Re: [Freesurfer] fcseed-sess error

2015-05-21 Thread Alexandra Tanner
Hi Doug,

It is a pretty small segmentation. In subject NNC0931 (the example we're
looking at) the segmentation has 54 voxels. fcseed-sess also didn't work
in subject NNC0901 -- in that subject the segmentation has 78 voxels. For
comparison, in one of the subjects where fcseed-sess completed without
error the segmentation has 89 voxels. Do you think this is an issue of
size?

Thanks!
Alex

 I'm not sure what is going wrong here, but it does not find any voxels
when the segmentation is mapped into the functional space. Can you look
at

 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz

 And see how many voxels it has? Is it possible that that is a really
small segmentation?

 doug


 On 05/21/2015 10:30 AM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,
 I'm running fcseed-sess to compute the time course in 12 different ROIs
(created with fcseed-config) across 27 subjects. I'm having an issue,
however, where fcseed-sess completes for a particular ROI in most
subjects
 but errors out for a few subjects (see log below). I saw someone had
the
 same issue in the mail archives
 (https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-August/032646.html)
so I checked the registration but everything seems to look fine. Any
other
 suggestions on how to fix this issue would be greatly appreciated! Thanks!
 Alex
 fcseed-config and fcseed-sess commands/logs:
 # /usr/local/freesurfer/dev/fsfast/bin/fcseed-config -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
-segid 1 -seg
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
-fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat -fsd
 resting -mean -force
 # ProjectDir /autofs/cluster/roffman/users/Stable5_PerRun
 # $Id: fcseed-config,v 1.8 2014/02/25 19:08:31 greve Exp $
 # Wed May 20 14:03:50 EDT 2015
 fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
fsd resting
 segstem
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol
RegDOF 6
 FillThresh .5
 DoMean 1
 DoSVD 0
 DoSqr 0
 MakeMask 0
 WMErode 0
 SVDSynth 0
 DoWM 0
 UseB0DC 0
 segidlist 1
 Tue May 19 17:40:27 EDT 2015
 Linux dauntless 2.6.32-504.1.3.el6.x86_64 #1 SMP Tue Nov 11 17:57:25
UTC
 2014 x86_64 x86_64 x86_64 GNU/Linux
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 cd /autofs/cluster/roffman/users/Stable5_PerRun
 /usr/local/freesurfer/dev/fsfast/bin/fcseed-sess
 -s NNC0931 -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
freesurfer-Linux-centos6_x86_64-dev-20150519
 mri_label2vol --seg
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
--reg
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
--temp
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
--fillthresh .5 --o
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
--pvf
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
PVF
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
Number of labels: 0
 Annot File:  (null)
 Template Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
Outut Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
Registration File:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
Fill Threshold: 0.5
 Label Vox Vol:  1
 ProjType:   (null)
 ProjTypeId: 0
 ProjStart:  0
 ProjStop:   0
 ProjDelta:  0.1
 Subject:  (null)
 Hemi: (null)
 UseNewASeg2Vol:  0
 DoLabelStatVol  0
 LabelCodeOffset  0
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 $Id: mri_label2vol.c,v 1.46 2014/12/08 21:11:54 greve Exp $
 Template RAS-to-Vox: 
 -0.3  -0.0  -0.0   36.0;
 -0.0  -0.0  -0.3   36.0;
 -0.0   0.3  -0.0   23.5;
 -0.0  -0.0  -0.0   1.0;
 Template Voxel Volume: 27
 nHits Thresh: 13.5
 Loading registration from
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
regio_read_register: loading lta
 RegMat: 
   0.99848   0.02007  -0.05128  -0.41633;
   0.04918   0.09388   0.99437  -30.67201;
 -0.02477   0.99538  -0.09275   5.35657;
   0.0   0.0   0.0   1.0;
 Label RAS-to-Vox: 
 -0.33283  -0.00669   0.01709   36.13877;
   0.00826  -0.33179   0.03092   34.21448;
   0.01639   0.03129   0.33146   13.27600;
   0.0   0.0   0.0   1.0;
 PVF
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
Computing PVF 27

[Freesurfer] fcseed-sess error

2015-05-21 Thread Alexandra Tanner
Hi Doug and Freesurfers,

I'm running fcseed-sess to compute the time course in 12 different ROIs
(created with fcseed-config) across 27 subjects. I'm having an issue,
however, where fcseed-sess completes for a particular ROI in most subjects
but errors out for a few subjects (see log below). I saw someone had the
same issue in the mail archives
(https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-August/032646.html)
so I checked the registration but everything seems to look fine. Any other
suggestions on how to fix this issue would be greatly appreciated!

Thanks!
Alex


fcseed-config and fcseed-sess commands/logs:

# /usr/local/freesurfer/dev/fsfast/bin/fcseed-config -cfg
/cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
-segid 1 -seg
lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
-fcname
lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat -fsd
resting -mean -force
# ProjectDir /autofs/cluster/roffman/users/Stable5_PerRun
# $Id: fcseed-config,v 1.8 2014/02/25 19:08:31 greve Exp $
# Wed May 20 14:03:50 EDT 2015

fcname lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
fsd resting
segstem
lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol
RegDOF 6
FillThresh .5
DoMean 1
DoSVD 0
DoSqr 0
MakeMask 0
WMErode 0
SVDSynth 0
DoWM 0
UseB0DC 0
segidlist 1



Tue May 19 17:40:27 EDT 2015
Linux dauntless 2.6.32-504.1.3.el6.x86_64 #1 SMP Tue Nov 11 17:57:25 UTC
2014 x86_64 x86_64 x86_64 GNU/Linux
setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
cd /autofs/cluster/roffman/users/Stable5_PerRun
/usr/local/freesurfer/dev/fsfast/bin/fcseed-sess
-s NNC0931 -cfg
/cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
freesurfer-Linux-centos6_x86_64-dev-20150519

mri_label2vol --seg
/cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
--reg
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
--temp
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
--fillthresh .5 --o
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
--pvf
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
PVF
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
Number of labels: 0
Annot File:  (null)
Template Volume:
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
Outut Volume:
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
Registration File:
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
Fill Threshold: 0.5
Label Vox Vol:  1
ProjType:   (null)
ProjTypeId: 0
ProjStart:  0
ProjStop:   0
ProjDelta:  0.1
Subject:  (null)
Hemi: (null)
UseNewASeg2Vol:  0
DoLabelStatVol  0
LabelCodeOffset  0
setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
$Id: mri_label2vol.c,v 1.46 2014/12/08 21:11:54 greve Exp $
Template RAS-to-Vox: 
-0.3  -0.0  -0.0   36.0;
-0.0  -0.0  -0.3   36.0;
-0.0   0.3  -0.0   23.5;
-0.0  -0.0  -0.0   1.0;
Template Voxel Volume: 27
nHits Thresh: 13.5
Loading registration from
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
regio_read_register: loading lta
RegMat: 
 0.99848   0.02007  -0.05128  -0.41633;
 0.04918   0.09388   0.99437  -30.67201;
-0.02477   0.99538  -0.09275   5.35657;
 0.0   0.0   0.0   1.0;
Label RAS-to-Vox: 
-0.33283  -0.00669   0.01709   36.13877;
 0.00826  -0.33179   0.03092   34.21448;
 0.01639   0.03129   0.33146   13.27600;
 0.0   0.0   0.0   1.0;
PVF
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
Computing PVF 27
mri_label2vol done
mri_binarize --i
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
--o
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/mask.nii
--match 1

$Id: mri_binarize.c,v 1.41 2014/08/17 17:47:29 greve Exp $
cwd /autofs/cluster/roffman/users/Stable5_PerRun
cmdline mri_binarize --i
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
--o
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/mask.nii
--match 1
sysname  Linux
hostname dauntless
machine  x86_64
user atanner

input 
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
frame  0
nErode3d   0
nErode2d   0
output
/autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/mask.nii

Re: [Freesurfer] fcseed-sess error

2015-05-21 Thread Alexandra Tanner
The voxel size for this functional sequence is 3x3x3mm

 What is the voxel size of your functional? 54 is small, but I would
 expect it to still work.

