TMFC is a MATLAB toolbox for SPM12 for task-modulated functional connectivity analysis.
TMFC toolbox implements:
- Beta-series correlations based on the least-squares separate appoach (BSC-LSS);
- Generalized psyhophysiological interactions (gPPI) with deconvolution procedure;
- Seed-to-voxel analysis and ROI-to-ROI analysis (to create FC matrices);
- Finite impulse response (FIR) task regression to remove co-activations;
- Graphical user interface (GUI) and command line interface (CLI);
- RAM control (allows to estimate model parameters in the whole-brain at a time without dividing into chunks);
- Parralel computations.
If you use TMFC toolbox, please cite this study:
Masharipov et al. "Comparison of whole-brain task-modulated functional connectivity methods for fMRI task connectomics." Commun Biol 7, 1402 (2024).
The current version of the toolbox is fully functional on MATLAB R2014a and later releases.
- Add SPM12 to your MATLAB path (in case the user has not already done so);
- Add TMFC toolbox to your MATLAB path (Home --> Set path --> Add with Subfolders --> Select TMFC_toolbox folder);
- Enter TMFC in command window to open TMFC GUI
or - See TMFC_command_window_example.m to run TMFC functions via command line.
To illustrate the use of TMFC toolbox, we provide simulated BOLD time series. Simulation was performed for 100 subjects and 100 ROIs.
Task design parameters:
- Event-related
- Two conditions (TaskA and TaskB)
- 40 events per condition
- Event duration = 1 s
- Random interstimulus interval (ISI) = 4-8 s (mean ISI = 6 s)
- Repetition time (TR) = 2 s
- Dummy scans: first 3 time points (6 s)
- Total scan time = 9.7 min
Simulation procedure is described in details in the referenced paper and here:
https://github.com/IHB-IBR-department/TMFC_simulations
To prepare example data and estimate basic GLMs run this code:
% BEFORE RUNNING THIS SCRIPT:
% 1) Set path to SPM12
% 2) Set path to TMFC_toolbox (Add with subfolders)
% 3) Change current working directory to: '...\TMFC_toolbox\examples'
%% Prepare example data and calculate basic first-level GLMs
clear
data.SF = 1; % Scaling Factor (SF) for co-activations: SF = SD_oscill/SD_coact
data.SNR = 1; % Signal-to-noise ratio (SNR): SNR = SD_signal/SD_noise
data.STP_delay = 0.2; % Short-term synaptic plasticity (STP) delay, [s]
data.N = 20; % Sample size (Select 20 subjects out of 100 to reduce computations)
data.N_ROIs = 100; % Number of ROIs
data.dummy = 3; % Remove first M dummy scans
data.TR = 2; % Repetition time (TR), [s]
data.model = 'AR(1)'; % Autocorrelation modeling
% Set path for stat folder
spm_jobman('initcfg');
data.stat_path = spm_select(1,'dir','Select a folder for data extraction and statistical analysis');
% Set path for simulated BOLD time series *.mat file
data.sim_path = fullfile(pwd,'data','SIMULATED_BOLD_EVENT_RELATED_[2s_TR]_[1s_DUR]_[6s_ISI]_[40_TRIALS].mat');
% Set path for task design *.mat file (stimulus onset times, SOTs)
data.sots_path = fullfile(pwd,'data','TASK_DESIGN_EVENT_RELATED_[2s_TR]_[1s_DUR]_[6s_ISI]_[40_TRIALS].mat');
% Generate *.nii images and calculate GLMs
prepare_example_data(data)
% Change current directory to new TMFC project folder
cd(data.stat_path)
This code creates *.nii files for 20 subjects (we select 20 subjects out of 100 and consider high SNR = 1 to reduce the number of computations).
Each *.nii file represents single time point and consists of 100 voxels. Each voxel correspons to one ROI. In this case, seed-to-voxel and ROI-to-ROI analyses are equivalent.
In real datasets, the number of voxels are not equal to the number of ROIs. However, all steps of TMFC analysis will be the same as described below.
Enter TMFC in command window to open TMFC GUI:
Click Settings button to open settings window:
- Choose between sequential and parallel computing (default: sequential computing)(change to parallel computing to speed up computations);
- Choose to store temporary files for GLM estimation on disk or in RAM (default: in RAM);
- Define Max RAM for GLM estimation (default: 2^32 = 4 GB)(change to 2^33 or 2^34 to speed up computations);
- Choose to perform seed-to-voxel and/or ROI-to-ROI analysis (default: both).
