Dear Dr. Greve,

Thanks a lot for your inputs on this.
In the manual-
https://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/QdecGroupAnalysis_freeview,
in qdec it shows there is an option to select 'Smoothing (FWHM)' under the
step 'Design'. Could you please share your thoughts if there is any optimal
value here I can choose which does a close comparison for the two different
voxel size (1.3 vs 1) or may be if I can compare without smoothing?
Thanks.

On Wed, Oct 5, 2016 at 3:21 PM, Douglas N Greve <gr...@nmr.mgh.harvard.edu>
wrote:

> I think the difference in voxel size (1mm vs 1.3mm) is problematic. You
> will get more smoothing with the 1.3mm (ie, partial volume effects), and
> that could easily show up in the thickness measurements
>
>
> On 10/05/2016 12:19 PM, Martin Juneja wrote:
> > Hi Dr. Greve,
> >
> > After I compare the two protocols (after using mri_info in FSL on raw
> > dicom file), I get following parameters used in both the protocols.
> > After looking at both the protocols parameters below, could you please
> > share your thoughts on whether parameters are in match enough to go
> > ahead and do the analysis i.e. patients data collected using protocol
> > 1 and controls data using protocol 2 or is it still a bad idea to
> compare.
> >
> > *Protocol 1:*
> >
> > INFO: loading series header info.
> >
> > INFO: sorting.
> >
> > RunNo = 1
> >
> > sdfiSameSlicePos() eps = 0.000001
> >
> > INFO: (256 256 176), nframes = 1, ismosaic=0
> >
> > sdfi->UseSliceScaleFactor 0
> >
> > datatype = 4, short=4, float=3
> >
> > PE Dir ROW ROW
> >
> > AutoAlign matrix detected
> >
> > AutoAlign Matrix ---------------------
> >
> >  1.00000 0.00000   0.00000   0.00000;
> >
> >  0.00000 1.00000   0.00000   0.00000;
> >
> >  0.00000 0.00000   1.00000   0.00000;
> >
> >  0.00000 0.00000   0.00000   1.00000;
> >
> > Volume information for IM-0001-0001-0001.dcm
> >
> > type: siemens_dicom
> >
> > dimensions: 256 x 256 x 176
> >
> >    voxel sizes: 1.000000, 1.000000, 1.000000
> >
> > type: SHORT (4)
> >
> > fov: 256.000
> >
> > dof: 0
> >
> > xstart: -128.0, xend: 128.0
> >
> > ystart: -128.0, yend: 128.0
> >
> > zstart: -88.0, zend: 88.0
> >
> > TR: 2100.00 msec, TE: 2.30 msec, TI: 1100.00 msec, flip angle: 12.00
> > degrees
> >
> > nframes: 1
> >
> > PhEncDir: ROW
> >
> > FieldStrength: 3.000000
> >
> > ras xform present
> >
> >     xform info: x_r =  -0.0000, y_r =  -0.0000, z_r =  -1.0000, c_r =
> >     2.5000
> >
> >   : x_a =  -1.0000, y_a =  -0.0000, z_a =  -0.0000, c_a =    14.0000
> >
> >   : x_s =   0.0000, y_s =  -1.0000, z_s =   0.0000, c_s =     2.0000
> >
> > Orientation   : PIL
> >
> > Primary Slice Direction: sagittal
> >
> > voxel to ras transform:
> >
> >   -0.0000  -0.0000  -1.0000    90.5000
> >
> >   -1.0000  -0.0000  -0.0000   142.0000
> >
> >     0.0000  -1.0000   0.0000   130.0000
> >
> >     0.0000   0.0000   0.0000     1.0000
> >
> > voxel-to-ras determinant -1
> >
> > ras to voxel transform:
> >
> >   -0.0000  -1.0000  -0.0000   142.0000
> >
> >   -0.0000  -0.0000  -1.0000   130.0000
> >
> >   -1.0000  -0.0000  -0.0000    90.5000
> >
> >   -0.0000  -0.0000  -0.0000     1.0000
> >
> >
> > *Protocol 2:*
> >
> > INFO: (256 256 128), nframes = 1, ismosaic=0
> >
> > sdfi->UseSliceScaleFactor 0
> >
> > datatype = 4, short=4, float=3
> >
> > PE Dir ROW ROW
> >
> > Volume information for IM-0001-0001-0001.dcm
> >
> > type: siemens_dicom
> >
> > dimensions: 256 x 256 x 128
> >
> >    voxel sizes: 1.000000, 1.000000, 1.330000
> >
> > type: SHORT (4)
> >
> > fov: 256.000
> >
> > dof: 0
> >
> > xstart: -128.0, xend: 128.0
> >
> > ystart: -128.0, yend: 128.0
> >
> > zstart: -64.0, zend: 64.0
> >
> > TR: 2100.00 msec, TE: 2.25 msec, TI: 1100.00 msec, flip angle: 12.00
> > degrees
> >
> > nframes: 1
> >
> > PhEncDir: ROW
> >
