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| This page provides some general recommendations for your group analysis. It is not directly related with the auditory dataset, but provides guidelines that have to be considered for any MEG/EEG experiment. <<TableOfContents(2,2)>> == Reminder == '''Averaging/contrasting MEG sensor data''' * MEG channels are not aligned across subjects (or sessions) because the physical position of channels varies with respect to the head. <<BR>>As a result, '''do not contrast/average MEG channel data across subjects or sessions'''. * However, even though this is not recommended for formal analysis, it can be extremely useful for data exploration. Most of channel patterns are spatially smooth and averaging across subjects will probably highlight interesting effects, and suggest time points and sensors with experimental effects. Examples include auditory/language signals (auditory cortices align reasonably well), attention effects (parietal/occipital alpha is fairly consistent across subjects) and most other perceptional/cognitive processes. * Note for maxfilter users: A good practice is to align all within-subject data to a reference fif file (align all sessions to a reference session). This will allow direct channel comparisons within-subject. Aligning data across subjects is not recommended since it can introduce large data distortions (though sometimes it may work well). * This does not apply to EEG because it uses standard channel configurations (e.g. 10-20). '''Averaging/contrasting cortical maps''' * Cortical maps have ambiguous signs across subjects: reconstructed sources depend heavily on the orientation of true cortical sources. Given the folding patterns of individual cortical anatomies vary considerably, cortical maps have subject-specific amplitude and sign ambiguities (e.g. positive vs. negative sources). This is true even if a standard anatomy is used for reconstruction. * As a result, to average/contrast cortical maps: * '''Across subjects: Rectify the cortical maps''' (absolute values) * '''Within subject: Do not rectify the cortical maps''' == Subject-level statistics == For one unique subject, test for significant differences between two experimental conditions: * Compare the '''single trials''' corresponding to each condition. * In most cases, you '''do not need to normalize''' the data. * Use '''independent tests'''. * For help with the implications of testing the '''relative or absolute values''', see: [[Tutorials/Difference|Difference]]. '''Sensor recordings''': * Not advised for MEG with multiple runs, correct for EEG. * '''A vs B''': * Never use an absolute value for testing recordings. * '''Parametric''' or '''non-parametric''' tests, independent, two-tailed, FDR-corrected. * Correct effect size, ambiguous sign. '''Constrained source maps''' (one value per vertex): * Use the non-normalized minimum norm maps for all the trials (current density maps, no Z-score). * '''A vs B''': * Null hypothesis H0: (A=B). * '''Parametric''' or '''non-parametric''' tests, independent, two-tailed, FDR-corrected. * Correct effect size, ambiguous sign. * '''|A| vs |B|''': * Null hypothesis H0: (|A|=|B|). * '''Non-parametric''' tests only, independent, two-tailed, FDR-corrected. * Incorrect effect size, meaningful sign. '''Unconstrained source maps''' (three values per vertex): * Use the non-normalized minimum norm maps for all the trials (current density maps, no Z-score). * We need to test the '''norm '''of the three orientations instead of testing the orientations separately. * '''Norm(A) vs. Norm(B)''': * Null hypothesis H0: (|A|=|B|). * '''Non-parametric''' tests only, independent, two-tailed, FDR-corrected. * Incorrect effect size, meaningful sign. '''Time-frequency maps''': * Test the non-normalized time-frequency maps for all the trials (no Z-score or ERS/ERD). * The values tested are power or magnitudes, all positive, so (A=B) and (|A|=|B|) are equivalent. * '''|A| vs |B|''': * Null hypothesis H0: (|A|=|B|) * '''Non-parametric''' tests only, independent, two-tailed, FDR-corrected. * Correct effect size, meaningful sign. == Group-level statistics [TODO] == ==== Subject averages ==== You need first to process the data separately for each subject: 1. Compute the ''' subject-level averages''', using the '''same number of trials''' for each subject.<<BR>> Sources: Average the non-normalized minimum norm maps (current density maps, no Z-score). 1. Sources and time-frequency: '''Normalize '''the data to bring the different subjects to the same range of values (Z-score normalization with respect to a baseline - never apply an absolute value here). 1. Sources computed on individual brains: '''Project '''the individual source maps on a template (see the [[Tutorials/CoregisterSubjects|coregistration tutorial]]). Not needed if the sources were estimated directly on the template anatomy. <<BR>>Note: We evaluated the alternative order (project the sources and then normalize): it doesn't seem to be making a significant difference. It's more practical then to normalize at the subject level before projecting the sources on the template, so that we have normalized maps to look at for each subject in the database. 1. Constrained sources: '''Smooth '''spatially the sources, to make sure the brain responses are aligned. '''Problem''': This is only possible after applying an absolute value, smoothing in relative values do not make sense, as the positive and negative signals and the two sides of a sulcus would cancel out. [TODO] ==== Group statistic ==== Two group analysis scenarios are possible: * '''One condition''' recorded for multiple subjects, comparison between '''two groups of subjects''': * Files A: Averages for group of subjects #1. * Files B: Averages for group of subjects #2. * Use '''independent tests''': Exactly the same options as for the single subject (described above) * '''Two conditions''' recorded for multiple subjects, comparison across '''all subjects''': * Files A: All subjects, average for condition A. * Files B: All subjects, average for condition B. * Use '''paired tests''' (= dependent tests), special cases listed below. ==== Paired tests ==== * '''Sensor recordings''': * '''(A-B=0)''': Parametric or non-parametric tests, two-tailed, FDR-corrected. * '''Constrained source maps''' (one value per vertex): * '''(A-B=0)''': Parametric or non-parametric tests, two-tailed, FDR-corrected. * '''(|A|-|B|=0)''': Non-parametric tests, two-tailed, FDR-corrected. * '''Unconstrained source maps''' (three values per vertex): * '''(Norm(A-B)=0)''': Non-parametric tests, __'''one-tailed'''__ (non-negative statistic), FDR-corrected. * '''(Norm(A)-Norm(B)=0)''': Non-parametric tests, two-tailed, FDR-corrected. * '''Time-frequency maps''': * '''(|A|-|B|=0)''': Non-parametric tests, two-tailed, FDR-corrected. * For help with '''relative/absolute options''', read the previous tutorial: [[Tutorials/Difference|Difference]]. |