Click OK.
See how to use TMFC functions via command line here.
TMFC toolbox has the following folder structure:
These folders and files will be created in the selected project path after performing corresponding analyses. To select TMFC project path and subjects click Subjects button.
Click Subjects button to open subject manager window:
Click Select subjects folder button and select folders for 20 subjects (inside "...\Example_data_SF_[1.00] SNR_[1.00] STP_[0.20]_AR(1)\GLMs" folder):
Click Select SPM.mat file for Subject #1 and select SPM.mat for the first subject ("...\GLMs\Subject_001\SPM.mat"), which contains information about the basic first-level GLM (typical GLM used for activation analysis):
Check selected subjects and click OK:
Finally, select a folder for the new TMFC project.
Click ROI_set button and define ROI set name:
Click OK and select 100 ROI masks (inside "...\Example_data_SF_[1.00] SNR_[1.00] STP_[0.20]_AR(1)\ROI_masks" folder):
Check selected ROIs and click OK:
In this example, single voxel represents a single ROI (i.e., ROI size = 1 voxel). In real data, each ROI will consist of several voxels. TMFC toolbox creates a "TMFC_project_folder\ROI_sets\ROI_set_name\Masked_ROIs" folder, which contains:
- Group_mean.nii file - Group mean binary mask (identifies voxels that have data across all subjects)
- ROI_name_masked.nii files - ROI mask files masked by Group_mean.nii file (reduce original ROI mask to voxels that have data across all subjects)
ROI masks which do not contain any voxels that have data across all subjects will be removed from the TMFC analysis. User can also remove heavily cropped ROIs.
You can define several ROI sets and switch between them. For example, push ROI_set button a second time and then push "Add new ROI set":
Define a name for the second ROI set (e.g., "20_ROIs) and select ROI masks for the second ROI set (e.g., select 20 ROIs). Now you can switch between ROI sets.
Click ROI_set button a third time and select "100_ROIs" set:
To perfrom beta-series correlation (BSC) analysis, we first need to calculate parameter estimates (betas) for individual trials using LSS regression.
Click LSS GLM button and select conditions of interest (individual betas will be calculated only for the selected conditions):
Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\LSS_regression" folder with subfolders for each subject. Subjects' subfolders will contain trial-wise beta images and SPM12 batches for individual trial GLMs.
To perform BSC-LSS analysis for selected ROI set, click BSC LSS button.
Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\ROI_sets\ROI_set_name\BSC_LSS" folder with three subfolders:
- Beta_series - containes beta series extracted for the selected ROI set (beta parameters are averaged across voxels for each ROI mask);
- ROI_to_ROI - containes BSC-LSS functional connectivity matrices (Person's r converted to Fisher's Z);
- Seed_to_voxel - containes voxel-by-voxel BSC-LSS images (*.nii files containing Fisher's Z values) calculated for each seed ROI.
NOTE: You don't need to recalculare LSS regression to perform the BSC-LSS analysis for a different ROI set. Just select a different ROI set by clicking the ROI set button and then click the BSC-LSS button.
By default, TMFC calculates contrasts for each condition of interest (Condition > Baseline). To calculate the functional connectivity difference between conditions (i.e., "Condition A > Condition B") click the BSC LSS button once again:
Define a new contrast by pressing "Add new" button, enter contrast title ("TaskA_vs_TaskB") and specify contrast weights ([1 -1]), and click OK:
Click OK to calculate the new contrast. Each time you need to calculate a new contrast, click the BSC LSS button. Contrast files will be stored in ROI_to_ROI and Seed_to_voxel subfolders.
You can use the SPM12 software to perform voxel-wise statistical inference. Click "Specify 2nd-level" button, select "One-sample t-test" and specify 20 contrast files for the "Cond_A_vs_Cond_B" contrast and the selected seed ROI from the ...\Seed_to_voxel\ROI_name subfolder.
In future releases, we will add a GUI window to perform ROI-to-ROI statistical inference. It will implement edge-wise FDR and Bonferroni correction, as well as network-based statistics (NBS) and threshold-free cluster enhancement (TFCE) with network-level FWE correction.
