CLARITY: fully-assembled biology
CLARITY: fully-assembled biology
批准号:
8727226
负责人:
Karl A. Deisseroth
金额:
$76.33万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-18 至 2017-08-31
关键词:
AchievementAddressAntibodiesBehaviorBiologicalBiologyBrainCellsChemical EngineeringCommunitiesDataData SetDatabasesDestinationsDevelopmentDisadvantagedDiseaseEducation and OutreachEducational process of instructingElectroencephalographyEnsureEventFoundationsFrightFunctional Magnetic Resonance ImagingGeneticGoalsHealthHumanHydrogelsImmunophenotypingInformation SystemsLeadLinkMammalsMapsMental disordersMethodologyMethodsMiningMissionModelingMolecularMolecular GeneticsMusNeocortexNeurobiologyNeuronsNeurosciencesOpticsOrganPatternPharmacologic SubstancePopulationPrimatesProcessPsychiatryRecording of previous eventsRecordsResearchResearch InfrastructureResolutionResourcesRewardsRodentSourceSpeedSystemTechnologyTissuesUrsidae FamilyVertebratesWithdrawalWorkZebrafishblindcomputer infrastructuredesigndisabilityexperienceimaging modalityinsightinstrumentationmacromoleculemillisecondmolecular phenotypeneural circuitnew technologynovel strategiesprogramsreconstructiontechnology developmenttool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Studying intact systems with both local precision and global scope is a fundamental unmet goal in biology. For example, in the study of the brain, efforts to determine connectivity of small patches of brain, though pioneering, are challenged by the fact that resulting maps will be nearly impossible to interpret because both the brainwide sources and destinations of traced wiring connections, as well as the activity of corresponding cells during behaviorally significant events, will remain unknown. Conversely molecular, electrophysiological, or imaging methods to record population activity are agnostic with regard to brain-wide wiring patterns of recorded cells, creating an enormous gap in understanding of function. We have now laid foundations for addressing this challenge, by integrating chemical engineering, computational optics, and molecular genetics in an approach termed CLARITY. We will develop the approach in the behaving vertebrate CNS, challenging for speed and complexity, but CLARITY will become applicable across biology as we develop platforms for zebrafish, rodents, and primates. In Aim 1, we bring chemical engineering tools to bear, rapidly transforming scattering and impermeable tissues into intact but transparent and macromolecule-permeable (antibody-compatible) form. In Aim 2, we develop activity-readout technology designed to extract volumetric activity (even in freely-moving mammals) that can then be linked to the global wiring and molecular phenotypes. This transformative technology will allow rapid extraction of systems information (dynamics, history, wiring, and molecular phenotypes) from large and intact biological tissues or organs without disassembly, down to millisecond-scale and cellular resolution. In Aim 3, we directly apply CLARITY to behaving mice and zebrafish, rapidly obtaining brain-wide activity patterns of every cell involved in disease-relevant states of fear an reward. This alone will be a milestone achievement in biology, but furthermore these data will also be linked to full molecular and global wiring information of those cells in the same brains, al publicly accessible for mining/searching. Finally in Aim 4 we design and build online datasets for zebrafish, mouse, and primate to broadly serve the community. Computational infrastructure will address handling and public access to the massive amount of data collected (among the largest datasets in all of biology), including the records of activity in every neuron in vertebrate brains
during specific experiences linked to molecular and global wiring information. We are experienced with technology outreach and education, and will leverage this experience to achieve the full transformative mission of this new technology.
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会议论文
An optical-genetic toolbox for monitoring and controlling diverse neuromodulatory circuits governing complex behaviors in primates
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批准号:10650669
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项目类别:
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资助金额:$134.24万
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财政年份:2023
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负责人:Karl A. Deisseroth
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依托单位:
Interaction of external inputs with internal dynamics: influence of brain states on neural computation and behavior
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批准号:10698364
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项目类别:
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资助金额:$6.0万
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财政年份:2021
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依托单位:
Interaction of external inputs with internal dynamics: influence of brain states on neural computation and behavior
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批准号:10047726
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项目类别:
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资助金额:$337.89万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Administrative Core
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批准号:10047727
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项目类别:
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资助金额:$23.65万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Research Project 1 - Developing and applying tools to probe internal state dynamics of perception and motivation
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批准号:10490239
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项目类别:
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资助金额:$113.22万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Administrative Core
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批准号:10490234
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项目类别:
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资助金额:$40.1万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Administrative Core
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批准号:10687135
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项目类别:
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资助金额:$24.84万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Research Project 1 - Developing and applying tools to probe internal state dynamics of perception and motivation
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批准号:10687144
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项目类别:
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资助金额:$83.03万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Interaction of external inputs with internal dynamics: influence of brain states on neural computation and behavior
-
批准号:10687134
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项目类别:
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资助金额:$382.03万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Research Project 1 - Developing and applying tools to probe internal state dynamics of perception and motivation
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批准号:10047732
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项目类别:
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资助金额:$43.51万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Interaction of external inputs with internal dynamics: influence of brain states on neural computation and behavior
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批准号:10490233
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项目类别:
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资助金额:$391.61万
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财政年份:2021
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负责人:Karl A. Deisseroth
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依托单位:
Channel Structure-Based Tools for Precise Interrogation of Circuitry and Behavior
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批准号:9901798
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项目类别:
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资助金额:$13.86万
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财政年份:2019
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负责人:Karl A. Deisseroth
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依托单位:
Structural and molecular identification of circuitry underlying joint processing of motivation and aversion
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批准号:10408098
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项目类别:
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资助金额:$63.32万
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财政年份:2018
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负责人:Karl A. Deisseroth
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依托单位:
Channel structure-based tools for precise interrogation of circuitry and behavior
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批准号:10319554
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项目类别:
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资助金额:$80.22万
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财政年份:2018
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负责人:Karl A. Deisseroth
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依托单位:
Channel structure-based tools for precise interrogation of circuitry and behavior
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批准号:9509649
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项目类别:
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资助金额:$78.86万
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财政年份:2018
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负责人:Karl A. Deisseroth
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依托单位:
Single-cell causality in origination, propagation, and resolution of drug-altered brain states
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批准号:10494005
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项目类别:
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资助金额:$30.05万
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财政年份:2017
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负责人:Karl A. Deisseroth
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依托单位:
Neural circuit dynamics of drug action
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批准号:9358977
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项目类别:
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资助金额:$295.15万
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财政年份:2017
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负责人:Karl A. Deisseroth
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依托单位:
Neural circuit dynamics of drug action:revealing, uncoupling, and restoring altered brain states
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批准号:10494001
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项目类别:
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资助金额:$232.78万
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财政年份:2017
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负责人:Karl A. Deisseroth
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依托单位:
Administrative Core
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批准号:10494002
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项目类别:
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资助金额:$13.0万
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财政年份:2017
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负责人:Karl A. Deisseroth
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依托单位:
Project 1
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批准号:9358981
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项目类别:
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资助金额:$29.95万
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财政年份:2017
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负责人:Karl A. Deisseroth
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依托单位:
海外基金