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Simultaneous recording with two Neuropixels probes

dataset
posted on 2024-02-16, 11:14 authored by Nicholas A. Steinmetz, Matteo CarandiniMatteo Carandini, Kenneth HarrisKenneth Harris

These data were obtained by Nick Steinmetz (nick[dot]steinmetz@gmail.com), in the CortexLab at UCL, and were published in Jun JJ, Steinmetz, NA, Siegle, JH, Denman, DJ, Bauza, M, Barbarits, B, Lee, AK et al. Fully integrated silicon probes for high-density recording of neural activity. Nature 2017.

Two "Phase3" Neuropixels probes were inserted into the brain of an awake, head-fixed mouse for about an hour and a half. These electrode arrays recorded 384 channels of neural data each at 30 kHz and <7 µV RMS noise levels. The sites are densely spaced in a "continuous tetrode"-like arrangement, so that each probe records from a 3.8 mm span of the brain.

One probe (referred to in the files as "posterior") recorded from visual cortex, hippocampus, visual thalamus, and some other part(s) of thalamus; the other probe ("frontal") recorded from motor cortex and striatum. Their approximate positions are indicated by green and red lines on atlas sections in the image raster831.jpg, left.

The data were spike-sorted automatically by Kilosort (software by M. Pachitariu) and manually by N. Steinmetz using Phy (manual phase; software by C. Rossant). In total 831 well-isolated individual neurons were identified.

In addition to neural data, a movie of the eye of the mouse was acquired at 100 Hz and a movie of the frontal aspect (face, forearms, anterior trunk) was recorded at 40 Hz. The mouse's forepaws rested on a wheel that could move left or right, and the movements of this wheel were recorded. Auditory and olfactory information was not recorded and the mouse was not guaranteed to be in silence or in an odor-free environment.

The experiments that were run

During the first phase of the recording, the mouse was shown various types of visual stimuli (described below) on three monitors placed around the mouse at right angles to each other, covering about +/-135 degrees azimuth and +/-35 degrees elevation. During the second phase of the recording, the monitors were turned off and the mouse was in complete or nearly-complete darkness.

Experiment 1: Large flashed bars

Bars consisted of a side-by-side black and white bar on grey background with alternating phase over time. Bars were vertical at each of 9 different azimuth positions covering the entire vertical extent (conditions 1-9); or were horizontal at each of 3 different elevation positions covering the entire horizontal extent (conditions 10-12). There was also a blank condition (13). Bars flashed at 4 Hz for 2 seconds each.

The data file experiment1stimInfo contains stimStarts, the onset of each stimulus; stimStops, the offset; and stimIDs, the condition number of each stimulus as described above. Units are in seconds, same timebase as the spikes.

In this and subsequent experiments, the "Protocol" struct has more details of the parameters of each condition, see fields "parnames", "pardefs", and "pars".

Experiment 2: Full-field oriented drifting gratings

Sine-wave modulated full-field drifting gratings of 16 drift directions (0:22.5:337.5) with 2 Hz temporal frequency and 0.08 cycles/degree spatial frequency displayed for 1.5 seconds (conditions 1-16) plus a blank condition (17). The data file experiment2stimInfo as above.

Experiment 3: Sparse noise stimuli for receptive field mapping

8 degree squares were displayed at random times for 1/6 of a second on each vertex of a 9x34 grid with 8 degree spacing covering the whole extent of the monitors. Background was grey and squares could be either white or black. The presentation consisted of three repeats of a single five-minute long pattern of squares.

The data file experiment3stimInfo contains "photodiodeFlips", the times when each of the 54006 arrays were presented, and "stimArray", the value of each square on each frame (1 = white, 0 = grey, -1 = black). There is also "stimEventTimes", a rearrangement of these data that you may find useful - it is a 9x34x2 cell array containing the list of onset times for each square turning white (in stimEventTimes{x,y,1}) and black (stimEventTimes{x,y,2}).

Experiment 4: Darkness, no stimulation

The data file spontaneousPeriodInfo contains the start and stop times of the darknes

Loading the data

The data is stored in a set of npy files. These are in folders that need to be unzipped first. They can be loaded with numpy in Python, or you will need the npy-matlab repository to load them in Matlab.

To load the data and make some plots, use the Matlab script script_dualPhase3.m. This script also contains documentation of what each file contains, so running through the script may be the easiest way to understand the data. Documentation of each file is also here.

Funding

Integration of internal and external signals in sensory cortex.

Wellcome Trust

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Integration of internal and external signals in sensory cortex.

Wellcome Trust

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Neural network analysis using a novel multichannel "SMART" neuroprobe.

Wellcome Trust

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