TMFC matrices (*.mat files) can be analysed in any MATLAB toolbox for ROI-to-ROI statistical inference. For example, you can use the network-based statistics (NBS) toolbox (https://www.nitrc.org/projects/nbs/).
To visualisaze the ROI-to-ROI results, enter this code in MATLAB command window:
% Select TMFC project path
tmfc.project_path = spm_select(1,'dir','Select TMFC project folder');
ROI_set_number = 1;
tmfc.ROI_set(ROI_set_number).set_name = '100_ROIs';
% Load BSC-LSS matrices for the 'TaskA_vs_TaskB' contrast (contrast # 3)
for i = 1:20
M(i).paths = struct2array(load(fullfile(tmfc.project_path,'ROI_sets',tmfc.ROI_set(ROI_set_number).set_name,'BSC_LSS','ROI_to_ROI',...
['Subject_' num2str(i,'%04.f') '_Contrast_0003_[TaskA_vs_TaskB].mat'])));
end
matrices = cat(3,M(:).paths);
% Perform one-sample t-test (two-sided, FDR-correction)
contrast = 1; % A > B effect
alpha = 0.001/2; % alpha = 0.001 thredhold corrected for two-sided comparison
correction = 'FDR'; % False Discovery Rate (FDR) correction (Benjamini–Hochberg procedure)
[thresholded_1,pval,tval,conval_1] = tmfc_ttest(matrices,contrast,alpha,correction);
contrast = -1; % B > A effect
[thresholded_2] = tmfc_ttest(matrices,contrast,alpha,correction);
% Plot BSC-LSS results
f1 = figure(1); f1.Position = [382,422,1063,299];
try
sgtitle('BSC-LSS results');
catch
suptitle('BSC-LSS results');
end
subplot(1,3,1); imagesc(conval_1); title('Group mean'); axis square; colorbar; caxis(tmfc_axis(conval_1,1));
subplot(1,3,2); imagesc(thresholded_1); title('A>B (pFDR<0.001)'); axis square; colorbar;
subplot(1,3,3); imagesc(thresholded_2); title('B>A (pFDR<0.001)'); axis square; colorbar;
colormap(subplot(1,3,2),'parula')
colormap(subplot(1,3,3),'parula')
colormap(subplot(1,3,1),'redblue')
set(findall(gcf,'-property','FontSize'),'FontSize',16)
Results for edge-wise inference with FDR-correction ("TaskA vs TaskB"):
Co-activations can spuriosly inflate TMFC estimates (see the referenced paper and Cole et al., 2019).
To remove co-activations, we can perform task regression with finite impulse response (FIR) functions prior to BSC analysis.
Click "FIR task regression" button and specify FIR window length and the number of FIR time bins:
Click OK. Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\FIR_regression" folder with subjects' subfolders. Subjects' subfolders will contain residuals (*.nii images), as well as SPM12 batches and SPM.mat files for FIR GLMs.
To perform BSC-LSS analysis after FIR task regression (using residual time series), click BSC LSS after FIR button. The following steps are similar to those for the BSC-LSS analysis.
To perform gPPI analysis, we first need to extract time series from the seed ROIs and calculate psyhophysiological interaction (PPI) terms.
Click "VOIs" button to extract time series for the selected ROI set. Select conditions of interest. All other conditions will be considered as nuisance conditions. TMFC toolbox uses SPM12 volume of interest (VOI) function to extract time series. It extracts the first eigenvariate for the seed ROI after removing effects of no interest (using nuisance regressors, such as motion regressors, aCompCorr regressors, regressors for conditions of no interest, etc), and performing whitening and high-pass filtering.
Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\ROI_sets\ROI_set_name\VOIs" folder with subjects' subfolders. Subjects' subfolders will contain SPM12 VOI .mat files.
Click "PPIs" button to calculate PPI terms using the deconvolution procedure (Gitelman et al., 2003). TMFC toolbox uses SPM12 Parametric Empirical Bayes (PEB) function to calulate PPI terms.
Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\ROI_sets\ROI_set_name\PPIs" folder with subjects' subfolders. Subjects' subfolders will contain SPM12 PPI .mat files.
Click "gPPI" button to perform gPPI analysis.
Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\ROI_sets\ROI_set_name\gPPI" folder with three subfolders:
- GLM_batches - containes SPM12 batches for gPPI GLMs;
- ROI_to_ROI - containes gPPI functional connectivity matrices (asymmetrical and symmetrical, symmetrization is carried out by averaging the upper and lower diagonal elements);
- Seed_to_voxel - containes voxel-by-voxel gPPI images calculated for each seed ROI.
