= Elekta-Neuromag recordings =
This tutorial describes how to process continuous Elekta-Neuromag MEG recordings. It is based on median nerve stimulation acquired at the Massachusetts General Hospital in 2005 with a Neuromag Vectorview 306 system. The sample dataset contains the results for one subject for both arms: 18 minutes, 300 stimulations per arm.

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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== Download and installation ==
 * '''Requirements''': You have already followed all the basic tutorials and you have a working copy of Brainstorm installed on your computer.
 * Go to the [[http://neuroimage.usc.edu/bst/download.php|Download]] page of this website and download the file '''sample_neuromag.zip'''
 * Unzip  it in a folder that is not in any of the  Brainstorm folders (program  folder or database folder). This is really  important that you always  keep your original data files in a separate  folder: the program folder  can be deleted when updating the software,  and the contents of the  database folder is supposed to be manipulated  only by the program  itself.
 * Start Brainstorm (Matlab scripts or stand-alone version)
 * Menu File > Create new protocol > '''TutorialNeuromag''', with the following options:
  * '''No, use individual anatomy''',
  * '''No, use one channel file per run'''.<<BR>><<BR>> {{attachment:createProtocol.gif||height="372",width="347"}}

== Import the anatomy ==
 * Right-click on the TutorialNeuromag folder > New subject > Subject01 (leave all the defaults).<<BR>><<BR>> {{attachment:createSubjectMenu.gif||height="165",width="343"}}  {{attachment:createSubject.gif||height="309",width="296"}}
 * Right-click on the subject node > Import anatomy folder:
  * Set the file format: "FreeSurfer folder"
  * Select the folder: '''sample_neuromag/anatomy'''
  * Number of vertices of the cortex surface: 15000 (default value) <<BR>><<BR>> {{attachment:mriImportMenu.gif||height="224",width="180"}}  {{attachment:mriFile.gif||height="167",width="362"}}
 * Set the 6 required fiducial points (indicated in MRI coordinates):
  * NAS: x=131,  y=232,  z=123
  * LPA: x=48,  y=136,  z=74
  * RPA: x=204,  y=131,  z=67
  * AC: x=127,  y=143,  z=118
  * PC: x=127,  y=117,  z=111
  * IH: x=127,  y=120,  z=167 (anywhere on the midsagittal plane)
 * 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.<<BR>><<BR>> {{attachment:anatomy.gif||height="248",width="400"}}

== Access the recordings ==
=== Link the FIF file to the database ===
 * The sample_neuromag package contains one run for one subject only.
 * Switch to the "functional data" view, the middle button in the toolbar above the database explorer.
 * Right click on the Subject01 > Review raw file: <<BR>><<BR>> {{attachment:reviewMenu.gif||height="159",width="210"}} {{attachment:reviewFile.gif||height="160",width="427"}}
  * Select the file format: '''MEG/EEG Neuromag FIFF (*.fif)'''
  * Pick the file: '''sample_neuromag/data/mind004_050924_median01_raw.fif'''
 * Select "Event channel" when asked about the events.<<BR>><<BR>> {{attachment:eventsImport.gif||height="157",width="280"}}
 * Then you have to select from which technical tracks you want to read the events. <<BR>><<BR>> {{attachment:eventsChannels.gif||height="165",width="375"}}
 * In this dataset, the tracks of interest are:
  * '''STI 001''': Contains the onsets of the electric stimulation of the '''right '''arm.
  * '''STI 002''': Contains the onsets of the electric stimulation of the '''left '''arm.
  * These are not standard settings, they depend on your acquisition setup. In most cases, you would rather import "events" defined with the Neuromag acquisition software, which are saved in tracks STI 014, STI 101, STI 201...
 * Select '''STI 001''' and '''STI 002'''. The full tracks are read, all the changes of values are detected from these two tracks and a list of events is created.
 * At the end, you're asked if you want to "Refine the registration with the head  points". This operation improves the initial MRI/MEG registration by fitting the head points digitized at the MEG acquisition and the scalp surface. Answer '''YES'''.<<BR>><<BR>> {{attachment:refine.gif||height="170",width="324"}} <<BR>>
 * Always make sure that the final registration looks good. The  yellow surface represents the inner surface of the MEG helmet and the  green dots represent the head points that were saved with the MEG  recordings. In this case the registration looks acceptable. If  you consider it is not the case, you can fix it manually: right-click on the channel file > MRI registration > Edit. <<BR>><<BR>> {{attachment:checkRegistrationFig.gif||height="199",width="218"}}

