MEG visual tutorial: Single subject

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 in simulateneous MEG/EEG recordings of 19 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 19 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.

License

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 DG, Henson RN, A multi-subject, multi-modal human neuroimaging dataset, Scientific Data (2015)

Any questions, please contact: rik.henson@mrc-cbu.cam.ac.uk

Presentation of the experiment

Experiment

• 19 subjects (three are excluded from the group analysis for various reasons)
• 6 acquisition runs (sessions) of approximately 10mins for each subject
• Presentation of series of images: familiar faces, unfamiliar faces, phase-scrambled faces
• 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

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 presetation are saved in the STI101 channel, with the following event codes:
  • Famous faces: 5, 6, 7
  • Unfamiliar faces: 13, 14, 15
  • Scrambled phase: 17, 18, 19

• The distribution includes MEG noise recordings acquired at a similar period, processed with MaxFilter 2.2 in a way similar to the subject recordings.

Subject anatomy

• MRI data acquired on a 3T Siemens TIM Trio: 1x1x1mm T1-weighted structural MRI

• Processed with FreeSurfer 5.3

Download and installation

• The data is hosted on the OpenfMRI website: https://openfmri.org/dataset/ds000117/

• Download all the files available for dowload 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 this package. 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 where you downloaded all the datasets.

• 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 put 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 will be later excluded from the EEG group analysis because the position of the electrodes is incorrect, so it was not the best example.

• Switch to the "anatomy" view.

• Right-click on the TutorialAuditory folder > New subject > sub002

  • Leave the default options you set 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 surface-based cortical atlases and the atlas of sub-cortical regions (ASEG).
  
  

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 FIF files in: Sub001/MEEG
    
    

• Events: Ignore
  We will read events for the stimulus channel and define trial definitions 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 the three fiducial points NAS/LPA/RPA. All the anatomical 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]
  
  

• Close all the windows (use the [X] button at the top-right corner of the Brainstorm window).

Import event markers

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 here illustrate 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, Value.
  Do not execute the process, we will add other processes to classify the markers.
  
  

• Add process Events > Merge events to create the labeled groups from numeric event codes (x3):

  • Famous: 5, 6, 7
  • Unfamiliar: 13, 14, 15
  • Scrambled: 17, 18, 19

• 

• Because the detection only looks for values, multiple events can be detected in one trial. For example, a value of 7 represents a Famous trial, but during the presentation another event 4101 event occurs. The value of channel STI101 goes from 7 to 4101, then back to 7. The reading
  another event occurred as well. The value went from 7 to 4101, for example, and then back to 7. In this case, the 7 would be counted twice.

• In the Record tab, menu Events > Detect multiple responses, remove the extra events

  • Response events: Famous

  • Minimum delay between events: 2200ms

  • Select Keep only the first event
    
    

• The stimulus presentation to the subject has a delay of 34.5ms, which can be corrected with an offset.

• In the Record tab, menu Events > Add time offset

  • Event names: Famous

  • Time offset: 34.5ms
    
    

• Complete these same steps (merge, detect multiple and add time offset) for types Unfamiliar and Scrambled.

Pre-processing

Spectral evaluation

• Drag and drop 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.
  
  

• 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: 293Hz, 307Hz, 314Hz, 321Hz, 328Hz.

  • 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 immediately after 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 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 correction with SSP

Artifact detection

In the record tab, run the following menus:

• Artifacts > Detect heartbeats: Channel name=EEG063, All file, Event name=cardiac

• In many of the other tutorials, you will have detected the blink category and used the SSP process to remove the blink artifact. In this experiment, we are particularly interested in the subject's response to seeing the stimulus. Therefore we will mark eyeblinks and other eye movements as BAD.

• Artifacts > Detect events above threshold: Channel name=EEG062, All file, Event name=blink_BAD, Maximum threshold=100, Threshold units=uV, Filter=[0.30,20.00]Hz, Use absolute value is checked
  
  
  
  

• Close all the windows (using the [X] button).

Heartbeats

• Empty the Process1 list (right-click > Clear list).