To remove co-activations with arbitrary shape of HRF function, we can combine FIR task regression with gPPI regression. The difference between classic gPPI GLM and gPPI-FIR GLM is that the latter uses finite impulse response (FIR) functions (instead of canonical HRF function) to model activations for conditions of interst and conditions of no interest. The FIR model allows to model activations with any possible hemodynamic response shape.
Click "gPPI-FIR" button to perform gPPI-FIR analysis.
Once the calculations are complete, TMFC toolbox will create a "...\TMFC_project_name\ROI_sets\ROI_set_name\gPPI-FIR" folder with three subfolders (GLM_batches, ROI_to_ROI, Seed_to_voxel).
To visualisaze the ROI-to-ROI results, enter this code in MATLAB command window:
% Select TMFC project path
tmfc.project_path = spm_select(1,'dir','Select TMFC project folder');
ROI_set_number = 1;
tmfc.ROI_set(ROI_set_number).set_name = '100_ROIs';
% Load gPPI-FIR matrices for the 'TaskA_vs_TaskB' contrast (contrast # 3)
clear M marices conval_1 thresholded_1
for i = 1:20
M(i).paths = struct2array(load(fullfile(tmfc.project_path,'ROI_sets',tmfc.ROI_set(ROI_set_number).set_name,'gPPI_FIR','ROI_to_ROI','symmetrical',...
['Subject_' num2str(i,'%04.f') '_Contrast_0003_[TaskA_vs_TaskB].mat'])));
end
matrices = cat(3,M(:).paths);
% Perform one-sample t-test (two-sided, FDR-correction)
contrast = 1; % A > B effect
[thresholded_1,pval,tval,conval_1] = tmfc_ttest(matrices,contrast,alpha,correction);
contrast = -1; % B > A effect
[thresholded_2] = tmfc_ttest(matrices,contrast,alpha,correction);
% Plot gPPI-FIR results
f2 = figure(2); f2.Position = [382,422,1063,299];
try
sgtitle('gPPI-FIR results');
catch
suptitle('gPPI-FIR results');
end
subplot(1,3,1); imagesc(conval_1); title('Group mean'); axis square; colorbar; caxis(tmfc_axis(conval_1,1));
subplot(1,3,2); imagesc(thresholded_1); title('A>B (pFDR<0.001)'); axis square; colorbar;
subplot(1,3,3); imagesc(thresholded_2); title('B>A (pFDR<0.001)'); axis square; colorbar;
colormap(subplot(1,3,2),'parula')
colormap(subplot(1,3,3),'parula')
colormap(subplot(1,3,1),'redblue')
set(findall(gcf,'-property','FontSize'),'FontSize',16)
Results for edge-wise inference with FDR-correction ("TaskA vs TaskB"):
TMFC toolbox uses information from SPM.mat files to obtain paths to fMRI files. If you estimated first-level GLMs and then moved the GLM and fMRI data folders to another location, you need to change paths in SPM.mat files.
Click Change paths button and select subjects for which you want to update the SPM.mat files. Enter the old path pattern (see SPM.swd field in SPM.mat file) and the new path pattern:
Click OK.
