def test_long_extraction():
fnirs_data_folder = mne.datasets.fnirs_motor.data_path()
fnirs_raw_dir = os.path.join(fnirs_data_folder, 'Participant-1')
raw_intensity = mne.io.read_raw_nirx(fnirs_raw_dir).load_data()
long_chans = get_long_channels(raw_intensity)
original_num_channels = len(raw_intensity.ch_names)
assert original_num_channels == 56
long_num_channels = len(long_chans.ch_names)
assert long_num_channels == 56 - 16
new_lens = source_detector_distances(long_chans.info)
assert np.min(new_lens) >= 0.01
# Now test for non standard short length
long_chans = get_long_channels(raw_intensity, min_dist=0.022)
long_num_channels = len(long_chans.ch_names)
assert long_num_channels > 16 # There are 8 SDs in this set * hbo/hbr
new_lens = source_detector_distances(long_chans.info)
assert np.max(new_lens) >= 0.022
# Check that we dont run on other types, eg eeg.
raw_intensity.pick(picks=range(2))
raw_intensity.set_channel_types({'S1_D1 760': 'eeg', 'S1_D1 850': 'eeg'},
verbose='error')
with pytest.raises(RuntimeError, match='NIRS signals only'):
_ = get_long_channels(raw_intensity)
def individual_analysis(bids_path, ID):
raw_intensity = read_raw_bids(bids_path=bids_path, verbose=False)
# Convert signal to haemoglobin and resample
raw_od = optical_density(raw_intensity)
raw_haemo = beer_lambert_law(raw_od)
raw_haemo.resample(0.3)
# Cut out just the short channels for creating a GLM repressor
sht_chans = get_short_channels(raw_haemo)
raw_haemo = get_long_channels(raw_haemo)
# Create a design matrix
design_matrix = make_first_level_design_matrix(raw_haemo, stim_dur=5.0)
# Append short channels mean to design matrix
design_matrix["ShortHbO"] = np.mean(sht_chans.copy().pick(picks="hbo").get_data(), axis=0)
design_matrix["ShortHbR"] = np.mean(sht_chans.copy().pick(picks="hbr").get_data(), axis=0)
# Run GLM
glm_est = run_GLM(raw_haemo, design_matrix)
# Define channels in each region of interest
# List the channel pairs manually
left = [[4, 3], [1, 3], [3, 3], [1, 2], [2, 3], [1, 1]]
right = [[6, 7], [5, 7], [7, 7], [5, 6], [6, 7], [5, 5]]
# Then generate the correct indices for each pair
groups = dict(
Left_Hemisphere=picks_pair_to_idx(raw_haemo, left, on_missing='ignore'),
Right_Hemisphere=picks_pair_to_idx(raw_haemo, right, on_missing='ignore'))
# Extract channel metrics
cha = glm_to_tidy(raw_haemo, glm_est, design_matrix)
cha["ID"] = ID # Add the participant ID to the dataframe
# Compute region of interest results from channel data
roi = pd.DataFrame()
for idx, col in enumerate(design_matrix.columns):
roi = roi.append(glm_region_of_interest(glm_est, groups, idx, col))
roi["ID"] = ID # Add the participant ID to the dataframe
# Contrast left vs right tapping
contrast_matrix = np.eye(design_matrix.shape[1])
basic_conts = dict([(column, contrast_matrix[i])
for i, column in enumerate(design_matrix.columns)])
contrast_LvR = basic_conts['Tapping/Left'] - basic_conts['Tapping/Right']
contrast = compute_contrast(glm_est, contrast_LvR)
con = glm_to_tidy(raw_haemo, contrast, design_matrix)
