PROCESSING YOUR EEG DATA
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- Anabel Lawson
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1 PROCESSING YOUR EEG DATA Step 1: Open your CNT file in neuroscan and mark bad segments using the marking tool (little cube) as mentioned in class. Mark any bad channels using hide skip and bad. Save the file. Step 2: Open Matlab. Change default directory to P:\EEG\Matlab. In the Current Folder window, find S1_EEG_Preprocess.m and double click. It will open in the editor window. Step 3: Run each cell in the script. Place your cursor at the top of the editor window, and then press the little button, or press Ctl Shift Enter to run the cell and advance to the next. Follow any instructions that appear in the popup box. Step 4: Open and run script S2_Identify_ICs_to_remove.m. This runs the ADJUST algorithm to remove ocular and other artifacts. a. For more information on this refer to the ADJUST Tutorial (appended to these instructions) b. Once you have determined which ICs to remove make sure to click the Accept button of the IC component so it changes to say Reject. After it changes hit OK and the window will close and the color above the headmap will change to a pinkish color. Step 5: IMPORTANT!!!! Once you finish using ADJUST to mark bad components (all pink on the component number), and close both windows with the head maps (by clicking OK on those windows), you must type the following in the command window: WriteICsToRemove (Case Sensitive). This last step saves your list of independent components that you selected for removal. You ll see a text file has been created named _ICs2Remove.txt (where is your file name) in the folder where the data are stored. Step 6: Your mission is complete for now. You have an epoched file that has removed bad segments, interpolated bad channels, removed crap at the end, and you have selected the independent components that need to be removed. Next, we ll be conducting re referencing, running the FFT using a Hamming window, and getting the average spectral power by site. This script is awaiting a few tweaks so that you get feedback and instruction as you go. I ll update you when it s read. Await further instructions!
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4 What is ICA? ICA is a "blind source separation" technique. ICA separates sources of activity that are mixed together at recording electrodes.
5 What is ICA? For EEG data Channel data (X) can be thought of as a weighted (W) combination of independent component activations (Wx), each of which has a scalp projection (W -1 ). You can think of ICs as putative sources of the scalp-recorded EEG.
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7 What is ADJUST? ADJUST= Automatic EEG artifact Detection based on the Joint Use of Spatial and Temporal features Automatic ICA-based algorithm that identifies artifact-related IC components Uses both spatial and temporal distributions Combines stereotyped features to efficiently and systematically reject an artifact Mognon, Jovicich, Bruzzone, & Buiatti, 2010
8 How does it work? EEG is decomposed into ICs (done in EEGlab) ICs defined only by statistical relationships. It knows nothing about where electrodes are Detectors are applied for 4 types of artifacts Computes class-specific spatial and temporal features on all ICs Each feature has a threshold dividing artifacts from non-artifacts For each detector, ICs identified as artifacts if features associated with the artifact exceed their respective threshold. Mognon, Jovicich, Bruzzone, & Buiatti, 2010
9 Features Spatial Average Difference (SAD) Temporal Kurtosis (TK) Maximum Epoch Variance (MEV) Spatial Eye Difference (SED) Generic Discontinuities Spatial Feature (GDSF)
10 Features Spatial Average Difference (SAD) Spatial topography of blink ICs Looks for higher amplitude in frontal vs. posterior areas Temporal Kurtosis (TK) Kurtosis over the IC time course Kurtosis is "peakedness" of the distribution (i.e. distribution of timepoints in the epoch) Looks for outliers in amplitude distribution typical of blinks Mognon, Jovicich, Bruzzone, & Buiatti, 2010
11 Features Maximum Epoch Variance (MEV) Is a ratio of variance in epoch with most variance compared to mean variance over all epochs Looks for slower fluctuations typical of vertical eye movement Spatial Eye Difference (SED) Looks for large amplitudes in frontal areas in antiphase typical of horizontal eye movement Generic Discontinuities Spatial Feature (GDSF) Looks for local spatial discontinuities Mognon, Jovicich, Bruzzone, & Buiatti, 2010
12 Where to begin? Pre-processing Clean file for non-stereotyped gross artifacts AKA Muscle activity and other external factors Variable spatial distribution that could take up a lot of ICs Low-Pass filtering, if appropriate for your data, can remove some artifacts and prevent so many ICs from capturing these higherfrequency noise artifacts ICA From EEGlab or, if not performed already, can be called from ADJUST Run ICA d files with ADJUST Import dataset into EEGLab Tools ADJUST Use script and select file OR
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14 Component Head Maps # of channels in EEG data = # of components Typically more true components than channels Multiple true components combined into a single ICA component We have 64 components because we had 64 channels ADJUST will highlight in red the components it identified as artifacts
15 Looking at an individual IC Head map IC activity plotted against trial Activity power spectrum Features and thresholds Press to Reject IC
16 Component Data Scroll Shows the activity of 64 components across epochs 10
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19 Eye blinks Features used Spatial Average Difference (SAD) Temporal Kurtosis (TK) Frontal distribution High power in delta frequency band In component data scroll high potentials with morphology of eye blink (like in EEG) can be observed
20 All have SAD and TK features over threshold All have a frontal distribution All have higher power in delta band
21 Look at Component Scroll for what IC 1 looks like High potentials with these morphology further suggest the IC component is in fact eye blink related
22 Vertical Eye Movement Features used Spatial Average Difference (SAD) Maximum Epoch Variance (MEV) Frontal distribution similar to that of an eye blink
23 Frontal distribution It appears that the artifact is mostly driven by what is happening around trial 200 SAD and MEV features are over threshold
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25 Horizontal Eye Movement Features used Spatial Eye Difference (SED) Maximum Epoch Variance (MEV) Frontal distribution in anti-phase (one positive and one negative)
26 Anti-phase, primarily frontal distribution In the IC Activity by trial, three sections stand out SED and MEV features are over threshold
27 Trial Trials
28 Generic Discontinuities Features used Generic Discontinuities Spatial Feature (GDSF) Maximum Epoch Variance (MEV) Variable distribution Sudden amplitude fluctuations with no spatial preference Could be present in as little as one or 2 trials, and limited to 1 channel In component data scroll weird activity in the trial plotted on the IC activity
29 GDSF and MEV features over threshold Variable distribution even at a single channel IC activity shows a lot of variability across epochs and doesn t show one as responsible
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31 GDSF and MEV features over threshold Variable distribution. In this case, present at a single channel In the IC Activity by trial, one section stands out
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33 So do we reject all of the ICs ADJUST tells us too? If ADJUST has identified a component as bad, we mark it as bad UNLESS there is clear evidence that over-rules that verdict. Additionally, we need to be looking for cases where ADJUST will miss artifacts Specially, lateral eye movements seem to be missed with some frequency in ERP tasks since folks don't make large movements.
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