Antonella Kis wrote:
> Dear Doug,
>
> Thank you very much for your valuable reply.
>
> I still have few questions on which I would like to ask your advise:
>
> QUESTION 1:
>
> While running the recall-all for all my subjects I also used the 
> -qcache option. I am not sure how this data is further used for my GLM 
> analysis.
>
> I will appreciate if you can confirm if in this case in order to do a  
> thickness-age correlation group  study I need to complete the 
> following steps:
>
> STEP 1:  Uncached Data: resamples each subjects data to fsaveragea 
> (into a common space), and Concatenating all the subjects' into a 
> single file by running
>
> mris_preproc --fsgd AGE_fsgd.fsgd \
> --target fsaverage --hemi lh \
> --meas thickness \
> --out lh.AGE.thickness.00.mgh
>
> STEP 2:  The independent variable is the thickness smoothed at various 
> FWHM (full-width/half-max), usually 0, 5, 10, 10, 20, and 25mm so run:
>
> mris_preproc --fsgd AGE_fsgd.fsgd \
> --cache-in thickness.fwhm10.fsaverage \
> --target fsaverage --hemi lh \
> --out lh.AGE.thickness.10.mgh
>
> STEP 3:  If I run the next step (I know is optional) where I can use 
> this data lh.AGE.thickness.10B.mgh? Is this a better data to be use 
> for my further steps?
You would use it in the same place that you would use 
lh.AGE.thickness.10.mgh. It is just a different way to compute it if you 
did not qcache.
>
> OPTIONAL: THIS WILL TAKE ABOUT 5 MINUTES
>
> mri_surf2surf --hemi lh \
> --s fsaverage \
> --sval lh.AGE.thickness.00.mgh \
> --fwhm 10 \
> --cortex \
> --tval lh.AGE.thickness.10B.mgh
>
> STEP 4:  GLM Analysis (mri_glmfit)
>
> mri_glmfit \
> --y lh.AGE.thickness.10.mgh \
> --fsgd AGE_fsgd.fsgd dods\
> --C lh-Avg-thickness-age-Cor.mtx \
> --surf fsaverage lh \
> --cortex \
> --glmdir lh.AGE.glmdir
>
> STEP 5: View the uncorrected significance map with tksurfer:
>
> tksurfer fsaverage lh inflated \
> -annot aparc.annot -fthresh 2 \
> -overlay lh.AGE.glmdir/lh-Avg-thickness-age-Cor/sig.mgh
>
>
> STEP  6: Viewing the medial surface, change the overlay threshold to 
> something very, very low (say, .01), View --> Configure --> Overlay, 
> set "Min" .01
>
> STEP 7:  CSD (Cluster Simulation Data)- Run the Simulation
>
> mri_glmfit-sim \
> --glmdir lh.AGE.glmdir \
> --sim mc-z 5 4 mc-z.negative \
> --sim-sign neg \
> --overwrite
>
> QUESTION 2: You mentioned that I should use the --cache option to 
> mri_glmfit-sim. How I should do this?  Do I need to change STEP 7?
Yes, use
mri_glmfit-sim \
--glmdir lh.AGE.glmdir \
--cache 4 neg \
--overwrite

>
> QUESTION 3:  How I can check my data to make sure that I have actual 
> activation above the voxel-wise threshold and how I can change my 
> threshold? Based on what I need to change my threshold? Do I change my 
> treshold until I find some activation?
Run tksurfer to view the sig.mgh file. Set the threshold to the one you 
used in mri_glmfit-sim using the view->configure->overlay. There are no 
hard and fast rules to setting thresholds, but people usually use p<.05 
or p<.01.

doug
>
>
> Thank you very much for your valuable help.
> Antonella
>
>
>
> ------------------------------------------------------------------------
> *From:* Douglas N Greve <gr...@nmr.mgh.harvard.edu>
> *To:* Antonella Kis <ator...@yahoo.com>
> *Cc:* "freesurfer@nmr.mgh.harvard.edu" <freesurfer@nmr.mgh.harvard.edu>
> *Sent:* Tuesday, August 16, 2011 12:04 PM
> *Subject:* Re: [Freesurfer] thickness-age correlation
>
>
>
> Antonella Kis wrote:
> > Dear Freesurfer experts,
> >
> > I am doing a thickness-age correlation group difference study 
> (patients versus controls. I would like to know if:
> >
> > 1) my contrast vector defined as 0 0 0.5 0.5 is correct in order to 
> test the change in thickness with age
> > 
> Yes.
> > 2)what is the best iteration number for the simulation? Should be 
> 5000 or 1000 or greater?
> > 
> 10,000 -- note that if you're doing a whole-hemisphere correction with 
> the monte-carlo simulation then you should use the pre-computed 
> results (use the --cache option to mri_glmfit-sim)
> > 3)why when I run the simulation for 5 iterations I've got zero clusters?
> > 
> You should look at your data to make sure that you have actual 
> activation above the voxel-wise threshold you have set. Also, only 5 
> clusters would not be enough to get a significant cluster anyway.
> > 4)can I derive the thickness from the significant clusters of glm 
> analysis? Do I need to run QDEC after GLM?
> > 
> If you mean that you want the average thickness from each subject for 
> a given cluster, then this information is generated with 
> mri_glmfit-sim in the csdbase.y.ocn.dat file.
>
> doug
> >  Thanks for any enlightenment.
> > Antonella
> >
> >  
> ------------------------------------------------------------------------
> >
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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 Fax: 617-726-7422
>
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>
>
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>

-- 
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

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