con["ID"] = ID # Add the participant ID to the dataframe
# Convert to uM for nicer plotting below.
cha["theta"] = [t * 1.e6 for t in cha["theta"]]
roi["theta"] = [t * 1.e6 for t in roi["theta"]]
con["effect"] = [t * 1.e6 for t in con["effect"]]
return raw_haemo, roi, cha, con
def test_GLM_system_test():
fnirs_data_folder = mne.datasets.fnirs_motor.data_path()
fnirs_raw_dir = os.path.join(fnirs_data_folder, 'Participant-1')
raw_intensity = mne.io.read_raw_nirx(fnirs_raw_dir).load_data()
raw_intensity.resample(1.0)
new_des = [des for des in raw_intensity.annotations.description]
new_des = ['Control' if x == "1.0" else x for x in new_des]
new_des = ['Tapping/Left' if x == "2.0" else x for x in new_des]
new_des = ['Tapping/Right' if x == "3.0" else x for x in new_des]
annot = mne.Annotations(raw_intensity.annotations.onset,
raw_intensity.annotations.duration, new_des)
raw_intensity.set_annotations(annot)
raw_intensity.annotations.crop(35, 2967)
raw_od = mne.preprocessing.nirs.optical_density(raw_intensity)
raw_haemo = mne.preprocessing.nirs.beer_lambert_law(raw_od)
short_chs = get_short_channels(raw_haemo)
raw_haemo = get_long_channels(raw_haemo)
design_matrix = make_first_level_design_matrix(raw_intensity,
hrf_model='spm',
stim_dur=5.0,
drift_order=3,
drift_model='polynomial')
design_matrix["ShortHbO"] = np.mean(
short_chs.copy().pick(picks="hbo").get_data(), axis=0)
design_matrix["ShortHbR"] = np.mean(
short_chs.copy().pick(picks="hbr").get_data(), axis=0)
glm_est = run_GLM(raw_haemo, design_matrix)
df = glm_to_tidy(raw_haemo, glm_est, design_matrix)
df = _tidy_long_to_wide(df)
a = (df.query('condition in ["Control"]').groupby(['condition', 'Chroma'
]).agg(['mean']))
# Make sure false positive rate is less than 5%
assert a["Significant"].values[0] < 0.05
assert a["Significant"].values[1] < 0.05
a = (df.query('condition in ["Tapping/Left", "Tapping/Right"]').groupby(
['condition', 'Chroma']).agg(['mean']))
# Fairly arbitrary cutoff here, but its more than 5%
assert a["Significant"].values[0] > 0.7
assert a["Significant"].values[1] > 0.7
assert a["Significant"].values[2] > 0.7
assert a["Significant"].values[3] > 0.7
left = [[1, 1], [1, 2], [1, 3], [2, 1], [2, 3], [2, 4], [3, 2], [3, 3],
[4, 3], [4, 4]]
right = [[5, 5], [5, 6], [5, 7], [6, 5], [6, 7], [6, 8], [7, 6], [7, 7],
[8, 7], [8, 8]]
groups = dict(Left_ROI=picks_pair_to_idx(raw_haemo, left),
Right_ROI=picks_pair_to_idx(raw_haemo, right))
df = pd.DataFrame()
for idx, col in enumerate(design_matrix.columns[:3]):
df = df.append(glm_region_of_interest(glm_est, groups, idx, col))
assert df.shape == (12, 8)
def test_long_extraction():
fnirs_data_folder = mne.datasets.fnirs_motor.data_path()
fnirs_raw_dir = os.path.join(fnirs_data_folder, 'Participant-1')
raw_intensity = mne.io.read_raw_nirx(fnirs_raw_dir).load_data()
long_chans = get_long_channels(raw_intensity)
original_num_channels = len(raw_intensity.ch_names)
assert original_num_channels == 56
long_num_channels = len(long_chans.ch_names)
assert long_num_channels == 56 - 16
new_lens = source_detector_distances(long_chans.info)
assert np.min(new_lens) >= 0.01
# Now test for non standard short length
long_chans = get_long_channels(raw_intensity, min_dist=0.022)
long_num_channels = len(long_chans.ch_names)
assert long_num_channels > 16 # There are 8 SDs in this set * hbo/hbr
new_lens = source_detector_distances(long_chans.info)
assert np.max(new_lens) >= 0.022
def test_short():
raw_intensity = _load_dataset()
with pytest.raises(RuntimeError, match="must be optical density"):
_ = short_channel_regression(raw_intensity)
raw_od = mne.preprocessing.nirs.optical_density(raw_intensity)
raw_od_corrected = short_channel_regression(raw_od)
assert 'fnirs_od' in raw_od_corrected
with pytest.raises(RuntimeError, match="long channels present"):
short_channel_regression(get_short_channels(raw_od))
with pytest.raises(RuntimeError, match="short channels present"):
short_channel_regression(get_long_channels(raw_od))
def analysis(fname, ID):
raw_intensity = read_raw_bids(bids_path=fname, verbose=False)
