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Unsupervised spike sorting for large scale, high density multielectrode arrays
by
Murino, Vittorio
, Hennig, Matthias H
, Maccione, Alessandro
, Francesca Cella Zanacchi
, Ullo, Simona
, Albert Puente Encinas
, Sona, Diego
, Bhalla, Upinder
, Jens-Oliver Muthmann
, Kepiro, Ibolya
, Martino Sorbaro
, Cesar Juarez Ramirez
, Berdondini, Luca
, Pirmoradian, Sahar
, Sernagor, Evelyne
, Hilgen, Gerrit
in
Neuroscience
/ Quality control
/ Retina
/ Retinal ganglion cells
2016
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Unsupervised spike sorting for large scale, high density multielectrode arrays
by
Murino, Vittorio
, Hennig, Matthias H
, Maccione, Alessandro
, Francesca Cella Zanacchi
, Ullo, Simona
, Albert Puente Encinas
, Sona, Diego
, Bhalla, Upinder
, Jens-Oliver Muthmann
, Kepiro, Ibolya
, Martino Sorbaro
, Cesar Juarez Ramirez
, Berdondini, Luca
, Pirmoradian, Sahar
, Sernagor, Evelyne
, Hilgen, Gerrit
in
Neuroscience
/ Quality control
/ Retina
/ Retinal ganglion cells
2016
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Do you wish to request the book?
Unsupervised spike sorting for large scale, high density multielectrode arrays
by
Murino, Vittorio
, Hennig, Matthias H
, Maccione, Alessandro
, Francesca Cella Zanacchi
, Ullo, Simona
, Albert Puente Encinas
, Sona, Diego
, Bhalla, Upinder
, Jens-Oliver Muthmann
, Kepiro, Ibolya
, Martino Sorbaro
, Cesar Juarez Ramirez
, Berdondini, Luca
, Pirmoradian, Sahar
, Sernagor, Evelyne
, Hilgen, Gerrit
in
Neuroscience
/ Quality control
/ Retina
/ Retinal ganglion cells
2016
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Unsupervised spike sorting for large scale, high density multielectrode arrays
Paper
Unsupervised spike sorting for large scale, high density multielectrode arrays
2016
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Overview
A new method for automated spike sorting for recordings with high density, large scale multielectrode arrays is presented. It is based on an efficient, low-dimensional representation of detected events by their estimated spatial current source locations and dominant spike shape features. Millions of events can be sorted in just minutes, and the full analysis chain scales roughly linearly with recording time. We demonstrate this method using recordings from the mouse retina with a 4,096 channel array, and present validation based on anatomical imaging and model-based quality control. Our analysis shows that it is feasible to reliably isolate the activity of hundreds to thousands of retinal ganglion cells in single recordings.
Publisher
Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
Subject
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