 On 05/21/2015 11:20 AM, Alexandra Tanner wrote:
 Hi Doug,

 It is a pretty small segmentation. In subject NNC0931 (the example we're
 looking at) the segmentation has 54 voxels. fcseed-sess also didn't work
 in subject NNC0901 -- in that subject the segmentation has 78 voxels.
 For
 comparison, in one of the subjects where fcseed-sess completed without
 error the segmentation has 89 voxels. Do you think this is an issue of
 size?

 Thanks!
 Alex

 I'm not sure what is going wrong here, but it does not find any voxels
 when the segmentation is mapped into the functional space. Can you look
 at
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz

 And see how many voxels it has? Is it possible that that is a really
 small segmentation?
 doug


 On 05/21/2015 10:30 AM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,
 I'm running fcseed-sess to compute the time course in 12 different
 ROIs
 (created with fcseed-config) across 27 subjects. I'm having an issue,
 however, where fcseed-sess completes for a particular ROI in most
 subjects
 but errors out for a few subjects (see log below). I saw someone had
 the
 same issue in the mail archives
 (https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-August/032646.html)
 so I checked the registration but everything seems to look fine. Any
 other
 suggestions on how to fix this issue would be greatly appreciated!
 Thanks!
 Alex
 fcseed-config and fcseed-sess commands/logs:
 # /usr/local/freesurfer/dev/fsfast/bin/fcseed-config -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
 -segid 1 -seg
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
 -fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
 -fsd
 resting -mean -force
 # ProjectDir /autofs/cluster/roffman/users/Stable5_PerRun
 # $Id: fcseed-config,v 1.8 2014/02/25 19:08:31 greve Exp $
 # Wed May 20 14:03:50 EDT 2015
 fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
 fsd resting
 segstem
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol
 RegDOF 6
 FillThresh .5
 DoMean 1
 DoSVD 0
 DoSqr 0
 MakeMask 0
 WMErode 0
 SVDSynth 0
 DoWM 0
 UseB0DC 0
 segidlist 1
 Tue May 19 17:40:27 EDT 2015
 Linux dauntless 2.6.32-504.1.3.el6.x86_64 #1 SMP Tue Nov 11 17:57:25
 UTC
 2014 x86_64 x86_64 x86_64 GNU/Linux
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 cd /autofs/cluster/roffman/users/Stable5_PerRun
 /usr/local/freesurfer/dev/fsfast/bin/fcseed-sess
 -s NNC0931 -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
 freesurfer-Linux-centos6_x86_64-dev-20150519
 mri_label2vol --seg
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
 --reg
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 --temp
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
 --fillthresh .5 --o
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
 --pvf
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
 PVF
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
 Number of labels: 0
 Annot File:  (null)
 Template Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
 Outut Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
 Registration File:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 Fill Threshold: 0.5
 Label Vox Vol:  1
 ProjType:   (null)
 ProjTypeId: 0
 ProjStart:  0
 ProjStop:   0
 ProjDelta:  0.1
 Subject:  (null)
 Hemi: (null)
 UseNewASeg2Vol:  0
 DoLabelStatVol  0
 LabelCodeOffset  0
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 $Id: mri_label2vol.c,v 1.46 2014/12/08 21:11:54 greve Exp $
 Template RAS-to-Vox: 
 -0.3  -0.0  -0.0   36.0;
 -0.0  -0.0  -0.3   36.0;
 -0.0   0.3  -0.0   23.5;
 -0.0  -0.0  -0.0   1.0;
 Template Voxel Volume: 27
 nHits Thresh: 13.5
 Loading registration from
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 regio_read_register: loading lta
 RegMat: 
0.99848   0.02007  -0.05128  -0.41633;
0.04918   0.09388   0.99437  -30.67201;
 -0.02477   0.99538  -0.09275   5.35657;
0.0   0.0   0.0   1.0;
 Label RAS-to-Vox: 
 -0.33283  -0.00669   0.01709   36.13877

Re: [Freesurfer] fcseed-sess error

2015-05-21 Thread Alexandra Tanner
I actually already tried rerunning fcseed-config and fcseed-sess lowering
the fillthresh (even brought it down to 0) and I still got the same error.
I just tried .05 to be thorough but no dice :(

 Try lowering the fillthreshold to .1 in fcseed-config (means you have to
 re-run fcseed-sess for all subjects, but see if it makes those two
 work). For such a small seed, it may even be better to use .05.

 On 05/21/2015 11:42 AM, Alexandra Tanner wrote:
 The voxel size for this functional sequence is 3x3x3mm

 What is the voxel size of your functional? 54 is small, but I would
 expect it to still work.

 On 05/21/2015 11:20 AM, Alexandra Tanner wrote:
 Hi Doug,

 It is a pretty small segmentation. In subject NNC0931 (the example
 we're
 looking at) the segmentation has 54 voxels. fcseed-sess also didn't
 work
 in subject NNC0901 -- in that subject the segmentation has 78 voxels.
 For
 comparison, in one of the subjects where fcseed-sess completed without
 error the segmentation has 89 voxels. Do you think this is an issue of
 size?

 Thanks!
 Alex

 I'm not sure what is going wrong here, but it does not find any
 voxels
 when the segmentation is mapped into the functional space. Can you
 look
 at
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz

 And see how many voxels it has? Is it possible that that is a really
 small segmentation?
 doug


 On 05/21/2015 10:30 AM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,
 I'm running fcseed-sess to compute the time course in 12 different
 ROIs
 (created with fcseed-config) across 27 subjects. I'm having an issue,
 however, where fcseed-sess completes for a particular ROI in most
 subjects
 but errors out for a few subjects (see log below). I saw someone had
 the
 same issue in the mail archives
 (https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-August/032646.html)
 so I checked the registration but everything seems to look fine. Any
 other
 suggestions on how to fix this issue would be greatly appreciated!
 Thanks!
 Alex
 fcseed-config and fcseed-sess commands/logs:
 # /usr/local/freesurfer/dev/fsfast/bin/fcseed-config -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
 -segid 1 -seg
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
 -fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
 -fsd
 resting -mean -force
 # ProjectDir /autofs/cluster/roffman/users/Stable5_PerRun
 # $Id: fcseed-config,v 1.8 2014/02/25 19:08:31 greve Exp $
 # Wed May 20 14:03:50 EDT 2015
 fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
 fsd resting
 segstem
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol
 RegDOF 6
 FillThresh .5
 DoMean 1
 DoSVD 0
 DoSqr 0
 MakeMask 0
 WMErode 0
 SVDSynth 0
 DoWM 0
 UseB0DC 0
 segidlist 1
 Tue May 19 17:40:27 EDT 2015
 Linux dauntless 2.6.32-504.1.3.el6.x86_64 #1 SMP Tue Nov 11 17:57:25
 UTC
 2014 x86_64 x86_64 x86_64 GNU/Linux
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 cd /autofs/cluster/roffman/users/Stable5_PerRun
 /usr/local/freesurfer/dev/fsfast/bin/fcseed-sess
 -s NNC0931 -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
 freesurfer-Linux-centos6_x86_64-dev-20150519
 mri_label2vol --seg
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
 --reg
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 --temp
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
 --fillthresh .5 --o
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
 --pvf
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
 PVF
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
 Number of labels: 0
 Annot File:  (null)
 Template Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
 Outut Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
 Registration File:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 Fill Threshold: 0.5
 Label Vox Vol:  1
 ProjType:   (null)
 ProjTypeId: 0
 ProjStart:  0
 ProjStop:   0
 ProjDelta:  0.1
 Subject:  (null)
 Hemi: (null)
 UseNewASeg2Vol:  0
 DoLabelStatVol  0
 LabelCodeOffset  0
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 $Id: mri_label2vol.c,v 1.46 2014/12/08 21:11:54 greve Exp $
 Template RAS-to-Vox: 
 -0.3  -0.0  -0.0   36.0;
 -0.0  -0.0  -0.3   36.0;
 -0.0   0.3  -0.0   23.5;
 -0.0  -0.0  -0.0   1.0

Re: [Freesurfer] fcseed-sess error

2015-05-21 Thread Alexandra Tanner
Hi Doug,

So I just tried making my ROI a little bit bigger in an earlier binarizing
step that created my segmentation, and when I ran fcseed-config and
fcseed-sess in this same subject it ran without error. I guess it was a
sizing issue! Let me know if you have any additional thoughts.

