dc.contributor.author | Prevedel, Robert | |
dc.contributor.author | Yoon, Young-Gyu | |
dc.contributor.author | Hoffman, Maximilian | |
dc.contributor.author | Pak, Nikita | |
dc.contributor.author | Wetzstein, Gordon | |
dc.contributor.author | Kato, Saul | |
dc.contributor.author | Schrödel, Tina | |
dc.contributor.author | Raskar, Ramesh | |
dc.contributor.author | Zimmer, Manuel | |
dc.contributor.author | Boyden, Edward S. | |
dc.contributor.author | Vaziri, Alipasha | |
dc.date.accessioned | 2015-12-10T23:10:39Z | |
dc.date.available | 2015-12-10T23:10:39Z | |
dc.date.issued | 2014-05-18 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/100180 | |
dc.description | Notes: 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.abstract | High-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.iso | en_US | en_US |
dc.publisher | Center for Brains, Minds and Machines (CBMM) | en_US |
dc.relation.ispartofseries | CBMM Memo Series;016 | |
dc.rights | Attribution-NonCommercial 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/us/ | * |
dc.subject | Microscopy | en_US |
dc.subject | Neuroscience | en_US |
dc.title | Simultaneous whole‐animal 3D imaging of neuronal activity using light‐field microscopy | en_US |
dc.type | Technical Report | en_US |
dc.type | Working Paper | en_US |
dc.type | Other | en_US |