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| = MEG visual tutorial: Single subject = | = MEG visual tutorial: Single subject (BIDS) = |
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| The aim of this tutorial is to reproduce in the Brainstorm environment the analysis described in the SPM tutorial "Multimodal, Multisubject data fusion". The data processed here consists in simulateneous MEG/EEG recordings of 16 subjects performing simple visual task on a large number of famous, unfamiliar and scrambled faces. The analysis is split in two tutorial pages: the present tutorial describes the detailed analysis of one single subject and another one that the describes the batch processing and group analysis of the 16 subjects. Note that the operations used here are not detailed, the goal of this tutorial is not to teach Brainstorm to a new inexperienced user. For in depth explanations of the interface and the theory, please refer to the introduction tutorials. |
The aim of this tutorial is to reproduce in the Brainstorm environment the analysis described in the SPM tutorial "[[ftp://ftp.mrc-cbu.cam.ac.uk/personal/rik.henson/wakemandg_hensonrn/Publications/SPM12_manual_chapter.pdf|Multimodal, Multisubject data fusion]]". The data processed here consists of simultaneous MEG/EEG recordings from 16 participants performing a simple visual recognition task from presentations of famous, unfamiliar and scrambled faces. The analysis is split in two tutorial pages: the present tutorial describes the detailed analysis of one single subject; the second tutorial describes batch processing and [[Tutorials/VisualGroup|group analysis of all 16 participants]]. Note that the operations used here are not detailed, the goal of this tutorial is not to introduce Brainstorm to new users. For in-depth explanations of the interface and theoretical foundations, please refer to the [[http://neuroimage.usc.edu/brainstorm/Tutorials#Get_started|introduction tutorials]]. |
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| These data are provided freely for research purposes only (as part of their Award of the BioMag2010 Data Competition). If you wish to publish any of these data, please acknowledge Daniel Wakeman and Richard Henson. The best single reference is: "Wakeman, D. G. & Henson, R. N. A multi-subject, multi-modal human neuroimaging dataset. Sci. Data 2:150001 doi: 10.1038/sdata.2015.1 (2015)." Any questions, please contact: rik.henson@mrc-cbu.cam.ac.uk |
This dataset was obtained from the OpenfMRI project (http://www.openfmri.org), accession #ds117. It is made available under the Creative Commons Attribution 4.0 International Public License. Please cite the following reference if you use these data: <<BR>>Wakeman DG, Henson RN, [[http://www.nature.com/articles/sdata20151|A multi-subject, multi-modal human neuroimaging dataset]], Scientific Data (2015) Any questions regarding the data, please contact: rik.henson@mrc-cbu.cam.ac.uk |
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| * 16 subjects * 6 runs (sessions) of approximately 10mins for each subject |
* 16 subjects (the original version of the dataset included 19 subjects, but 3 were excluded from the group analysis for [[http://neuroimage.usc.edu/brainstorm/Tutorials/VisualSingleOrig%23Bad%5Fsubjects|various reasons]]) * 6 acquisition runs (aka sessions) of approximately 10mins for each subject |
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| * The subject has to judge the left-right symmetry of each stimulus * Total of nearly 300 trials in total for each of the 3 conditions |
* Participants had to judge the left-right symmetry of each stimulus * Total of nearly 300 trials for each of the 3 conditions |
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| * MEG data have been "cleaned" using Signal-Space Separation as implemented in MaxFilter 2.1. * A Polhemus digitizer was used to digitise three fiducial points and a large number of other points across the scalp, which can be used to coregister the M/EEG data with the structural MRI image. |
* MEG data have been "cleaned" using Signal-Space Separation as implemented in MaxFilter 2.2. * A Polhemus device was used to digitize three fiducial points and a large number of other points across the scalp, which can be used to coregister the M/EEG data with the structural MRI image. * Stimulation triggers: The triggers related with the visual presentation are saved in the STI101 channel, with the following event codes (bit 3 = face, bit 4 = unfamiliar, bit 5 = scrambled): * Famous faces: 5 (00101), 6 (00110), 7 (00111) * Unfamiliar faces: 13 (01101), 14 (01110), 15 (01111) * Scrambled images: 17 (10001), 18 (10010), 19 (10011) * Delays between the trigger in STI101 and the actual presentation of stimulus: '''34.5ms''' * The data distribution includes MEG noise recordings acquired around the dates of the experiment, processed with MaxFilter 2.2 in the same way as the experimental data. |
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| * MRI data acquired on a 3T Siemens TIM Trio: 1x1x1mm T1-weighted structural MRI. * The face was removed from the strucural images for anonymization purposes. * Processed with FreeSurfer 5.3. |
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| * '''Requirements''': You have already followed all the introduction tutorials and you have a working copy of Brainstorm installed on your computer. * The data is hosted on this FTP site (use an FTP client such as FileZilla, not your web browser): <<BR>>ftp://ftp.mrc-cbu.cam.ac.uk/personal/rik.henson/wakemandg_hensonrn/ * Download only the following folders (about 75Gb): * EmptyRoom: * Publications: * SubXX/T1: * SubXX/MEEG: * README.TXT: * License and dataset description * Go to the Download page of the Brainstorm website, and download the file: sample_group.zip |
* First, make sure you have enough space on your hard drive, at least '''350Gb''': * Raw files: '''100Gb''' * Processed files: '''250Gb''' * The data is hosted on the OpenfMRI website: https://openfmri.org/dataset/ds000117/ * Download all the files available from this website (approximately 160Gb):<<BR>>'''ds117_metadata.tgz''', '''ds117_sub001_raw.tgz''', ..., '''ds117_sub019_raw.tgz''' * Unzip all the .tgz files in the same folder. * The FreeSurfer segmentations of the T1 images are not part of the OpenfMRI distribution. You can either process them by yourself, or download the result of the segmentation from the Brainstorm website. <<BR>>Go to the [[http://neuroimage.usc.edu/bst/download.php|Download]] page, and download the file: '''sample_group_freesurfer.zip'''<<BR>>Unzip this file in the same folder as the other files. * We will use the following files from this distribution: * '''/anatomy/subXXX/''': Segmentation folders generated with FreeSurfer. * '''/emptyroom/090707_raw_st.fif''': MEG empty room measurements, processed with MaxFilter. * '''/ds117/subXXX/MEG/*_sss.fif''': MEG and EEG recordings, processed with MaxFilter. * '''/README''': License and dataset description. * Reminder: Do not save the downloaded files in the Brainstorm folders (program or database folders). * Start Brainstorm (Matlab scripts or stand-alone version). For help, see the [[Installation]] page. * Select the menu File > Create new protocol. Name it "'''TutorialVisual'''" and select the options: * "'''No, use individual anatomy'''", * "'''No, use one channel file per condition'''". == Import the anatomy == This page explains how to import and process subject '''#002''' only. Subject #001 was not the best example because it will be later excluded from the EEG group analysis (incorrect electrodes positions). * Switch to the "anatomy" view. * Right-click on the TutorialVisual folder > New subject > '''sub002''' * Leave the default options you defined for the protocol. * Right-click on the subject node > Import anatomy folder: * Set the file format: "FreeSurfer folder" * Select the folder: '''anatomy/freesurfer/sub002''' (from sample_group_freesurfer.zip) * Number of vertices of the cortex surface: 15000 (default value) * The two sets of fiducials we usually have to define interactively are here automatically set. * '''NAS/LPA/RPA''': The file Anatomy/Sub01/fiducials.m contains the definition of the nasion, left and right ears. The anatomical points used by the authors are the same as the ones we recommend in the Brainstorm [[CoordinateSystems|coordinates systems page]]. * '''AC/PC/IH''': Automatically identified using the SPM affine registration with an MNI template. * If you want to double-check that all these points were correctly marked after importing the anatomy, right-click on the MRI > Edit MRI. * At the end of the process, make sure that the file "cortex_15000V" is selected (downsampled pial surface, that will be used for the source estimation). If it is not, double-click on it to select it as the default cortex surface. Do not worry about the big holes in the head surface, parts of MRI have been remove voluntarily for anonymization purposes.<<BR>><<BR>> {{attachment:anatomy_import.gif||width="613",height="384"}} * All the anatomical atlases [[Tutorials/LabelFreeSurfer|generated by FreeSurfer]] were automatically imported: the cortical atlases (Desikan-Killiany, Mindboggle, Destrieux, Brodmann) and the sub-cortical regions (ASEG atlas). <<BR>><<BR>> {{attachment:anatomy_atlas.gif||width="550",height="211"}} == Access the recordings == === Link the recordings === We need to attach the continuous .fif files containing the recordings to the database. * Switch to the "functional data" view. * Right-click on the subject folder > '''Review raw file'''. * Select the file format: "'''MEG/EEG: Neuromag FIFF (*.fif)'''" * Select the first file in the MEG folder for subject 002: '''sub002/MEEG/run_01_sss.fif''' <<BR>><<BR>> {{attachment:review_raw.gif||width="542",height="202"}} * Events:''' Ignore'''. We will read the stimulus triggers later.<<BR>><<BR>> {{attachment:review_ignore.gif||width="330",height="186"}} * Refine registration now? '''NO''' <<BR>>The head points that are available in the FIF files contain all the points that were digitized during the MEG acquisition, including the ones corresponding to the parts of the face that have been removed from the MRI. If we run the fitting algorithm, all the points around the nose will not match any close points on the head surface, leading to a wrong result. We will first remove the face points and then run the registration manually. === Channel classification === A few non-EEG channels are mixed in with the EEG channels, we need to change this before applying any operation on the EEG channels. * Right-click on the channel file > '''Edit channel file'''. Double-click on a cell to edit it. * Change the type of '''EEG062''' to '''EOG '''(electrooculogram). * Change the type of '''EEG063 '''to '''ECG '''(electrocardiogram). * Change the type of '''EEG061''' and '''EEG064''' to '''NOSIG'''. Close the window and save the modifications. <<BR>><<BR>> {{attachment:channel_edit.gif||width="561",height="252"}} === MRI registration === At this point, the registration MEG/MRI is based only on the three anatomical landmarks NAS/LPA/RPA. All the MRI scans were anonymized (defaced) and for some subjects the nasion could not be defined properly. We will try to refine this registration using the additional head points that were digitized (only the points above the nasion). * Right-click on the channel file > '''Digitized head points > Remove points below nasion'''.