This page provides some general recommendations for your event-related analysis. It is not directly related with the auditory dataset, but provides guidelines you should consider for any MEG/EEG experiment. <<BR>>We do not provide standard analysis pipelines for resting or steady state recordings yet, but we will add a few examples soon in the section [[http://neuroimage.usc.edu/brainstorm/Tutorials#Other_analysis_scenarios|Other analysis scenarios]] of the tutorials page. <<TableOfContents(3,2)>> == What is your question? == The most appropriate analysis pipeline for your data depends on the question you are trying to answer. Before defining what are the main steps of your analysis, you should be able to state clearly the question you want to answer with your recordings. ==== What dimension? ==== * MEG/EEG recordings * Cortical sources * Individual anatomy or template * Constrained (one value per vertex) or unconstrained (three values per grid point) * Full cortex or regions of interests * Frequency or time-frequency maps ==== What kind of experiment? ==== * '''Single subject''': Contrast two experimental conditions across trials, for one single subject. * Files A: Single trials for condition A. * Files B: Single trials for condition B. * '''Group analysis, within subject''': Contrast two conditions A and B measured for each subject. * Files A: Subject-level averages for condition A (all the subjects). * Files B: Subject-level averages for condition B (all the subjects). * '''Group analysis, between subjects''': Contrast two groups of subjects for one condition. * Files A: Subject-level averages for group #1. * Files B: Subject-level averages for group #2. ==== What level of precision? ==== * Difference of averages * Statistically significant differences between conditions or groups ==== What statistical test? ==== * '''A = B''' * Tests the null hypothesis H0:(A=B) against the alternative hypothesis H1:(A<<HTML(≠)>>B) * Correct effect size: We identify correctly '''where and when''' the conditions are different. * Ambiguous sign: We cannot say which condition is stronger. * '''Power(A) = Power(B)''' * Tests the null hypothesis H0:(Power(A)=Power(B)) against the alternative hypothesis H1:(Power(A)<<HTML(≠)>>Power(B)) * Incorrect effect size: Doesn't detect correctly the effects when A and B have opposite signs. * Correct sign: We can identify correctly which condition has a '''stronger response'''. * Power(x) = |x|<<HTML(<SUP>2</SUP>)>>, where |x| represents the modulus of the values: * Absolute value for scalar values (recordings, constrained sources, time-frequency maps) * Norm of the three orientations for unconstrained sources. == Common pre-processing pipeline == Most event-related studies can start with the pipeline we've introduced in these tutorials. 1. Import the anatomy of the subject (or use a template for all the subjects). 1. Access the recordings: * Link the continuous recordings to the Brainstorm database. * Prepare the channel file: co-register sensors and MRI, edit type and name of channels. * Edit the event markers: fix the delays of the triggers, mark additional events. 1. Pre-process the signals: * Evaluate the quality of the recordings with a power spectral density plot (PSD). * Apply frequency filters (low-pass, high-pass, notch). * Identify bad channels and bad segments. * Correct for artifacts with SSP or ICA. 1. Import the recordings in the database: epochs around some markers of interest. == EEG recordings == === Average === * Average the epochs across acquisition runs: OK. * Average the epochs across subjects: OK. * Electrodes are in the same standard positions for all the subjects (e.g. 10-20). * Never use an absolute value for averaging or contrasting sensor-level data. * Group averages: Use the same number of trials for all the subjects. === Statistics: Single subject === * '''A ='''''' B''' * '''Parametric '''or '''non-parametric''' t-test, '''independent''', two-tailed, FDR-corrected. * Use as many trials as possible for A and B: No need to have an equal number of trials. === Statistics: Group analysis, within subject === * '''A ='''''' B''' * '''First-level statistic''': Average * For each subject, compute the sensor average for conditions A and B. * Use the same number of trials for all the averages. * '''Second-level statistic''': t-test * '''Parametric''' or '''non-parametric''' t-test, '''paired''', two-tailed, FDR-corrected. === Statistics: Group analysis, between subjects === * '''A ='''''' B''' * '''First-level statistic''': Average * For each subject, compute the sensor average for conditions A and B. * Use the same number of trials for all the averages. * '''Second-level statistic''': t-test * '''Parametric''' or '''non-parametric''' t-test, '''independent''', two-tailed, FDR-corrected. == MEG recordings == === Average === * Average the epochs within each acquisition runs: OK. * Averaging across acquisition runs: Not advised because the head of the subject may move between runs. * Averaging across subjects: Strongly discouraged because the shape of the heads vary but the sensors are fixed. One sensor does not correspond to the same brain region for different subjects. * Tolerance for data exploration: Averaging across runs and subjects can be useful for identifying time points and sensors with interesting effects but should be avoided for formal analysis. * Note for Elekta/MaxFilter users: You can align all sessions to a reference session, this will allow direct channel comparisons within-subject. Not recommended across subjects. * Never use an absolute value for averaging or contrasting sensor-level data. * Group averages: Use the same number of trials for all the sessions. === Statistics: Single subject === * '''A ='''''' B''' * '''Parametric '''or '''non-parametric''' t-test, '''independent''', two-tailed, FDR-corrected. * Use as many trials as possible for A and B: No need to have an equal number of trials. === Statistics: Group analysis === * Not recommended with MEG recordings: do your analysis in source space. == Constrained cortical sources == === Average: Single subject === 1. '''Sensor average''': Compute one sensor-level average''' '''per acquisition session and condition. <<BR>>Use the '''same number of trials''' for all the averages. 