Difference between revisions of "Workshops"
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Image:Kaspar_Podgorski.jpg|Kaspar Podgorski, Janelia Research Campus | Image:Kaspar_Podgorski.jpg|Kaspar Podgorski, Janelia Research Campus | ||
Image:Nico_Pegard.jpg|Nico Pegard, UNC Chapel Hill | Image:Nico_Pegard.jpg|Nico Pegard, UNC Chapel Hill | ||
| − | + | Image:Sutter.png|Rick Ayer, Sutter Instrument | |
Image:Emily_Gibson.jpg|Emily Gibson, UC Denver | Image:Emily_Gibson.jpg|Emily Gibson, UC Denver | ||
Image:Andrea.png|Andrea Giovannucci, UNC Chapel Hill | Image:Andrea.png|Andrea Giovannucci, UNC Chapel Hill | ||
Image:Simon.jpg|Simon Schultz, Imperial college London | Image:Simon.jpg|Simon Schultz, Imperial college London | ||
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== 2019 Speakers == | == 2019 Speakers == | ||
Revision as of 14:24, 18 March 2020
The Nemonic project holds a yearly workshops at UC Santa Barbara to help train personnel from other institutions on how to create and use novel multiphoton neuroimaging instrumentation developed by the Nemonic consortium.
Contents
2020 Information
Kaspar Podgorski, Janelia Research Campus
Nico Pegard, UNC Chapel Hill
Rick Ayer, Sutter Instrument
Emily Gibson, UC Denver
Andrea Giovannucci, UNC Chapel Hill
Simon Schultz, Imperial college London
2019 Speakers
Kaspar Podgorski, Janelia Research Campus
Nico Pegard, UNC Chapel Hill
Darcy Peterka, Columbia
Emily Gibson, UC Denver
Andrea Giovannucci, UNC Chapel Hill
Simon Schultz, Imperial college London
2019 Workshop Slideshows
Fast and scalable calcium imaging data analysis with CaImAn - Andrea Giovannucci
Robotically automated, two-photon targeted patch clamp physiology - Simon Schultz
High Speed Two-Photon Tomography - Kaspar Podgorski
Extending multiphoton microscopy to 3D brain imaging in freely moving mice - Emily Gibson
Darcy Peterka's 2019 Nemonic workshop talk - Darcy Peterka
2019 Related Papers and Files
CaImAn: an open source tool for scalable calcium imaging data analysis[1]
Robotic Automation of In Vivo Two-Photon Targeted Whole-Cell Patch-Clamp Electrophysiology[2]
Progress in automating patch clamp cellular physiology[3]
ABLE: An Activity-Based Level Set Segmentation Algorithm for Two-Photon Calcium Imaging Data[4]
High speed functional imaging with source localized multifocal two-photon microscopy[5]
Building a two-photon microscope is easy[6]
2019 Nemonic workshop schedule[7]
See Also