<<BR>><<BR>> {{attachment:channel_remove.gif||width="329",height="194"}} * Right-click on the channel file > '''MRI registration > Refine using head points'''.<<BR>><<BR>> {{attachment:channel_refine.gif||width="294",height="173"}} * MEG/MRI registration, before (left) and after (right) this automatic registration procedure: <<BR>><<BR>> {{attachment:registration.gif||width="236",height="209"}} {{attachment:registration_final.gif||width="237",height="208"}} * Right-click on the channel file > MRI registration > EEG: Edit...<<BR>>Click on ['''Project electrodes on surface'''], then close the figure to save the modifications.<<BR>><<BR>> {{attachment:channel_project.gif||width="477",height="207"}} === Read stimulus triggers === We need to read the stimulus markers from the STI channels. The following tasks can be done in an interactive way with menus in the Record tab, as in the introduction tutorials. We will illustrate here how to do this with the pipeline editor, it will be easier to batch it for all the runs and all the subjects. * In Process1, select the "Link to raw file", click on [Run]. * Select process '''Events > Read from channel''', Channel: '''STI101''', Detection mode: '''Bit'''.<<BR>>Do not execute the process, we will add other processes to classify the markers.<<BR>><<BR>> {{attachment:raw_read_events.gif||width="499",height="290"}} * We want to create three categories of events, based on their numerical codes: * '''Famous faces''': 5 (00101), 6 (00110), 7 (00111) => Bit 3 only * '''Unfamiliar faces''': 13 (01101), 14 (01110), 15 (01111) => Bit 3 and 4 * '''Scrambled images''': 17 (10001), 18 (10010), 19 (10011) => Bit 5 only * We will start by creating the category "Unfamiliar" (combination of events "3" and "4") and remove the remove the initial events. Then we just have to rename the remaining "3" in "Famous", and all the "5" in "Scrambled". * Add process '''Events > Group by name''': "'''Unfamiliar=3,4'''", Delay=0, '''Delete original events''' * Add process '''Events > Rename event''': 3 => Famous * Add process '''Events > Rename event''': 5 => Scrambled <<BR>><<BR>> {{attachment:events_merge.gif||width="532",height="402"}} * Add process '''Events > Add time offset''' to correct for the presentation delays:<<BR>>Event names: "'''Famous, Unfamiliar, Scrambled'''", Time offset = '''34.5ms'''<<BR>><<BR>> {{attachment:events_offset.gif||width="348",height="355"}} * Finally run the script. Double-click on the recordings to make sure the labels were detected correctly. You can delete the unwanted events that are left in the recordings (1,2,9,13): <<BR>><<BR>> {{attachment:events_display.gif||width="595",height="194"}} == Pre-processing == === Spectral evaluation === * Keep the "Link to raw file" in Process1. * Run process '''Frequency > Power spectrum density (Welch)''' with the options illustrated below. <<BR>><<BR>> {{attachment:psd_process.gif||width="669",height="314"}} * Right-click on the PSD file > Power spectrum. <<BR>><<BR>> {{attachment:psd_plot.gif||width="408",height="235"}} * The MEG sensors look awful, because of one small segment of data located around 248s. Open the MEG recordings and scroll to 248s (just before the first Unfamiliar event). <<BR>><<BR>> {{attachment:psd_error.gif||width="527",height="183"}} * In these recordings, the continuous head tracking was activated, but it starts only at the time of the stimulation (248s) while the acquisition of the data starts 20s before (226s). The first 20s do not have head localization coils (HPI) coils activity and are not corrected by MaxFilter. After 248s, the HPI coils are on, and MaxFilter filters them out. The transition between the two states is not smooth and creates important distortions in the spectral domain. For a proper evaluation of the recordings, we should '''compute the PSD only after the HPI coils are turned on'''. * Run process '''Events > Detect cHPI activity (Elekta)'''. This detects the changes in the cHPI activity from channel STI201 and marks all the data without head localization as bad. <<BR>><<BR>> {{attachment:psd_badsegment.gif||width="503",height="234"}} * Re-run the process '''Frequency > Power spectrum density (Welch)'''. All the bad segments are excluded from the computation, therefore the PSD is now estimated only with the data '''after 248s'''. <<BR>><<BR>> {{attachment:psd_fix.gif||width="668",height="283"}} * Observations: * Three groups of sensors, from top to bottom: EEG, MEG gradiometers, MEG magnetometers. * Power lines: '''50 '''Hz and harmonics * Alpha peak around 10 Hz * Artifacts due to Elekta electronics (HPI coils): '''293'''Hz, '''307'''Hz, '''314'''Hz, '''321'''Hz, '''328'''Hz. * Peak from unknown source at '''103.4Hz''' in the MEG only. * Suspected bad EEG channels: '''EEG016''' * Close all the windows. === Remove line noise === * Keep the "Link to raw file" in Process1. * Select process '''Pre-process > Notch filter''' to remove the line noise (50-200Hz).<<BR>>Add the process '''Frequency > Power spectrum density (Welch)'''. <<BR>><<BR>> {{attachment:notch_process.gif||width="562",height="262"}} * Double-click on the PSD for the new continuous file to evaluate the quality of the correction. <<BR>><<BR>> {{attachment:notch_result.gif||width="566",height="215"}} * Close all the windows (use the [X] button at the top-right corner of the Brainstorm window). === EEG reference and bad channels === * Right-click on link to the processed file ("Raw | notch(50Hz ...") > '''EEG > Display time series'''. * Select channel '''EEG016''' and mark it as '''bad''' (using the popup menu or pressing the Delete key). <<BR>><<BR>> {{attachment:channel_bad.gif||width="587",height="214"}} * In the Record tab, menu '''Artifacts > Re-reference EEG''' > "AVERAGE". <<BR>><<BR>> {{attachment:channel_ref.gif||width="535",height="270"}} * At the end, the window "select active projectors" is open to show the new re-referencing projector. Just close this window. To get it back, use the menu Artifacts > Select active projectors. == Artifact detection == === Heartbeats: Detection === * Empty the Process1 list (right-click > Clear list). * Drag and drop the continuous processed file ("Raw | notch(50Hz...)") to the Process1 list. * Run process''' Events > Detect heartbeats''': Channel name='''EEG063''', All file, Event name=cardiac <<BR>><<BR>> {{attachment:detect_cardiac.gif||width="310",height="230"}} === Eye blinks: Detection === * In many of the other tutorials, we detect the blinks and remove them with SSP. In this experiment, we are particularly interested in the subject's response to seeing the stimulus. Therefore we will exclude from the analysis all the recordings contaminated with blinks or other eye movements. * Run process '''Artifacts > Detect events above threshold''': <<BR>>Event name='''blink_BAD''', Channel='''EEG062''', All file, Maximum threshold='''100''', Threshold units='''uV''', Filter='''[0.30,20.00]Hz''', '''Use absolute value of signal'''.<<BR>><<BR>> {{attachment:detect_blinks.gif||width="285",height="455"}} * Inspect visually the two new cateogries of events: cardiac and blink_BAD.<<BR>><<BR>> {{attachment:detect_display.gif||width="655",height="237"}} * Close all the windows (using the [X] button). === Heartbeats: Correction with SSP === * Keep the "Raw | notch" file selected in Process1. * Select process '''Artifacts > SSP: Heartbeats''' > Sensor type: '''MEG MAG''' * Add process '''Artifacts > SSP: Heartbeats''' > Sensor type: '''MEG GRAD''' - Run the execution <<BR>><<BR>> {{attachment:ssp_ecg_process.gif||width="293",height="225"}} * Double-click on the continuous file to show all the MEG sensors. <<BR>>In the Record tab, select sensors "Left-temporal". * Menu Artifacts > Select active projectors. * In category '''cardiac/MEG MAG''': Select '''component #1''' and view topography. * In category '''cardiac/MEG GRAD''': Select '''component #1 '''and view topography. <<BR>><<BR>> {{attachment:ssp_ecg_topo.gif||width="604",height="175"}} * Make sure that selecting the two components removes the cardiac artifact. Then click '''[Save]'''. === Additional bad segments === * Process1>Run: Select the process "'''Events > Detect other artifacts'''". This should be done separately for MEG and EEG to avoid confusion about which sensors are involved in the artifact. <<BR>><<BR>> {{attachment:detect_other.gif||width="486",height="253"}} * Display the MEG sensors. Review the segments that were tagged as artifact, determine if each event represents an artifact and then mark the time of the artifact as BAD. This can be done by selecting the time window around the artifact, then right-click > '''Reject time segment'''. Note that this detection process marks 1-second segments but the artifact can be shorter.<<BR>><<BR>> {{attachment:artifacts_mark_bad.png||width="640"}} * Once all the events in the two categories are reviewed and bad segments are marked, the two categories (1-7Hz and 40-240Hz) can be deleted. * Do this detection and review again for the EEG. === SQUID jumps === MEG signals recorded with Elekta-Neuromag systems frequently contain SQUID jumps ([[http://neuroimage.usc.edu/brainstorm/Tutorials/BadSegments?highlight=(squid)#Elekta-Neuromag_SQUID_jumps|more information]]). These sharp steps followed by a change of baseline value are easy to identify visually but more complicated to detect automatically. The process "Detect other artifacts" usually detects most of them in the category "1-7Hz". If you observe that some are skipped, you can try re-running it with a higher sensitivity. It is important to review all the sensors and all the time in each run to be sure these events are marked as bad segments. . {{attachment:detect_jumps.gif||width="547",height="214"}} == Epoching and averaging == === Import epochs === * Keep the "Raw | notch" file selected in Process1. * Select process: '''Import recordings > Import MEG/EEG: Events''' (do not run immediately)<<BR>>Event names "Famous, Unfamiliar, Scrambled", All file, Epoch time=[-500,1200]ms * Add process: '''Pre-process > Remove DC offset''': Baseline=[-500,-0.9]ms - Run execution.<<BR>><<BR>> {{attachment:import_epochs.gif||width="647",height="399"}} === Average by run === * In Process1, select all the imported trials. * Run process: '''Average > Average files''': '''By trial groups (folder average)''' <<BR>><<BR>> {{attachment:average_process.gif||width="478",height="504"}} === Review EEG ERP === * EEG evoked response (famous, scrambled, unfamiliar): <<BR>><<BR>> {{attachment:average_topo.gif||width="684",height="392"}} * Open the [[Tutorials/ChannelClusters|Cluster tab]] and create a cluster with the channel '''EEG065''' (button [NEW IND]).<<BR>><<BR>> {{attachment:cluster_create.gif||width="569",height="166"}} * Select the cluster, select the three average files, right-click > '''Clusters time series''' (Overlay:Files). <<BR>><<BR>> {{attachment:cluster_display.gif||width="658",height="220"}} * Basic observations for EEG065 (right parieto-occipital electrode): * Around 170ms (N170): greater negative deflection for Famous than Scrambled faces. * After 250ms: difference between Famous and Unfamiliar faces. == Source estimation == === MEG noise covariance: Empty room recordings === The minimum norm model we will use next to estimate the source activity can be improved by modeling the the noise contaminating the data. The section shows how to [[Tutorials/NoiseCovariance|estimate the noise covariance]] in different ways for EEG and MEG. For the MEG recordings we will use the empty room measurements we have, and for the EEG we will compute it from the pre-stimulus baselines we have in all the imported epochs. * Create a new subject: '''emptyroom''' * Right-click on the new subject > '''Review raw file'''.