> > FieldStrength: 3.000000
> >
> > ras xform present
> >
> >     xform info: x_r =  -0.0202, y_r =   0.0424, z_r =  -0.9989, c_r =
> >   -23.2439
> >
> >   : x_a =  -0.9989, y_a =  -0.0441, z_a =   0.0184, c_a =    53.2183
> >
> >   : x_s =   0.0433, y_s =  -0.9981, z_s =  -0.0432, c_s =   -12.5170
> >
> > Orientation   : PIL
> >
> > Primary Slice Direction: sagittal
> >
> > voxel to ras transform:
> >
> >   -0.0202   0.0424  -1.3285    58.9497
> >
> >   -0.9989  -0.0441   0.0244   185.1541
> >
> >     0.0433  -0.9981  -0.0575   113.3820
> >
> >     0.0000   0.0000   0.0000     1.0000
> >
> > voxel-to-ras determinant -1.33
> >
> > ras to voxel transform:
> >
> >   -0.0202  -0.9989   0.0433   181.2290
> >
> >     0.0424  -0.0441  -0.9981   118.8377
> >
> >   -0.7511   0.0138  -0.0325    45.4015
> >
> >   -0.0000  -0.0000  -0.0000     1.0000
> >
> > Thanks a lot.
> >
> > On Mon, Oct 3, 2016 at 11:42 AM, Douglas N Greve
> > <gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>> wrote:
> >
> >     I would still say no -- the differences could still be due to
> >     differences in acquisition parameters
> >
> >
> >     On 10/03/2016 02:30 PM, Martin Juneja wrote:
> >     > Thanks Dr. Harms and Dr. Greve.
> >     > So can I do the cortical thickness comparison if we have healthy
> >     > controls data from the same scanner but acquired using different
> >     > protocol e.g. if we get access of age-matched healthy controls data
> >     > from another lab who used the same scanner?
> >     >
> >     > Thanks.
> >     >
> >     > On Fri, Sep 30, 2016 at 12:02 PM, Douglas N Greve
> >     > <gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>
> >     <mailto:gr...@nmr.mgh.harvard.edu
> >     <mailto:gr...@nmr.mgh.harvard.edu>>> wrote:
> >     >
> >     >     You can do the comparison, but the interpretation is
> >     difficult. If you
> >     >     see a difference, how do you know it is not due to the scanner?
> >     >     There's
> >     >     not much you can do ...
> >     >
> >     >
> >     >     On 09/29/2016 02:54 PM, Martin Juneja wrote:
> >     >     > Hello FS experts,
> >     >     >
> >     >     > I have a data set of 20 subjects (patients) collected at
> >     location-1
> >     >     > with 3T Siemens scanner. Also, I have a set of age-matched 20
> >     >     subjects
> >     >     > (controls) collected at location-2 with 3T Siemens scanner.
> >     >     >
> >     >     > I am interested in comparing cortical thickness between
> >     controls and
> >     >     > patients using FreeSurfer but I am not sure if I can do
> >     that since I
> >     >     > have both the data sets collected at two different locations.
> >     >     >
> >     >     > I would really appreciate any inputs on this.
> >     >     >
> >     >     > I tried to find some papers on scanner differences but all
> >     I could
> >     >     > find was between 1.5 T vs 3T or 3T vs 7T. Is there any
> special
> >     >     > covariates I need to define for this purpose (if so then at
> >     >     which step
> >     >     > during analysis?) or is it not possible at all?
> >     >     >
> >     >     > Thanks.
> >     >     >
> >     >     >
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> >     >     --
> >     >     Douglas N. Greve, Ph.D.
> >     >     MGH-NMR Center
> >     > gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>
> >     <mailto:gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu
> >>
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> >     --
> >     Douglas N. Greve, Ph.D.
> >     MGH-NMR Center
> >     gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>
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> --
> Douglas N. Greve, Ph.D.
> MGH-NMR Center
> gr...@nmr.mgh.harvard.edu
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