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U24NS146314

Cooperative Agreement

Overview

Grant Description
HUMAN BRAIN SINGLE-CELL GENOMICS EXPLORER - PROJECT SUMMARY / ABSTRACT THERE HAS BEEN AN EXPLOSION OF GENOMICS DATA IN NEUROSCIENCE THAT BRIDGES INSIGHTS FROM SINGLE-CELL GENOMIC DATA TO BRAIN FUNCTION AND DISEASES. DATA ON HUNDREDS OF MILLIONS OF CELLS ARE BEING GENERATED BY CONSORTIA SUCH AS BICAN/BICCN, PYSCHENCODE, SEA-AD, SCORCH, AND SSPSYGENE. AS MANY DIFFERENT CELL TAXONOMIES ARE BEING GENERATED, THE NEUROSCIENCE FIELD NEEDS A SINGLE-CELL BRAIN RESOURCE FOR RESEARCHERS TO EXPLORE AND USE AS A REFERENCE MODEL FOR THEIR DATASETS. A HUGE SEMI-MANUAL EFFORT WOULD BE NOT ONLY NEARLY IMPOSSIBLE GIVEN THE DATA SIZE, BUT ALSO WOULD QUICKLY BECOME OBSOLETE. ONLY AUTOMATED EFFORTS WILL BE ABLE TO ADDRESS THE NEED FOR A DURABLE, FLEXIBLE, AND NIMBLE NEUROSCIENCE CELL REFERENCE. WE PROPOSE TO USE CUTTING-EDGE AI TECHNIQUES TO BUILD A UNIVERSAL CELL EMBEDDING FOR BRAIN (UCE-BRAIN), A FOUNDATIONAL BRAIN CELL TAXONOMY MODEL ACROSS HUNDREDS OF MILLIONS OF CELLS. WE WILL DEVELOP THE UCSC HUMAN BRAIN SINGLE-CELL GENOMICS EXPLORER TO ENABLE USERS TO ACCESS AND INTERACTIVELY EXPLORE THE UCE-BRAIN, THE REFERENCE CELL TAXONOMY, AS WELL AS MAP NEW DATA INTO THE REFERENCE. THE DATA EXPLORER WILL BE CAPABLE OF INTERACTIVE DATA VISUALIZATION OF THE HUNDREDS OF MILLIONS OF CELLS IN A 2D EMBEDDING SPACE; THE CELL CURATOR WILL EXPLORE THE BICAN TAXONOMY ANNOTATIONS AS WELL AS GATHERING COMMUNITY-DRIVEN CELL TYPES; THE CELL MAPPER WILL OFFER TWO METHODS TO MAP NEW DATA TO THE REFERENCE MODELS AND VISUALIZE THE RESULTS; AND TOOLS AND DOCUMENTATION. WE WILL INCORPORATE A LARGE LANGUAGE MODEL (LLM) INTO THE CELL CURATOR AND CELL MAPPER TO PARSE USERS’ REQUESTS, PROVIDE A NATURAL LANGUAGE SUMMARY OF THE RESULTS IN A CHATBOT-STYLE INTERACTION, AND INTEGRATE USER FEEDBACK. OUR TEAM’S DIVERSE EXPERTISE AND STRONG HISTORY OF SUCCESSFUL COLLABORATION WILL ENSURE THE SUCCESS OF THE PROJECT. AIM 1. CONSTRUCT FOUNDATION MODELS FOR HUMAN BRAIN CELLS WE WILL DEVELOP UCE-BRAIN, A BRAIN-SPECIFIC FOUNDATION MODEL THAT WILL CREATE HIGH QUALITY UNIVERSAL REPRESENTATIONS OF BRAIN SINGLE CELL DATA. WE WILL BUILD UCE-BRAIN CLUSTERS THAT ARE MOST CONSISTENT WITH BICAN TAXONOMY IN GOLD-STANDARD PUBLICATIONS, WHILE STILL ALLOWING THE CLUSTERS TO EVOLVE IN RESPONSE TO NEW DATASETS. AIM 2. MAPPING NEW DATA INTO THE REFERENCE CELL TYPE TAXONOMY. WE WILL OFFER TWO METHODS FOR USERS TO MAP AND ANNOTATE THEIR DATA. ONE METHOD WILL ALLOW USERS TO UPLOAD THEIR DATA TO A SERVER TO MAP TO UCE-BRAIN. A SECOND METHOD WILL ALLOW USERS WITH SENSITIVE DATA TO MAP TO A STRIPPED-DOWN MODEL ON THEIR LAPTOPS. AIM 3. DEVELOP THE CELL CURATOR TO PROMOTE COMMUNITY ANNOTATION OF THE REFERENCE CELL TYPE TAXONOMY. THE CELL CURATOR TOOL WILL ENABLE USERS TO INSPECT AND CURATE THE REFERENCE CELL CLUSTERS. WE WILL CONDUCT EFFORTS TO FOSTER THE NEUROSCIENCE RESEARCH COMMUNITY’S CONTRIBUTIONS. AIM 4. DEVELOP THE UCSC BRAIN EXPLORER WEBSITE AND HARMONIZE SINGLE-CELL SEQUENCING DATA. THE UCSC BRAIN EXPLORER WEBSITE SERVES AS THE GATEWAY TO ALL FUNCTIONALITY AND RESOURCES DEVELOPED IN THIS APPLICATION. DATA HARMONIZATION WILL OCCUR ON TERRA, WHERE WE WILL PROCESS DATASETS USING THE BICAN/BICCN PIPELINES. WE WILL INTEGRATE GOOGLE ANALYTICS TO TRACK AGGREGATED USER INTERACTIONS.
Funding Goals