• Drag and drop the continuous processed file ("Raw | notch(50Hz...)") to the Process1 list.
• Select the following processes and run the pipeline:

  • Artifacts > SSP: Heartbeats > Sensor type: MEG MAG

  • Artifacts > SSP: Heartbeats > Sensor type: MEG GRAD
    
    

• 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, 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 SENSOR ARTIFACTS (SQUID JUMPS): Because of the different sensor technologies, one can expect that the different MEG systems may produce different types of artifact. With the Neuromag system, used for this experiment, one can see an artifact produced by the sensors which is exaggerated by the pre-processing completed with Max Filter, seen here in the examples below. The spacial filtering of Max Filter causes the artifact to be speard across most sensors and also spread a bit in time. Ideally, the offending should be marked bad before applying the Max Filter. In the case of this dataset, we have the artifacts - sometimes more frequent than others. The 1-7Hz artifact detection employed here will usually catch them, but it is important to review all the sensors and all the time in each recording to be sure these events are marked as bad segments.
  
  
  

Prepare all runs

Complete the above steps for Runs 2-6:
Access the recordings
Pre-processing
Artifact detection

Epoching and averaging

Import epochs

• Drag and drop the 6 pre-processed raw folders in Process1 > Run

• Run the two processes together: Import recordings > Import MEG/EEG: Events and Pre-process > Remove DC offset
  
  

Average

• Drag and drop all the imported trials in Process1.

• Run > Average > Average files: By trial groups (folder average)
  
  

Review EEG ERP

• EEG evoked response (famous, scrambled, unfamiliar):
  
  

• Make a cluster with channel EEG065 and overlay the channel across the three conditions.

  • Display the EEG time series for one of the averages.

  • Select EEG065

  • In the Cluster tab, select the new selection button (NEW SEL) and check the box, overlay conditions
    
    

• Select the cluster then select three average files and right click > Clusters time series
  
  

• Around 170ms (N170) there is a greater negative deflection for Famous than Scrambled faces and as well as a difference between Famous and Unfamiliar faces after 250ms.

Empty room recordings

MEG

For this dataset, one empty room recording will be used for all subjects.

• Create a new subject: emptyroom

• Create a link to the raw file: sample_group/emptyroom/090707_raw_st.fif

• Apply the same notch filter as for the data

• Compute the noise covariance. Right-click on Raw | notch > Noise covariance > Compute from recordings

• Copy the noise covariance to Sub001. Right-click on the Noise covariance > Copy to other subjects
  
  

EEG

Compute a EEG noise covariance for EACH RUN using the EEG recordings and merge it with the existing noise covariance, which contains the noise covariance for MEG.

• Expand the folder run_01_sss_notch to see the imported files. Select all imported trials, Right-click > Noise covariance > Compute from recordings, Time window=[-300,0]ms, Sensor types=EEG, select Merge.

• Repeat for runs 2-6.

Source estimation

Head Model

We will compute one head model file which contains both the Overlapping Spheres (MEG) model and OpenMEEG BEM (EEG) model. To compute the OpenMEEG BEM on the EEG, it is necessary to prepare the BEM surfaces.

• Switch to the "Anatomy" view. Right-click on Sub001 > Generate BEM surfaces. Select the default values. If you have memory errors while generating the model (below), you can reduce the number of vertices in these BEM surfaces.
  
  

• Switch back to the "Functional" view. Drag and drop the 6 imported trial folders in Process1.

• Run > Sources > Compute head model: Overlapping spheres (MEG) and OpenMEEG BEM (EEG). It will take quite a long time to compute the BEM models using the default values.

Source Model

• Drop all imported files into the Process1 box

• MEG: Run > Sources > Compute sources, Sensor types=MEG, Leave all the default options to calculate a wMNE solution with constrained dipole orientation. Click Run.

• EEG: Run > Sources > Compute sources, Sensor types=EEG, Leave all the default options to calculate a wMNE solution with constrained dipole orientation.

Other subjects

• sub001: Bad registration
• sub006:
• sub016:

Scripting

Corresponding script in the Brainstorm distribution:
TODO: Coming soon.

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