Please see:
TMFC_command_window_example.m
clc
clear
close all
% BEFORE RUNNING THIS SCRIPT:
% 1) Set path to SPM12
% 2) Set path to TMFC_toolbox (Add with subfolders)
% 3) Change current working directory to: '...\TMFC_toolbox\examples'
cd(fileparts(matlab.desktop.editor.getActiveFilename)); % Set path to '...\TMFC_toolbox\examples'
%% Prepare example data and calculate basic first-level GLMs
data.SF = 1; % Scaling Factor (SF) for co-activations: SF = SD_oscill/SD_coact
data.SNR = 1; % Signal-to-noise ratio (SNR): SNR = SD_signal/SD_noise
data.STP_delay = 0.2; % Short-term synaptic plasticity (STP) delay, [s]
data.N = 20; % Sample size (Select 20 subjects out of 100 to reduce computations)
data.N_ROIs = 100; % Number of ROIs
data.dummy = 3; % Remove first M dummy scans
data.TR = 2; % Repetition time (TR), [s]
data.model = 'AR(1)'; % Autocorrelation modeling
% Set path for stat folder
spm_jobman('initcfg');
data.stat_path = spm_select(1,'dir','Select a folder for data extraction and statistical analysis');
% Set path for simulated BOLD time series *.mat file
data.sim_path = fullfile(pwd,'data','SIMULATED_BOLD_EVENT_RELATED_[2s_TR]_[1s_DUR]_[6s_ISI]_[40_TRIALS].mat');
% Set path for task design *.mat file (stimulus onset times, SOTs)
data.sots_path = fullfile(pwd,'data','TASK_DESIGN_EVENT_RELATED_[2s_TR]_[1s_DUR]_[6s_ISI]_[40_TRIALS].mat');
% Generate *.nii images and calculate GLMs
prepare_example_data(data)
% Change current directory to new TMFC project folder
cd(data.stat_path)
%% Setting up computation parameters
% Sequential or parallel computing (0 or 1)
tmfc.defaults.parallel = 1; % Parallel
% Store temporaty files during GLM estimation in RAM or on disk
tmfc.defaults.resmem = true; % RAM
% How much RAM can be used at the same time during GLM estimation
tmfc.defaults.maxmem = 2^32; % 4 GB
% Seed-to-voxel and ROI-to-ROI analyses
tmfc.defaults.analysis = 1;
%% Setting up paths
% The path where all results will be saved
tmfc.project_path = data.stat_path;
% Define paths to individual subject SPM.mat files
% tmfc.subjects(1).path = '...\Your_study\Subjects\sub_001\stat\Standard_GLM\SPM.mat';
% tmfc.subjects(2).path = '...\Your_study\Subjects\sub_002\stat\Standard_GLM\SPM.mat';
% tmfc.subjects(3).path = '...\Your_study\Subjects\sub_003\stat\Standard_GLM\SPM.mat';
% etc
% Alternativelly, use tmfc_select_subjects_GUI to select subjects
% Go to GLMs subfolder and select 20 subjects
SPM_check = 1; % Check SPM.mat files
[paths] = tmfc_select_subjects_GUI(SPM_check);
for i = 1:length(paths)
tmfc.subjects(i).path = paths{i};
end
clear SPM_check paths
%% Select ROIs
% Use tmfc_select_ROIs_GUI to select ROIs
%
% The tmfc_select_ROIs_GUI function creates group binary mask based on
% 1st-level masks (SPM.VM) and applies it to all selected ROIs. Empty ROIs
% will be removed. Masked ROIs will be limited to only voxels which have
% data for all subjects. The dimensions, orientation, and voxel sizes of
% the masked ROI images will be adjusted according to the group binary mask
%
% Go to ROI_masks subfolder and select 100 ROIs
[ROI_set] = tmfc_select_ROIs_GUI(tmfc);
tmfc.ROI_set(1) = ROI_set;
clear ROI_set
%% LSS regression
% Define conditions of interest
% tmfc.LSS.conditions(1).sess = 1;
% tmfc.LSS.conditions(1).number = 1;
% tmfc.LSS.conditions(2).sess = 1;
% tmfc.LSS.conditions(2).number = 2;
% Alternatively, use tmfc_LSS_GUI to select conditions of interest
[conditions] = tmfc_LSS_GUI(tmfc.subjects(1).path);
tmfc.LSS.conditions = conditions;
% Run LSS regression
start_sub = 1; % Start from the 1st subject
[sub_check] = tmfc_LSS(tmfc,start_sub);
clear conditions
%% BSC-LSS
% Extract and correlate mean beta series for conditions of interest
ROI_set_number = 1; % Select ROI set
[sub_check,contrasts] = tmfc_BSC(tmfc,ROI_set_number);
% Update contrasts info
% The tmfc_BSC function creates default contrasts for each
% condition of interest (i.e., Condition > Baseline)
tmfc.ROI_set(ROI_set_number).contrasts.BSC = contrasts;
% Define new contrasts:
tmfc.ROI_set(ROI_set_number).contrasts.BSC(3).title = 'TaskA_vs_TaskB';
tmfc.ROI_set(ROI_set_number).contrasts.BSC(4).title = 'TaskB_vs_TaskA';
tmfc.ROI_set(ROI_set_number).contrasts.BSC(3).weights = [1 -1];
tmfc.ROI_set(ROI_set_number).contrasts.BSC(4).weights = [-1 1];
% Calculate new contrasts
type = 3; % BSC-LSS
contrast_number = [3,4]; % Calculate contrasts #3 and #4
[sub_check] = tmfc_ROI_to_ROI_contrast(tmfc,type,contrast_number,ROI_set_number);
[sub_check] = tmfc_seed_to_voxel_contrast(tmfc,type,contrast_number,ROI_set_number);
% Load BSC-LSS matrices for the 'TaskA_vs_TaskB' contrast (contrast # 3)
for i = 1:data.N
M(i).paths = struct2array(load(fullfile(tmfc.project_path,'ROI_sets',tmfc.ROI_set(ROI_set_number).set_name,'BSC_LSS','ROI_to_ROI',...