<<BR>>Select file: '''sample_group/emptyroom/090707_raw_st.fif '''<<BR>>Do not apply default transformation, Ignore event channel.<<BR>><<BR>> {{attachment:noise_review.gif||width="506",height="164"}} * Select this new file in Process1 and run process '''Pre-process > Notch filter''': '''50 100 150 200Hz'''. When using empty room measurements to compute the noise covariance, they must be processed exactly in the same way as the other recordings. <<BR>><<BR>> {{attachment:noise_notch.gif||width="436",height="225"}} * Right-click on the filtered noise recordings > '''Noise covariance > Compute from recordings''': <<BR>><<BR>> {{attachment:noise_compute.gif||width="649",height="240"}} * Right-click on the '''Noise covariance > Copy to other subjects '''<<BR>><<BR>> {{attachment:noise_copy.gif||width="273",height="126"}} === EEG noise covariance: Pre-stimulus baseline === * In folder sub002/run_01_sss_notch, select all the imported the imported trials, right-click > '''Noise covariance > Compute from recordings''', Time=[-500,-0.9]ms, '''EEG only''', '''Merge'''. {{attachment:noise_eeg.gif||width="650",height="280"}} * This computes the noise covariance only for EEG, and combines it with the existing MEG information. {{attachment:noise_display.gif||width="375",height="223"}} === BEM layers === We will compute a [[Tutorials/TutBem|BEM forward model]] to estimate the brain sources from the EEG recordings. For this, we need some layers defining the separation between the different tissues of the head (scalp, inner skull, outer skull). * Go to the anatomy view (first button above the database explorer). * Right-click on the subject folder > '''Generate BEM surfaces''': The number of vertices to use for each layer depends on your computing power and the accuracy you expect. You can try for instance with '''1082 vertices '''(scalp) and '''642 vertices '''(outer skull and inner skull). <<BR>><<BR>> {{attachment:anatomy_bem.gif||width="603",height="232"}} === Forward model: EEG and MEG === * Go back to the functional view (second button above the database explorer). * Model used: Overlapping spheres for MEG, OpenMEEG BEM for EEG ([[Tutorials/HeadModel|more information]]). * In folder sub002/run_01_sss_notch, right-click on the channel file > '''Compute head model'''.<<BR>>Keep all the default options . Expect this to take a while...<<BR>><<BR>> {{attachment:headmodel_compute.gif||width="643",height="313"}} === Inverse model: Minimum norm estimates === * Right-click on the new head model > '''Compute sources [2016]''': '''MEG MAG + GRAD''' (default options) <<BR>><<BR>> {{attachment:sources_compute.gif||width="626",height="406"}} * Right-click on the new head model > '''Compute sources [2016]''': '''EEG''' (default bad channels). * At the end we have two inverse operators, that are shared for all the files of the run (single trials and averages). If we wanted to look at the run-level source averages, we could normalize the source maps with a Z-score wrt baseline. In this tutorial, we will first average across runs and normalize the subject-level averages. This will be done in the next tutorial (group analysis).<<BR>><<BR>> {{attachment:sources_files.gif||width="243",height="147"}} == Time-frequency analysis == We will compute the time-frequency decomposition of each trial using Morlet wavelets, and average the power of the Morlet coefficients for each condition and each run separately. We will restrict the computation to the MEG magnetometers and the EEG channels to limit the computation time and disk usage. * In Process1, select the imported trials "Famous" for run#01. * Run process '''Frequency > Time-frequency (Morlet wavelets)''': Sensor types=MEG MAG,EEG <<BR>>Not normalized, Frequency='''Log(6:20:60)''', Measure=Power, '''Save average''' <<BR>><<BR>> {{attachment:tf_process.gif||width="628",height="479"}} * Double-click on the file to display it. In the Display tab, select the option "Hide edge effects" to exclude form the display all the values that could not be estimated in a reliable way. Let's extract only the good values from this file (-200ms to +900ms). <<BR>><<BR>> {{attachment:tf_display.gif||width="270",height="155"}} * In Process1, select the time-frequency file. * Run process '''Extract > Extract time''': Time window='''[-200, 900]ms''', '''Overwrite input files''' <<BR>><<BR>> {{attachment:tf_cut.gif||width="411",height="197"}} * Display the file again, observe that all the possibly bad values are gone. <<BR>><<BR>> {{attachment:tf_cutdisplay.gif||width="410",height="178"}} * You can display all the sensors at once (MEG MAG or EEG): right-click > 2D Layout (maps).<<BR>><<BR>> {{attachment:tf_2dlayout.gif||width="653",height="270"}} * Repeat these steps for other conditions (Scrambled and Unfamiliar) and the other runs (2-6). There is no way with this process to compute all the averages at once, as we did with the process "Average files". This will be easier to run from a script. * If we wanted to look at the run-level source averages, we could normalize these time-frequency maps. In this tutorial, we will first average across runs and normalize the subject-level averages. This will be done in the next tutorial (group analysis). == Scripting == We have now all the files we need for the group analysis ([[Tutorials/VisualGroup|next tutorial]]). We need to repeat the same operations for all the runs and all the subjects. Some of these steps are '''fully automatic''' and take a lot of time (filtering, computing the forward model), they should be executed from a script. However, we recommend you always '''review manually''' some of the pre-processing steps (selection of the bad segments and bad channels, SSP/ICA components). Do not trust blindly any fully automated cleaning procedure. For the strict reproducibility of this analysis, we provide a script that processes all the 19 subjects: '''brainstorm3/toolbox/script/tutorial_visual_single.m''' (execution time: 10-30 hours)<<BR>>Report for the first subject: [[http://neuroimage.usc.edu/bst/examples/report_TutorialVisual_sub001.html|report_TutorialVisual_sub001.html]] <<HTML(<div style="border:1px solid black; background-color:#EEEEFF; width:720px; height:500px; overflow:scroll; padding:10px; font-family: Consolas,Menlo,Monaco,Lucida Console,Liberation Mono,DejaVu Sans Mono,Bitstream Vera Sans Mono,Courier New,monospace,sans-serif; font-size: 13px; white-space: pre;">)>><<EmbedContent("http://neuroimage.usc.edu/bst/viewcode.php?f=tutorial_visual_single.m")>><<HTML(</div >)>> <<BR>>You should note that this is not the result of a fully automated procedure. The bad channels were identified manually and are defined for each run in the script. The bad segments were detected automatically, confirmed manually for each run and saved in external files distributed with the Brainstorm package sample_group_freesurfer.zip (sample_group/brainstorm/bad_segments/*.mat). All the process calls (bst_process) were generated automatically using with the script generator (menu '''Generate .m script''' in the pipeline editor). Everything else was added manually (loops, bad channels, file copies). == Bad subjects == After evaluating the results for the 19 subjects, 3 subjects were excluded from the analysis: * '''sub001''': Error during the digitization of the EEG electrodes with the Polhemus (the same electrode was clicked twice). This impacts only the EEG, this subject could be used for MEG analysis. <<BR>><<BR>> {{attachment:bad_sub001.gif||width="274",height="158"}} * '''sub005''': Too many blinks or other eye movements. <<BR>> <<BR>> {{attachment:bad_sub005.gif||width="430",height="164"}} * '''sub016''': Too many blinks or other eye movements. <<BR>> <<BR>> {{attachment:bad_sub016.jpg||width="430",height="152"}} Make sure you don't include these subjects in the group analysis. <<EmbedContent("http://neuroimage.usc.edu/bst/get_prevnext.php?prev=&next=Tutorials/VisualGroup")>> |
MEG visual tutorial: Single subject (BIDS)
Authors: Francois Tadel, Elizabeth Bock.
The aim of this tutorial is to reproduce in the Brainstorm environment the analysis described in the SPM tutorial "Multimodal, Multisubject data fusion". The data processed here consists of simultaneous MEG/EEG recordings from 16 participants performing a simple visual recognition task from presentations of famous, unfamiliar and scrambled faces.
The analysis is split in two tutorial pages: the present tutorial describes the detailed analysis of one single subject; the second tutorial describes batch processing and group analysis of all 16 participants.
Note that the operations used here are not detailed, the goal of this tutorial is not to introduce Brainstorm to new users. For in-depth explanations of the interface and theoretical foundations, please refer to the introduction tutorials.
Contents
License
This dataset was obtained from the OpenfMRI project (http://www.openfmri.org), accession #ds117. It is made available under the Creative Commons Attribution 4.0 International Public License. Please cite the following reference if you use these data:
Wakeman DG, Henson RN, A multi-subject, multi-modal human neuroimaging dataset, Scientific Data (2015)
Any questions regarding the data, please contact: rik.henson@mrc-cbu.cam.ac.uk
Presentation of the experiment
Experiment
16 subjects (the original version of the dataset included 19 subjects, but 3 were excluded from the group analysis for various reasons)
- 6 acquisition runs (aka sessions) of approximately 10mins for each subject
- Presentation of series of images: familiar faces, unfamiliar faces, phase-scrambled faces
- Participants had to judge the left-right symmetry of each stimulus
- Total of nearly 300 trials for each of the 3 conditions
MEG acquisition
Acquisition at 1100Hz with an Elekta-Neuromag VectorView system (simultaneous MEG+EEG).
- Recorded channels (404):
- 102 magnetometers
- 204 planar gradiometers
- 70 EEG electrodes recorded with a nose reference.
MEG data have been "cleaned" using Signal-Space Separation as implemented in MaxFilter 2.2.
- A Polhemus device was used to digitize three fiducial points and a large number of other points across the scalp, which can be used to coregister the M/EEG data with the structural MRI image.
- Stimulation triggers: The triggers related with the visual presentation are saved in the STI101 channel, with the following event codes (bit 3 = face, bit 4 = unfamiliar, bit 5 = scrambled):
- Famous faces: 5 (00101), 6 (00110), 7 (00111)
- Unfamiliar faces: 13 (01101), 14 (01110), 15 (01111)
- Scrambled images: 17 (10001), 18 (10010), 19 (10011)
Delays between the trigger in STI101 and the actual presentation of stimulus: 34.5ms
The data distribution includes MEG noise recordings acquired around the dates of the experiment, processed with MaxFilter 2.2 in the same way as the experimental data.
Subject anatomy
- MRI data acquired on a 3T Siemens TIM Trio: 1x1x1mm T1-weighted structural MRI.
- The face was removed from the strucural images for anonymization purposes.
Processed with FreeSurfer 5.3.
Download and installation
First, make sure you have enough space on your hard drive, at least 350Gb:
Raw files: 100Gb
Processed files: 250Gb
The data is hosted on the OpenfMRI website: https://openfmri.org/dataset/ds000117/
Download all the files available from this website (approximately 160Gb):
ds117_metadata.tgz, ds117_sub001_raw.tgz, ..., ds117_sub019_raw.tgz- Unzip all the .tgz files in the same folder.