Thanks again for your help!

Best,
Alex

 I actually already tried rerunning fcseed-config and fcseed-sess
lowering
 the fillthresh (even brought it down to 0) and I still got the same
error.
 I just tried .05 to be thorough but no dice :(

 Try lowering the fillthreshold to .1 in fcseed-config (means you have
to
 re-run fcseed-sess for all subjects, but see if it makes those two
work). For such a small seed, it may even be better to use .05. On
05/21/2015 11:42 AM, Alexandra Tanner wrote:
 The voxel size for this functional sequence is 3x3x3mm
 What is the voxel size of your functional? 54 is small, but I would
expect it to still work.
 On 05/21/2015 11:20 AM, Alexandra Tanner wrote:
 Hi Doug,
 It is a pretty small segmentation. In subject NNC0931 (the example
we're
 looking at) the segmentation has 54 voxels. fcseed-sess also didn't
work
 in subject NNC0901 -- in that subject the segmentation has 78
voxels.
 For
 comparison, in one of the subjects where fcseed-sess completed without
 error the segmentation has 89 voxels. Do you think this is an issue of
 size?
 Thanks!
 Alex
 I'm not sure what is going wrong here, but it does not find any voxels
 when the segmentation is mapped into the functional space. Can you look
 at
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
And see how many voxels it has? Is it possible that that is a
really
 small segmentation?
 doug
 On 05/21/2015 10:30 AM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,
 I'm running fcseed-sess to compute the time course in 12 different
ROIs
 (created with fcseed-config) across 27 subjects. I'm having an
issue,
 however, where fcseed-sess completes for a particular ROI in most
subjects
 but errors out for a few subjects (see log below). I saw someone had
 the
 same issue in the mail archives
 (https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-August/032646.html)
 so I checked the registration but everything seems to look fine. Any
other
 suggestions on how to fix this issue would be greatly appreciated!
Thanks!
 Alex
 fcseed-config and fcseed-sess commands/logs:
 # /usr/local/freesurfer/dev/fsfast/bin/fcseed-config -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
 -segid 1 -seg
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
 -fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
-fsd
 resting -mean -force
 # ProjectDir /autofs/cluster/roffman/users/Stable5_PerRun
 # $Id: fcseed-config,v 1.8 2014/02/25 19:08:31 greve Exp $ # Wed
May 20 14:03:50 EDT 2015
 fcname
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.dat
 fsd resting
 segstem
 lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol
 RegDOF 6
 FillThresh .5
 DoMean 1
 DoSVD 0
 DoSqr 0
 MakeMask 0
 WMErode 0
 SVDSynth 0
 DoWM 0
 UseB0DC 0
 segidlist 1
 Tue May 19 17:40:27 EDT 2015
 Linux dauntless 2.6.32-504.1.3.el6.x86_64 #1 SMP Tue Nov 11 17:57:25
 UTC
 2014 x86_64 x86_64 x86_64 GNU/Linux
 setenv SUBJECTS_DIR /cluster/roffman/users/Stable5_PerRun
 cd /autofs/cluster/roffman/users/Stable5_PerRun
 /usr/local/freesurfer/dev/fsfast/bin/fcseed-sess
 -s NNC0931 -cfg
 /cluster/roffman/users/Stable5_PerRun/FC_Analyses/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.cfg
 freesurfer-Linux-centos6_x86_64-dev-20150519
 mri_label2vol --seg
 /cluster/roffman/users/Stable5_PerRun/NNC0931/mri/lh_7Network_6_FPCN_inferiorparietal_supramarginal_Vtx126184_sm04.bin.vol.mgz
 --reg
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 --temp
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
 --fillthresh .5 --o
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
 --pvf
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
 PVF
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/pvf.nii
 Number of labels: 0
 Annot File:  (null)
 Template Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/template.nii
 Outut Volume:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/tmp.fcseed-sess.7514/seg.nii
 Registration File:
 /autofs/cluster/roffman/users/Stable5_PerRun/NNC0931/resting/014/register.dof6.lta
 Fill Threshold: 0.5
 Label Vox Vol:  1
 ProjType:   (null)
 ProjTypeId: 0
 ProjStart:  0
 ProjStop:   0
 ProjDelta:  0.1
 Subject:  (null)
 Hemi: (null)
 UseNewASeg2Vol:  0
 DoLabelStatVol  0
 LabelCodeOffset  0
 setenv

[Freesurfer] Talairach coordinate discrepancy mri_surfcluster vs tksurfer

2015-04-02 Thread Alexandra Tanner
Hi Doug and Freesurfers,

I ran mri_surfcluster to generate coordinates for cluster maxima from a
functional surface analysis. The summary text file generated by
mri_surfcluster lists a bunch of information about the clusters, including
talairach coordinates for each cluster peak (see example below). I
visualized these max vertices in tksurfer by entering the VtxMax given
in the summary file into the Vertex Index field in the tksurfer tools
window. I'm noticing, however, that the talairach coordinates given in the
tksurfer tools window (Vertex Talairach) after entering the vertex index
are not the same as the coordinates listed in the summary file. Seems the
coordinates are off by .5 - 1 millimeter or so, which I know is not much,
but I'm curious if anyone knows the reason for this discrepancy?
Additionally, if we want to use the peaks for seeds in a functional
connectivity analysis which set of coordinates is more accurate?

Any insight would be greatly appreciated!

Best,
Alex

Ex. Summary text file:
# ClusterNo  Max   VtxMax   Size(mm^2)  TalX   TalY   TalZNVtxs
   1   33.019  124877   1219.98 30.7   21.1   -1.4  2841
   2   27.538  116676   1406.49  7.6   23.7   38.1  2923
   3   25.380  109387   3977.58 41.9   31.2   26.7  7023
   4   24.404   86863   3241.21 31.5  -60.2   39.0  7288
   5  -20.441  104109   1903.13  5.5   20.5   -7.4  3923
   6   18.118  141781600.75  5.5  -23.0   26.4  1553

Cluster 1 Vertex Talairach coordinates from tksurfer tools: (29.88  20.79 
-1.32)



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[Freesurfer] [Fwd: Re: Modeling cortical thickness question]

2014-12-10 Thread Alexandra Tanner
Hi Doug,
Thanks for your response! Please see Josh's follow-up question below.
Thanks again for your help!

Best,
Alex

 Original Message 
Subject: Re: [Fwd: Re: [Freesurfer] Modeling cortical thickness question]
From:Roffman, Joshua L.,M.D. jroff...@partners.org
Date:Wed, December 10, 2014 11:52 am
To:  Alexandra Tanner atan...@nmr.mgh.harvard.edu
--

Maybe...if we take this approach I guess we would want the cube root of
age, not age cubed? The relationship we are testing is whether y=x^3
(where x is age and y is cortical thickness). So if we took the cube root
of both sides, that might be closer to what we want?

(Alex: could you forward this to the list)

Thx
Josh

Sent from my iPhone

 On Dec 10, 2014, at 9:32 AM, Alexandra Tanner
atan...@nmr.mgh.harvard.edu wrote:

 Hi Josh,
 Below is Doug's response...does this answer your question?

 Thanks,
 Alex

  Original Message 
 Subject: Re: [Freesurfer] Modeling cortical thickness question
 From:Douglas N Greve gr...@nmr.mgh.harvard.edu
 Date:Tue, December 9, 2014 4:48 pm
 To:  freesurfer@nmr.mgh.harvard.edu
 --


 Do you mean a polynomial of age? If so, just add age age^2 and age^3 as
 variables in the FSGD file
 doug

 On 12/09/2014 02:04 PM, Alexandra Tanner wrote:
 Hello Freesurfers,

 Our group is wondering if any of you know whether it is possible to model
 cortical thickness as a third order polynomial? The specific question is:
 we are looking at whether there is a hyperbolic relationship between
 cortical thickness and date of birth among a cohort of individuals born
 over a 6 year period. Any insights would be greatly appreciated!