1. '''Sources''': Estimate sources for each average (constrained, no normalization). 1. '''Source average''': Average the source-level session averages to get one subject average. 1. '''Low-pass filter''' your evoked responses (optional). 1. '''Normalize '''the subject min-norm averages: Z-score vs. baseline (no absolute value).<<BR>>Justification: The amplitude range of current densities may vary between subjects because of anatomical or experimental differences. This normalization helps bringing the different subjects to the same range of values. 1. '''Do not rectify the cortical maps''', but display them as absolute values if needed. === Average: Group analysis === 1. '''Subject averages''': Compute within-subject averages for all the subjects, as described above. 1. '''Rectify''' the cortical maps (apply an absolute value). <<BR>>Justification: Cortical maps have ambiguous signs across subjects: reconstructed sources depend heavily on the orientation of true cortical sources. Given the folding patterns of individual cortical anatomies vary considerably, cortical maps have subject-specific amplitude and sign ambiguities. This is true even if a standard anatomy is used for reconstruction. 1. '''Project '''the individual source maps on a template (only when using the individual brains). <<BR>> For more details, see tutorial: [[Tutorials/CoregisterSubjects|Group analysis: Subject coregistration]]. 1. '''Smooth '''spatially the sources.<<BR>>Justification: The effects observed with constrained cortical maps may be artificially very focal, not overlapping very well between subjects. Smoothing the cortical maps may help the activated regions overlap between subjects. 1. '''Group average''': Compute grand averages of all the subjects. === Difference of averages: Within subject === 1. '''Subject averages''': Compute within-subject averages for conditions A and B, as described above. 1. '''Subject difference''': Compute the difference between conditions for each subject (A-B). 1. '''Rectify''' the difference of source maps (apply an absolute value). 1. '''Project '''the individual difference on a template (only when using the individual brains). 1. '''Smooth '''spatially the sources. 1. '''Group average''': Compute grand averages of all the subjects: average_subjects(|Ai-Bi|). === Difference of averages: Between subjects === 1. '''Subject averages''': Compute within-subject averages for conditions A and B, as described above. 1. '''Grand averages''': Compute the group-level averages for groups #1 and #2 as described in "Average: Group analysis" 1. '''Difference''': Compute the difference between group-level averages: avg(|A1|)-avg(|A2|) 1. '''Limitations''': Because we rectify the source maps before computing the difference, we lose the ability to detect the differences between equal values of opposite signs. And we cannot keep the sign because we are averaging across subjects. Therefore, many effects are not detected correctly. === Statistics: Single subject === 1. '''Sources''': Compute source maps for each trial (constrained, no normalization) 1. '''Statistics''': Compare all the trials of condition A vs all the trials of condition B.<<BR>>Use as many trials as possible for A and B: No need to have an equal number of trials. 1. '''A = B''' * '''Parametric''' or '''non-parametric''' t-test, '''independent''', two-tailed, FDR-corrected. * Indicates when and where there is a significant effect (but not in which direction). 1. '''|A| = |B|''' * '''Non-parametric''' tests only, '''independent''', test absolute values, two-tailed, FDR-corrected. * Indicates which condition corresponds to a stronger brain response (for a known effect). === Statistics: Group analysis, within subject === * '''|A - B| = 0''' : Parametric 1. '''Sources''': Compute source maps for each trial (constrained, no normalization) 1. '''First-level statistic''': Compute a t-statistic for the source maps of all the trials A vs B. * Process2 "Test > Compute t-statistic": no absolute values, independant, equal variance. * Use as many trials as possible for A and B: No need to have an equal number of trials. * With a high number of trials (n>30), t-values follow approximately a N(0,1) distribution. 1. '''Low-pass filter''' your evoked responses (optional). 1. '''Rectify '''the individual t-statistic (we're giving up the sign across subjects). 1. '''Project '''the individual t-statistic on a template (only when using the individual brains). 1. '''Smooth '''spatially the t-statistic maps. 1. '''Second-level statistic''': Compute a one-sampled chi-square test based on the t-statistics. * Process1: "Test > Parametric test against zero": One-sampled Chi-square test * This tests for '''|A-B|'''=0 using a Chi-square test: X = sum(|t<<HTML(<SUB>)>>i<<HTML(</SUB>)>>|^2) ~ Chi2(N<<HTML(<SUB>)>>subj<<HTML(</SUB>)>>) * Indicates when and where there is a significant effect (but not in which direction). * '''|A - B| = 0 ''': Non-parametric 1. '''Rectified differences''': Proceed as described in ''Difference of averages: Between subjects'', but stop before the computation of the grand averages (#6) and compute a test instead.<<BR>>You obtain one |A<<HTML(<SUB>)>>i<<HTML(</SUB>)>>-B<<HTML(<SUB>)>>i<<HTML(</SUB>)>>| value for each subject, test these values against zero. 1. '''Non-parametric''' one-sample test, one-tailed, FDR-corrected. 1. Indicates when and where there is a significant effect (but not in which direction). * '''|A| = |B|''' 1. '''Rectified subject averages''': Proceed as described in ''Average: Group analysis'', but stop before the grand average (#5). You obtain two averages per subject (A<<HTML(<SUB>)>>i<<HTML(</SUB>)>> and B<<HTML(<SUB>)>>i<<HTML(</SUB>)>>). 1. '''Non-parametric''' two-sample test, '''paired''', test absolute values, two-tailed, FDR-corrected. 1. Indicates which condition corresponds to a stronger brain response (for a known effect). === Statistics: Group analysis, between subjects === * '''|A| = |B|''' * '''Subject averages''': Compute within-subject averages for A and B, as described above.