=== Review the recordings ===
 * Right-click on the "Link to raw file" to see what types of channels are available:<<BR>><<BR>> {{attachment:listTypes.gif||height="341",width="332"}}
  * '''MEG (all)''': Represents all the MEG sensors in the file (magnetometers and gradiometers)
  * '''MEG (magnetometers)''': 101 magnetometers (sensor names ending with a "1")
  * '''MEG (gradiometers)''': 202 planar gradiometers (sensor names ending with "2" or "3")
  * '''ECG''': Electro-cardiogram
  * '''EOG''': Electro-oculogram
  * '''Stim''': All the stimulation lines
 * Double-click on the file to display all the MEG sensors.
 * In the Record tab, look at the list of the available default display configurations for the Neuromag Vectorview MEG systems. If you would like to use different combinations of sensors, you can create your own combinations with the entry "Edit montages..."<<BR>><<BR>> {{attachment:montages.gif||height="333",width="457"}}

== Pre-processing ==
=== Evaluate the recordings ===
 * Drag and drop the "Link to raw file" into the Process1 list.
 * Select the process "'''Frequency > Power spectrum density'''", configure it as follows:<<BR>><<BR>> {{attachment:processPsd.gif||height="358",width="487"}}
 * In all the processes, the types of sensors can be specified using the following convention:
  * '''MEG''': All the MEG sensors
  * '''MEG MAG''': All the magnetometers
  * '''MEG GRAD''': All the gradiometers
  * '''MEG GRAD2''': Only the first axial gradiometer on each chip (name ends with a "2")
  * '''MEG GRAD3''': Only the second axial gradiometer on each chip  (name ends with a "3")
 * Double-click on the PSD file to display it.<<BR>><<BR>> {{attachment:processPsdView.gif||height="179",width="383"}}
 * This power spectrum shows that there is no MEG sensor that is clearly bad, but some sensors show a strong contamination from the power lines (60Hz and harmonics).

=== Remove: 60Hz and harmonics ===
 * __Preliminary note__: This process is very time and resource consuming. If you are not planning to analyze anything specifically around 60Hz, you may want to skip this section and and the long computation time associated with it. It is described here as a reference for users who would need it.
 * The standard procedure illustrated for removing the 60Hz power line noise illustrated in the CTF-based introduction tutorial would be simply to run the process "Pre-process > Notch filter"  on the continuous file. However, this case is a bit more complicated.
  * If you try to run this process without selecting the option "Process the entire file at once", you would get the following error. The file already contains some SSP projectors, created by one of the Neuromag progams. Using these projectors requires all the sensors, and running frequency filters requires all the time samples at once. As a consequence, the entire file must be read in one block in order to apply frequency filters on it. <<BR>><<BR>> {{attachment:sinError.gif||height="234",width="658"}}
  * Alternatively, if you try with the  option "Process the entire file at once", you would probably crash Matlab or freeze your computer because of a lack of memory. The file is already large and this process requires to create a lot of matrices of the same size in memory. Do not try this unless you have at least 24Gb of memory available on your computer.
  * The solution is to re-write an intermediate file with the SSP projectors applied, that you will be able to process easily after.
 * Select the "Link to raw file" in Process1 and run process "'''Artifacts > Apply SSP and CTF compensation'''". This creates a new .fif file which is an exact copy of the original .fif file, but with the SSP projectors applied to the recordings values (instead of being just saved as linear operators on the side).<<BR>><<BR>> {{attachment:processApplySsp.gif||height="145",width="270"}}
 * Clear the Process1 list and select the new continuous file "'''Raw | clean'''"
 * Run the process  "'''Pre-process > Notch filter'''", configured as follows:<<BR>>(this may take a while complete...)<<BR>><<BR>> {{attachment:processSin.gif||height="274",width="336"}}
 * To evaluate the results of this process, select the last file generated ('''"Raw | clean | notch"''') and run again the process "'''Frequency > Power spectrum density'''".<<BR>><<BR>> {{attachment:processPsd2.gif||height="351",width="396"}}
 * You should observe a significant decrease of the contributions of the removed frequencies (60Hz, 120Hz, 180Hz) compared with the original spectrum. <<BR>><<BR>> {{attachment:processPsdView2.gif||height="202",width="425"}}