 Thanks,
 Alex
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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer

 --
 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: https://gate.nmr.mgh.harvard.edu/filedrop2
 www.nmr.mgh.harvard.edu/facility/filedrop/index.html
 Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/

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[Freesurfer] Modeling cortical thickness question

2014-12-09 Thread Alexandra Tanner
Hello Freesurfers,

Our group is wondering if any of you know whether it is possible to model
cortical thickness as a third order polynomial? The specific question is:
we are looking at whether there is a hyperbolic relationship between
cortical thickness and date of birth among a cohort of individuals born
over a 6 year period. Any insights would be greatly appreciated!

Thanks,
Alex
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addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



Re: [Freesurfer] funcroi calculating percent signal change

2013-11-01 Thread Alexandra Tanner
Hi Doug,

Thanks, this seems to work!

Quick question -- in the past we've done ROI analyses where we've
functionally constrained our labels. When calculating percent signal
change we would take the output from funcroi-table-sess divide it by the
output of funcroi-table-sess with no -c flag (the baseline offset value)
and multiply by 100. Is this also a correct method for calculating percent
signal change? I've tried it for the current ROI I'm using and compared my
calculated value to the value I got by adding -m cespct and the numbers
I'm getting are not the same (ex. 0.0159 vs 0.01444 for one subject). Is
-m cespct more accurate? Thanks!

Best,
Alex



 Hi Alex, if you use -m cespct it will report the mean percent signal
 change within the ROI. Does this work?
 doug


 On 10/31/2013 02:37 PM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,

 I would like to calculate percent signal change within an anatomical ROI
 for a group of subjects in Freesurfer 5.0. We are not functionally
 constraining our ROI, however, we do want to calculate the percent
 signal
 change across the entire region in each of our conditions (the contrasts
 we are using are condition-vs-fixation). Below are examples of the
 commands I've run for one of our conditions:

 funcroi-config -analysis SIRP_Stable5 -label lh.7Network_6.PFC.label
 -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg

 funcroi-sess -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg
 -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED

 funcroi-table-sess -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg
 -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED
 -o
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/18ActiveFolate_12Placebo_PreAndPost_7Tpost/lh_7Networks_6_PFC_1vFix
 -c Cond1vFix

 Is it necessary to now generate the mean functional baseline offset
 value
 within the ROI in order to calculate percent signal change if our
 contrast
 is comparing condition-vs-fixation? Any clarification on when the offset
 value is needed would be greatly appreciated!

 Thanks,
 Alex





 --
 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: https://gate.nmr.mgh.harvard.edu/filedrop2
 www.nmr.mgh.harvard.edu/facility/filedrop/index.html
 Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/




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Re: [Freesurfer] funcroi calculating percent signal change

2013-11-01 Thread Alexandra Tanner
Great, thanks for the clarification Doug!

Best,
Alex


 It depends on how are you defining percent contrast. What you are are
 slightly different methods.

 Using -m cespct is equivalent to computing
 100*Sum(contrast_i/baseline_i)/N where i is a voxel in the ROI
 Your method is equivalent to computing 100*Sum(contrast_i)/Sum(baseline_i)

 So they will be close but not exact. Which one is better? Hard to say. I
 would tend toward -m cespect

 doug



 On 11/01/2013 01:43 PM, Alexandra Tanner wrote:
 Hi Doug,

 Thanks, this seems to work!

 Quick question -- in the past we've done ROI analyses where we've
 functionally constrained our labels. When calculating percent signal
 change we would take the output from funcroi-table-sess divide it by the
 output of funcroi-table-sess with no -c flag (the baseline offset value)
 and multiply by 100. Is this also a correct method for calculating
 percent
 signal change? I've tried it for the current ROI I'm using and compared
 my
 calculated value to the value I got by adding -m cespct and the numbers
 I'm getting are not the same (ex. 0.0159 vs 0.01444 for one subject). Is
 -m cespct more accurate? Thanks!

 Best,
 Alex


 Hi Alex, if you use -m cespct it will report the mean percent signal
 change within the ROI. Does this work?
 doug


 On 10/31/2013 02:37 PM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,

 I would like to calculate percent signal change within an anatomical
 ROI
 for a group of subjects in Freesurfer 5.0. We are not functionally
 constraining our ROI, however, we do want to calculate the percent
 signal
 change across the entire region in each of our conditions (the
 contrasts
 we are using are condition-vs-fixation). Below are examples of the
 commands I've run for one of our conditions:

 funcroi-config -analysis SIRP_Stable5 -label lh.7Network_6.PFC.label
 -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg

 funcroi-sess -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg
 -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED

 funcroi-table-sess -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg
 -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED
 -o
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/18ActiveFolate_12Placebo_PreAndPost_7Tpost/lh_7Networks_6_PFC_1vFix
 -c Cond1vFix

 Is it necessary to now generate the mean functional baseline offset
 value
 within the ROI in order to calculate percent signal change if our
 contrast
 is comparing condition-vs-fixation? Any clarification on when the
 offset
 value is needed would be greatly appreciated!

 Thanks,
 Alex




 --
 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: https://gate.nmr.mgh.harvard.edu/filedrop2
 www.nmr.mgh.harvard.edu/facility/filedrop/index.html
 Outgoing:
 ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/





 --
 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: https://gate.nmr.mgh.harvard.edu/filedrop2
 www.nmr.mgh.harvard.edu/facility/filedrop/index.html
 Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/




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addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



[Freesurfer] funcroi calculating percent signal change

2013-10-31 Thread Alexandra Tanner
Hi Doug and Freesurfers,

I would like to calculate percent signal change within an anatomical ROI
for a group of subjects in Freesurfer 5.0. We are not functionally
constraining our ROI, however, we do want to calculate the percent signal
change across the entire region in each of our conditions (the contrasts
we are using are condition-vs-fixation). Below are examples of the
commands I've run for one of our conditions:

funcroi-config -analysis SIRP_Stable5 -label lh.7Network_6.PFC.label -roi
/cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg

funcroi-sess -roi
/cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg
-sf
/cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED

funcroi-table-sess -roi
/cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/SIRP_lh_7Networks_6_PFC.roicfg
-sf
/cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED
-o
/cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/Anatomical_roicfg_103113/18ActiveFolate_12Placebo_PreAndPost_7Tpost/lh_7Networks_6_PFC_1vFix
-c Cond1vFix

Is it necessary to now generate the mean functional baseline offset value
within the ROI in order to calculate percent signal change if our contrast
is comparing condition-vs-fixation? Any clarification on when the offset
value is needed would be greatly appreciated!

Thanks,
Alex



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addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
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but does not contain patient information, please contact the sender and properly
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[Freesurfer] Make an average activation map of 2 scans

2013-08-23 Thread Alexandra Tanner
Hi Freesurfers,

Does anyone know how to make an average activation map of two subjects
without running a group analysis? I have 15 subjects that each have a pre
and a post scan (30 scans total) and we would like to combine the pre and
post bold runs for each subject to generate an averaged AllvFix activation
map for each pair (so I would end up with 1 activation map per subject
pair of the pre and post bold runs averaged together -- 15 maps total).
Originally I tried treating each of my subject pairs as a group and ran
isxconcat-sess and mri_glmfit on each pair (N=2), but because my N was so
small the osgm map looked very strange and wispy.

Because I'm trying to combine a pre and post scan for the same subject, is
it possible to register the post subject's bold scans to the pre subject
(or vice versa) so that we can treat all the bold runs as one subject and
run selxavg3-sess referencing the pre and post bold runs in the runlist
file? Any clarification or suggestions would be greatly appreciated!