['Subject_' num2str(i,'%04.f') '_Contrast_0003_[TaskA_vs_TaskB].mat'])));
end
matrices = cat(3,M(:).paths);
% Perform one-sample t-test (two-sided, FDR-correction)
contrast = 1; % A > B effect
alpha = 0.001/2; % alpha = 0.001 thredhold corrected for two-sided comparison
correction = 'FDR'; % False Discovery Rate (FDR) correction (Benjamini–Hochberg procedure)
[thresholded_1,pval,tval,conval_1] = tmfc_ttest(matrices,contrast,alpha,correction);
contrast = -1; % B > A effect
[thresholded_2] = tmfc_ttest(matrices,contrast,alpha,correction);
% Plot BSC-LSS results
f1 = figure(1); f1.Position = [382,422,1063,299];
try
sgtitle('BSC-LSS results');
catch
suptitle('BSC-LSS results');
end
subplot(1,3,1); imagesc(conval_1); title('Group mean'); axis square; colorbar; caxis(tmfc_axis(conval_1,1));
subplot(1,3,2); imagesc(thresholded_1); title('A>B (pFDR<0.001)'); axis square; colorbar;
subplot(1,3,3); imagesc(thresholded_2); title('B>A (pFDR<0.001)'); axis square; colorbar;
colormap(subplot(1,3,2),'parula')
colormap(subplot(1,3,3),'parula')
colormap(subplot(1,3,1),'redblue')
set(findall(gcf,'-property','FontSize'),'FontSize',16)
clear type contrasts contrast_number
%% FIR task regression (regress out co-activations and save residual time series)
% FIR window length in [s]
tmfc.FIR.window = 24;
% Number of FIR time bins
tmfc.FIR.bins = 24;
% Run FIR task regression
[sub_check] = tmfc_FIR(tmfc,start_sub);
%% LSS regression after FIR task regression (use residual time series)
% Define conditions of interest
tmfc.LSS_after_FIR.conditions = tmfc.LSS.conditions;
% Run LSS regression
[sub_check] = tmfc_LSS_after_FIR(tmfc,start_sub);
%% BSC-LSS after FIR task regression (use residual time series)
% Extract and correlate mean beta series for conditions of interest
ROI_set_number = 1; % Select ROI set
[sub_check,contrasts] = tmfc_BSC_after_FIR(tmfc,ROI_set_number);
% Update contrasts info
% The tmfc_BSC_after_FIR function creates default contrasts for each
% condition of interest (i.e., Condition > Baseline)
tmfc.ROI_set(ROI_set_number).contrasts.BSC_after_FIR = contrasts;
% Define new contrast:
tmfc.ROI_set(ROI_set_number).contrasts.BSC_after_FIR(3).title = 'TaskA_vs_TaskB';
tmfc.ROI_set(ROI_set_number).contrasts.BSC_after_FIR(4).title = 'TaskB_vs_TaskA';
tmfc.ROI_set(ROI_set_number).contrasts.BSC_after_FIR(3).weights = [1 -1];
tmfc.ROI_set(ROI_set_number).contrasts.BSC_after_FIR(4).weights = [-1 1];
% Calculate new contrast
type = 4; % BSC-LSS after FIR
contrast_number = [3,4]; % Calculate contrast #3 and #4
[sub_check] = tmfc_ROI_to_ROI_contrast(tmfc,type,contrast_number,ROI_set_number);
[sub_check] = tmfc_seed_to_voxel_contrast(tmfc,type,contrast_number,ROI_set_number);
% Load BSC-LSS (after FIR) matrices for the 'TaskA_vs_TaskB' contrast (contrast # 3)
clear M marices conval_1 thresholded_1
for i = 1:data.N
M(i).paths = struct2array(load(fullfile(tmfc.project_path,'ROI_sets',tmfc.ROI_set(ROI_set_number).set_name,'BSC_LSS_after_FIR','ROI_to_ROI',...