=== Heartbeats and eye blinks ===
Signal Space Projection (SSP) is a method for projecting the recordings away from stereotyped artifacts, such as eye blinks and heartbeats.

 * Double-click on the last continuous file you got to display all the '''MEG '''recordings.<<BR>>("Raw | clean | notch" with the notch filter, or "Link to raw file" without)
 * Right-click on the link > '''ECG '''> Display time series, to look at the heartbeats.
 * Right-click on the link > '''EOG '''> Display time series, to look at the eye movements.
 * From the SSP menu in the Record tab, run the automatic detections:
  * '''Detect  heartbeats:''' Select channel '''ECG 063''', event name "cardiac".<<BR>><<BR>> {{attachment:processDetectEcg.gif||height="214",width="310"}}
  * '''Detect eye blinks:''' Select channel '''EOG 062''', event name "blink".<<BR>><<BR>> {{attachment:processDetectEog.gif||height="213",width="309"}}
  * '''Remove simultaneous:''' To avoid capturing ocular artifacts in the cardiac SSP.<<BR>>Remove events named: "'''cardiac'''"<<BR>>When too close from events: "'''blink'''"<<BR>>Minimum delay between events: '''250ms'''.<<BR>><<BR>> {{attachment:processRemoveSimult.gif||height="234",width="309"}}
 * Review the traces of ECG/EOG channels and make sure the events detected make sense.<<BR>><<BR>> {{attachment:processDetectAfter.gif||height="240",width="229"}}
 * From the same menu, run the following processes, separately for GRAD and MAG:
  * '''Compute SSP: Heartbeats''': Event "cardiac", sensor types="'''MEG MAG'''", use existing SSP.<<BR>>(select component #1) <<BR>><<BR>> {{attachment:sspEcgMag.gif||height="218",width="560"}}
  * '''Compute SSP: Heartbeats''': Event "cardiac", sensor types="'''MEG GRAD'''", use existing SSP.<<BR>>(select component #1) <<BR>><<BR>> {{attachment:sspEcgGrad.gif||height="219",width="561"}}
  * '''Compute SSP: Eyeblinks''': Event "blink", sensor types="'''MEG MAG'''", use existing SSP.<<BR>>(select component #1) <<BR>><<BR>> {{attachment:sspEogMag.gif||height="218",width="560"}}
  * '''Compute SSP: Eyeblinks''': Event "blink", sensor types="'''MEG GRAD'''", use existing SSP.<<BR>>(select component #1)<<BR>><<BR>> {{attachment:sspEogGrad.gif||height="218",width="560"}}
 * For more information regarding this SSP method, refer to this tutorial:<<BR>>[[Tutorials/TutRawSsp|Detect and remove artifacts]].
 * At this stage, you should also review the entire file (pressing repeatedly F3) to detect any obvious bad segment in the recordings. If you detect any, select the time window to mark as bad, right click on the figure > Reject time segment.