Thanks,
Alex




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Re: [Freesurfer] funcroi-table-sess error

2013-08-12 Thread Alexandra Tanner
Hi Doug,

I was running the command out of the $SUBJECTS_DIR. I created a log folder
in the $SUBJECTS_DIR and then the command ran smoothly! Thanks!

Best,
Alex


 Hi Alex, are you running it from the project folder? It is looking for a
 folder called log in the current directory. It should be creating this
 folder (bug). So, if you run it from the project folder, the log folder
 will be there. Or can create a log folder in your current directory
 (mkdir log)

 doug

 On 7/30/13 2:03 PM, Alexandra Tanner wrote:
 Dear Doug and Freesurfers,

 I am attempting to run funcroi-table-sess on a set of subjects but keep
 getting an error message I've never seen before:

 funcroi-table-sess -roi
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/ctx.lh.insula.aparc+aseg_2vFix.roicfg
 -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED
 -c Cond2vFix -o
 /cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/18ActiveFolate_12Placebo_PreAndPost_7Tpost/ctx_lh_insula_aparc+aseg_2vFix


 log/funcroi-table-sess.log
 log/funcroi-table-sess.log: No such file or directory.


 Funcroi-sess ran without error, as did funcroi-config. I've run this
 analysis many times in the past and have never had this problem so I am
 at
 a loss as to what is going wrong. Any help would be greatly appreciated!

 Thanks,
 Alex








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[Freesurfer] funcroi-table-sess error

2013-07-30 Thread Alexandra Tanner
Dear Doug and Freesurfers,

I am attempting to run funcroi-table-sess on a set of subjects but keep
getting an error message I've never seen before:

funcroi-table-sess -roi
/cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/ctx.lh.insula.aparc+aseg_2vFix.roicfg
-sf
/cluster/roffman/users/Stable5_PerRun/Subject_Files/30_ActiveFolateAndPlacebo_PostPrePAIRED
-c Cond2vFix -o
/cluster/roffman/users/Stable5_PerRun/ROI_Analysis/FB12/18ActiveFolate_12Placebo_PreAndPost_7Tpost/ctx_lh_insula_aparc+aseg_2vFix


log/funcroi-table-sess.log
log/funcroi-table-sess.log: No such file or directory.


Funcroi-sess ran without error, as did funcroi-config. I've run this
analysis many times in the past and have never had this problem so I am at
a loss as to what is going wrong. Any help would be greatly appreciated!

Thanks,
Alex



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Re: [Freesurfer] Contrast file for cortical thickness 2 group 1 covariate analysis

2013-04-08 Thread Alexandra Tanner

Hi Doug,

I apologize if my last email was a bit confusing/lacking in information.
Dr. Roffman gives a more thorough explanation of what we're trying to
achieve (see below). Hopefully this gives you a better idea of what we're
asking -- thanks!


We are looking at the relationship between age and cortical thickness in two
independent groups (each n=22).

We are not interested in mapping the difference in slopes for the
age-thickness relationship between group 1 and group 2.  Rather, we are
interested in mapping the significance of the difference in the
age-thickness correlation strength between group 1 and group 2.  Two
distributions can have a similar slope, but the R2 for one group can be
very different than the R2 for the other group, based on how tightly the
datapoints conform to the best fit line for each group.  That appears to
be the case for our data.

If we are using an ROI approach, we see that in group 1, within the left
inferior frontal gyrus, when we look at Pearson's r for the relationship
between cortical thickness and age, we get r=.717 (p=.0002).  In group 2,
within the same region, Pearson's r=.169 (p=.452).  We can test for a
difference in correlation strength between two groups by performing a
Fisher r-to-z transformation.  With 22 subjects in each group, this yields
a z score of 2.25, and p=.0244, indicating that the correlation is
significantly stronger in group 1 than in group 2.

The question is whether we can apply this approach in a vertex-wise manner
and see where across the brain there are differences in age-thickness
correlation strength between the two groups.


Any advice would be greatly appreciated!

Best,
Alex




 Hi Alex, I'm not sure I understand what you mean. What is the strength
 of the thickness/age relationship if not the slope between thickness and
 age?
 doug




 On 04/05/2013 03:56 PM, Alexandra Tanner wrote:
 Dear Doug and Freesurfers,

 I'm running a group cortical thickness analysis covaried by age, and
 we're
 curious if there is a way to correlate thickness and age within groups
 and
 then look at whether or not there is a difference in the strength of the
 thickness/age relationship between groups. Originally the contrast file
 we
 used was the group-x-age.mtx (0 0 1 -1) looking at whether or not there
 was a difference between the group age slopes, but we then realized
 we're
 not interested in whether the slopes of the relationships are different,
 but rather if the strength of the cortical thickness/age relationship
 differs between groups.

 I ran mri_glmfit with an fsgd file that was set up as follows:
 GroupDescriptorFile 1
 Title OSGM
 Class Group1
 Class Group2
 Variables Age
 Input subject1 Group1 30
 Input subject2 Group2 40

 I've taken a look at the wiki
 (http://surfer.nmr.mgh.harvard.edu/fswiki/Fsgdf2G1V) and can't seem to
 find a contrast file that does what we're looking for. Any advice on
 what
 sort of contrast file we should use, or whether we need to run a
 different
 analysis than glmfit, would be greatly appreciated! Thanks!

 Best,
 Alex



 --
 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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[Freesurfer] Contrast file for cortical thickness 2 group 1 covariate analysis

2013-04-05 Thread Alexandra Tanner
Dear Doug and Freesurfers,

I'm running a group cortical thickness analysis covaried by age, and we're
curious if there is a way to correlate thickness and age within groups and
then look at whether or not there is a difference in the strength of the
thickness/age relationship between groups. Originally the contrast file we
used was the group-x-age.mtx (0 0 1 -1) looking at whether or not there
was a difference between the group age slopes, but we then realized we're
not interested in whether the slopes of the relationships are different,
but rather if the strength of the cortical thickness/age relationship
differs between groups.

I ran mri_glmfit with an fsgd file that was set up as follows:
GroupDescriptorFile 1
Title OSGM
Class Group1
Class Group2
Variables Age
Input subject1 Group1 30
Input subject2 Group2 40

I've taken a look at the wiki
(http://surfer.nmr.mgh.harvard.edu/fswiki/Fsgdf2G1V) and can't seem to
find a contrast file that does what we're looking for. Any advice on what
sort of contrast file we should use, or whether we need to run a different
analysis than glmfit, would be greatly appreciated! Thanks!

Best,
Alex
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Re: [Freesurfer] mergecontrasts-sess group map

2012-11-30 Thread Alexandra Tanner
Hi Doug,

So if I run a group analysis with each contrast separately, would I then
be running mri_concat to do a conjunction of the group sig maps? Also, can
I merge more than 2 contrasts at once when using mri_concat? Thanks!

Alex


 Hi Alex, unfortunately, you cannot compute a conjunction with the CES.
That's the problem with trying to do group-wise multi-variate analysis.
Another thing you can do is to do a group analysis with each contrast
separately, then do a conjunction of the group sig maps.
 doug

 On 11/29/2012 03:39 PM, Alexandra Tanner wrote:
 Thanks for the clarification! So I will rerun mergecontrasts-sess using
the ces image on my subjects and then run mri_vol2surf and mri_concat
to
 get the group map. Thanks for your help!
 Best,
 Alex
 Usually the contrast effects size (ces) (in SPM this is the CON image,
in FSL it is the COPE image). Univariate maps are usually passed up to
the group level (the conjunction done with mergecontrasts is
 multivariate).
 doug
 On 11/29/2012 01:05 PM, Alexandra Tanner wrote:
 Hi Doug,
 Thanks for the response! Just out of curiosity, what map is typically
used
 for group analyses? Should I have used a map other than sig on the
individual subject level as well?
 Thanks!
 Alex
 You'll have to run mri_vol2surf on each one separately to bring it into
 the fsaverage space, then mri_concat to stack all of the maps into one
 file. At that point you can compute a mean (also with mri_concat).
Generally, one does not do group analysis on sig maps though. doug
 On 11/27/2012 05:08 PM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,
 I recently used mergecontrasts-sess to merge two contrasts of an
analysis
 in 50 different subjects. The command ran on each subject
 individually
 and
 created a sig.nii and sig.ovpl file within a merged contrast folder
for
 each subject. I'd now like to look at an average map of the merged
contrasts across all 50 subjects.
 Does anyone know how to go about getting this average map for my group
 of
 50 subjects?
 Command I ran to get the sig.nii/sig.ovpl file for each subject:
mergecontrasts-sess -mergedcontrast Merge_7vFix_1vFix -conjunction
andor
 -analysis SIRP_Stable5 -contrast Cond7vFix 3 pos 0 -contrast Cond1vFix
 3
 pos 0 -map sig -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/50_MTH_Subjects
-df
 /cluster/roffman/users/Stable5_PerRun
 Any help would be greatly appreciated!
 Thanks,
 Alex
 --
 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/
 --
 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/

 --
 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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addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
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but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



Re: [Freesurfer] mergecontrasts-sess group map

2012-11-29 Thread Alexandra Tanner

Hi Doug,

Thanks for the response! Just out of curiosity, what map is typically used
for group analyses? Should I have used a map other than sig on the
individual subject level as well?