<<BR>>You obtain two averages per subject (A<<HTML(<SUB>)>>i<<HTML(</SUB>)>> and B<<HTML(<SUB>)>>i<<HTML(</SUB>)>>). * '''Non-parametric''' two-sample test, '''independent''', test absolute values, two-tailed, FDR. * Indicates which condition corresponds to a stronger brain response (for a known effect). === Design considerations === * Use within-subject designs whenever possible (i.e. collect two conditions A and B for each subject), then contrast data at the subject level before comparing data between subjects. * Such designs are not only statistically optimal, but also ameliorate the between-subject sign ambiguities as contrasts can be constructed within each subject. == Unconstrained cortical sources == Three values for each grid point, corresponding to the three dipoles orientations (X,Y,Z). <<BR>>We want only one statistic and one p-value per grid point in output. === Average: Single subject [???] === 1. '''Sensor average''': Compute one sensor-level average''' '''per acquisition session and condition. <<BR>>Use the '''same number of trials''' for all the averages. 1. '''Sources''': Estimate sources for each average (unconstrained, no normalization). 1. '''Source average''': Average the source-level session averages to get one subject average. 1. '''Low-pass filter''' your evoked responses (optional). 1. '''Normalize '''the subject min-norm averages: Z-score vs. baseline (no absolute value).<<BR>>'''[???]''' HOW TO NORMALIZE UNCONSTRAINED MAPS WRT BASELINE? === Average: Group analysis [???] === 1. '''Subject averages''': Compute within-subject averages for all the subjects, as described above. 1. '''Flatten''' the cortical map: compute the norm of the three orientations at each grid point. 1. '''Project '''the individual source maps on a template (only when using the individual brains). 1. '''Group average''': Compute grand averages of all the subjects. === Difference of averages: Within subject [???] === 1. '''Subject averages''': Compute within-subject averages for conditions A and B, as described above. 1. '''Subject difference''': Compute the difference between conditions for each subject (A-B). 1. '''Flatten''' the cortical map: compute the norm of the three orientations at each grid point. 1. '''Project '''the individual difference on a template. 1. '''Group average''': Compute grand averages of all the subjects: average_subjects(|Ai-Bi|). === Difference of averages: Between subjects [???] === 1. '''Subject averages''': Compute within-subject averages for conditions A and B, as described above. 1. '''Grand averages''': Compute the group-level averages for groups #1 and #2 as described in "Average: Group analysis" 1. '''Difference''': Compute the difference between group-level averages: avg(|A1|)-avg(|A2|) 1. '''Limitations''': Because we rectify the source maps before computing the difference, we lose the ability to detect the differences between equal values of opposite signs. And we cannot keep the sign because we are averaging across subjects. Therefore, many effects are not detected correctly. === Statistics: Single subject [???] === 1. '''Sources''': Compute source maps for each trial (unconstrained, no normalization) 1. '''Statistics''': Compare all the trials of condition A vs all the trials of condition B.<<BR>>Use as many trials as possible for A and B: No need to have an equal number of trials. 1. '''|A| = |B|''' * '''Non-parametric''' tests only, '''independent''', test norm, two-tailed, FDR-corrected. * Indicates which condition corresponds to a stronger brain response (for a known effect). === Statistics: Group analysis, within subject [???] === * '''|A - B| = 0''' : Parametric 1. '''Sources''': Compute source maps for each trial (unconstrained, no normalization) 1. '''First-level statistic''': Compute a t-statistic for the source maps of all the trials A vs B. * Process2 "Test > Compute t-statistic": no absolute values, independant, equal variance. * Use as many trials as possible for A and B: No need to have an equal number of trials. * With a high number of trials (n>30), t-values follow approximately a N(0,1) distribution. 1. '''Low-pass filter''' your evoked responses (optional). 1. '''Rectify '''the individual t-statistic (we're giving up the sign across subjects). 1. '''Project '''the individual t-statistic on a template (when using ). 1. '''Smooth '''spatially the t-statistic maps. 1. '''Second-level statistic''': Compute a one-sampled Chi-square test based on the t-statistics. * Process1: "Test > Parametric test against zero": One-sampled Chi-square test * This tests for '''|A-B|'''=0 using a Chi-square test: X = sum(|t<<HTML(<SUB>)>>i<<HTML(</SUB>)>>|^2) ~ Chi2(N<<HTML(<SUB>)>>subj<<HTML(</SUB>)>>) * Indicates when and where there is a significant effect (but not in which direction). * '''|A - B| = 0 ''': Non-parametric 1. '''Rectified differences''': Proceed as described in ''Difference of averages: Between subjects'', but stop before the computation of the grand averages (#6) and compute a test instead.<<BR>>You obtain one |A<<HTML(<SUB>)>>i<<HTML(</SUB>)>>-B<<HTML(<SUB>)>>i<<HTML(</SUB>)>>| value for each subject, test these values against zero. 1. '''Non-parametric''' one-sample test, one-tailed, FDR-corrected. 1. Indicates when and where there is a significant effect (but not in which direction). * '''|A| = |B|''' 1. '''Subject averages''': Compute within-subject averages for A and B, as described above.<<BR>>You obtain two averages per subject (A<<HTML(<SUB>)>>i<<HTML(</SUB>)>> and B<<HTML(<SUB>)>>i<<HTML(</SUB>)>>). 1. '''Non-parametric''' two-sample test, '''paired''', test absolute values, two-tailed, FDR-corrected. 1. Indicates which condition corresponds to a stronger brain response (for a known effect). === Statistics: Group analysis, between subjects [???] === * '''|A| = |B|''' * '''Subject averages''': Compute within-subject averages for A and B, as described above.