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Fit V1 cell

Learning objectives

  • Learn how to combine GLM with other modeling approach.
  • Review previous tutorials.
import jax
import math
import os
import matplotlib.pyplot as plt
import nemos as nmo
import numpy as np
import pynapple as nap
import requests
import tqdm
import workshop_utils

# required for second order methods (BFGS, Newton-CG)
jax.config.update("jax_enable_x64", True)
# configure plots some
plt.style.use(workshop_utils.STYLE_FILE)

Data Streaming

path = workshop_utils.data.download_data("m691l1.nwb", "https://osf.io/xesdm/download",
                                         '../data')

Pynapple

data = nap.load_file(path)
print(data)
epochs = data["epochs"]
spikes = data["units"]
stimulus = data["whitenoise"]
  • stimulus is white noise shown at 40 Hz
  • white noise is a good stimulus for mapping basic stimulus properties of V1 simple cells
fig, ax = plt.subplots(1, 1, figsize=(12,4))
ax.imshow(stimulus[0], cmap='Greys_r')
stimulus.shape
print(spikes)
spikes = spikes[[34]]
  • goal is to predict the neuron's response to this white noise stimuli
  • several ways we could do this, what do you think?

Spike-triggered average

  • compute spike-triggered average to visualize receptive field.
sta = nap.compute_event_trigger_average(spikes, stimulus, binsize=0.025,
                                        windowsize=(-0.15, 0.0))
sta
sta[1, 0]
  • visualize spike-triggered average and decide on our spatial filter.
fig, axes = plt.subplots(1, len(sta), figsize=(3*len(sta),3))
for i, t in enumerate(sta.t):
    axes[i].imshow(sta[i,0], vmin = np.min(sta), vmax = np.max(sta),
                   cmap='Greys_r')
    axes[i].set_title(str(t)+" s")
receptive_field = np.mean(sta.get(-0.125, -0.05), axis=0)[0]

fig, ax = plt.subplots(1, 1, figsize=(4,4))
ax.imshow(receptive_field, cmap='Greys_r')
  • use the spike-triggered average to preprocess our visual input.
# element-wise multiplication and sum
print((receptive_field * stimulus[0]).sum())
# dot product of flattened versions
print(np.dot(receptive_field.flatten(), stimulus[0].flatten()))
filtered_stimulus = np.einsum('t h w, h w -> t', stimulus, receptive_field)
# add the extra dimension for feature
filtered_stimulus = np.expand_dims(filtered_stimulus, 1)
fig, ax = plt.subplots(1, 1, figsize=(12,4))
ax.plot(filtered_stimulus)

Preparing data for nemos

  • get counts and filtered_stimulus into proper shape for nemos
# grab spikes from when we were showing our stimulus, and bin at 1 msec
# resolution
bin_size = .001
counts = spikes.restrict(filtered_stimulus.time_support).count(bin_size)
print(counts.rate)
print(filtered_stimulus.rate)
print(counts[:5])
print(filtered_stimulus[:5])
filtered_stimulus = workshop_utils.data.fill_forward(counts, filtered_stimulus)
filtered_stimulus
  • Set up the basis and prepare the temporal predictor for the GLM.
basis = nmo.basis.RaisedCosineBasisLog(8)
window_size = 100
time, basis_kernels = basis.evaluate_on_grid(window_size)
time *= bin_size * window_size
convolved_input = nmo.utils.convolve_1d_trials(basis_kernels, filtered_stimulus)
# convolved_input has shape (n_time_pts, n_features, n_basis_funcs), and
# n_features is the singleton dimension from filtered_stimulus, so let's
# squeeze it out:
convolved_input = np.squeeze(convolved_input)
# and, as also described in the head direction tutorial, when doing this we
# need to remove the first window_size time points from the neuron counts and
# the last time point from the convolved input:
counts = counts[window_size:]
convolved_input = convolved_input[:-1]
# and grab the counts for our single neuron
counts = counts[:, 0]

Fitting the GLM

  • Fit the GLM
model = workshop_utils.model.GLM(regularizer=nmo.regularizer.UnRegularized(solver_name="LBFGS"))
model.fit(convolved_input, counts)
  • Examine the resulting temporal filter
temp_weights = np.einsum('b, t b -> t', model.coef_, basis_kernels)
plt.plot(time, temp_weights)

Further exercises

Total running time of the script: ( 0 minutes 0.000 seconds)

Download Python source code: 04_v1_cells_code.py

Download Jupyter notebook: 04_v1_cells_code.ipynb

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