Difference between revisions of "Workshops"
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This workshop is planned take place from 8am – 12 pm Pacific time, February 22nd-24th, 2021. An exact schedule will be released once our speaker line-up is set. | This workshop is planned take place from 8am – 12 pm Pacific time, February 22nd-24th, 2021. An exact schedule will be released once our speaker line-up is set. | ||
− | '''Application: [[File:Nemonic_Workshop_Feb22-24_2021. | + | '''Application: [[File:Nemonic_Workshop_Feb22-24_2021.pdf]]''' |
== 2020 Speakers == | == 2020 Speakers == |
Revision as of 11:58, 21 December 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
2021 Application
This workshop is planned take place from 8am – 12 pm Pacific time, February 22nd-24th, 2021. An exact schedule will be released once our speaker line-up is set.
Application: File:Nemonic Workshop Feb22-24 2021.pdf
2020 Speakers
2020 Videos
2020 Workshop Slideshows
Open Platforms for Two- and Three-Photon Microscopy - Rick Ayer
Fast and scalable brain imaging data at single-cell resolution - Andrea Giovannucci
3D-SHOT with Computer Generated Holography at high speed and with high performance - Nicolas Pegard
Advances in two-dimensional spatial frequency modulation imaging - Jeff Squier
2020 Related Resources
https://www.youtube.com/watch?v=DLTaqzz8hJM&feature=youtu.be
2019 Speakers
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 Resources
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]
See Also