Thanks!
Alex



 You'll have to run mri_vol2surf on each one separately to bring it into
 the fsaverage space, then mri_concat to stack all of the maps into one
 file. At that point you can compute a mean (also with mri_concat).
 Generally, one does not do group analysis on sig maps though.
 doug


 On 11/27/2012 05:08 PM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,

 I recently used mergecontrasts-sess to merge two contrasts of an
 analysis
 in 50 different subjects. The command ran on each subject individually
 and
 created a sig.nii and sig.ovpl file within a merged contrast folder for
 each subject. I'd now like to look at an average map of the merged
 contrasts across all 50 subjects.
 Does anyone know how to go about getting this average map for my group
 of
 50 subjects?

 Command I ran to get the sig.nii/sig.ovpl file for each subject:
 mergecontrasts-sess -mergedcontrast Merge_7vFix_1vFix -conjunction andor
 -analysis SIRP_Stable5 -contrast Cond7vFix 3 pos 0 -contrast Cond1vFix 3
 pos 0 -map sig -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/50_MTH_Subjects -df
 /cluster/roffman/users/Stable5_PerRun

 Any help would be greatly appreciated!

 Thanks,
 Alex



 --
 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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The information in this e-mail is intended only for the person to whom it is
addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



Re: [Freesurfer] mergecontrasts-sess group map

2012-11-29 Thread Alexandra Tanner
Thanks for the clarification! So I will rerun mergecontrasts-sess using
the ces image on my subjects and then run mri_vol2surf and mri_concat to
get the group map. Thanks for your help!

Best,
Alex

 Usually the contrast effects size (ces) (in SPM this is the CON image,
 in FSL it is the COPE image). Univariate maps are usually passed up to
 the group level (the conjunction done with mergecontrasts is
 multivariate).
 doug


 On 11/29/2012 01:05 PM, Alexandra Tanner wrote:
 Hi Doug,

 Thanks for the response! Just out of curiosity, what map is typically
 used
 for group analyses? Should I have used a map other than sig on the
 individual subject level as well?

 Thanks!
 Alex


 You'll have to run mri_vol2surf on each one separately to bring it into
 the fsaverage space, then mri_concat to stack all of the maps into one
 file. At that point you can compute a mean (also with mri_concat).
 Generally, one does not do group analysis on sig maps though.
 doug


 On 11/27/2012 05:08 PM, Alexandra Tanner wrote:
 Hi Doug and Freesurfers,

 I recently used mergecontrasts-sess to merge two contrasts of an
 analysis
 in 50 different subjects. The command ran on each subject individually
 and
 created a sig.nii and sig.ovpl file within a merged contrast folder
 for
 each subject. I'd now like to look at an average map of the merged
 contrasts across all 50 subjects.
 Does anyone know how to go about getting this average map for my group
 of
 50 subjects?

 Command I ran to get the sig.nii/sig.ovpl file for each subject:
 mergecontrasts-sess -mergedcontrast Merge_7vFix_1vFix -conjunction
 andor
 -analysis SIRP_Stable5 -contrast Cond7vFix 3 pos 0 -contrast Cond1vFix
 3
 pos 0 -map sig -sf
 /cluster/roffman/users/Stable5_PerRun/Subject_Files/50_MTH_Subjects
 -df
 /cluster/roffman/users/Stable5_PerRun

 Any help would be greatly appreciated!

 Thanks,
 Alex


 --
 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/





 --
 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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The information in this e-mail is intended only for the person to whom it is
addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



[Freesurfer] mergecontrasts-sess group map

2012-11-27 Thread Alexandra Tanner
Hi Doug and Freesurfers,

I recently used mergecontrasts-sess to merge two contrasts of an analysis
in 50 different subjects. The command ran on each subject individually and
created a sig.nii and sig.ovpl file within a merged contrast folder for
each subject. I'd now like to look at an average map of the merged
contrasts across all 50 subjects.
Does anyone know how to go about getting this average map for my group of
50 subjects?

Command I ran to get the sig.nii/sig.ovpl file for each subject:
mergecontrasts-sess -mergedcontrast Merge_7vFix_1vFix -conjunction andor
-analysis SIRP_Stable5 -contrast Cond7vFix 3 pos 0 -contrast Cond1vFix 3
pos 0 -map sig -sf
/cluster/roffman/users/Stable5_PerRun/Subject_Files/50_MTH_Subjects -df
/cluster/roffman/users/Stable5_PerRun

Any help would be greatly appreciated!

Thanks,
Alex
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contains patient information, please contact the Partners Compliance HelpLine at
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Re: [Freesurfer] mris_anatomical_stats on multiple subjects

2012-09-05 Thread Alexandra Tanner
Hi again,

This is a follow-up question to my previous email -- the method I used may
not be the most efficient or the correct way to extract cortical thickness
from manually created ROIs. I'm unfamiliar with how to obtain thickness
data from a label, so I'm not sure if what I did is correct or if first I
must convert my label to volume or to an annotation file. If anyone knows
a better or more accurate way to measure thickness from the ROI I'd really
appreciate your advice!

Best,
Alex

 Hi Doug and Freesurfers,

 I'm currently working on extracting thickness measurements from an ROI I
manually created. I created my ROI label in tksurfer and applied the label
 to each subject I'd like to extract thickness data from using
 mri_label2label. I then used the following command to generate a stats
file, with the thickness measurement, from my label:
 mris_anatomical_stats  -f something.stats  -l something.label  subjid
?h
 (http://surfer.nmr.mgh.harvard.edu/fswiki/tksurfer_labeledit).

 This generated a stats file that gave me the average thickness for my
ROI
 in my subject. I was wondering if there is a way to run the same
command,
 but on multiple subjects at once, so as not to have to run this command
on
 each individual subject. Any suggestions would be greatly appreciated!

 Best,
 Alex
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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer








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The information in this e-mail is intended only for the person to whom it is
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contains patient information, please contact the Partners Compliance HelpLine at
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but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



[Freesurfer] mris_anatomical_stats on multiple subjects

2012-09-04 Thread Alexandra Tanner
Hi Doug and Freesurfers,

I'm currently working on extracting thickness measurements from an ROI I
manually created. I created my ROI label in tksurfer and applied the label
to each subject I'd like to extract thickness data from using
mri_label2label. I then used the following command to generate a stats
file, with the thickness measurement, from my label:
mris_anatomical_stats  -f something.stats  -l something.label  subjid  ?h
(http://surfer.nmr.mgh.harvard.edu/fswiki/tksurfer_labeledit).

This generated a stats file that gave me the average thickness for my ROI
in my subject. I was wondering if there is a way to run the same command,
but on multiple subjects at once, so as not to have to run this command on
each individual subject. Any suggestions would be greatly appreciated!