<<BR>>You obtain two averages per subject (A<<HTML(<SUB>)>>i<<HTML(</SUB>)>> and B<<HTML(<SUB>)>>i<<HTML(</SUB>)>>). * '''Non-parametric''' two-sample test, '''independent''', test absolute values, two-tailed, FDR. * Indicates which condition corresponds to a stronger brain response (for a known effect). == Regions of interest (scouts) [???] == === Statistics: Single subject === * Even within-subject cortical maps have sign ambiguities. MEG has limited spatial resolution and sources in opposing sulcal/gyral areas are reconstructed with inverted signs (constrained orientations only). Averaging activity in cortical regions of interest (scouts) would thus lead to signal cancelation. To avoid this brainstorm uses algorithms to manipulate the sign of individual sources before averaging within a cortical region. Unfortunately, this introduces an amplitude and sign ambiguity in the time course when summarizing scout activity. * As a result, '''perform any interesting within-subject average/contrast before computing an average scout time series'''. * Then consider as constrained or unconstrained source maps. === Statistics: Group analysis, within subject === * Comparison of scout time series between subjects is tricky because there is no way to avoid sign ambiguity for different subjects. Thus there are no clear recommendations. Rectifying before comparing scout time series between subjects can be a good idea or not depending on different cases. Having a good understanding of the data (multiple inspections across channels/sources/subjects) can offer hints whether rectifying the scout time series is a good idea. Using unconstrained cortical maps to create the scout time series can ameliorate ambiguity concerns. == Time-frequency maps == === Average: Single subject === 1. '''Time-frequency maps''': Compute time-frequency maps for each trial. * Apply the default measure: magnitude for Hilbert transform, power for Morlet wavelets. * Do not normalize the source maps: no Z-score or ERS/ERD. * The values are all strictly positive, there is no sign ambiguity as for recordings or sources. 1. '''Average''' all the time-frequency maps together, for each condition separately. * If you are averaging time-frequency maps computed on sensor-level data, the same limitations apply as for averaging sensor level data (see sections about MEG and EEG recordings above). === Average: Group analysis [???] === 1. '''Subject averages''': Compute within-subject averages for all the subjects, as described above. 1. '''Normalize''': '''[???]''' Zscore, ERD/ERS, or FieldTrip?<<BR>>Justification: The amplitude range of current densities may vary between subjects because of anatomical or experimental differences. This normalization helps bringing the different subjects to the same range of values. 1. '''Group average''': Compute grand averages of all the subjects. === Difference of averages === 1. '''Group average''': Compute the averages for conditions A and B as in ''Average: Group analysis''. 1. '''Difference''': Compute the difference between group-level averages: avg(A)-avg(B). === Statistics: Single subject [???] === 1. '''Time-frequency maps''': Compute time-frequency maps for each trial. * Apply the default measure: magnitude for Hilbert transform, power for Morlet wavelets. * Do not normalize the source maps: no Z-score or ERS/ERD. * The values are all strictly positive, there is no sign ambiguity as for recordings or sources. 1. '''Statistics''': Compare all the trials of condition A vs all the trials of condition B.<<BR>>Use as many trials as possible for A and B: No need to have an equal number of trials. 1. '''A = B''' '''[???]''' * '''Parametric''' or '''non-parametric''' t-test, '''independent''', two-tailed, FDR-corrected. '''[???]''' * Indicates both where there is a significant effect and what is its direction (no sign ambiguity). === Statistics: Group analysis, within subject [???] === * '''A = B ''''''[???]''' 1. '''Subject averages''': Compute within-subject averages for all subjects, as described above. 1. '''Parametric''' or '''non-parametric''' t-test, '''independent''', two-tailed, FDR-corrected. '''[???]''' 1. Indicates both where there is a significant effect and what is its direction (no sign ambiguity). |
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| The following inconsistencies are still present in the documentation. We are actively working on these issues and will update this tutorial as soon as we found solutions. * [Group analysis] Unconstrained sources: How to compute a Z-score? * Zscore(A): Normalizes each orientation separately, which doesn't make much sense. * Zscore(Norm(A)): Gets rid of the signs, forbids the option of a signed test H0:(Norm(A-B)=0) |
The following inconsistencies are still present in the documentation. We are actively working on these issues and will update this tutorial as soon as we found solutions. * [Group analysis] Unconstrained sources: How to normalize wrt baseline with a Z-score? * Zscore(A): Normalizes each orientation separately, we cannot take the norm of it after. * Zscore(|A|): Gets rid of the signs, forbids the option of a signed test H0:(Norm(A-B)=0) |
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| * We would need a way to normalize across the three orientations are the same time. * [Group analysis] Constrained sources: How do we smooth? * Group analysis benefits a lot from smoothing the source maps before computing statistics. * However this requires to apply an absolute value first. How do we do? |
* We need a way to normalize across the three orientations are the same time. |
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| * Norm(A)-Norm(B): Cannot detect correctly the differences * (A-B): We test individually each orientation, which doesn't make much sense. * We would need a test for the three orientations at once. |
* |A|-|B|: Cannot detect correctly the difference. * |A-B|: Cannot be computed because the trials are not paired. * We need a test for the three orientations at the same time. * [Group analysis] Unconstrained sources:Can we use parametric tests? * Time-frequency maps: * Can we use parametric tests for (A-B=0) ? Does (A-B) ~ normal distribution? * Do we need to normalize the time-frequency maps when testing across subjects? * If yes, how to normalize the time-frequency maps? (Z-score, ERS/ERD, divide by std) |
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| <<EmbedContent("http://neuroimage.usc.edu/bst/get_prevnext.php?prev=Tutorials/Statistics&next=Tutorials/Connectivity")>> <<EmbedContent(http://neuroimage.usc.edu/bst/get_feedback.php?Tutorials/GroupAnalysis)>> |
<<EmbedContent("http://neuroimage.usc.edu/bst/get_prevnext.php?prev=Tutorials/Statistics&next=Tutorials/Scripting")>> <<EmbedContent(http://neuroimage.usc.edu/bst/get_feedback.php?Tutorials/Workflows)>> |
Tutorial 27: Workflows
[TUTORIAL UNDER DEVELOPMENT: NOT READY FOR PUBLIC USE]
Authors: Francois Tadel, Elizabeth Bock, Dimitrios Pantazis, Richard Leahy, Sylvain Baillet
This page provides some general recommendations for your event-related analysis. It is not directly related with the auditory dataset, but provides guidelines you should consider for any MEG/EEG experiment.
We do not provide standard analysis pipelines for resting or steady state recordings yet, but we will add a few examples soon in the section Other analysis scenarios of the tutorials page.
Contents
What is your question?
