TY - JOUR
T1 - Unsupervised Spike Sorting for Large-Scale, High-Density Multielectrode Arrays
AU - Hilgen, Gerrit
AU - Sorbaro, Martino
AU - Pirmoradian, Sahar
AU - Muthmann, Jens Oliver
AU - Kepiro, Ibolya Edit
AU - Ullo, Simona
AU - Ramirez, Cesar Juarez
AU - Puente Encinas, Albert
AU - Maccione, Alessandro
AU - Berdondini, Luca
AU - Murino, Vittorio
AU - Sona, Diego
AU - Cella Zanacchi, Francesca
AU - Sernagor, Evelyne
AU - Hennig, Matthias Helge
PY - 2017/3/7
Y1 - 2017/3/7
N2 - We present a method for automated spike sorting for recordings with high-density, large-scale multielectrode arrays. Exploiting the dense sampling of single neurons by multiple electrodes, an efficient, low-dimensional representation of detected spikes consisting of estimated spatial spike locations and dominant spike shape features is exploited for fast and reliable clustering into single units. Millions of events can be sorted in minutes, and the method is parallelized and scales better than quadratically with the number of detected spikes. Performance is demonstrated using recordings with a 4,096-channel array and validated using anatomical imaging, optogenetic stimulation, and model-based quality control. A comparison with semi-automated, shape-based spike sorting exposes significant limitations of conventional methods. Our approach demonstrates that it is feasible to reliably isolate the activity of up to thousands of neurons and that dense, multi-channel probes substantially aid reliable spike sorting.
AB - We present a method for automated spike sorting for recordings with high-density, large-scale multielectrode arrays. Exploiting the dense sampling of single neurons by multiple electrodes, an efficient, low-dimensional representation of detected spikes consisting of estimated spatial spike locations and dominant spike shape features is exploited for fast and reliable clustering into single units. Millions of events can be sorted in minutes, and the method is parallelized and scales better than quadratically with the number of detected spikes. Performance is demonstrated using recordings with a 4,096-channel array and validated using anatomical imaging, optogenetic stimulation, and model-based quality control. A comparison with semi-automated, shape-based spike sorting exposes significant limitations of conventional methods. Our approach demonstrates that it is feasible to reliably isolate the activity of up to thousands of neurons and that dense, multi-channel probes substantially aid reliable spike sorting.
KW - electrophysiology
KW - high-density multielectrode array
KW - neural cultures
KW - retina
KW - spike sorting
UR - http://www.scopus.com/inward/record.url?scp=85014523793&partnerID=8YFLogxK
U2 - 10.1016/j.celrep.2017.02.038
DO - 10.1016/j.celrep.2017.02.038
M3 - Article
C2 - 28273464
AN - SCOPUS:85014523793
SN - 2211-1247
VL - 18
SP - 2521
EP - 2532
JO - Cell Reports
JF - Cell Reports
IS - 10
ER -