The FreeSurfer segmentations of the T1 images are not part of the OpenfMRI distribution. You can either process them by yourself, or download the result of the segmentation from the Brainstorm website.
Go to the Download page, and download the file: sample_group_freesurfer.zip
Unzip this file in the same folder as the other files.- We will use the following files from this distribution:
/anatomy/subXXX/: Segmentation folders generated with FreeSurfer.
/emptyroom/090707_raw_st.fif: MEG empty room measurements, processed with MaxFilter.
/ds117/subXXX/MEG/*_sss.fif: MEG and EEG recordings, processed with MaxFilter.
/README: License and dataset description.
- Reminder: Do not save the downloaded files in the Brainstorm folders (program or database folders).
Start Brainstorm (Matlab scripts or stand-alone version). For help, see the Installation page.
Select the menu File > Create new protocol. Name it "TutorialVisual" and select the options:
"No, use individual anatomy",
"No, use one channel file per condition".
Import the anatomy
This page explains how to import and process subject #002 only. Subject #001 was not the best example because it will be later excluded from the EEG group analysis (incorrect electrodes positions).
- Switch to the "anatomy" view.
Right-click on the TutorialVisual folder > New subject > sub002
- Leave the default options you defined for the protocol.
Right-click on the subject node > Import anatomy folder:
Set the file format: "FreeSurfer folder"
Select the folder: anatomy/freesurfer/sub002 (from sample_group_freesurfer.zip)
- Number of vertices of the cortex surface: 15000 (default value)
- The two sets of fiducials we usually have to define interactively are here automatically set.
NAS/LPA/RPA: The file Anatomy/Sub01/fiducials.m contains the definition of the nasion, left and right ears. The anatomical points used by the authors are the same as the ones we recommend in the Brainstorm coordinates systems page.
AC/PC/IH: Automatically identified using the SPM affine registration with an MNI template.
If you want to double-check that all these points were correctly marked after importing the anatomy, right-click on the MRI > Edit MRI.
At the end of the process, make sure that the file "cortex_15000V" is selected (downsampled pial surface, that will be used for the source estimation). If it is not, double-click on it to select it as the default cortex surface. Do not worry about the big holes in the head surface, parts of MRI have been remove voluntarily for anonymization purposes.
All the anatomical atlases generated by FreeSurfer were automatically imported: the cortical atlases (Desikan-Killiany, Mindboggle, Destrieux, Brodmann) and the sub-cortical regions (ASEG atlas).
Access the recordings
Link the recordings
We need to attach the continuous .fif files containing the recordings to the database.
- Switch to the "functional data" view.
Right-click on the subject folder > Review raw file.
Select the file format: "MEG/EEG: Neuromag FIFF (*.fif)"
Select the first file in the MEG folder for subject 002: sub002/MEEG/run_01_sss.fif
Events: Ignore. We will read the stimulus triggers later.
Refine registration now? NO
The head points that are available in the FIF files contain all the points that were digitized during the MEG acquisition, including the ones corresponding to the parts of the face that have been removed from the MRI. If we run the fitting algorithm, all the points around the nose will not match any close points on the head surface, leading to a wrong result. We will first remove the face points and then run the registration manually.
Channel classification
A few non-EEG channels are mixed in with the EEG channels, we need to change this before applying any operation on the EEG channels.
Right-click on the channel file > Edit channel file. Double-click on a cell to edit it.
Change the type of EEG062 to EOG (electrooculogram).
Change the type of EEG063 to ECG (electrocardiogram).
Change the type of EEG061 and EEG064 to NOSIG. Close the window and save the modifications.
MRI registration
At this point, the registration MEG/MRI is based only on the three anatomical landmarks NAS/LPA/RPA. All the MRI scans were anonymized (defaced) and for some subjects the nasion could not be defined properly. We will try to refine this registration using the additional head points that were digitized (only the points above the nasion).
Right-click on the channel file > Digitized head points > Remove points below nasion.
Right-click on the channel file > MRI registration > Refine using head points.
MEG/MRI registration, before (left) and after (right) this automatic registration procedure:
Right-click on the channel file > MRI registration > EEG: Edit...
Click on [Project electrodes on surface], then close the figure to save the modifications.
Read stimulus triggers
We need to read the stimulus markers from the STI channels. The following tasks can be done in an interactive way with menus in the Record tab, as in the introduction tutorials. We will illustrate here how to do this with the pipeline editor, it will be easier to batch it for all the runs and all the subjects.
- In Process1, select the "Link to raw file", click on [Run].
Select process Events > Read from channel, Channel: STI101, Detection mode: Bit.
Do not execute the process, we will add other processes to classify the markers.
- We want to create three categories of events, based on their numerical codes:
Famous faces: 5 (00101), 6 (00110), 7 (00111) => Bit 3 only
Unfamiliar faces: 13 (01101), 14 (01110), 15 (01111) => Bit 3 and 4
Scrambled images: 17 (10001), 18 (10010), 19 (10011) => Bit 5 only
- We will start by creating the category "Unfamiliar" (combination of events "3" and "4") and remove the remove the initial events. Then we just have to rename the remaining "3" in "Famous", and all the "5" in "Scrambled".
Add process Events > Group by name: "Unfamiliar=3,4", Delay=0, Delete original events
Add process Events > Rename event: 3 => Famous
Add process Events > Rename event: 5 => Scrambled
Add process Events > Add time offset to correct for the presentation delays:
Event names: "Famous, Unfamiliar, Scrambled", Time offset = 34.5ms
Finally run the script. Double-click on the recordings to make sure the labels were detected correctly. You can delete the unwanted events that are left in the recordings (1,2,9,13):
Pre-processing
Spectral evaluation
- Keep the "Link to raw file" in Process1.
Run process Frequency > Power spectrum density (Welch) with the options illustrated below.
Right-click on the PSD file > Power spectrum.
The MEG sensors look awful, because of one small segment of data located around 248s. Open the MEG recordings and scroll to 248s (just before the first Unfamiliar event).
In these recordings, the continuous head tracking was activated, but it starts only at the time of the stimulation (248s) while the acquisition of the data starts 20s before (226s). The first 20s do not have head localization coils (HPI) coils activity and are not corrected by MaxFilter. After 248s, the HPI coils are on, and MaxFilter filters them out. The transition between the two states is not smooth and creates important distortions in the spectral domain. For a proper evaluation of the recordings, we should compute the PSD only after the HPI coils are turned on.
Run process Events > Detect cHPI activity (Elekta). This detects the changes in the cHPI activity from channel STI201 and marks all the data without head localization as bad.
Re-run the process Frequency > Power spectrum density (Welch). All the bad segments are excluded from the computation, therefore the PSD is now estimated only with the data after 248s.
- Observations:
- Three groups of sensors, from top to bottom: EEG, MEG gradiometers, MEG magnetometers.
Power lines: 50 Hz and harmonics
- Alpha peak around 10 Hz
Artifacts due to Elekta electronics (HPI coils): 293Hz, 307Hz, 314Hz, 321Hz, 328Hz.
Peak from unknown source at 103.4Hz in the MEG only.
Suspected bad EEG channels: EEG016
- Close all the windows.
Remove line noise
- Keep the "Link to raw file" in Process1.
Select process Pre-process > Notch filter to remove the line noise (50-200Hz).
Add the process Frequency > Power spectrum density (Welch).
Double-click on the PSD for the new continuous file to evaluate the quality of the correction.
- Close all the windows (use the [X] button at the top-right corner of the Brainstorm window).
EEG reference and bad channels
Right-click on link to the processed file ("Raw | notch(50Hz ...") > EEG > Display time series.
Select channel EEG016 and mark it as bad (using the popup menu or pressing the Delete key).
In the Record tab, menu Artifacts > Re-reference EEG > "AVERAGE".
At the end, the window "select active projectors" is open to show the new re-referencing projector. Just close this window. To get it back, use the menu Artifacts > Select active projectors.
Artifact detection
Heartbeats: Detection
Empty the Process1 list (right-click > Clear list).
- Drag and drop the continuous processed file ("Raw | notch(50Hz...)") to the Process1 list.
Run process Events > Detect heartbeats: Channel name=EEG063, All file, Event name=cardiac
Eye blinks: Detection
- In many of the other tutorials, we detect the blinks and remove them with SSP. In this experiment, we are particularly interested in the subject's response to seeing the stimulus. Therefore we will exclude from the analysis all the recordings contaminated with blinks or other eye movements.
Run process Artifacts > Detect events above threshold:
Event name=blink_BAD, Channel=EEG062, All file, Maximum threshold=100, Threshold units=uV, Filter=[0.30,20.00]Hz, Use absolute value of signal.
Inspect visually the two new cateogries of events: cardiac and blink_BAD.
- Close all the windows (using the [X] button).
Heartbeats: Correction with SSP
- Keep the "Raw | notch" file selected in Process1.
Select process Artifacts > SSP: Heartbeats > Sensor type: MEG MAG
Add process Artifacts > SSP: Heartbeats > Sensor type: MEG GRAD - Run the execution
Double-click on the continuous file to show all the MEG sensors.
In the Record tab, select sensors "Left-temporal".Menu Artifacts > Select active projectors.
In category cardiac/MEG MAG: Select component #1 and view topography.
In category cardiac/MEG GRAD: Select component #1 and view topography.
Make sure that selecting the two components removes the cardiac artifact. Then click [Save].
Additional bad segments
Process1>Run: Select the process "Events > Detect other artifacts". This should be done separately for MEG and EEG to avoid confusion about which sensors are involved in the artifact.
Display the MEG sensors. Review the segments that were tagged as artifact, determine if each event represents an artifact and then mark the time of the artifact as BAD. This can be done by selecting the time window around the artifact, then right-click > Reject time segment. Note that this detection process marks 1-second segments but the artifact can be shorter.
- Once all the events in the two categories are reviewed and bad segments are marked, the two categories (1-7Hz and 40-240Hz) can be deleted.
- Do this detection and review again for the EEG.
SQUID jumps
MEG signals recorded with Elekta-Neuromag systems frequently contain SQUID jumps (more information). These sharp steps followed by a change of baseline value are easy to identify visually but more complicated to detect automatically.
The process "Detect other artifacts" usually detects most of them in the category "1-7Hz". If you observe that some are skipped, you can try re-running it with a higher sensitivity. It is important to review all the sensors and all the time in each run to be sure these events are marked as bad segments.
Epoching and averaging
Import epochs
- Keep the "Raw | notch" file selected in Process1.
Select process: Import recordings > Import MEG/EEG: Events (do not run immediately)
Event names "Famous, Unfamiliar, Scrambled", All file, Epoch time=[-500,1200]msAdd process: Pre-process > Remove DC offset: Baseline=[-500,-0.9]ms - Run execution.
Average by run
- In Process1, select all the imported trials.