['Subject_' num2str(i,'%04.f') '_Contrast_0003_[TaskA_vs_TaskB].mat'])));
end
matrices = cat(3,M(:).paths);
% Perform one-sample t-test (two-sided, FDR-correction)
contrast = 1; % A > B effect
[thresholded_1,pval,tval,conval_1] = tmfc_ttest(matrices,contrast,alpha,correction);
contrast = -1; % B > A effect
[thresholded_2] = tmfc_ttest(matrices,contrast,alpha,correction);
% Plot BSC-LSS (after FIR) results
f2 = figure(2); f2.Position = [382,422,1063,299];
try
sgtitle('BSC-LSS (after FIR task regression) results');
catch
suptitle('BSC-LSS (after FIR task regression) results');
end
subplot(1,3,1); imagesc(conval_1); title('Group mean'); axis square; colorbar; caxis(tmfc_axis(conval_1,1));
subplot(1,3,2); imagesc(thresholded_1); title('A>B (pFDR<0.001)'); axis square; colorbar;
subplot(1,3,3); imagesc(thresholded_2); title('B>A (pFDR<0.001)'); axis square; colorbar;
colormap(subplot(1,3,2),'parula')
colormap(subplot(1,3,3),'parula')
colormap(subplot(1,3,1),'redblue')
set(findall(gcf,'-property','FontSize'),'FontSize',16)
clear type contrasts contrast_number
%% BGFC
% Calculate background functional connectivity (BGFC)
[sub_check] = tmfc_BGFC(tmfc,ROI_set_number,start_sub);
%% gPPI
% Define conditions of interest
[conditions] = tmfc_gPPI_GUI(tmfc.subjects(1).path);
tmfc.ROI_set(ROI_set_number).gPPI.conditions = conditions;
clear conditions
% VOI extraction
[sub_check] = tmfc_VOI(tmfc,ROI_set_number,start_sub);
% PPI calculation
[sub_check] = tmfc_PPI(tmfc,ROI_set_number,start_sub);
% gPPI calculation
[sub_check,contrasts] = tmfc_gPPI(tmfc,ROI_set_number,start_sub);
% Update contrasts info
% The tmfc_gPPI function creates default contrasts for each
% condition of interest (i.e., Condition > Baseline)
tmfc.ROI_set(ROI_set_number).contrasts.gPPI = contrasts;
% Define new contrasts:
tmfc.ROI_set(ROI_set_number).contrasts.gPPI(3).title = 'TaskA_vs_TaskB';
tmfc.ROI_set(ROI_set_number).contrasts.gPPI(4).title = 'TaskB_vs_TaskA';
tmfc.ROI_set(ROI_set_number).contrasts.gPPI(3).weights = [1 -1];
tmfc.ROI_set(ROI_set_number).contrasts.gPPI(4).weights = [-1 1];
% Calculate new contrasts
type = 1; % gPPI
contrast_number = [3,4]; % Calculate contrasts #3 and #4
[sub_check] = tmfc_ROI_to_ROI_contrast(tmfc,type,contrast_number,ROI_set_number);
[sub_check] = tmfc_seed_to_voxel_contrast(tmfc,type,contrast_number,ROI_set_number);
% Load gPPI matrices for the 'TaskA_vs_TaskB' contrast (contrast # 3)
clear M marices conval_1 thresholded_1
for i = 1:data.N
M(i).paths = struct2array(load(fullfile(tmfc.project_path,'ROI_sets',tmfc.ROI_set(ROI_set_number).set_name,'gPPI','ROI_to_ROI','symmetrical',...
