Mul$ Voxel Pa,ern Analysis (fmri) Mul$ Variate Pa,ern Analysis (more generally) Magic Voxel Pa,ern Analysis (probably not!)

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Mul$ Voxel Pa,ern Analysis (fmri) Mul$ Variate Pa,ern Analysis (more generally) Magic Voxel Pa,ern Analysis (probably not!)

all MVPA really shows is that there are places where, in most people s brain, ac$vity differs when they re doing one thing as opposed to another. Have you decoded something about orangeness vs appleness or are there poten$al confounds? The mathema$cs are sound and the method does work, but the trouble is what the results mean.

GLMA oppositesigned varia$ons cancel MVPA oppositesigned varia$ons sum (unless you do something fancier to make them not do so)

Counterac$ng? Be,er design Linear regression (e.g., of RT) Be,er (more careful) interpreta$on Not OK: Brain region A represents informa$on X OK: Brain region A can predict behavior Y ; Rela$onship between brain Region A and behavior Y follows model Z. Poten$ally problema$c: distributed representa$ons with posi$vely and nega$vely voxel signs Probably OK: methods that do not discard sign/direc$on of individual effects

Individual differences and MVPA?

238 rs-fcmri scans (3 T; con$nuous rest) from typically developing par$cipants ranging in age from 7 to 30 years Blood oxygen level dependent (BOLD) $me courses were generated for 160 regions of interest (ROIs) derived from a series of meta-analyses of task-related fmri studies that cover much of the brain All possible interregional temporal correla$ons, or func$onal connec$ons (n = 12,720), were computed for each individual. reduced the number of features to the 200 func$onal connec$ons most reliably different between children and adults in each round of leave-one-out cross-valida$on Binary SVM classifica/on of individuals as either children or adults was 91% accurate (permuta/on test, P < 0.0001; 90% sensi/ve; 92% specific). For independent replica$on, the same analyses were also carried out on two other large-scale developmental func$onal connec$vity data sets with somewhat different characteris$cs. Turn analysis inside out which brain regions predict maturity?

Davis et al. but could also get significant MVPA results even if it really only varied along one dimension

Davis et al. but could also get significant MVPA results even if it really only varied along one dimension

Davis et al. How do you test for mul$dimensionality? - Look for effects based on the supposed dimensions (and possibly regress out) - If including both dimensions improves accuracy, then be,er evidence for mul$dimensionality - Requires models/ hypotheses of what dimensions are

In many cases,mvpa tests may be providing informa$on that is largely assumed by the group-level sta$s$cal maps already reported in most papers (e.g., Rissman et al., 2010): experimental effects vary across voxels. As formal tests of this variability, MVPA results may be more sensi$ve indicators of heterogeneity of response across regions or voxels within a region. However, knowledge of this variability does not confer any special theore/cal status to the results in and of itself. Instead, to make conclusions about the dimensionality or content of the ac$va$on pa,erns that s$muli elicit, it is important to incorporate addi$onal methods that explicitly measure these aspects of the ac$va$on pa,erns, such as encoding models, classifier-based tests of dimensionality, and mul$dimensional scaling. Or as Frank put it: We just can t throw MVPA at some data, with no hypothesis in mind, and expect it to crack the code for us. In other words, MVPA can t tell the theory behind the classified pa,erns. GLMA vs MVPA?