241 and 284.
