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dc.contributor.authorPrevedel, Robert
dc.contributor.authorYoon, Young-Gyu
dc.contributor.authorHoffman, Maximilian
dc.contributor.authorPak, Nikita
dc.contributor.authorWetzstein, Gordon
dc.contributor.authorKato, Saul
dc.contributor.authorSchrödel, Tina
dc.contributor.authorRaskar, Ramesh
dc.contributor.authorZimmer, Manuel
dc.contributor.authorBoyden, Edward S.
dc.contributor.authorVaziri, Alipasha
dc.date.accessioned2015-12-10T23:10:39Z
dc.date.available2015-12-10T23:10:39Z
dc.date.issued2014-05-18
dc.identifier.urihttp://hdl.handle.net/1721.1/100180
dc.descriptionNotes: Robert Prevedel*, Young‐Gyu Yoon*, Maximilian Hoffmann, Nikita Pak, Gordon Wetzstein, Saul Kato, Tina Schrödel, Ramesh Raskar, Manuel Zimmer, Edward S Boyden** & Alipasha Vaziri** (* equal contributions, ** co-corresponding authors)en_US
dc.description.abstractHigh-speed, large-scale three-dimensional (3D) imaging of neuronal activity poses a major challenge in neuroscience. Here we demonstrate simultaneous functional imaging of neuronal activity at single-neuron resolution in an entire Caenorhabditis elegans and in larval zebrafish brain. Our technique captures the dynamics of spiking neurons in volumes of ~700 μm × 700 μm × 200 μm at 20 Hz. Its simplicity makes it an attractive tool for high-speed volumetric calcium imaging.en_US
dc.language.isoen_USen_US
dc.publisherCenter for Brains, Minds and Machines (CBMM)en_US
dc.relation.ispartofseriesCBMM Memo Series;016
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subjectMicroscopyen_US
dc.subjectNeuroscienceen_US
dc.titleSimultaneous whole‐animal 3D imaging of neuronal activity using light‐field microscopyen_US
dc.typeTechnical Reporten_US
dc.typeWorking Paperen_US
dc.typeOtheren_US


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