== Epoching and averaging ==
=== Import the recordings ===
 * Right-click on the raw link > Import in database.<<BR>><<BR>> {{attachment:importPopup.gif||height="298",width="193"}}
 * The following figure appears, that asks how to import these recordings in the Brainstorm database.<<BR>><<BR>> {{attachment:importOptions.gif||height="364",width="580"}}
  * '''Time window''': Time range of interest, keep all the time definition.
  * '''Split''': Useful to import continuous recordings without events. We do not need this here.
  * '''Events selection''': Check the "Use events" option, and select both '''STI 001 '''and '''STI 002'''. The values in the parenthesis represent the number of occurrences of each event.
  * '''Epoch time''': Time instants that will be extracted before an after each event, to create the epochs that will be saved in the database. Set it to [-100, +300] ms
  * '''Use Signal Space Projections''': Save and use the SSP vectors created by MaxFilter, MNE and Brainstorm. Keep this option selected.
  * '''Remove DC Offset''': Check this option, and select: Time range: [-100, 0] ms. <<BR>>For each epoch, this will: compute the average of each channel over the baseline (pre-stimulus interval: -100ms to 0ms), then subtract it from the channel at all the times in [-100,+300]ms.
  * '''Resample recordings''': Keep this unchecked
  * '''Create a separate folder for each epoch type''': If selected, a new folder is created for each event type (here, it will create two folders "STI 001" and "STI 002"). If not selected, all the epochs from all the selected events are saved in the same folder.
  * Click on [Import] and wait.
 * Rename the condition "'''STI_001_5'''" and "'''STI_002''''''_5'''" into respectively "'''Right'''" and "'''Left'''" (Right-click > Rename, or press F2, or click twice waiting a while before the two clicks).
 * Rename the groups of trials to '''Left''' and '''Right'''.<<BR>><<BR>> {{attachment:rename.gif||height="105",width="225"}}
 * At this stage, you should review the trials one after the other (press F3 to jump to the next file), separately for the magnetometers and the gradiometers, to make sure that you don't have any bad trial that have been imported. If you find a bad trial: right-click on the file or on the figure > Reject trial.

=== Averaging ===
 * Drag and drop all the left and right trials to the Process1 tab.
 * Run the process '''Average > Average files > By condition''': <<BR>><<BR>> {{attachment:processAverage.gif||height="452",width="451"}}
 * Double-click on the Left and Right averages to display all the MEG sensors:<<BR>><<BR>> {{attachment:averageArtifact.gif||height="196",width="480"}}

=== Stimulation artifact ===
 * We see clearly our evoked responses in these figures, but the stimulation artifact between 0ms and 4ms causes the automatic scaling of the figures to be too high, especially for the right stimulation. This effect would get a lot worse when displaying the sources for these files. To get a better display of these averages, we can cut these peaks at 0ms by replacing the values with linear interpolations.
 * Select the averages for the Left and Right condition in the Process1 tab.
 * Run the process '''Artifacts > Cut stimulation artifact''': 0-4ms, overwrite<<BR>><<BR>> {{attachment:processCut.gif||height="239",width="471"}}
 * Now you can display the Left and Right averages correctly: Right-click on the file > MEG (All) > Display time series.
 * Display the 2D topographies for each average: Right-click on the file > MEG (All) > 2D Sensor cap (or press CTRL+T from the time series figures).
 * You can also add a low-pass filter at 100Hz for the visualization.<<BR>><<BR>> {{attachment:reviewAverages.gif||height="378",width="791"}}
 * Everything looks ok, the time series figures show a clean signal with a very high SNR, and the topographies at the first response peak (about 22ms) show an activity on the left side for the Right condition, and on the right side for the Left condition.

== Gradiometers & magnetometers ==
==== Scaling factor ====
Magnetometers  record values in Tesla (T), while gradiometers record values in Tesla per meter (T/m). The range of values obtained is not the same, therefore it is difficult to represent the two types of signals in the same figures.

We can convert the gradiometers values from T/m to T by multiplying them with the distance between the two gradiometer coils (0.0168 meters on the VectorView MEG system). But this still produces values that are too small to be represented with the same scale as the magnetometers. A more practical multiplication factor of '''0.04''' was proposed by Matti Hamalainen.