# Delete annotation labeled 15, as these just signify the start and end of experiment.
raw_intensity.annotations.delete(
raw_intensity.annotations.description == '15.0')
# sanitize event names
raw_intensity.annotations.description[:] = [
d.replace('/', '_') for d in raw_intensity.annotations.description
]
# Convert signal to haemoglobin and just keep hbo
raw_od = optical_density(raw_intensity)
raw_haemo = beer_lambert_law(raw_od, ppf=0.1)
raw_haemo.resample(0.5, npad="auto")
# Cut out just the short channels for creating a GLM regressor
short_chans = get_short_channels(raw_haemo)
raw_haemo = get_long_channels(raw_haemo)
# Create a design matrix
design_matrix = make_first_level_design_matrix(raw_haemo,
hrf_model='fir',
stim_dur=1.0,
fir_delays=range(10),
drift_model='cosine',
high_pass=0.01,
oversampling=1)
# Add short channels as regressor in GLM
for chan in range(len(short_chans.ch_names)):
design_matrix[f"short_{chan}"] = short_chans.get_data(chan).T
# Run GLM
glm_est = run_glm(raw_haemo, design_matrix)
# Create a single ROI that includes all channels for example
rois = dict(AllChannels=range(len(raw_haemo.ch_names)))
# Calculate ROI for all conditions
conditions = design_matrix.columns
# Compute output metrics by ROI
df_ind = glm_est.to_dataframe_region_of_interest(rois, conditions)
df_ind["ID"] = ID
df_ind["theta"] = [t * 1.e6 for t in df_ind["theta"]]
return df_ind, raw_haemo, design_matrix
def individual_analysis(bids_path):
# Read data with annotations in BIDS format
raw_intensity = read_raw_bids(bids_path=bids_path, verbose=False)
raw_intensity = get_long_channels(raw_intensity, min_dist=0.01)
# Convert signal to optical density and determine bad channels
raw_od = optical_density(raw_intensity)
sci = scalp_coupling_index(raw_od, h_freq=1.35, h_trans_bandwidth=0.1)
raw_od.info["bads"] = list(compress(raw_od.ch_names, sci < 0.5))
raw_od.interpolate_bads()
# Downsample and apply signal cleaning techniques
raw_od.resample(0.8)
raw_od = temporal_derivative_distribution_repair(raw_od)
# Convert to haemoglobin and filter
raw_haemo = beer_lambert_law(raw_od, ppf=0.1)
raw_haemo = raw_haemo.filter(0.02,
0.3,
h_trans_bandwidth=0.1,
l_trans_bandwidth=0.01,
verbose=False)
# Apply further data cleaning techniques and extract epochs
raw_haemo = enhance_negative_correlation(raw_haemo)
# Extract events but ignore those with
# the word Ends (i.e. drop ExperimentEnds events)
events, event_dict = events_from_annotations(raw_haemo,
verbose=False,
regexp='^(?![Ends]).*$')
epochs = Epochs(raw_haemo,
events,
event_id=event_dict,
tmin=-5,
tmax=20,
reject=dict(hbo=200e-6),
reject_by_annotation=True,
proj=True,
baseline=(None, 0),
detrend=0,
preload=True,
verbose=False)
return raw_haemo, epochs
def individual_analysis(bids_path, ID):
raw_intensity = read_raw_bids(bids_path=bids_path, verbose=False)
raw_intensity.annotations.delete(
raw_intensity.annotations.description == '15.0')
# sanitize event names
raw_intensity.annotations.description[:] = [
d.replace('/', '_') for d in raw_intensity.annotations.description
]
# Convert signal to haemoglobin and resample
raw_od = optical_density(raw_intensity)
raw_haemo = beer_lambert_law(raw_od, ppf=0.1)
raw_haemo.resample(0.3)
# Cut out just the short channels for creating a GLM repressor
sht_chans = get_short_channels(raw_haemo)
raw_haemo = get_long_channels(raw_haemo)
# Create a design matrix
design_matrix = make_first_level_design_matrix(raw_haemo, stim_dur=5.0)
# Append short channels mean to design matrix
design_matrix["ShortHbO"] = np.mean(
sht_chans.copy().pick(picks="hbo").get_data(), axis=0)
design_matrix["ShortHbR"] = np.mean(
sht_chans.copy().pick(picks="hbr").get_data(), axis=0)
# Run GLM
glm_est = run_glm(raw_haemo, design_matrix)
# Extract channel metrics
cha = glm_est.to_dataframe()
# Add the participant ID to the dataframes
cha["ID"] = ID
# Convert to uM for nicer plotting below.
cha["theta"] = [t * 1.e6 for t in cha["theta"]]