Best,
Alex
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but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



Re: [Freesurfer] Help removing marking from DICOM/.nii files

2012-08-22 Thread Alexandra Tanner

Hi Doug,

Thanks for the quick reply! It seems the value of the writing is much
higher than any value elsewhere in the image (over 4000). Instructions on
how to replace this value with values of nearby voxels would be great --
hopefully that will allow us to run the autorecon1 command on it.

Thanks,
Alex



 Hi Alex, there's no way to erase it in a way that you can recover the
 underlying signal. I'm surprised that such small things are causing the
 talairach to crash. If the writing is always the same value and that
 value does not appear in other parts of the image,  you might be able
 to  replace the value with values of nearby voxels. Let me know if you
 need some instructions on this.
 doug

 On 08/22/2012 02:08 PM, Alexandra Tanner wrote:
 Hi Doug,

 I'm currently working with 4-6 year old clinical pediatric non-Siemens
 DICOM files that I'm unpacking and preprocessing in freesurfer. So far
 we've been able to unpack the DICOMS to .nii format and successfully
 begin
 the autorecon process for our first few subjects. We've noticed, when
 looking at the raw scans for some of our subjects, however, there is
 writing (probably information from the scan console) included in the
 images, and in some slices, slightly overlapping with the outer edge of
 the skull/brain. When attempting to run the autorecon1 on these scans,
 the
 command terminates during the talairach transform. We're thinking, since
 we don't have this issue with all of our subjects, the writing may be
 what
 is causing the problem.

 I'm wondering if you know of any way to remove the writing from the
 images
 (I tried seeing if I could erase the lettering in tkmedit but it seems
 it
 can't be erased manually). Attached is a screenshot of a coronal slice
 with the writing. Any suggestions would be greatly appreciated!

 Thanks,
 Alex


 --
 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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Re: [Freesurfer] Clinical DICOM files

2012-08-20 Thread Alexandra Tanner
Hi Doug,

Thanks! Do you know what command line I should use with dcmunpack? I can't
specify the run number since I don't currently have that information for
my scan, only the DICOM files. Typically when we unpack our Siemens files
we use the following command line: unpacksdcmdir -src source -targ
target -run last MEMPRAGE scan MPRAGE COR blah -- for this scan
should I be converting to mgh/mgz instead?

Thanks,
Alex

 dcmunpack will convert them to whatever file format you want (don't use
 COR though).
 doug

 On 08/20/2012 09:51 AM, Alexandra Tanner wrote:
 Thanks Bruce. I see that because these are not Siemens scans I need to
 use
 the command dcmunpack instead of unpacksdcmdir, however, if the DICOM
 files are already saved on our cluster do the files need to be unpacked
 or
 simply converted to COR format using mri_convert? Thanks!

 Best,
 Alex

 Hi Alex
 The dicoms should be enough
 Bruce



 On Aug 16, 2012, at 4:10 PM, Alexandra Tanner
 atan...@nmr.mgh.harvard.edu  wrote:

 Dear Doug,

 We're getting T1 DICOM files from the Clinical PACS System (via mi2b2)
 and
 would like to pull them info the freesurfer stream to get cortical
 thickness. In order to run the standard unpacking commands, do we need
 any
 other files besides the DICOM files themselves? Of note, these scans
 were
 acquired on a variety of clinical scanners at MGH.
 Any suggestions you have would be greatly appreciated!

 Thanks,
 Alex
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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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[Freesurfer] Talairach transform error

2012-08-20 Thread Alexandra Tanner
Dear Doug,

As I mentioned in a previous email, I'm currently working with T1 DICOM
files from the Clinical PACS System that I'd like to pull into the
freesurfer stream to get cortical thickness. I've unpacked the data,
converting the DICOM files to mgz format, and successfully ran the first
recon-all command: recon-all -i input -s subject -force. I then
proceeded to run the recon-all -autorecon-all -s subject command on my
subject, but the command terminated about 5 minutes in and I received the
following error message:

#
#@# Talairach Failure Detection Mon Aug 20 13:53:21 EDT 2012
/autofs/cluster/roffman/users/Stable5_PerRun/Subject2/mri

 talairach_afd -T 0.005 -xfm transforms/talairach.xfm

ERROR: talairach_afd: Talairach Transform: transforms/talairach.xfm
***FAILED*** (p=0., pval=0.  threshold=0.0050)
Linux compute-0-35 2.6.32-220.23.1.el6.x86_64 #1 SMP Mon Jun 18 18:58:52
BST 2012 x86_64 x86_64 x86_64 GNU/Linux

recon-all -s Subject2 exited with ERRORS at Mon Aug 20 13:53:21 EDT 2012


I tried viewing the talairach.xfm file in tkregister2, as I saw someone
else who received the same error message was instructed to do, but no
image would load (in the coronal and horizontal views the screen remained
black and had one thin strip of grey in the center; the sagittal view
brought up a blank white screen).

We know that our data is intact because Dr. Roffman is able to view images
of this subject on his computer using the mi2b2 software, so do you think
it is possible that somewhere earlier, either in the recon or the
dcmunpack stages, there was an error with the data that wasn't recognized
until doing the talairach transformation?

Also, something else I noticed when looking at our subject's data, the
talairach.xfm and talairach.auto.xfm files are different, even though for
all other subjects I've run recons on they are the same -- could this be a
contributing factor?

I'm unsure how to proceed with the unpacking since I'm currently unable to
perform any edits to the talairach registration to try and fix the error,
so any suggestions would be very helpful and greatly appreciated!

Thanks,
Alex



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[Freesurfer] Clinical DICOM files

2012-08-16 Thread Alexandra Tanner
Dear Doug,

We're getting T1 DICOM files from the Clinical PACS System (via mi2b2) and
would like to pull them info the freesurfer stream to get cortical
thickness. In order to run the standard unpacking commands, do we need any
other files besides the DICOM files themselves? Of note, these scans were
acquired on a variety of clinical scanners at MGH.
Any suggestions you have would be greatly appreciated!

Thanks,
Alex
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but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



[Freesurfer] Talairach registration

2012-08-10 Thread Alexandra Tanner
Hi Doug,

I'm currently looking into doing surface edits on past data and I heard
someone mention that one should never scale the brain when editing the
talairach registration. I was wondering if this was true, or if it's okay
to scale the brain so long as you check the scaling in all 3 dimensions
after doing so. Any input would be great!

Thanks,
Alex
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Re: [Freesurfer] Talairach registration

2012-08-10 Thread Alexandra Tanner

Thanks Doug! What do you mean by registering to an individual? Is editing
the talairach registration for each individual subject not the same thing?

Thanks,
Alex

 Hi Alex, it is fine to scale the brain for the tal registration. It is
 when registering to an individual that one must be very careful with
 scaling.
 doug

 On 08/10/2012 08:51 AM, Alexandra Tanner wrote:
 Hi Doug,

 I'm currently looking into doing surface edits on past data and I heard
 someone mention that one should never scale the brain when editing the
 talairach registration. I was wondering if this was true, or if it's
 okay
 to scale the brain so long as you check the scaling in all 3 dimensions
 after doing so. Any input would be great!

 Thanks,
 Alex



 --
 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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addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



Re: [Freesurfer] Freesurfer Question

2012-07-25 Thread Alexandra Tanner
Hi Doug,

Sorry for all the confusion, I misunderstood what we were looking for.
Right now what we want is the volume measurement in each of the
subcortical regions for each subject, which you suggested with the
asegstats2table command.

Thanks so much for your help!
Alex


 Hi Alex, what do you mean by a thickness map of the subcortical region?
 The subcortical structure are usually characterized by simple volume
 measurements (eg, hippocampus has a volume of XXX mm3). There are tools
 out there to do voxel based morphometry. Is this what you mean?
 doug

 On 07/24/2012 03:02 PM, Alexandra Tanner wrote:
 Hi Doug,

 We don't want to do ROIs because we're trying to get a thickness map of
 the entire subcortical region of the brain.