The most appropriate analysis pipeline for your data depends on the question you are trying to answer. Before defining what are the main steps of your analysis, you should be able to state clearly the question you want to answer with your recordings.
What dimension?
- MEG/EEG recordings
- Cortical sources
- Individual anatomy or template
- Constrained (one value per vertex) or unconstrained (three values per grid point)
- Full cortex or regions of interests
- Frequency or time-frequency maps
What kind of experiment?
Single subject: Contrast two experimental conditions across trials, for one single subject.
- Files A: Single trials for condition A.
- Files B: Single trials for condition B.
Group analysis, within subject: Contrast two conditions A and B measured for each subject.
- Files A: Subject-level averages for condition A (all the subjects).
- Files B: Subject-level averages for condition B (all the subjects).
Group analysis, between subjects: Contrast two groups of subjects for one condition.
- Files A: Subject-level averages for group #1.
- Files B: Subject-level averages for group #2.
What level of precision?
- Difference of averages
- Statistically significant differences between conditions or groups
What statistical test?
A = B
Tests the null hypothesis H0:(A=B) against the alternative hypothesis H1:(A≠B)
Correct effect size: We identify correctly where and when the conditions are different.
- Ambiguous sign: We cannot say which condition is stronger.
Power(A) = Power(B)
Tests the null hypothesis H0:(Power(A)=Power(B)) against the alternative hypothesis H1:(Power(A)≠Power(B))
- Incorrect effect size: Doesn't detect correctly the effects when A and B have opposite signs.
Correct sign: We can identify correctly which condition has a stronger response.
Power(x) = |x|2, where |x| represents the modulus of the values:
- Absolute value for scalar values (recordings, constrained sources, time-frequency maps)
- Norm of the three orientations for unconstrained sources.
Common pre-processing pipeline
Most event-related studies can start with the pipeline we've introduced in these tutorials.
- Import the anatomy of the subject (or use a template for all the subjects).
- Access the recordings:
- Link the continuous recordings to the Brainstorm database.
- Prepare the channel file: co-register sensors and MRI, edit type and name of channels.
- Edit the event markers: fix the delays of the triggers, mark additional events.
- Pre-process the signals:
- Evaluate the quality of the recordings with a power spectral density plot (PSD).
- Apply frequency filters (low-pass, high-pass, notch).
- Identify bad channels and bad segments.
- Correct for artifacts with SSP or ICA.
- Import the recordings in the database: epochs around some markers of interest.
EEG recordings
Average
- Average the epochs across acquisition runs: OK.
- Average the epochs across subjects: OK.
- Electrodes are in the same standard positions for all the subjects (e.g. 10-20).
- Never use an absolute value for averaging or contrasting sensor-level data.
- Group averages: Use the same number of trials for all the subjects.
Statistics: Single subject
A = B
Parametric or non-parametric t-test, independent, two-tailed, FDR-corrected.
- Use as many trials as possible for A and B: No need to have an equal number of trials.
Statistics: Group analysis, within subject
A = B
First-level statistic: Average
- For each subject, compute the sensor average for conditions A and B.
- Use the same number of trials for all the averages.
Second-level statistic: t-test
Parametric or non-parametric t-test, paired, two-tailed, FDR-corrected.
Statistics: Group analysis, between subjects
A = B
First-level statistic: Average
- For each subject, compute the sensor average for conditions A and B.
- Use the same number of trials for all the averages.
Second-level statistic: t-test
Parametric or non-parametric t-test, independent, two-tailed, FDR-corrected.
MEG recordings
Average
- Average the epochs within each acquisition runs: OK.
- Averaging across acquisition runs: Not advised because the head of the subject may move between runs.
- Averaging across subjects: Strongly discouraged because the shape of the heads vary but the sensors are fixed. One sensor does not correspond to the same brain region for different subjects.
- Tolerance for data exploration: Averaging across runs and subjects can be useful for identifying time points and sensors with interesting effects but should be avoided for formal analysis.
- Note for Elekta/MaxFilter users: You can align all sessions to a reference session, this will allow direct channel comparisons within-subject. Not recommended across subjects.
- Never use an absolute value for averaging or contrasting sensor-level data.
- Group averages: Use the same number of trials for all the sessions.
Statistics: Single subject
A = B
Parametric or non-parametric t-test, independent, two-tailed, FDR-corrected.
- Use as many trials as possible for A and B: No need to have an equal number of trials.
Statistics: Group analysis
- Not recommended with MEG recordings: do your analysis in source space.
Constrained cortical sources
Average: Single subject
Sensor average: Compute one sensor-level average per acquisition session and condition.
Use the same number of trials for all the averages.Sources: Estimate sources for each average (constrained, no normalization).
Source average: Average the source-level session averages to get one subject average.
Low-pass filter your evoked responses (optional).
Normalize the subject min-norm averages: Z-score vs. baseline (no absolute value).
Justification: The amplitude range of current densities may vary between subjects because of anatomical or experimental differences. This normalization helps bringing the different subjects to the same range of values.Do not rectify the cortical maps, but display them as absolute values if needed.
Average: Group analysis
Subject averages: Compute within-subject averages for all the subjects, as described above.
Rectify the cortical maps (apply an absolute value).
Justification: Cortical maps have ambiguous signs across subjects: reconstructed sources depend heavily on the orientation of true cortical sources. Given the folding patterns of individual cortical anatomies vary considerably, cortical maps have subject-specific amplitude and sign ambiguities. This is true even if a standard anatomy is used for reconstruction.Project the individual source maps on a template (only when using the individual brains).
For more details, see tutorial: Group analysis: Subject coregistration.Smooth spatially the sources.
Justification: The effects observed with constrained cortical maps may be artificially very focal, not overlapping very well between subjects. Smoothing the cortical maps may help the activated regions overlap between subjects.Group average: Compute grand averages of all the subjects.
Difference of averages: Within subject
Subject averages: Compute within-subject averages for conditions A and B, as described above.
Subject difference: Compute the difference between conditions for each subject (A-B).
