Unfortunately, that did not fix the problem.

Here is what I did
1)gtmseg --s 128_S_0225_v06 --keep-cc # noerrors
2)gtmseg --s 128_S_0225_v06 --keep-cc --no-xcerseg  # no errors

3)mri_gtmpvc --i t12pet.nii.gz --psf 4 --auto-mask PSF+2 0.01 --seg
gtmseg.mgz --reg output.lta --default-seg-merge --replace 252 251 --replace
253 251 --replace 254 251 --replace 255 251 --mgx 0.01 --o gtmpvcrcc.output
Loading input t12pet.nii.gz
  done loading input 1 frames
ERROR: item 251 appears as both source and target seg id in replacement list

$Id: mri_gtmpvc.c,v 1.52.2.5 2015/08/28 19:00:13 greve Exp $
setenv SUBJECTS_DIR /analysis/software_test/fs6pvc
cd /analysis/software_test/fs6pvc/128_S_0225_v06/mri
mri_gtmpvc --i t12pet.nii.gz --psf 4 --auto-mask PSF+2 0.01 --seg
gtmseg.mgz --reg output.lta --default-seg-merge --replace 252 251 --replace
253 251 --replace 254 251 --replace 255 251 --mgx 0.01 --o gtmpvcrcc.output
sysname  Linux
hostname
machine  x86_64
user
vgthresh   0.001000
nReplace   22
0.0000 0.0000 0.0000 0.0000 0.0000 0.0000
9 avail.processors, using 9
Creating output directory gtmpvcrcc.output
Loading seg for gtm gtmseg.mgz
Loading seg ctab gtmseg.ctab
Reading gtmseg.lta
Replacing 22
ERROR: CheckSegTissueType() no entry for seg 192
Failed tissue type check

Thank you for looking into this,
Pradeep


On Fri, Jan 29, 2016 at 10:13 AM, Douglas N Greve <gr...@nmr.mgh.harvard.edu
> wrote:

> I think I see the problem. When you run gtmseg, you need to add
> --keep-cc. You can rerun it using the previous command line, but add
> --keep-cc and --no-xcerseg. The second option tells it not to redo the
> extracerebral segmentation (which won't change with CC)
>
> On 01/29/2016 11:21 AM, Pradeep wrote:
> > Thank you for the response.
> >
> > Here is my full command log with error
> >
> >
> > $gtmseg --s 128_S_0225_v06 --keep-hypo --keep-cc
> >
> > $ mri_gtmpvc --i t12pet.nii.gz --psf 4 --auto-mask PSF+2 0.01 --seg
> > gtmseg.mgz --reg output.lta --default-seg-merge --mgx 0.01 --o
> > gtmpvccc.output
> > Loading input t12pet.nii.gz
> >   done loading input 1 frames
> >
> > $Id: mri_gtmpvc.c,v 1.52.2.5 2015/08/28 19:00:13 greve Exp $
> > setenv SUBJECTS_DIR /analysis/software_test/fs6pvc
> > cd /analysis/software_test/fs6pvc/******/mri
> > mri_gtmpvc --i t12pet.nii.gz --psf 4 --auto-mask PSF+2 0.01 --seg
> > gtmseg.mgz --reg output.lta --default-seg-merge --mgx 0.01 --o
> > gtmpvccc.output
> > sysname  Linux
> > hostname server
> > machine  x86_64
> > user     user
> > vgthresh   0.001000
> > nReplace   18
> > 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000
> > 9 avail.processors, using 9
> > Creating output directory gtmpvccc.output
> > Loading seg for gtm gtmseg.mgz
> > Loading seg ctab gtmseg.ctab
> > Reading gtmseg.lta
> > Replacing 18
> > ERROR: CheckSegTissueType() no entry for seg 192
> > Failed tissue type check
> >
> >
> > Thanks,
> > Pradeep
> >
> >
> > On Thu, Jan 28, 2016 at 5:34 PM, Douglas N Greve
> > <gr...@nmr.mgh.harvard.edu <mailto:gr...@nmr.mgh.harvard.edu>> wrote:
> >
> >
> >
> >     On 01/28/2016 06:50 PM, Pradeep wrote:
> >     > Hello Doug,
> >     >
> >     > I have used the gtmseg with --keep-cc  flag and the
> >     corresponding ctab
> >     > files showed the labels but the mri_gtmpvc step failed.
> >     > ****
> >     > Loading seg for gtm gtmseg.mgz
> >     > Loading seg ctab gtmseg.ctab
> >     > Reading gtmseg.lta
> >     > Replacing 18
> >     > ERROR: CheckSegTissueType() no entry for seg 192
> >     > Failed tissue type check
> >     > ****
> >     What is your mri_gtmpvc command line? What is the rest of the
> terminal
> >     output?
> >     > My objective is to use the combination of all CC's as a reference
> >     > region and obtain the PVC results, which would be listed in
> >     gtm.stats.dat
> >     It will be best to combine them when running mri_gtmpvc using
> >     --replace,
> >     eg, --replace 252 251 --replace 253 251 --replace 254 251
> >     --replace 255 251
> >     this will cause all segments of the CC to appear to be a single
> >     segment
> >     (251).
> >     >
> >     > Also, I read in the previous email discussions that the default
> >     > ref-region Pons is 'PVC'ed'. So if I want to calculate the SUVR
> with
> >     > another ROI as a reference region,
> >     > would it be OK take a ratio of the ROI's in gtm.stats.dat table.
> >     Yes, or you can spec the new region, eg --rescale 251
> >     >
> >     > Thanks,
> >     > Pradeep
> >     >
> >     > On Mon, Jan 11, 2016 at 9:25 AM, 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:
> >     >
> >     >
> >     >     If you want to use partial volume correction, then you are
> >     better off
> >     >     using mri_gtmpvc with the bbr registration, something like
> >     >
> >     >     1. To start, run
> >     >
> >     >     gtmseg --s subject
> >     >
> >     >     This will take a couple of hours and produces some files needed
> >     >     for GTM
> >     >     PVC (which is used for GTM, MG, RBV).
> >     >
> >     >     2. You'd then register the PET to the anatomical with
> bbregister
> >     >     (probably with --t2 weighting). Make sure to save the output
> >     as an LTA
> >     >     (--lta). I usually use the mean TAC as the input. You can do
> >     this in
> >     >     parallel with #1.
> >     >
> >     >     3. You'd then run mri_gtmpvc, something like
> >     >
> >     >     mri_gtmpvc --i pet.nii.gz --psf PSF --auto-mask PSF+2 .01 --seg
> >     >     gtmseg.mgz
> >     >     --reg reg.lta --default-seg-merge  --o gtmpvc.output
> >     >
> >     >     PSF is the point-spread FWHM of the scanner; reg.lta is the
> >     >     registration from #2. By default, this will scale by pons.
> >     The output
> >     >     will be gtm.stats.dat and gtm.nii.gz. They both basically
> >     have the
> >     >     same information. gtm.stats.dat is an easy to read text
> >     file. Where
> >     >     each row is an ROI, something like:
> >     >
> >     >     9   17 Left-Hippocampus subcort_gm       473
> >     >     174.083        1.406       0.1216
> >     >
> >     >     9 = nineth row
> >     >     17 = index for RO
> >     >     Left-Hippocampus = name of ROI
> >     >     subcort_gm = tissue class
> >     >     473 = number of PET voxels in the ROI
> >     >     174 = variance reduction factor for ROI (based on GLM/SGTM)
> >     >     1.406 = PVC uptake of ROI relative to Pons
> >     >     0.1216 = resdiual varaince across voxels in the ROI
> >     >
> >     >     gtm.nii.gz is a nifti file with each "voxel" being an ROI.
> >     The value
> >     >     is the PVC uptake of ROI relative to Pons. These can easily be
> >     >     concatenated together (mri_concat) and used as input to
> >     mri_glmfit
> >     >     for group analysis.
> >     >
> >     >
> >     >
> >     >
> >     >     On 01/08/2016 04:22 AM, Benjamin Spurny wrote:
> >     >     > Dear Freesurfer experts!
> >     >     >
> >     >     > I am currently working on PET analysis using FS
> >     >     >
> >     >     > I coregistered my PET with the processed MR using bbregister,
> >     >     > transfered it to a surface using mri_vol2surf
> >     >     > and now createt an overlay in freeview with the
> >     lh.inflated and
> >     >     used the
> >     >     > labels from the lh.aparc.a2009s.annot file.
> >     >     >
> >     >     > In freeview i get the corresponding BP value for each
> >     vertex now but
> >     >     > is there a way to get a list of vertices with the
> >     corresponding
> >     >     BP value
> >     >     > and the corresponding ROI this vertex belongs to?
> >     >     > Or is there a better to do this analyis?
> >     >     >
> >     >     > Many thanks in advance!
> >     >     >
> >     >     > Benjamin
> >     >     >
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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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