(1) TO SUPPORT EXTRAMURAL RESEARCH FUNDED BY THE NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE (NINDS) INCLUDING: BASIC RESEARCH THAT EXPLORES THE FUNDAMENTAL STRUCTURE AND FUNCTION OF THE BRAIN AND THE NERVOUS SYSTEM, RESEARCH TO UNDERSTAND THE CAUSES AND ORIGINS OF PATHOLOGICAL CONDITIONS OF THE NERVOUS SYSTEM WITH THE GOAL OF PREVENTING THESE DISORDERS, RESEARCH ON THE NATURAL COURSE OF NEUROLOGICAL DISORDERS, IMPROVED METHODS OF DISEASE PREVENTION, NEW METHODS OF DIAGNOSIS AND TREATMENT, DRUG DEVELOPMENT, DEVELOPMENT OF NEURAL DEVICES, CLINICAL TRIALS, AND RESEARCH TRAINING IN BASIC, TRANSLATIONAL AND CLINICAL NEUROSCIENCE. THE INSTITUTE IS THE LARGEST FUNDER OF BASIC NEUROSCIENCE IN THE US AND SUPPORTS RESEARCH ON TOPICS INCLUDING BUT NOT LIMITED TO: DEVELOPMENT OF THE NERVOUS SYSTEM, INCLUDING NEUROGENESIS AND PROGENITOR CELL BIOLOGY, SIGNAL TRANSDUCTION IN DEVELOPMENT AND PLASTICITY, AND PROGRAMMED CELL DEATH, SYNAPSE FORMATION, FUNCTION, AND PLASTICITY, LEARNING AND MEMORY, CHANNELS, TRANSPORTERS, AND PUMPS, CIRCUIT FORMATION AND MODULATION, BEHAVIORAL AND COGNITIVE NEUROSCIENCE, SENSORIMOTOR LEARNING, INTEGRATION AND EXECUTIVE FUNCTION, NEUROENDOCRINE SYSTEMS, SLEEP AND CIRCADIAN RHYTHMS, AND SENSORY AND MOTOR SYSTEMS. IN ADDITION, THE INSTITUTE SUPPORTS BASIC, TRANSLATIONAL AND CLINICAL STUDIES ON A NUMBER OF DISORDERS OF THE NERVOUS SYSTEM INCLUDING (BUT NOT LIMITED TO): STROKE, TRAUMATIC INJURY TO THE BRAIN, SPINAL CORD AND PERIPHERAL NERVOUS SYSTEM, NEURODEGENERATIVE DISORDERS, MOVEMENT DISORDERS, BRAIN TUMORS, CONVULSIVE DISORDERS, INFECTIOUS DISORDERS OF THE BRAIN AND NERVOUS SYSTEM, IMMUNE DISORDERS OF THE BRAIN AND NERVOUS SYSTEM, INCLUDING MULTIPLE SCLEROSIS, DISORDERS RELATED TO SLEEP, AND PAIN. PROGRAMMATIC AREAS, WHICH ARE PRIMARILY SUPPORTED BY THE DIVISION OF NEUROSCIENCE, ARE ALSO SUPPORTED BY THE DIVISION OF EXTRAMURAL ACTIVITIES, THE DIVISION OF TRANSLATIONAL RESEARCH, THE DIVISION OF CLINICAL RESEARCH, THE OFFICE OF TRAINING AND WORKFORCE DEVELOPMENT, THE OFFICE OF PROGRAMS TO ENHANCE NEUROSCIENCE WORKFORCE DEVELOPMENT, AND THE OFFICE OF INTERNATIONAL ACTIVITIES. (2) TO EXPAND AND IMPROVE THE SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. TO UTILIZE THE SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM, TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Place of Performance
Santa Cruz, California 950641077 United States
Geographic Scope
Single Zip Code
Analysis Notes
Amendment Since initial award the total obligations have increased 99% from $1,866,838 to $3,712,398.
Santa Cruz University Of California was awarded Universal Brain Cell Taxonomy Explorer - AI-Powered Neuroscience Resource Cooperative Agreement U24NS146314 worth $3,712,398 from National Eye Institute in September 2025 with work to be completed primarily in Santa Cruz California United States. The grant has a duration of 3 years and was awarded through assistance program 93.867 Vision Research. The Cooperative Agreement was awarded through grant opportunity Human Brain Single-cell Genomics Explorer (U24 - Clinical Trial Not Allowed).

Status
(Ongoing)

Last Modified 8/20/25

Period of Performance
9/1/25
Start Date
8/31/28
End Date
0% Complete

Funding Split
$3.7M
Federal Obligation
$0.0
Non-Federal Obligation
$3.7M
Total Obligated
100.0% Federal Funding
0.0% Non-Federal Funding

Activity Timeline

Interactive chart of timeline of amendments to U24NS146314

Transaction History

Modifications to U24NS146314

Additional Detail

Award ID FAIN
U24NS146314
SAI Number
U24NS146314-868553611
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NQ00 NIH National Institute of Neurological Disorders and Stroke
Funding Office
75NW00 NIH National Eye Institute
Awardee UEI
VXUFPE4MCZH5
Awardee CAGE
1CV82
Performance District
CA-19
Senators
Dianne Feinstein
Alejandro Padilla
Modified: 8/20/25