Rectify the difference of source maps (apply an absolute value).
Project the individual difference on a template (only when using the individual brains).
Smooth spatially the sources.
Group average: Compute grand averages of all the subjects: average_subjects(|Ai-Bi|).
Difference of averages: Between subjects
Subject averages: Compute within-subject averages for conditions A and B, as described above.
Grand averages: Compute the group-level averages for groups #1 and #2 as described in "Average: Group analysis"
Difference: Compute the difference between group-level averages: avg(|A1|)-avg(|A2|)
Limitations: Because we rectify the source maps before computing the difference, we lose the ability to detect the differences between equal values of opposite signs. And we cannot keep the sign because we are averaging across subjects. Therefore, many effects are not detected correctly.
Statistics: Single subject
Sources: Compute source maps for each trial (constrained, no normalization)
Statistics: Compare all the trials of condition A vs all the trials of condition B.
Use as many trials as possible for A and B: No need to have an equal number of trials.A = B
Parametric or non-parametric t-test, independent, two-tailed, FDR-corrected.
- Indicates when and where there is a significant effect (but not in which direction).
|A| = |B|
Non-parametric tests only, independent, test absolute values, two-tailed, FDR-corrected.
- Indicates which condition corresponds to a stronger brain response (for a known effect).
Statistics: Group analysis, within subject
|A - B| = 0 : Parametric
Sources: Compute source maps for each trial (constrained, no normalization)
First-level statistic: Compute a t-statistic for the source maps of all the trials A vs B.
Process2 "Test > Compute t-statistic": no absolute values, independant, equal variance.
- Use as many trials as possible for A and B: No need to have an equal number of trials.
With a high number of trials (n>30), t-values follow approximately a N(0,1) distribution.
Low-pass filter your evoked responses (optional).
Rectify the individual t-statistic (we're giving up the sign across subjects).
Project the individual t-statistic on a template (only when using the individual brains).
Smooth spatially the t-statistic maps.
Second-level statistic: Compute a one-sampled chi-square test based on the t-statistics.
Process1: "Test > Parametric test against zero": One-sampled Chi-square test
This tests for |A-B|=0 using a Chi-square test: X = sum(|ti|^2) ~ Chi2(Nsubj)
- Indicates when and where there is a significant effect (but not in which direction).
|A - B| = 0 : Non-parametric
Rectified differences: Proceed as described in Difference of averages: Between subjects, but stop before the computation of the grand averages (#6) and compute a test instead.
You obtain one |Ai-Bi| value for each subject, test these values against zero.Non-parametric one-sample test, one-tailed, FDR-corrected.
- Indicates when and where there is a significant effect (but not in which direction).
|A| = |B|
Rectified subject averages: Proceed as described in Average: Group analysis, but stop before the grand average (#5). You obtain two averages per subject (Ai and Bi).
Non-parametric two-sample test, paired, test absolute values, two-tailed, FDR-corrected.
- Indicates which condition corresponds to a stronger brain response (for a known effect).
Statistics: Group analysis, between subjects
|A| = |B|
Subject averages: Compute within-subject averages for A and B, as described above.
You obtain two averages per subject (Ai and Bi).Non-parametric two-sample test, independent, test absolute values, two-tailed, FDR.
- Indicates which condition corresponds to a stronger brain response (for a known effect).
Design considerations
- Use within-subject designs whenever possible (i.e. collect two conditions A and B for each subject), then contrast data at the subject level before comparing data between subjects.
- Such designs are not only statistically optimal, but also ameliorate the between-subject sign ambiguities as contrasts can be constructed within each subject.
Unconstrained cortical sources
Three values for each grid point, corresponding to the three dipoles orientations (X,Y,Z).
We want only one statistic and one p-value per grid point in output.
Average: Single subject [???]
Sensor average: Compute one sensor-level average per acquisition session and condition.
Use the same number of trials for all the averages.Sources: Estimate sources for each average (unconstrained, no normalization).
Source average: Average the source-level session averages to get one subject average.
Low-pass filter your evoked responses (optional).
Normalize the subject min-norm averages: Z-score vs. baseline (no absolute value).
[???] HOW TO NORMALIZE UNCONSTRAINED MAPS WRT BASELINE?
Average: Group analysis [???]
Subject averages: Compute within-subject averages for all the subjects, as described above.
Flatten the cortical map: compute the norm of the three orientations at each grid point.
Project the individual source maps on a template (only when using the individual brains).
Group average: Compute grand averages of all the subjects.
Difference of averages: Within subject [???]
Subject averages: Compute within-subject averages for conditions A and B, as described above.
Subject difference: Compute the difference between conditions for each subject (A-B).
Flatten the cortical map: compute the norm of the three orientations at each grid point.
Project the individual difference on a template.
Group average: Compute grand averages of all the subjects: average_subjects(|Ai-Bi|).
Difference of averages: Between subjects [???]
Subject averages: Compute within-subject averages for conditions A and B, as described above.
Grand averages: Compute the group-level averages for groups #1 and #2 as described in "Average: Group analysis"
Difference: Compute the difference between group-level averages: avg(|A1|)-avg(|A2|)
Limitations: Because we rectify the source maps before computing the difference, we lose the ability to detect the differences between equal values of opposite signs. And we cannot keep the sign because we are averaging across subjects. Therefore, many effects are not detected correctly.
Statistics: Single subject [???]
Sources: Compute source maps for each trial (unconstrained, no normalization)
Statistics: Compare all the trials of condition A vs all the trials of condition B.
Use as many trials as possible for A and B: No need to have an equal number of trials.|A| = |B|
Non-parametric tests only, independent, test norm, two-tailed, FDR-corrected.
- Indicates which condition corresponds to a stronger brain response (for a known effect).
Statistics: Group analysis, within subject [???]
|A - B| = 0 : Parametric
Sources: Compute source maps for each trial (unconstrained, no normalization)
First-level statistic: Compute a t-statistic for the source maps of all the trials A vs B.
