File: left_cerebellum_volume_source.py

package info (click to toggle)
python-mne 1.3.0%2Bdfsg-1
  • links: PTS, VCS
  • area: main
  • in suites: bookworm
  • size: 100,172 kB
  • sloc: python: 166,349; pascal: 3,602; javascript: 1,472; sh: 334; makefile: 236
file content (70 lines) | stat: -rw-r--r-- 2,190 bytes parent folder | download
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
# -*- coding: utf-8 -*-
"""
.. _ex-cerebellum-source-space:

==============================================
Generate a left cerebellum volume source space
==============================================

Generate a volume source space of the left cerebellum and plot its vertices
relative to the left cortical surface source space and the FreeSurfer
segmentation file.
"""

# Author: Alan Leggitt <alan.leggitt@ucsf.edu>
#
# License: BSD-3-Clause

# %%

import mne
from mne import setup_source_space, setup_volume_source_space
from mne.datasets import sample

print(__doc__)

data_path = sample.data_path()
subjects_dir = data_path / 'subjects'
subject = 'sample'
aseg_fname = subjects_dir / 'sample' / 'mri' / 'aseg.mgz'

# %%
# Setup the source spaces

# setup a cortical surface source space and extract left hemisphere
surf = setup_source_space(subject, subjects_dir=subjects_dir, add_dist=False)
lh_surf = surf[0]

# setup a volume source space of the left cerebellum cortex
volume_label = 'Left-Cerebellum-Cortex'
sphere = (0, 0, 0, 0.12)
lh_cereb = setup_volume_source_space(
    subject, mri=aseg_fname, sphere=sphere, volume_label=volume_label,
    subjects_dir=subjects_dir, sphere_units='m')

# Combine the source spaces
src = surf + lh_cereb

# %%
# Plot the positions of each source space

fig = mne.viz.plot_alignment(subject=subject, subjects_dir=subjects_dir,
                             surfaces='white', coord_frame='mri',
                             src=src)
mne.viz.set_3d_view(fig, azimuth=180, elevation=90,
                    distance=0.30, focalpoint=(-0.03, -0.01, 0.03))

# %%
# You can export source positions to a NIfTI file::
#
#     >>> nii_fname = 'mne_sample_lh-cerebellum-cortex.nii'
#     >>> src.export_volume(nii_fname, mri_resolution=True)
#
# And display source positions in freeview::
#
#    >>> from mne.utils import run_subprocess
#    >>> mri_fname = subjects_dir + '/sample/mri/brain.mgz'
#    >>> run_subprocess(['freeview', '-v', mri_fname, '-v',
#                        '%s:colormap=lut:opacity=0.5' % aseg_fname, '-v',
#                        '%s:colormap=jet:colorscale=0,2' % nii_fname,
#                        '-slice', '157 75 105'])