Run process: Average > Average files: By trial groups (folder average)
Review EEG ERP
EEG evoked response (famous, scrambled, unfamiliar):
Open the Cluster tab and create a cluster with the channel EEG065 (button [NEW IND]).
Select the cluster, select the three average files, right-click > Clusters time series (Overlay:Files).
- Basic observations for EEG065 (right parieto-occipital electrode):
- Around 170ms (N170): greater negative deflection for Famous than Scrambled faces.
- After 250ms: difference between Famous and Unfamiliar faces.
Source estimation
MEG noise covariance: Empty room recordings
The minimum norm model we will use next to estimate the source activity can be improved by modeling the the noise contaminating the data. The section shows how to estimate the noise covariance in different ways for EEG and MEG. For the MEG recordings we will use the empty room measurements we have, and for the EEG we will compute it from the pre-stimulus baselines we have in all the imported epochs.
Create a new subject: emptyroom
Right-click on the new subject > Review raw file.
Select file: sample_group/emptyroom/090707_raw_st.fif
Do not apply default transformation, Ignore event channel.
Select this new file in Process1 and run process Pre-process > Notch filter: 50 100 150 200Hz. When using empty room measurements to compute the noise covariance, they must be processed exactly in the same way as the other recordings.
Right-click on the filtered noise recordings > Noise covariance > Compute from recordings:
Right-click on the Noise covariance > Copy to other subjects
EEG noise covariance: Pre-stimulus baseline
In folder sub002/run_01_sss_notch, select all the imported the imported trials, right-click > Noise covariance > Compute from recordings, Time=[-500,-0.9]ms, EEG only, Merge.
This computes the noise covariance only for EEG, and combines it with the existing MEG information.
BEM layers
We will compute a BEM forward model to estimate the brain sources from the EEG recordings. For this, we need some layers defining the separation between the different tissues of the head (scalp, inner skull, outer skull).
- Go to the anatomy view (first button above the database explorer).
Right-click on the subject folder > Generate BEM surfaces: The number of vertices to use for each layer depends on your computing power and the accuracy you expect. You can try for instance with 1082 vertices (scalp) and 642 vertices (outer skull and inner skull).
Forward model: EEG and MEG
- Go back to the functional view (second button above the database explorer).
Model used: Overlapping spheres for MEG, OpenMEEG BEM for EEG (more information).
In folder sub002/run_01_sss_notch, right-click on the channel file > Compute head model.
Keep all the default options . Expect this to take a while...
Inverse model: Minimum norm estimates
Right-click on the new head model > Compute sources [2016]: MEG MAG + GRAD (default options)
Right-click on the new head model > Compute sources [2016]: EEG (default bad channels).
At the end we have two inverse operators, that are shared for all the files of the run (single trials and averages). If we wanted to look at the run-level source averages, we could normalize the source maps with a Z-score wrt baseline. In this tutorial, we will first average across runs and normalize the subject-level averages. This will be done in the next tutorial (group analysis).
Time-frequency analysis
We will compute the time-frequency decomposition of each trial using Morlet wavelets, and average the power of the Morlet coefficients for each condition and each run separately. We will restrict the computation to the MEG magnetometers and the EEG channels to limit the computation time and disk usage.
- In Process1, select the imported trials "Famous" for run#01.
Run process Frequency > Time-frequency (Morlet wavelets): Sensor types=MEG MAG,EEG
Not normalized, Frequency=Log(6:20:60), Measure=Power, Save average
Double-click on the file to display it. In the Display tab, select the option "Hide edge effects" to exclude form the display all the values that could not be estimated in a reliable way. Let's extract only the good values from this file (-200ms to +900ms).
- In Process1, select the time-frequency file.
Run process Extract > Extract time: Time window=[-200, 900]ms, Overwrite input files
Display the file again, observe that all the possibly bad values are gone.
You can display all the sensors at once (MEG MAG or EEG): right-click > 2D Layout (maps).
- Repeat these steps for other conditions (Scrambled and Unfamiliar) and the other runs (2-6). There is no way with this process to compute all the averages at once, as we did with the process "Average files". This will be easier to run from a script.
- If we wanted to look at the run-level source averages, we could normalize these time-frequency maps. In this tutorial, we will first average across runs and normalize the subject-level averages. This will be done in the next tutorial (group analysis).
Scripting
We have now all the files we need for the group analysis (next tutorial). We need to repeat the same operations for all the runs and all the subjects. Some of these steps are fully automatic and take a lot of time (filtering, computing the forward model), they should be executed from a script.
However, we recommend you always review manually some of the pre-processing steps (selection of the bad segments and bad channels, SSP/ICA components). Do not trust blindly any fully automated cleaning procedure.
For the strict reproducibility of this analysis, we provide a script that processes all the 19 subjects: brainstorm3/toolbox/script/tutorial_visual_single.m (execution time: 10-30 hours)
Report for the first subject: report_TutorialVisual_sub001.html
1 function tutorial_visual_single(bids_dir, reports_dir)
2 % TUTORIAL_VISUAL_SINGLE: Runs the Brainstorm/SPM group analysis pipeline (single subject, BIDS version).
3 %
4 % ONLINE TUTORIALS: https://neuroimage.usc.edu/brainstorm/Tutorials/VisualSingle
5 %
6 % INPUTS:
7 % - bids_dir: Path to folder ds000117 (https://openneuro.org/datasets/ds000117)
8 % |- derivatives/freesurfer/sub-XX : Segmentation folders generated with FreeSurfer
9 % |- derivatives/meg_derivatives/sub-XX/ses-meg/meg/*.fif : MEG+EEG recordings (processed with MaxFilter's SSS)
10 % |- derivatives/meg_derivatives/sub-emptyroom/ses-meg/meg/*.fif : Empty room measurements
11 % - reports_dir: If defined, exports all the reports as HTML to this folder
12
13 % @=============================================================================
14 % This function is part of the Brainstorm software:
15 % https://neuroimage.usc.edu/brainstorm
16 %
17 % Copyright (c) University of Southern California & McGill University
18 % This software is distributed under the terms of the GNU General Public License
19 % as published by the Free Software Foundation. Further details on the GPLv3
20 % license can be found at http://www.gnu.org/copyleft/gpl.html.
21 %
22 % FOR RESEARCH PURPOSES ONLY. THE SOFTWARE IS PROVIDED "AS IS," AND THE
23 % UNIVERSITY OF SOUTHERN CALIFORNIA AND ITS COLLABORATORS DO NOT MAKE ANY
24 % WARRANTY, EXPRESS OR IMPLIED, INCLUDING BUT NOT LIMITED TO WARRANTIES OF
25 % MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE, NOR DO THEY ASSUME ANY
26 % LIABILITY OR RESPONSIBILITY FOR THE USE OF THIS SOFTWARE.
27 %
28 % For more information type "brainstorm license" at command prompt.
29 % =============================================================================@
30 %
31 % Author: Francois Tadel, Elizabeth Bock, 2016-2018
32
33
34 %% ===== SCRIPT VARIABLES =====
35 % Full list of subjects to process
36 SubjectNames = {'sub-01', 'sub-02', 'sub-03', 'sub-04', 'sub-05', 'sub-06', 'sub-07', 'sub-08', ...
37 'sub-09', 'sub-10', 'sub-11', 'sub-12', 'sub-13', 'sub-14', 'sub-15', 'sub-16'};
38 % Empty-room dates for each subject (so that we can match automatically recordings with empty-room)
39 EmptyRoomSubj = 'sub-emptyroom';
40 AcquisitionDates = {'09-Apr-2009', '06-May-2009', '11-May-2009', '18-May-2009', '15-May-2009', '15-May-2009', '15-May-2009', '15-May-2009', ...
41 '15-May-2009', '15-May-2009', '01-Jun-2009', '01-Jun-2009', '01-Jun-2009', '26-Nov-2009', '08-Dec-2009', '08-Dec-2009'};
42 % Bad channels {iSubj} = {Run01, Run02, Run03, Run04, Run05, Run06}
43 BadChannels{1} = {'EEG016', 'EEG070', 'EEG050',{'EEG008','EEG050'}, [], []};
44 BadChannels{2} = {{'EEG027', 'EEG030', 'EEG038'}, 'EEG010', 'EEG010', 'EEG010', 'EEG010', 'EEG010'};
45 BadChannels{3} = {{'EEG008','EEG017'}, {'EEG008','EEG017'}, {'EEG008','EEG017'}, {'EEG008','EEG017'}, {'EEG008','EEG017','EEG001'}, {'EEG008','EEG017','EEG020'}};
46 BadChannels{4} = {{'EEG038'}, {'EEG038','EEG001','EEG016'}, {'EEG038','EEG001','EEG016'}, {'EEG038','EEG001'}, {'EEG038','EEG001','EEG016'}, {'EEG038','EEG001','EEG016'}};
47 BadChannels{5} = {'EEG001', 'EEG001', [], [], [], []};
48 BadChannels{6} = {'EEG068', [], 'EEG004', [], [], []};
49 BadChannels{7} = {[], [], {'EEG004','EEG008'}, {'EEG004','EEG008'},{'EEG004','EEG008','EEG043','EEG045','EEG047'}, {'EEG004','EEG008'}};
50 BadChannels{8} = {[], [], [], [], [], []};
51 BadChannels{9} = {[], 'EEG004', 'EEG004', [], 'EEG004', 'EEG004'};
52 BadChannels{10} = {[], [], [], [], [], []};
53 BadChannels{11} = {{'EEG010','EEG050'}, 'EEG050', 'EEG050', 'EEG050', 'EEG050', 'EEG050'};
54 BadChannels{12} = {{'EEG024','EEG057'}, {'EEG024','EEG057'}, {'EEG024','EEG057'}, {'EEG024','EEG057','EEG070'}, {'EEG024','EEG057'}, {'EEG024','EEG057','EEG070'}};
55 BadChannels{13} = {'EEG009', 'EEG009', {'EEG009','EEG057','EEG69'}, 'EEG009', {'EEG009','EEG044'}, {'EEG009','EEG044'}};
56 BadChannels{14} = {'EEG029', 'EEG029', 'EEG029', {'EEG004','EEG008','EEG016','EEG029'}, {'EEG004','EEG008','EEG016','EEG029'}, {'EEG004','EEG008','EEG016','EEG029'}};
57 BadChannels{15} = {'EEG038', 'EEG038', 'EEG038', 'EEG038', {'EEG054','EEG038'}, 'EEG038'};
58 BadChannels{16} = {'EEG008', 'EEG008', 'EEG008', 'EEG008', 'EEG008', 'EEG008'};
59 % SSP components to remove {iSubj} = {sRun01, sRun02, sRun03, sRun03, sRun04, sRun05, sRun06}, sRun0X={ECG_GRAD,ECG_MAG}
60 SspSelect{1} = {{1,1}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
61 SspSelect{2} = {{1,1}, {1,1}, {1,1}, {1,1}, {3,1}, {1,1}};
62 SspSelect{3} = {{[],1}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
63 SspSelect{4} = {{[],1}, {[],1}, {[],1}, {[],1}, {[],1}, {[],1}};
64 SspSelect{5} = {{2,1}, {1,1}, {1,1}, {[],1}, {1,1}, {1,1}};
65 SspSelect{6} = {{2,1}, {2,1}, {1,1}, {2,1}, {1,1}, {2,1}};
66 SspSelect{7} = {{1,1}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
67 SspSelect{8} = {{1,1}, {1,1}, {[],1}, {2,1}, {1,1}, {2,1}};
68 SspSelect{9} = {{1,1}, {1,1}, {[],1}, {[],1}, {1,1}, {1,1}};
69 SspSelect{10} = {{1,1}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
70 SspSelect{11} = {{[],1}, {[],1}, {[],1}, {[],1}, {[],[]}, {[],[]}};
71 SspSelect{12} = {{[1,2],[1,2]}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
72 SspSelect{13} = {{[],[]}, {[],[]}, {[],[]}, {[],[]}, {[],[]}, {[],[]}};
73 SspSelect{14} = {{1,1}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
74 SspSelect{15} = {{1,1}, {1,1}, {1,1}, {1,1}, {1,1}, {1,1}};
75 SspSelect{16} = {{1,1}, {1,1}, {1,1}, {2,1}, {1,1}, {1,1}};
76
77
78 %% ===== CREATE PROTOCOL =====
79 % Start brainstorm without the GUI
80 if ~brainstorm('status')
81 brainstorm nogui
82 end
83 % Output folder for reports
84 if (nargin < 2) || isempty(reports_dir) || ~isdir(reports_dir)
85 reports_dir = [];
86 end
87 % You have to specify the folder in which the tutorial dataset is unzipped
88 if (nargin < 1) || isempty(bids_dir) || ~file_exist(bids_dir) || ~file_exist(bst_fullfile(bids_dir, 'derivatives')) || ~file_exist(bst_fullfile(bids_dir, 'dataset_description.json'))
89 error('The first argument must be the full path to the tutorial folder.');
90 end
91 % The protocol name has to be a valid folder name (no spaces, no weird characters...)