In the time series figure and for Elekta-Neuromag systems (all versions), the gradiometer values are always multiplied by 0.04. This is an empirical scaling factor that is used for visualization only, it is never saved in the recordings and is not used for any other purpose.

==== Magnetic interpolation ====
 * You can also display the MEG MAG (top) and MEG GRAD (bottom) sensors separately: <<BR>><<BR>> {{attachment:averageMagGrad.gif||height="319",width="467"}}
 * The topographies look very similar, because all the values are re-interpolated on a surface of virtual magnetometers. To display the real values for the different types of sensors, without this magnetic interpolation, use the menus "No magnetic interpolation".
 * Right-click on Left > MEG (mag) > No magnetic interpolation > 2D Sensor cap. <<BR>><<BR>> {{attachment:averageMagNointerp.gif||height="196",width="235"}}
 * Repeat the same operation for "MEG (gradiometers)". You now have three options, because it is not possible to display at the same time the values for the two planar gradiometers:
  * Grad 2: First gradiometer, sensor names ending with "2"
  * Grad 3: Second gradiometer, sensor names ending with "3"
  * Grad norm: Norm of the two gradiometers => sqrt(grad2^2^ + grad3^2^)
 * The three options side-by-side at 22ms (grad 2, grad3, norm): <<BR>><<BR>> {{attachment:averageGradNointerp2.gif||height="165",width="542"}}

== Source estimation ==
We need now to calculate a source model for these recordings, using a noise covariance matrix calculated from the pre-stimulation baselines. This process is not detailed a lot here because it is very similar to what is shown in the CTF-based introduction tutorials.

==== Head model ====
 * Right-click on the channel file > Compute head model.<<BR>><<BR>> {{attachment:headmodelMenu.gif||height="196",width="228"}}
 * Use the overlapping spheres model and keep all of the options at their default values.<<BR>><<BR>> {{attachment:headmodelOptions.gif||height="247",width="222"}}
 * For more information: [[Tutorials/TutHeadModel|Head model tutorial]].

==== Noise covariance ====
 * Select all the Left and Right trials, right-click > Noise covariance > Compute from recordings.<<BR>><<BR>> {{attachment:noisecovPopup.gif||height="188",width="420"}}
 * Leave all the default options and click [OK]. <<BR>><<BR>> {{attachment:noisecovOptions.gif||height="374",width="382"}}
 * For more information: [[Tutorials/TutNoiseCov|Noise covariance tutorial]].

==== Inverse model ====
 * Right-click on the headmodel > Compute sources.<<BR>><<BR>> {{attachment:inversePopup.gif||height="131",width="224"}}
 * Select wMNE and all the default options. This will run a source reconstruction grouping the information from the magnetometers and the gradiometers into the same model. This is the recommended procedure, but you can also estimate sources for the two types of sensors separately if needed. <<BR>><<BR>> {{attachment:inverseOptions.gif||height="233",width="207"}}
 * A shared inversion kernel is created in the ''(Common files)'' folder, and a link node is now visible for each recording file, single trials and averages. <<BR>><<BR>> {{attachment:inverseFiles.gif||height="239",width="229"}}
 * For more information: [[Tutorials/TutSourceEstimation|Source estimation tutorial]].

==== Scouts ====
You can easily reproduce exactly the same results as the ones presented in the introduction tutorials. Place scouts to capture the activity in the primary and secondary somatosensory areas to track the processing of the electric stimulations in time, at the surface surface of the brain.

{{attachment:final.gif||height="419",width="842"}}

== Scripting ==
The operations described in this tutorial can be reproduced from a Matlab script, available in the Brainstorm distribution: '''brainstorm3/toolbox/script/tutorial_neuromag.m '''

== Discussion ==
 * Combining magneto+gradiometers: http://neuroimage.usc.edu/forums/showthread.php?1900

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