In vivo intracellular recording in the mouse V1 during passive visual stimulations and audiovisual discrimination task

Whole cell recordings (Vm channel) performed in the layer 2/3 primary visual cortex (V1) of awake mice. Recordings are performed in current clamp (Im channel). A local ECoG was placed on the dura in the vincinity of the recorded neuron. Vistim channels indicate the orientation of the drifting grating (Vistim 1 frequency), contrast (Vistim 1 amplitude), temporal frequency (Vistim 2 frequency), and spatial frquency (Vistim 2 amplitude). The diode signal indicates the exact timing of the stimulus presentation. The two mouse channels (Mouse1 adn Mouse2) indicate the movement of the spherical treadmill on which the animal is standing. In the behavior database, the mice are performing a behavioral task (additional information can be found in those files: licking channel, auditory channel (one of two tones) reward (laser channel)). The script and the data are using an Igor Pro format. For converting the two mouse signals into locomotion, please refer to the script AnalysisMouseWaveProc.ipf or the functions imbeded in LoadExperiments 2013.ipf . Those data have been used for the article Einstein et al., 2017 (https://doi.org/10.1523/JNEUROSCI.3868-16.2017). The excel sheet provides additional information about the recording. If you want to open the ibw files directly in Matlab, use IBWread, m file