92 ProtocolName = 'TutorialVisual';
93 % Delete existing protocol
94 gui_brainstorm('DeleteProtocol', ProtocolName);
95 % Create new protocol
96 gui_brainstorm('CreateProtocol', ProtocolName, 0, 0);
97 % Set visualization filters: 40Hz low-pass, no high-pass
98 panel_filter('SetFilters', 1, 40, 0, [], 0, [], 0, 0);
99 % Set colormap: local color scale
100 bst_colormaps('SetMaxMode', 'meg', 'local');
101 bst_colormaps('SetMaxMode', 'eeg', 'local');
102
103
104 %% ===== PRE-PROCESS AND IMPORT =====
105 for iSubj = 1:16
106 % Start a new report (one report per subject)
107 bst_report('Start');
108 disp(sprintf('\n===== IMPORT: SUBJECT #%d =====\n', iSubj));
109
110 % If subject already exists: delete it
111 [sSubject, iSubject] = bst_get('Subject', SubjectNames{iSubj});
112 if ~isempty(sSubject)
113 db_delete_subjects(iSubject);
114 end
115
116 % ===== FILES TO IMPORT =====
117 % Build the path of the files to import
118 AnatDir = fullfile(bids_dir, 'derivatives', 'freesurfer', SubjectNames{iSubj}, 'ses-mri', 'anat');
119 DataDir = fullfile(bids_dir, 'derivatives', 'meg_derivatives', SubjectNames{iSubj}, 'ses-meg', 'meg');
120 % Check if the folder contains the required files
121 if ~file_exist(AnatDir)
122 error(['The folder "' AnatDir '" does not exist.']);
123 end
124 if ~file_exist(DataDir)
125 error(['The folder "' DataDir '" does not exist.']);
126 end
127
128 % ===== ANATOMY =====
129 % Process: Import anatomy folder
130 bst_process('CallProcess', 'process_import_anatomy', [], [], ...
131 'subjectname', SubjectNames{iSubj}, ...
132 'mrifile', {AnatDir, 'FreeSurfer'}, ...
133 'nvertices', 15000);
134
135 % ===== PROCESS EACH RUN =====
136 for iRun = 1:6
137 % Files to import
138 FifFile = bst_fullfile(DataDir, sprintf('%s_ses-meg_task-facerecognition_run-%02d_proc-sss_meg.fif', SubjectNames{iSubj}, iRun));
139
140 % ===== LINK CONTINUOUS FILE =====
141 % Process: Create link to raw file
142 sFileRaw = bst_process('CallProcess', 'process_import_data_raw', [], [], ...
143 'subjectname', SubjectNames{iSubj}, ...
144 'datafile', {FifFile, 'FIF'}, ...
145 'channelreplace', 1, ...
146 'channelalign', 0);
147 % Set acquisition date
148 panel_record('SetAcquisitionDate', sFileRaw.iStudy, AcquisitionDates{iSubj});
149
150 % ===== PREPARE CHANNEL FILE =====
151 % Process: Set channels type
152 bst_process('CallProcess', 'process_channel_settype', sFileRaw, [], ...
153 'sensortypes', 'EEG061, EEG064', ...
154 'newtype', 'NOSIG');
155 bst_process('CallProcess', 'process_channel_settype', sFileRaw, [], ...
156 'sensortypes', 'EEG062', ...
157 'newtype', 'EOG');
158 bst_process('CallProcess', 'process_channel_settype', sFileRaw, [], ...
159 'sensortypes', 'EEG063', ...
160 'newtype', 'ECG');
161
162 % Process: Remove head points
163 sFileRaw = bst_process('CallProcess', 'process_headpoints_remove', sFileRaw, [], ...
164 'zlimit', 0);
165 % Process: Refine registration
166 sFileRaw = bst_process('CallProcess', 'process_headpoints_refine', sFileRaw, []);
167 % Process: Project electrodes on scalp
168 sFileRaw = bst_process('CallProcess', 'process_channel_project', sFileRaw, []);
169
170 % Process: Snapshot: Sensors/MRI registration
171 bst_process('CallProcess', 'process_snapshot', sFileRaw, [], ...
172 'target', 1, ... % Sensors/MRI registration
173 'modality', 1, ... % MEG (All)
174 'orient', 1, ... % left
175 'Comment', sprintf('MEG/MRI Registration: Subject #%d, Run #%d', iSubj, iRun));
176 bst_process('CallProcess', 'process_snapshot', sFileRaw, [], ...
177 'target', 1, ... % Sensors/MRI registration
178 'modality', 4, ... % EEG
179 'orient', 1, ... % left
180 'Comment', sprintf('EEG/MRI Registration: Subject #%d, Run #%d', iSubj, iRun));
181
182 % ===== IMPORT TRIGGERS =====
183 % Process: Read from channel
184 bst_process('CallProcess', 'process_evt_read', sFileRaw, [], ...
185 'stimchan', 'STI101', ...
186 'trackmode', 2, ... % Bit: detect the changes for each bit independently
187 'zero', 0);
188 % Process: Group by name
189 bst_process('CallProcess', 'process_evt_groupname', sFileRaw, [], ...
190 'combine', 'Unfamiliar=3,4', ...
191 'dt', 0, ...
192 'delete', 1);
193 % Process: Rename event
194 bst_process('CallProcess', 'process_evt_rename', sFileRaw, [], ...
195 'src', '3', ...
196 'dest', 'Famous');
197 % Process: Rename event
198 bst_process('CallProcess', 'process_evt_rename', sFileRaw, [], ...
199 'src', '5', ...
200 'dest', 'Scrambled');
201 % Process: Add time offset
202 bst_process('CallProcess', 'process_evt_timeoffset', sFileRaw, [], ...
203 'info', [], ...
204 'eventname', 'Famous, Unfamiliar, Scrambled', ...
205 'offset', 0.0345);
206 % Process: Delete events
207 bst_process('CallProcess', 'process_evt_delete', sFileRaw, [], ...
208 'eventname', '1,2,6,7,8,9,10,11,12,13,14,15,16');
209 % Process: Detect cHPI activity (Elekta):STI201
210 bst_process('CallProcess', 'process_evt_detect_chpi', sFileRaw, [], ...
211 'eventname', 'chpi_bad', ...
212 'channelname', 'STI201', ...
213 'method', 'off'); % Mark as bad when the HPI coils are OFF
214
215 % ===== FREQUENCY FILTERS =====
216 % Process: Notch filter: 50Hz 100Hz 150Hz 200Hz
217 sFileClean = bst_process('CallProcess', 'process_notch', sFileRaw, [], ...
218 'freqlist', [50, 100, 150, 200], ...
219 'sensortypes', 'MEG, EEG', ...
220 'read_all', 0);
221 % Process: Power spectrum density (Welch)
222 sFilesPsd = bst_process('CallProcess', 'process_psd', [sFileRaw, sFileClean], [], ...
223 'timewindow', [], ...
224 'win_length', 4, ...
225 'win_overlap', 50, ...
226 'sensortypes', 'MEG, EEG', ...
227 'edit', struct(...
228 'Comment', 'Power', ...
229 'TimeBands', [], ...
230 'Freqs', [], ...
231 'ClusterFuncTime', 'none', ...
232 'Measure', 'power', ...
233 'Output', 'all', ...
234 'SaveKernel', 0));
235 % Process: Snapshot: Frequency spectrum
236 bst_process('CallProcess', 'process_snapshot', sFilesPsd, [], ...
237 'target', 10, ... % Frequency spectrum
238 'Comment', sprintf('Power spctrum: Subject #%d, Run #%d', iSubj, iRun));
239
240 % ===== BAD CHANNELS =====
241 if ~isempty(BadChannels{iSubj}{iRun})
242 % Process: Set bad channels
243 bst_process('CallProcess', 'process_channel_setbad', sFileClean, [], ...
244 'sensortypes', BadChannels{iSubj}{iRun});
245 end
246
247 % ===== EEG REFERENCE =====
248 % Process: Re-reference EEG
249 bst_process('CallProcess', 'process_eegref', sFileClean, [], ...
250 'eegref', 'AVERAGE', ...
251 'sensortypes', 'EEG');
252
253 % ===== DETECT ARTIFACTS ======
254 % Process: Detect heartbeats
255 bst_process('CallProcess', 'process_evt_detect_ecg', sFileClean, [], ...
256 'channelname', 'EEG063', ...
257 'timewindow', [], ...
258 'eventname', 'cardiac');
259 % Different amplitude thresholds for different subjects
260 if strcmpi(SubjectNames{iSubj}, 'sub-05')
261 thresholdMAX = 50;
262 else
263 thresholdMAX = 100;
264 end
265 % Process: Detect: blink_BAD - Detects all events where the amplitude exceeds 100uV
266 bst_process('CallProcess', 'process_evt_detect_threshold', sFileClean, [], ...
