On 03/20/2013 12:09 PM, Laura M. Tully wrote:
> Sorry -  meant to respond to list.
>
> Thanks for the response Doug - I have a few follow up questions I hope 
> you can clarify:
>
>       * is the xxx.ocn.annot file created by mri_glmfit-sim considered
>         a "label" by freesurfer?
>
It is an annotation
>
>       * or does it need to be converted to a label before I can use
>         mri_segstats to extract the betas from the cluster(s) in the
>         xxx.ocn.annot?
>
No
>
>       * I tried using the following command line to attempt to extract
>         the betas from the cluster annotation file created by
>         mri_glmfit-sim, but received an error:
>
>     mri_segstats --i beta.mgh --annot fsaverage hemi
>     contrast/xxx.ocn.annot --avgwf avgwf.dat
>
That looks correct. Did it work? Add --excludeid 0 to keep it from 
reporting on non-clusters
>
>
>       * how does one convert an xxx.ocn.annot file to a label?
>
If needed, use mri_annotation2label
>
>       * If I have run 3 different glms looking at the relationship
>         between thickness and 3 different behavioral variables, and
>         found 1 (or more) cluster in each glm using mri_glmfit-sim can
>         I create 1 annotation/label with all the clusters from the
>         separate glms and then extract the betas from that one
>         annotation using mri_segstats? Or do I need to treat each glm
>         separately?
>
It is probably easiest if you treat each glm separately. You can break 
the annotations into separate labels, then recombine the labels into 
another annotation (mris_label2annot), but it is a lot of work.
>
>      *
>
>
>       * I saw on the listserv some references to matlab functions that
>         can calculate r square and partial correlations for glms with
>         more than one predictor variable (e.g pcc between thickness
>         and behavioral variable 1; pcc between thickness and
>         behavioral variable2; Rsq for overall model) but I could not
>         find the .m scripts for the functions (MRIread
>         or fast_glm_pcc?) - would these functions be appropriate and
>         if so where might I find them?
>
Yes. They are in $FREESURFER_HOME/matlab and $FREESURFER_HOME/fsfast/toolbox
doug
>
>      *
>
>     Thanks in advance for your help!
>
>     Laura.
>
>
>     On Wed, Mar 20, 2013 at 8:29 AM, Douglas N Greve
>     <gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>> wrote:
>
>
>         On 03/20/2013 10:17 AM, Laura M. Tully wrote:
>         > Hi,
>         >
>         > I wanted to re-post my questions from a couple of days ago
>         below, but
>         > with some more specific questions following a search through the
>         > archives.
>         >
>         > I want to be able to extract the beta values from a cluster
>         identified
>         > using mc-z in a group by behavioral variable interaction so
>         that I can
>         > 1) plot the relationship of thickness to behavioral variable
>         data by
>         > group in that cluster, 2) conduct post hoc tests to examine the
>         > interaction, and 3) calculate the Rsquare and partial
>         correlations for
>         > each variable in the glm (i.e. how much variation in
>         thickness is
>         > explained by my behavioral variable).
>         >
>         > To extract the beta values from a cluster identified by mc-z
>         would I
>         > treat the cluster like a label and use mri_segstats to
>         extract the
>         > beta weights from the cluster? Would I need to make a label
>         of all the
>         > clusters that I want to do this for first?
>         You can do it label by label. Or, if the annotation created by
>         mri_glmfit-sim has all the clusters you want, you can use that
>         (also in
>         mri_segstats). You can also create an annotation from
>         individual labels
>         with mris_label2annot.
>         >
>         > Is there a way to calculate the basic statistics for the glm and
>         > extract in table form? i.e. Fs and ps for peaks of each
>         cluster? What
>         > about Rsquare, or the correlation between thickness and my
>         behavioral
>         > variable in the clusters? or would I need to compute these
>         outside of
>         > freesurfer using the extracted betas?
>         You will need to do it outside of FS. What are Fs and ps?
>         doug
>
>         >
>         > Thank you!
>         >
>         > Laura.
>         >
>         >
>         >
>         >
>         >
>         >
>         > On Mon, Mar 18, 2013 at 5:05 PM, Laura M. Tully
>         > <tully.la...@googlemail.com
>         <mailto:tully.la...@googlemail.com>
>         <mailto:tully.la...@googlemail.com
>         <mailto:tully.la...@googlemail.com>>> wrote:
>         >
>         >     Hi Freesurfer experts,
>         >
>         >     I'm hoping you can help me understand how to interpret
>         >     interactions in clusters identified in whole brain
>         analysis using
>         >     glmfit and glmfit-sim. Below I describe what I've done
>         and what
>         >     I'd like to be able to do. Any suggestions would be most
>         appreciated!
>         >
>         >       * I have two groups (patients, controls) and a behavioral
>         >         variable of interest (social functioning). I am
>         interested in
>         >         cortical thickness differences between groups (main
>         effect of
>         >         group), whether cortical thickness relate to social
>         >         functioning across the group (main effect of social
>         >         functioning), and whether this relationship differs
>         by group
>         >         (group x social functioning interaction).
>         >       * I ran whole brain analysis using mri_glmfit with
>         group and
>         >         functioning as variables of interest whilst controlling
>         >         for/regressing out gender, age, and mean thickness.
>         i.e. 4
>         >         classes (conmale,confemale, ptmale, ptfemale) and 3
>         continuous
>         >         variables (age, AvgThickness, Functioning) = 16
>         regressors.
>         >       * I tested the group x functioning interaction with the
>         >         following contrast - is it correct?