Process2 "Test > Compute t-statistic": no absolute values, independant, equal variance.
- Use as many trials as possible for A and B: No need to have an equal number of trials.
With a high number of trials (n>30), t-values follow approximately a N(0,1) distribution.
Low-pass filter your evoked responses (optional).
Rectify the individual t-statistic (we're giving up the sign across subjects).
Project the individual t-statistic on a template (when using ).
Smooth spatially the t-statistic maps.
Second-level statistic: Compute a one-sampled Chi-square test based on the t-statistics.
Process1: "Test > Parametric test against zero": One-sampled Chi-square test
This tests for |A-B|=0 using a Chi-square test: X = sum(|ti|^2) ~ Chi2(Nsubj)
- Indicates when and where there is a significant effect (but not in which direction).
|A - B| = 0 : Non-parametric
Rectified differences: Proceed as described in Difference of averages: Between subjects, but stop before the computation of the grand averages (#6) and compute a test instead.
You obtain one |Ai-Bi| value for each subject, test these values against zero.Non-parametric one-sample test, one-tailed, FDR-corrected.
- Indicates when and where there is a significant effect (but not in which direction).
|A| = |B|
Subject averages: Compute within-subject averages for A and B, as described above.
You obtain two averages per subject (Ai and Bi).Non-parametric two-sample test, paired, test absolute values, two-tailed, FDR-corrected.
- Indicates which condition corresponds to a stronger brain response (for a known effect).
Statistics: Group analysis, between subjects [???]
|A| = |B|
Subject averages: Compute within-subject averages for A and B, as described above.
You obtain two averages per subject (Ai and Bi).Non-parametric two-sample test, independent, test absolute values, two-tailed, FDR.
- Indicates which condition corresponds to a stronger brain response (for a known effect).
Regions of interest (scouts) [???]
Statistics: Single subject
- Even within-subject cortical maps have sign ambiguities. MEG has limited spatial resolution and sources in opposing sulcal/gyral areas are reconstructed with inverted signs (constrained orientations only). Averaging activity in cortical regions of interest (scouts) would thus lead to signal cancelation. To avoid this brainstorm uses algorithms to manipulate the sign of individual sources before averaging within a cortical region. Unfortunately, this introduces an amplitude and sign ambiguity in the time course when summarizing scout activity.
As a result, perform any interesting within-subject average/contrast before computing an average scout time series.
- Then consider as constrained or unconstrained source maps.
Statistics: Group analysis, within subject
- Comparison of scout time series between subjects is tricky because there is no way to avoid sign ambiguity for different subjects. Thus there are no clear recommendations. Rectifying before comparing scout time series between subjects can be a good idea or not depending on different cases. Having a good understanding of the data (multiple inspections across channels/sources/subjects) can offer hints whether rectifying the scout time series is a good idea. Using unconstrained cortical maps to create the scout time series can ameliorate ambiguity concerns.
Time-frequency maps
Average: Single subject
Time-frequency maps: Compute time-frequency maps for each trial.
- Apply the default measure: magnitude for Hilbert transform, power for Morlet wavelets.
- Do not normalize the source maps: no Z-score or ERS/ERD.
- The values are all strictly positive, there is no sign ambiguity as for recordings or sources.
Average all the time-frequency maps together, for each condition separately.
- If you are averaging time-frequency maps computed on sensor-level data, the same limitations apply as for averaging sensor level data (see sections about MEG and EEG recordings above).
Average: Group analysis [???]
Subject averages: Compute within-subject averages for all the subjects, as described above.
Normalize: [???] Zscore, ERD/ERS, or FieldTrip?
Justification: The amplitude range of current densities may vary between subjects because of anatomical or experimental differences. This normalization helps bringing the different subjects to the same range of values.Group average: Compute grand averages of all the subjects.
Difference of averages
Group average: Compute the averages for conditions A and B as in Average: Group analysis.
Difference: Compute the difference between group-level averages: avg(A)-avg(B).
Statistics: Single subject [???]
Time-frequency maps: Compute time-frequency maps for each trial.
- Apply the default measure: magnitude for Hilbert transform, power for Morlet wavelets.
- Do not normalize the source maps: no Z-score or ERS/ERD.
- The values are all strictly positive, there is no sign ambiguity as for recordings or sources.
Statistics: Compare all the trials of condition A vs all the trials of condition B.
Use as many trials as possible for A and B: No need to have an equal number of trials.A = B [???]
Parametric or non-parametric t-test, independent, two-tailed, FDR-corrected. [???]
- Indicates both where there is a significant effect and what is its direction (no sign ambiguity).
Statistics: Group analysis, within subject [???]
A = B [???]
Subject averages: Compute within-subject averages for all subjects, as described above.
Parametric or non-parametric t-test, independent, two-tailed, FDR-corrected. [???]
- Indicates both where there is a significant effect and what is its direction (no sign ambiguity).
Workflow: Current problems [TODO]
The following inconsistencies are still present in the documentation. We are actively working on these issues and will update this tutorial as soon as we found solutions.
- [Group analysis] Unconstrained sources: How to normalize wrt baseline with a Z-score?
- Zscore(A): Normalizes each orientation separately, we cannot take the norm of it after.
- Zscore(|A|): Gets rid of the signs, forbids the option of a signed test H0:(Norm(A-B)=0)
See also the tutorial: Source estimation
- We need a way to normalize across the three orientations are the same time.
- [Single subject] Unconstrained sources: How do compare two conditions with multiple trials?
- |A|-|B|: Cannot detect correctly the difference.
- |A-B|: Cannot be computed because the trials are not paired.
- We need a test for the three orientations at the same time.
- [Group analysis] Unconstrained sources:Can we use parametric tests?
- Time-frequency maps:
- Can we use parametric tests for (A-B=0) ? Does (A-B) ~ normal distribution?
- Do we need to normalize the time-frequency maps when testing across subjects?
- If yes, how to normalize the time-frequency maps? (Z-score, ERS/ERD, divide by std)