267 'eventname', 'blink_BAD', ...
268 'channelname', 'EEG062', ...
269 'timewindow', [], ...
270 'thresholdMAX', thresholdMAX, ...
271 'units', 3, ... % uV (10^-6)
272 'bandpass', [0.3, 20], ...
273 'isAbsolute', 1, ...
274 'isDCremove', 0);
275
276 % ===== SSP COMPUTATION =====
277 % Process: SSP ECG: cardiac
278 bst_process('CallProcess', 'process_ssp_ecg', sFileClean, [], ...
279 'eventname', 'cardiac', ...
280 'sensortypes', 'MEG GRAD', ...
281 'usessp', 1, ...
282 'select', SspSelect{iSubj}{iRun}{1});
283 bst_process('CallProcess', 'process_ssp_ecg', sFileClean, [], ...
284 'eventname', 'cardiac', ...
285 'sensortypes', 'MEG MAG', ...
286 'usessp', 1, ...
287 'select', SspSelect{iSubj}{iRun}{2});
288 % Process: Snapshot: SSP projectors
289 bst_process('CallProcess', 'process_snapshot', sFileClean, [], ...
290 'target', 2, ...
291 'Comment', sprintf('Subject #%d, Run #%d', iSubj, iRun)); % SSP projectors
292
293 % ===== IMPORT BAD EVENTS =====
294 % Get bad segments: this is typically done manually, not from a script
295 BadSegments = GetBadSegments(iSubj, iRun);
296 % Process: Import from file
297 bst_process('CallProcess', 'process_evt_import', sFileClean, [], ...
298 'evtfile', {BadSegments, 'ARRAY-TIMES'}, ...
299 'evtname', 'BAD');
300
301 % ===== IMPORT TRIALS =====
302 % Process: Import MEG/EEG: Events
303 sFilesEpochs = bst_process('CallProcess', 'process_import_data_event', sFileClean, [], ...
304 'subjectname', SubjectNames{iSubj}, ...
305 'condition', '', ...
306 'eventname', 'Famous, Scrambled, Unfamiliar', ...
307 'timewindow', [], ...
308 'epochtime', [-0.5, 1.2], ...
309 'createcond', 0, ...
310 'ignoreshort', 1, ...
311 'usectfcomp', 1, ...
312 'usessp', 1, ...
313 'freq', [], ...
314 'baseline', [-0.5, -0.0009]);
315
316 % ===== AVERAGE: RUN =====
317 % Process: Average: By trial group (folder average)
318 sFilesAvg = bst_process('CallProcess', 'process_average', sFilesEpochs, [], ...
319 'avgtype', 5, ... % By trial group (folder average)
320 'avg_func', 1, ... % Arithmetic average: mean(x)
321 'weighted', 0, ...
322 'keepevents', 0);
323 % Process: Snapshot: Recordings time series
324 bst_process('CallProcess', 'process_snapshot', sFilesAvg, [], ...
325 'target', 5, ... % Recordings time series
326 'modality', 4, ... % EEG
327 'time', 0.11, ...
328 'Comment', sprintf('Subject #%d, Run #%d', iSubj, iRun));
329 % Process: Snapshot: Recordings topography
330 bst_process('CallProcess', 'process_snapshot', sFilesAvg, [], ...
331 'target', 6, ... % Recordings topography (one time)
332 'modality', 4, ... % EEG
333 'time', 0.11, ...
334 'Comment', sprintf('Subject #%d, Run #%d', iSubj, iRun));
335
336 % ===== COMPUTE NOISECOV: EEG =====
337 % Process: Compute covariance (noise or data)
338 bst_process('CallProcess', 'process_noisecov', sFilesEpochs, [], ...
339 'baseline', [-0.5, -0.0009], ...
340 'sensortypes', 'EEG', ...
341 'target', 1, ... % Noise covariance (covariance over baseline time window)
342 'dcoffset', 1, ... % Block by block, to avoid effects of slow shifts in data
343 'identity', 0, ...
344 'copycond', 0, ...
345 'copysubj', 0, ...
346 'replacefile', 1); % Replace
347 end
348
349 % Save report
350 ReportFile = bst_report('Save', []);
351 if ~isempty(reports_dir) && ~isempty(ReportFile)
352 bst_report('Export', ReportFile, bst_fullfile(reports_dir, ['report_' ProtocolName '_' SubjectNames{iSubj} '.html']));
353 end
354 end
355
356
357 %% ===== EMPTY ROOM RECORDINGS =====
358 disp(sprintf('\n===== IMPORT: EMPTY-ROOM =====\n'));
359 % Loop on all the noise sessions
360 NoiseFiles = {};
361 for ses = {'20090409', '20090506', '20090511', '20090515', '20090518', '20090601', '20091126', '20091208'}
362 NoiseFiles{end+1} = fullfile(bids_dir, 'derivatives', 'meg_derivatives', EmptyRoomSubj, ['ses-' ses{1}], 'meg', ['sub-emptyroom_ses-' ses{1} '_task-noise_proc-sss_meg.fif']);
363 end
364 % Process: Create link to raw file
365 sFilesNoise = bst_process('CallProcess', 'process_import_data_raw', [], [], ...
366 'subjectname', EmptyRoomSubj, ...
367 'datafile', {NoiseFiles, 'FIF'}, ...
368 'channelreplace', 1, ...
369 'channelalign', 0);
370 % Process: Notch filter: 50Hz 100Hz 150Hz 200Hz
371 sFileNoiseClean = bst_process('CallProcess', 'process_notch', sFilesNoise, [], ...
372 'freqlist', [50, 100, 150, 200], ...
373 'sensortypes', 'MEG, EEG', ...
374 'read_all', 0);
375 % Process: Compute noise covariance
376 bst_process('CallProcess', 'process_noisecov', sFileNoiseClean, [], ...
377 'baseline', [], ...
378 'sensortypes', 'MEG', ...
379 'target', 1, ... % Noise covariance (covariance over baseline time window)
380 'dcoffset', 1, ... % Block by block, to avoid effects of slow shifts in data
381 'identity', 0, ...
382 'copycond', 1, ...
383 'copysubj', 1, ...
384 'copymatch', 1, ...
385 'replacefile', 2); % Merge
386
387
388 %% ===== SOURCE ESTIMATION =====
389 % Start a new report (one report for the source estimation of all the subjects)
390 bst_report('Start');
391 % Loop on the subjects: This loop is separated from the previous one, because we should
392 % compute the BEM surfaces after importing all the runs, so that the registration is done
393 % using the high resolution head surface, instead of the smooth scalp BEM layer.
394 for iSubj = 1:length(SubjectNames)
395 disp(sprintf('\n===== SOURCES: SUBJECT #%d =====\n', iSubj));
396
397 % ===== BEM SURFACES =====
398 % Process: Generate BEM surfaces
399 bst_process('CallProcess', 'process_generate_bem', [], [], ...
400 'subjectname', SubjectNames{iSubj}, ...
401 'nscalp', 1082, ...
402 'nouter', 642, ...
403 'ninner', 642, ...
404 'thickness', 4, ...
405 'method', 'brainstorm');
406
407 % ===== SELECT ALL AVERAGES =====
408 % Process: Select data files in: */*
409 sFilesAvg = bst_process('CallProcess', 'process_select_files_data', [], [], ...
410 'subjectname', SubjectNames{iSubj});
411 % Process: Select file comments with tag: Avg
412 sFilesAvg = bst_process('CallProcess', 'process_select_tag', sFilesAvg, [], ...
413 'tag', 'Avg'); % Select only the files with the tag
414
415 % ===== COMPUTE HEAD MODELS =====
416 % Process: Compute head model (only for the first run of the subject)
417 bst_process('CallProcess', 'process_headmodel', sFilesAvg(1), [], ...
418 'sourcespace', 1, ... % Cortex surface
419 'meg', 3, ... % Overlapping spheres
420 'eeg', 3, ... % OpenMEEG BEM
421 'ecog', 1, ... %
422 'seeg', 1, ... %
423 'openmeeg', struct(...
424 'BemSelect', [1, 1, 1], ...
425 'BemCond', [1, 0.0125, 1], ...
426 'BemNames', {{'Scalp', 'Skull', 'Brain'}}, ...
427 'BemFiles', {{}}, ...
428 'isAdjoint', 0, ...
429 'isAdaptative', 1, ...
430 'isSplit', 0, ...
431 'SplitLength', 4000));
432 % Get all the runs for this subject (ie the list of the study indices)
433 iStudyOther = setdiff(unique([sFilesAvg.iStudy]), sFilesAvg(1).iStudy);
434 % Copy the forward model file to the other runs
435 sHeadmodel = bst_get('HeadModelForStudy', sFilesAvg(1).iStudy);
436 for iStudy = iStudyOther
437 db_add(iStudy, sHeadmodel.FileName);
438 end
439
440 % ===== COMPUTE SOURCES: MEG =====
441 % Process: Compute sources [2018]
442 sAvgSrcMeg = bst_process('CallProcess', 'process_inverse_2018', sFilesAvg, [], ...
443 'output', 1, ... % Kernel only: shared
444 'inverse', struct(...
445 'Comment', 'MN: MEG ALL', ...
446 'InverseMethod', 'minnorm', ...
447 'InverseMeasure', 'amplitude', ...
448 'SourceOrient', {{'fixed'}}, ...
449 'Loose', 0.2, ...
450 'UseDepth', 1, ...
451 'WeightExp', 0.5, ...
452 'WeightLimit', 10, ...
453 'NoiseMethod', 'reg', ...
454 'NoiseReg', 0.1, ...
455 'SnrMethod', 'fixed', ...
456 'SnrRms', 1e-06, ...
457 'SnrFixed', 3, ...
458 'ComputeKernel', 1, ...
459 'DataTypes', {{'MEG GRAD', 'MEG MAG'}}));
460 % Process: Snapshot: Sources (one time) - Loop only to get a correct comment for the report
461 for i = 1:length(sAvgSrcMeg)
462 bst_process('CallProcess', 'process_snapshot', sAvgSrcMeg(i), [], ...
463 'target', 8, ... % Sources (one time)
464 'orient', 4, ... % bottom
465 'time', 0.11, ...
466 'threshold', 20, ...
467 'Comment', ['MEG sources: ' sFilesAvg(i).FileName]);
468 end
469
470 % ===== COMPUTE SOURCES: EEG =====
471 % Process: Compute sources [2018]
472 sAvgSrcEeg = bst_process('CallProcess', 'process_inverse_2018', sFilesAvg, [], ...
473 'output', 1, ... % Kernel only: shared
474 'inverse', struct(...
475 'Comment', 'MN: EEG', ...
476 'InverseMethod', 'minnorm', ...
477 'InverseMeasure', 'amplitude', ...