>         >
>         >     0000000000000.50.5-0.5-0.5
>         >
>         >       * I then ran mri_glmfit-sim to identify clusters that
>         survive
>         >         multiple comparisons. This revealed 4 clusters (3 in
>         LH; 1 in
>         >         RH) that represent regions showing significant group x
>         >         functioning interaction.
>         >       * I visualized the clusters in tksurfer, and by
>         loading the
>         >         y.fsgd file was able to visualize the plotted data
>         to get a
>         >         sense of the interaction, but this is as much as I
>         know in
>         >         terms of how to examine interactions in the cluster
>         data......
>         >
>         >     My specifc questions include:
>         >
>         >       * I understand that the values in xxx.sig.cluster.mgh
>         overlay
>         >         reflect log10 p values, the signs of which indicate the
>         >         direction of the relationship (i.e. -3 = negative
>         correlation
>         >         between thickness & variable) but I'm not sure how to
>         >         interpret this in the context of an interaction with
>         group?
>         >       * I understand that the values in xxx.y.ocn.dat
>         contain the
>         >         average thickness value for each subject in that
>         cluster and
>         >         that in a simple between groups test this data could
>         be used
>         >         to conduct post hoc t-tests to show the direction of the
>         >         difference, but again I'm not sure how to use this
>         data in the
>         >         context of the interaction. What do the values
>         represent in a
>         >         group x variable interaction?
>         >
>         >     Ideally, I'd like to extract the contrast estimates for each
>         >     subject in the group x functioning contrast and plot it
>         in another
>         >     program and conduct pairwise comparisons (t-tests) in
>         order to get
>         >     a better understanding of the interaction). I'm not sure
>         how to do
>         >     this - is it possible? My thinking is that I do
>         something similar
>         >     in fMRI analysis in spm where I can plot the contrasts in a
>         >     significant cluster and then extract both the average
>         contrast
>         >     estimates for each group and the contrast estimates for each
>         >     individual subject.
>         >
>         >     Thanks in advance!
>         >
>         >     Laura.
>         >
>         >
>         >     --
>         >     --
>         >     Laura M. Tully, MA
>         >     Social Neuroscience & Psychopathology, Harvard University
>         >     Center for the Assessment and Prevention of Prodromal
>         States, UCLA
>         >     Semel Institute of Neuroscience
>         > ltu...@mednet.ucla.edu <mailto:ltu...@mednet.ucla.edu>
>         <mailto:ltu...@mednet.ucla.edu <mailto:ltu...@mednet.ucla.edu>>
>         > ltu...@fas.harvard.edu <mailto:ltu...@fas.harvard.edu>
>         <mailto:ltu...@fas.harvard.edu <mailto:ltu...@fas.harvard.edu>>
>         > 310-267-0170 <tel:310-267-0170> <tel:310-267-0170
>         <tel:310-267-0170>>
>         >     --
>         >     My musings as a young clinical scientist:
>         > http://theclinicalbrain.blogspot.com/
>         >     Follow me on Twitter: @tully_laura
>         >
>         >
>         >
>         >
>         > --
>         > --
>         > Laura M. Tully, MA
>         > Social Neuroscience & Psychopathology, Harvard University
>         > Center for the Assessment and Prevention of Prodromal
>         States, UCLA
>         > Semel Institute of Neuroscience
>         > ltu...@mednet.ucla.edu <mailto:ltu...@mednet.ucla.edu>
>         <mailto:ltu...@mednet.ucla.edu <mailto:ltu...@mednet.ucla.edu>>
>         > ltu...@fas.harvard.edu <mailto:ltu...@fas.harvard.edu>
>         <mailto:ltu...@fas.harvard.edu <mailto:ltu...@fas.harvard.edu>>
>         > 310-267-0170 <tel:310-267-0170>
>         > --
>         > My musings as a young clinical scientist:
>         > http://theclinicalbrain.blogspot.com/
>         > Follow me on Twitter: @tully_laura
>         >
>         >
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>         --
>         Douglas N. Greve, Ph.D.
>         MGH-NMR Center
>         gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>
>         Phone Number: 617-724-2358 <tel:617-724-2358>
>         Fax: 617-726-7422 <tel:617-726-7422>
>
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>
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>     -- 
>     --
>     Laura M. Tully, MA
>     Social Neuroscience & Psychopathology, Harvard University
>     Center for the Assessment and Prevention of Prodromal States, UCLA
>     Semel Institute of Neuroscience
>     ltu...@mednet.ucla.edu <mailto:ltu...@mednet.ucla.edu>
>     ltu...@fas.harvard.edu <mailto:ltu...@fas.harvard.edu>
>     310-267-0170 <tel:310-267-0170>
>     -- 
>     My musings as a young clinical scientist:
>     http://theclinicalbrain.blogspot.com/
>     Follow me on Twitter: @tully_laura
>
>
>
>
> -- 
> --
> Laura M. Tully, MA
> Social Neuroscience & Psychopathology, Harvard University
> Center for the Assessment and Prevention of Prodromal States, UCLA 
> Semel Institute of Neuroscience
> ltu...@mednet.ucla.edu <mailto:ltu...@mednet.ucla.edu>
> ltu...@fas.harvard.edu <mailto:ltu...@fas.harvard.edu>
> 310-267-0170
> -- 
> My musings as a young clinical scientist: 
> http://theclinicalbrain.blogspot.com/
> Follow me on Twitter: @tully_laura

-- 
Douglas N. Greve, Ph.D.
MGH-NMR Center
gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html
Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/

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