On 11/04/2016 07:25 AM, Alshikho, Mohamad J. wrote:
>
>  Dear FS experts,
>
>  I ran surface based analysis using PET maps, and the pipeline 
> reported, in FS list, by multiple colleagues as  the following:
>
> ·spmregister --s subj --mov pet.nii --reg reg.dat --out pet_t1.mgh
>
> ·mris_preproc --target fsaverage --hemi lh --iv subj1/ubject1_pet.nii 
> subject1/pet/pet_2_T1_register.dat ..... --projfrac 0.5 --out lh.mgh
>
> ·mri_surf2surf --hemi lh --s fsaverage --fwhm 6 --cortex --sval lh.mgh 
> --tval lh.sm6.mgh
>
> ·mri_glmfit--y lh.sm6.mgh--fsgd fsgd.txt--C 2gc0.mtx --surf fsaverage 
> lh --cortex --glmdir lh.glmdir//
>
> ·then mri_glmfit-sim to correct for multiple comparison.
>
> I wanted to know the correct usage of the flag “*_projfrac_*” in the 
> command "*_mris_preproc_*":
>
> My understanding is that this flag control running the surface based 
> analysis far from the surface (i.e. close to the surface or deep in 
> the white matter)
>
> ·If it is 0.5 èthat means the surface based analysis is running in the 
> middle area between white and pial
>
> ·if it is zero èthe surface based analysis is running close to white 
> matter
>
> ·if it is +1 èthat means the surface based analysis is running close 
> to the pial
>
> ·if it is -1 èthat means the surface based analysis is running deep in 
> the white matter
>
> Kindly:
>
> 1.Is this correct?
>
Yes
>
> 2.Can I  use values like -2 or -3 ... etc to run the analysis deep in 
> the white matter. I aim to run surface based analysis on multiple 
> layers of the brain deep from the pial to investigate how the PET 
> signal is going to change between these layers?
>
In principle, yes, but often what happens is that when you follow the 
normal vector into the white matter that far, you end up in GM or CSF 
and not WM.
>
> 3.What is the difference between the flag "*_projfrac_*" and the flag 
> "*_projdis_*"
>
projdist will project an absolute distance (in mm). projfrac will 
project a fraction of the thickness (as you describe above)
>
> 4.If I replace the PET maps in the previous pipeline by diffusion 
> maps? Is it keep valid for diffusion data?
>
I guess it depends on what you mean by "valid". As I mention above, it 
will not necessarily sample WM, and that probably invalidates it somewhat
>
> Many Thank!
>
> Mohamad
>
>
>
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-- 
Douglas N. Greve, Ph.D.
MGH-NMR Center
gr...@nmr.mgh.harvard.edu
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