['Subject_' num2str(i,'%04.f') '_Contrast_0003_[TaskA_vs_TaskB].mat'])));
end
matrices = cat(3,M(:).paths);
% Perform one-sample t-test (two-sided, FDR-correction)
contrast = 1; % A > B effect
[thresholded_1,pval,tval,conval_1] = tmfc_ttest(matrices,contrast,alpha,correction);
contrast = -1; % B > A effect
[thresholded_2] = tmfc_ttest(matrices,contrast,alpha,correction);
% Plot gPPI results
f3 = figure(3); f3.Position = [382,422,1063,299];
try
sgtitle('gPPI results');
catch
suptitle('gPPI results');
end
subplot(1,3,1); imagesc(conval_1); title('Group mean'); axis square; colorbar; caxis(tmfc_axis(conval_1,1));
subplot(1,3,2); imagesc(thresholded_1); title('A>B (pFDR<0.001)'); axis square; colorbar;
subplot(1,3,3); imagesc(thresholded_2); title('B>A (pFDR<0.001)'); axis square; colorbar;
colormap(subplot(1,3,2),'parula')
colormap(subplot(1,3,3),'parula')
colormap(subplot(1,3,1),'redblue')
set(findall(gcf,'-property','FontSize'),'FontSize',16)
clear type contrasts contrast_number
%% gPPI-FIR (gPPI model with psychological regressors defined by FIR functions)
% Define FIR parameters for gPPI-FIR
tmfc.ROI_set(ROI_set_number).gPPI_FIR.window = 24; % FIR window length in [s]
tmfc.ROI_set(ROI_set_number).gPPI_FIR.bins = 24; % Number of FIR time bins
% gPPI-FIR calculation
[sub_check,contrasts] = tmfc_gPPI_FIR(tmfc,ROI_set_number,start_sub);
% Update contrasts info
% The tmfc_gPPI_FIR function creates default contrasts for each
% condition of interest (i.e., Condition > Baseline)
tmfc.ROI_set(ROI_set_number).contrasts.gPPI_FIR = contrasts;
% Define new contrasts:
tmfc.ROI_set(ROI_set_number).contrasts.gPPI_FIR(3).title = 'TaskA_vs_TaskB';
tmfc.ROI_set(ROI_set_number).contrasts.gPPI_FIR(4).title = 'TaskB_vs_TaskA';
tmfc.ROI_set(ROI_set_number).contrasts.gPPI_FIR(3).weights = [1 -1];
tmfc.ROI_set(ROI_set_number).contrasts.gPPI_FIR(4).weights = [-1 1];
% Calculate new contrasts
type = 2; % gPPI-FIR
contrast_number = [3,4]; % Calculate contrasts #3 and #4
[sub_check] = tmfc_ROI_to_ROI_contrast(tmfc,type,contrast_number,ROI_set_number);
[sub_check] = tmfc_seed_to_voxel_contrast(tmfc,type,contrast_number,ROI_set_number);
% Load gPPI-FIR matrices for the 'TaskA_vs_TaskB' contrast (contrast # 3)
clear M marices conval_1 thresholded_1
for i = 1:data.N
M(i).paths = struct2array(load(fullfile(tmfc.project_path,'ROI_sets',tmfc.ROI_set(ROI_set_number).set_name,'gPPI_FIR','ROI_to_ROI','symmetrical',...
['Subject_' num2str(i,'%04.f') '_Contrast_0003_[TaskA_vs_TaskB].mat'])));
end
matrices = cat(3,M(:).paths);
% Perform one-sample t-test (two-sided, FDR-correction)
contrast = 1; % A > B effect
[thresholded_1,pval,tval,conval_1] = tmfc_ttest(matrices,contrast,alpha,correction);
contrast = -1; % B > A effect
[thresholded_2] = tmfc_ttest(matrices,contrast,alpha,correction);
% Plot gPPI-FIR results
f4 = figure(4); f4.Position = [382,422,1063,299];
try
sgtitle('gPPI-FIR results');
catch
suptitle('gPPI-FIR results');
end
subplot(1,3,1); imagesc(conval_1); title('Group mean'); axis square; colorbar; caxis(tmfc_axis(conval_1,1));
subplot(1,3,2); imagesc(thresholded_1); title('A>B (pFDR<0.001)'); axis square; colorbar;
subplot(1,3,3); imagesc(thresholded_2); title('B>A (pFDR<0.001)'); axis square; colorbar;
colormap(subplot(1,3,2),'parula')
colormap(subplot(1,3,3),'parula')
colormap(subplot(1,3,1),'redblue')
set(findall(gcf,'-property','FontSize'),'FontSize',16)
clear type contrasts contrast_number
%% Save TMFC project *.mat file
save(fullfile(data.stat_path,'TMFC_project.mat'),'tmfc');