Skip to main content
Fig. 5 | Bioelectronic Medicine

Fig. 5

From: Framework for automated sorting of neural spikes from Neuralynx-acquired tetrode recordings in freely-moving mice

Fig. 5

Hippocampal CA1 recordings in freely-moving mice. a, b, Representative single-units showing the firing rates along the length of the track (left panels), average waveform in each channel of a tetrode (next-to-left panels), autocorrelogram (next-to-right panels; pink lines represent refractory period), and amplitudes of spikes over time (right panels). Automated units are displayed in green and manual units are shown in black. a, Representative single-units likely representing the same putative neuron sorted with automated and manual methods. b, Similar units likely to represent different neurons across automated and manual methods. c, Number of single-units per recording session using the automated framework (green) or the manual method (black). d, Population of place cells recorded from mice (n = 4) running the linear track. Each row represents normalized spike activity of one single-unit, where rows are organized by the position of the peak firing rate for each unit along the linear track. Sorted populations of place cells appear similar across automated and manual methods

Back to article page