return raw_haemo, cha
# As observed above, some channels have greater specificity to the desired
# brain region than other channels.
# Thus, when doing a region of interest analysis you may wish to give extra
# weight to channels with greater sensitivity to the desired ROI.
# This can be done by manually specifying the weights used in the region of
# interest function call.
# The details of the GLM analysis will not be described here, instead view the
# :ref:`fNIRS GLM tutorial <tut-fnirs-hrf>`. Instead, comments are provided
# for the weighted region of interest function call.
# Basic pipeline, simplified for example
raw_od = optical_density(raw)
raw_haemo = beer_lambert_law(raw_od)
raw_haemo.resample(0.3).pick("hbo") # Speed increase for web server
sht_chans = get_short_channels(raw_haemo)
raw_haemo = get_long_channels(raw_haemo)
design_matrix = make_first_level_design_matrix(raw_haemo, stim_dur=13.0)
design_matrix["ShortHbO"] = np.mean(
sht_chans.copy().pick(picks="hbo").get_data(), axis=0)
glm_est = run_glm(raw_haemo, design_matrix)
# First we create a dictionary for each region of interest.
# Here we include all channels in each ROI, as we will later be applying
# weights based on their specificity to the brain regions of interest.
rois = dict()
rois["Audio_weighted"] = range(len(glm_est.ch_names))
rois["Visual_weighted"] = range(len(glm_est.ch_names))
# Next we compute the specificity for each channel to the auditory and visual cortex.
spec_aud = fold_landmark_specificity(
raw_haemo,
# %% # Import and preprocess data # -------------------------- # # We read in the data and convert to haemoglobin concentration. fnirs_data_folder = mne.datasets.fnirs_motor.data_path() fnirs_raw_dir = os.path.join(fnirs_data_folder, 'Participant-1') raw = mne.io.read_raw_nirx(fnirs_raw_dir, verbose=True).load_data() raw = optical_density(raw) raw.resample(1.5) raw = beer_lambert_law(raw, ppf=0.1) raw = raw.pick(picks="hbo") raw = get_long_channels(raw, min_dist=0.025, max_dist=0.045) raw # %% # Process data with FOOOF # ----------------------- # # Next we estimate the power spectral density of the data and pass this to # the FOOOF algorithm. # # I recommend using the FOOOF algorithm as provided by the authors rather # than reimplementation or custom plotting etc. Their code is of excellent # quality, well maintained, thoroughly documented, and they have considered # many edge cases. #
def individual_analysis(bids_path, ID):
raw_intensity = read_raw_bids(bids_path=bids_path, verbose=False)
# Delete annotation labeled 15, as these just signify the start and end of experiment.
raw_intensity.annotations.delete(raw_intensity.annotations.description == '15.0')
# sanitize event names
raw_intensity.annotations.description[:] = [
d.replace('/', '_') for d in raw_intensity.annotations.description]
# Convert signal to haemoglobin and resample
raw_od = optical_density(raw_intensity)
raw_haemo = beer_lambert_law(raw_od, ppf=0.1)
raw_haemo.resample(0.3)
# Cut out just the short channels for creating a GLM repressor
sht_chans = get_short_channels(raw_haemo)
raw_haemo = get_long_channels(raw_haemo)
# Create a design matrix
design_matrix = make_first_level_design_matrix(raw_haemo, stim_dur=5.0)
# Append short channels mean to design matrix
design_matrix["ShortHbO"] = np.mean(sht_chans.copy().pick(picks="hbo").get_data(), axis=0)
design_matrix["ShortHbR"] = np.mean(sht_chans.copy().pick(picks="hbr").get_data(), axis=0)
# Run GLM
glm_est = run_glm(raw_haemo, design_matrix)
# Define channels in each region of interest
# List the channel pairs manually
left = [[4, 3], [1, 3], [3, 3], [1, 2], [2, 3], [1, 1]]
right = [[8, 7], [5, 7], [7, 7], [5, 6], [6, 7], [5, 5]]
# Then generate the correct indices for each pair
groups = dict(
Left_Hemisphere=picks_pair_to_idx(raw_haemo, left, on_missing='ignore'),
Right_Hemisphere=picks_pair_to_idx(raw_haemo, right, on_missing='ignore'))
# Extract channel metrics
cha = glm_est.to_dataframe()
# Compute region of interest results from channel data
roi = glm_est.to_dataframe_region_of_interest(groups,
design_matrix.columns,
demographic_info=True)
# Define left vs right tapping contrast
contrast_matrix = np.eye(design_matrix.shape[1])
basic_conts = dict([(column, contrast_matrix[i])
for i, column in enumerate(design_matrix.columns)])
contrast_LvR = basic_conts['Tapping_Left'] - basic_conts['Tapping_Right']
# Compute defined contrast
contrast = glm_est.compute_contrast(contrast_LvR)
con = contrast.to_dataframe()
# Add the participant ID to the dataframes
roi["ID"] = cha["ID"] = con["ID"] = ID
# Convert to uM for nicer plotting below.
cha["theta"] = [t * 1.e6 for t in cha["theta"]]
roi["theta"] = [t * 1.e6 for t in roi["theta"]]
con["effect"] = [t * 1.e6 for t in con["effect"]]
return raw_haemo, roi, cha, con