478 'SourceOrient', {{'fixed'}}, ...
479 'Loose', 0.2, ...
480 'UseDepth', 1, ...
481 'WeightExp', 0.5, ...
482 'WeightLimit', 10, ...
483 'NoiseMethod', 'reg', ...
484 'NoiseReg', 0.1, ...
485 'SnrMethod', 'fixed', ...
486 'SnrRms', 1e-06, ...
487 'SnrFixed', 3, ...
488 'ComputeKernel', 1, ...
489 'DataTypes', {{'EEG'}}));
490 % Process: Snapshot: Sources (one time) - Loop only to get a correct comment for the report
491 for i = 1:length(sAvgSrcEeg)
492 bst_process('CallProcess', 'process_snapshot', sAvgSrcEeg(i), [], ...
493 'target', 8, ... % Sources (one time)
494 'orient', 4, ... % bottom
495 'time', 0.11, ...
496 'threshold', 10, ...
497 'Comment', ['EEG sources: ' sFilesAvg(i).FileName]);
498 end
499 end
500 % Save report
501 ReportFile = bst_report('Save', []);
502 if ~isempty(reports_dir) && ~isempty(ReportFile)
503 bst_report('Export', ReportFile, bst_fullfile(reports_dir, ['report_' ProtocolName '_sources.html']));
504 end
505
506
507 %% ===== TIME-FREQUENCY =====
508 % Start a new report (one report for the time-frequency of all the subjects)
509 bst_report('Start');
510 % List of conditions to process separately
511 AllConditions = {'Famous', 'Scrambled', 'Unfamiliar'};
512 % Channels to display in the screen capture, by order of preference (if the first channel is bad, use the following)
513 SelChannel = {'EEG070','EEG060','EEG065','EEG050','EEG003'};
514 % Compute one separate time-frequency average for each subject/run/condition
515 for iSubj = 1:length(SubjectNames)
516 disp(sprintf('\n===== TIME-FREQUENCY: SUBJECT #%d =====\n', iSubj));
517 for iRun = 1:6
518 % Process: Select data files in: Subject/Run
519 sTrialsAll = bst_process('CallProcess', 'process_select_files_data', [], [], ...
520 'subjectname', SubjectNames{iSubj}, ...
521 'condition', sprintf('sub-%02d_ses-meg_task-facerecognition_run-%02d_proc-sss_meg_notch', iSubj, iRun));
522 % Loop on the conditions
523 for iCond = 1:length(AllConditions)
524 % Comment describing this average
525 strComment = [SubjectNames{iSubj}, ' / ', sprintf('run_%02d', iRun), ' / ', AllConditions{iCond}];
526 disp(['BST> ' strComment]);
527 % Find the first good channel in the display list
528 if isempty(BadChannels{iSubj}{iRun})
529 iSel = 1;
530 else
531 iSel = find(~ismember(SelChannel,BadChannels{iSubj}{iRun}), 1);
532 end
533 % Process: Select file comments with tag: Avg
534 sTrialsCond = bst_process('CallProcess', 'process_select_tag', sTrialsAll, [], ...
535 'tag', [AllConditions{iCond}, '_trial'], ...
536 'search', 1, ... % Search the file names
537 'select', 1); % Select only the files with the tag
538 % Process: Time-frequency (Morlet wavelets), averaged across trials
539 sTimefreq = bst_process('CallProcess', 'process_timefreq', sTrialsCond, [], ...
540 'sensortypes', 'MEG MAG, EEG', ...
541 'edit', struct(...
542 'Comment', ['Avg: ' AllConditions{iCond} ', Power, 6-60Hz'], ...
543 'TimeBands', [], ...
544 'Freqs', [6, 6.8, 7.6, 8.6, 9.7, 11, 12.4, 14, 15.8, 17.9, 20.2, 22.8, 25.7, 29, 32.7, 37, 41.7, 47.1, 53.2, 60], ...
545 'MorletFc', 1, ...
546 'MorletFwhmTc', 3, ...
547 'ClusterFuncTime', 'none', ...
548 'Measure', 'power', ...
549 'Output', 'average', ...
550 'RemoveEvoked', 0, ...
551 'SaveKernel', 0), ...
552 'normalize', 'none'); % None: Save non-standardized time-frequency maps
553 % Process: Extract time: [-200ms,900ms]
554 sTimefreq = bst_process('CallProcess', 'process_extract_time', sTimefreq, [], ...
555 'timewindow', [-0.2, 0.9], ...
556 'overwrite', 1);
557 % Screen capture of one sensor
558 hFigTf = view_timefreq(sTimefreq.FileName, 'SingleSensor', SelChannel{iSel});
559 bst_report('Snapshot', hFigTf, strComment, 'Time-frequency', [200, 200, 400, 250]);
560 close(hFigTf);
561 end
562 end
563 end
564 % Save report
565 ReportFile = bst_report('Save', []);
566 if ~isempty(reports_dir) && ~isempty(ReportFile)
567 bst_report('Export', ReportFile, bst_fullfile(reports_dir, ['report_' ProtocolName '_timefreq.html']));
568 end
569 end
570
571
572
573
574 %% ===== SUPPORT FUNCTIONS =====
575 function BadSeg = GetBadSegments(iSubj, iRun)
576 BadSegments{1} = {...
577 [247.867 248.185; 598.999 598.999; 598.999 598.999; 611.999 611.999; 612.999 612.999; 613.999 613.999; 616.999 616.999; 617.999 617.999; 623.999 623.999; 715.209 715.467], ...
578 [84.791 85.166], ...
579 [79.183 80.167], ...
580 [64.309 65.185], ...
581 [90.958 91.167; 178.005 178.355; 293.282 295.919; 312.298 316.479; 353.835 357.716], ...
582 [60.292 66.802; 69.975 71.210; 105.233 107.586; 108.822 109.506; 376.225 376.325]};
583 BadSegments{2} = {...
584 [223.806 224.199; 279.772 279.895; 453.241 455.108; 692.423 692.593], ...
585 [65.298 66.194; 304.727 306.178; 399.165 400.732], ...
586 [203.141 205.085; 281.579 287.883; 420.395 421.128], ...
587 [387.118 388.229; 440.318 441.900; 554.825 558.744], ...
588 [71.000 80.999; 82.750 87.367; 149.528 149.667; 264.747 267.995; 368.415 371.973; 376.263 378.763; 398.334 401.551; 537.410 541.645], ...
589 [38.000 47.999; 47.825 50.046; 61.298 61.384; 249.653 253.379; 282.917 283.820; 286.135 287.616; 298.167 300.196; 328.254 329.511; 335.957 337.817; 478.277 480.707]};
590 BadSegments{3} = {...
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671 [85.991 87.179; 88.999 88.999; 89.999 89.999; 92.966 93.027; 93.999 93.999; 107.999 107.999; 110.999 110.999; 111.971 112.025; 118.999 118.999; 121.999 121.999; 122.999 122.999; 166.999 166.999; 168.957 169.035; 173.999 173.999; 174.999 174.999; 175.957 176.035; 198.999 198.999; 199.999 199.999; 202.999 202.999; 203.999 203.999; 205.999 205.999; 207.999 207.999; 208.999 208.999; 210.974 211.044; 211.999 211.999; 212.999 212.999; 232.984 233.023; 234.999 234.999; 235.999 235.999; 236.999 236.999; 239.958 240.044; 240.999 240.999], ...
672 [71.132 72.227], ...
673 [98.134 98.827; 110.497 110.814; 114.000 117.272; 279.999 279.999; 279.999 279.999; 280.999 280.999; 282.999 282.999; 283.999 283.999; 284.999 284.999; 286.999 286.999; 287.999 287.999; 288.999 288.999; 289.999 289.999; 291.966 292.044; 292.999 292.999; 346.999 346.999; 437.608 437.646; 518.988 519.104; 522.969 523.015; 534.999 534.999; 536.967 537.029; 562.725 563.426]};
674 BadSegments{15} = {...
675 [66.755 67.172; 257.988 258.042; 258.714 259.385; 260.958 261.044; 265.931 266.062; 267.968 268.022; 268.978 269.033; 270.992 271.031; 272.964 273.017; 273.968 274.030; 275.975 276.059; 276.970 277.046; 288.976 289.038; 289.984 290.015; 295.994 296.025; 296.982 297.013; 300.966 301.152; 364.730 364.800], ...
676 [46.531 46.555; 65.156 66.148; 87.535 87.642; 183.896 183.934; 294.342 294.375; 330.004 330.528; 333.785 333.815; 345.177 345.203; 399.544 399.573; 480.964 480.980], ...
677 [53.557 54.175; 148.851 149.136], ...
678 [43.681 44.214; 361.255 361.587; 409.462 411.021], ...
679 [90.868 91.130; 410.935 411.044], ...
680 [64.786 65.141; 132.385 132.786; 177.735 178.252; 278.747 278.902; 313.959 314.028; 314.970 315.031]};
681 BadSegments{16} = {...
682 [38.958 44.335; 305.280 312.826; 324.778 326.067; 393.183 398.367; 403.410 422.854], ...
683 [49.726 50.251; 58.675 65.465; 263.918 264.088; 321.795 322.195; 522.881 523.081], ...
684 [61.245 62.325; 65.628 65.905; 315.686 317.275; 335.184 336.449; 387.870 388.117; 389.892 390.062], ...
685 [56.020 57.255; 60.711 61.096; 64.353 64.924; 73.202 73.757; 76.134 76.844; 95.625 96.859; 171.436 172.625; 178.359 178.715; 212.828 213.415; 352.425 352.617; 367.755 369.097; 488.400 489.426], ...
686 [71.665 72.513; 76.347 77.181; 127.134 128.862], ...
687 [46.190 47.209; 53.461 55.752; 194.317 194.510; 213.101 213.240; 216.356 216.442; 225.962 226.286; 245.163 245.464; 252.041 253.422; 254.648 254.856; 292.966 294.340; 340.928 341.067; 346.298 346.452]};
688 BadSeg = BadSegments{iSubj}{iRun}';
689 end
690
You should note that this is not the result of a fully automated procedure. The bad channels were identified manually and are defined for each run in the script. The bad segments were detected automatically, confirmed manually for each run and saved in external files distributed with the Brainstorm package sample_group_freesurfer.zip (sample_group/brainstorm/bad_segments/*.mat).
All the process calls (bst_process) were generated automatically using with the script generator (menu Generate .m script in the pipeline editor). Everything else was added manually (loops, bad channels, file copies).
Bad subjects
After evaluating the results for the 19 subjects, 3 subjects were excluded from the analysis:
sub001: Error during the digitization of the EEG electrodes with the Polhemus (the same electrode was clicked twice). This impacts only the EEG, this subject could be used for MEG analysis.
sub005: Too many blinks or other eye movements.
sub016: Too many blinks or other eye movements.
Make sure you don't include these subjects in the group analysis.