 Prior to trying this, we ran a within subjects paired analysis that gave
 us thickness maps of cortical surface. We ran these commands to look at
 the thickness maps in each of our two groups:

 mris_preproc --target fsaverage1 --hemi lh --meas thickness --out
 /cluster/roffman/users/Stable5_PerRun/Analyses_Patients/15_ActiveFolate_PreAndPostPAIRED_Structural/LH/lh.paired-diff.thickness.mgh
 --fsgd
 /cluster/roffman/users/fsgd/15_ActiveFolate_PreAndPostPAIRED_Structural.fsgd
 --paired-diff

 mri_glmfit --glmdir lh.paired-diff --y lh.paired-diff.thickness.mgh
 --fsgd
 /cluster/roffman/users/fsgd/15_ActiveFolate_PreAndPostPAIRED_Structural.fsgd
 --C /cluster/roffman/users/fsgd/Top_Minus_Bottom.mtx

 cd
 /cluster/roffman/users/Stable5_PerRun/Analyses_Patients/15_ActiveFolate_PreAndPostPAIRED_Structural/LH

 mri_glmfit --glmdir lh.paired-diff.sm05 --y lh.paired-diff.thickness.mgh
 --fsgd
 /cluster/roffman/users/fsgd/15_ActiveFolate_PreAndPostPAIRED2_Structural.fsgd
 –osgm

 (and then the same for our second group)


 And then we ran these commands to get a thickness map for the
 interaction
 between the two groups:

 mris_preproc --target fsaverage1 --hemi lh --meas thickness --out
 /cluster/roffman/users/Stable5_PerRun/Analyses_Patients/22_ActiveFolateAndPlacebo_PreAndPostPAIRED_Structural/LH/lh.paired-diff.thickness.mgh
 --fsgd
 /cluster/roffman/users/fsgd/22_ActiveFolateAndPlacebo_PreAndPostPAIRED_Structural.fsgd
 –paired-diff

 mri_surf2surf --s fsaverage1 --hemi lh --fwhm 5 --sval
 lh.paired-diff.thickness.mgh --tval lh.paired-diff.thickness.sm05.mgh

 mri_glmfit --glmdir lh.paired-diff.sm05 --y
 lh.paired-diff.thickness.sm05.mgh --fsgd
 /cluster/roffman/users/fsgd/22_ActiveFolateAndPlacebo_PreAndPostPAIRED2_Structural.fsgd
 --C /cluster/roffman/users/fsgd/Top_Minus_Bottom.mtx


 Basically what we're wondering is if there's a way to do the same type
 of
 paired within subjects analyses on the same data that will instead
 generate volume thickness maps of the subcortical brain.
 I hope this clarifies my question a bit better, and if anyone has any
 ideas that'd be great!

 Thanks,
 Alex


 Hi Alex, do you want to do it on an ROI basis? If so, you can use
 asegstats2table to create a table of your subjects at the two time
 points, then import this table into SPSS. Or you can run the table
 through mri_glmfit to do the paired-t analysis.
 doug

 On 07/24/2012 01:56 PM, Alexandra Tanner wrote:
 Hi Doug,

 Yes, sorry about that! I realized after I'd sent the email to you that
 I
 should've sent the email to the freesurfer list as well.

 We were hoping to look at volume in subcortical regions of the brain
 --
 basal ganglia, hippocampus, amygdala, etc. Do know if there are
 commands
 to do the within subjects paired analysis this way? And if so, what
 they
 are?

 Thanks so much!
 Alex

 Hi Alexandra, what structure are you looking to analyze? Ie, the
 volume
 of what? The volume of cortex?
 doug
 ps. In the future, please post such questions to the freesurfer list
 as
 it gives others the opportunity to answer and to learn. thanks!

 On 07/23/2012 12:03 PM, Alexandra Tanner wrote:
 Hi Mr. Greve,

 My name is Alex Tanner, I'm the new CRC for Dr. Roffman in the Brain
 Genomics Lab. I had a question regarding conducting volume analyses.
 On
 the freesurfer wiki there are commands that show how to conduct
 Paired
 Analyses to look at average surface, and I was curious if it was
 possible
 to do a paired analysis looking at volume instead.
 Any information you have would be very helpful.

 Thanks so much!

 Best,

 Alexandra Tanner
 Clinical Research Coordinator
 Laboratory for Brain Genomics
 Division of Psychiatric Neuroimaging
 Massachusetts General Hospital
 149 13th Street
 Charlestown, MA 02129
 (p) 617.643.3215


 --
 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



 --
 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

Re: [Freesurfer] Freesurfer Question

2012-07-24 Thread Alexandra Tanner
Hi Doug,

Yes, sorry about that! I realized after I'd sent the email to you that I
should've sent the email to the freesurfer list as well.

We were hoping to look at volume in subcortical regions of the brain --
basal ganglia, hippocampus, amygdala, etc. Do know if there are commands
to do the within subjects paired analysis this way? And if so, what they
are?

Thanks so much!
Alex

 Hi Alexandra, what structure are you looking to analyze? Ie, the volume
 of what? The volume of cortex?
 doug
 ps. In the future, please post such questions to the freesurfer list as
 it gives others the opportunity to answer and to learn. thanks!

 On 07/23/2012 12:03 PM, Alexandra Tanner wrote:
 Hi Mr. Greve,

 My name is Alex Tanner, I'm the new CRC for Dr. Roffman in the Brain
 Genomics Lab. I had a question regarding conducting volume analyses. On
 the freesurfer wiki there are commands that show how to conduct Paired
 Analyses to look at average surface, and I was curious if it was
 possible
 to do a paired analysis looking at volume instead.
 Any information you have would be very helpful.

 Thanks so much!

 Best,

 Alexandra Tanner
 Clinical Research Coordinator
 Laboratory for Brain Genomics
 Division of Psychiatric Neuroimaging
 Massachusetts General Hospital
 149 13th Street
 Charlestown, MA 02129
 (p) 617.643.3215



 --
 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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The information in this e-mail is intended only for the person to whom it is
addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
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Re: [Freesurfer] Freesurfer Question

2012-07-24 Thread Alexandra Tanner
Hi Doug,

We don't want to do ROIs because we're trying to get a thickness map of
the entire subcortical region of the brain.

Prior to trying this, we ran a within subjects paired analysis that gave
us thickness maps of cortical surface. We ran these commands to look at
the thickness maps in each of our two groups:

mris_preproc --target fsaverage1 --hemi lh --meas thickness --out
/cluster/roffman/users/Stable5_PerRun/Analyses_Patients/15_ActiveFolate_PreAndPostPAIRED_Structural/LH/lh.paired-diff.thickness.mgh
--fsgd
/cluster/roffman/users/fsgd/15_ActiveFolate_PreAndPostPAIRED_Structural.fsgd
--paired-diff

mri_glmfit --glmdir lh.paired-diff --y lh.paired-diff.thickness.mgh --fsgd
/cluster/roffman/users/fsgd/15_ActiveFolate_PreAndPostPAIRED_Structural.fsgd
--C /cluster/roffman/users/fsgd/Top_Minus_Bottom.mtx

cd
/cluster/roffman/users/Stable5_PerRun/Analyses_Patients/15_ActiveFolate_PreAndPostPAIRED_Structural/LH

mri_glmfit --glmdir lh.paired-diff.sm05 --y lh.paired-diff.thickness.mgh
--fsgd
/cluster/roffman/users/fsgd/15_ActiveFolate_PreAndPostPAIRED2_Structural.fsgd
–osgm

(and then the same for our second group)


And then we ran these commands to get a thickness map for the interaction
between the two groups:

mris_preproc --target fsaverage1 --hemi lh --meas thickness --out
/cluster/roffman/users/Stable5_PerRun/Analyses_Patients/22_ActiveFolateAndPlacebo_PreAndPostPAIRED_Structural/LH/lh.paired-diff.thickness.mgh
--fsgd
/cluster/roffman/users/fsgd/22_ActiveFolateAndPlacebo_PreAndPostPAIRED_Structural.fsgd
–paired-diff

mri_surf2surf --s fsaverage1 --hemi lh --fwhm 5 --sval
lh.paired-diff.thickness.mgh --tval lh.paired-diff.thickness.sm05.mgh

mri_glmfit --glmdir lh.paired-diff.sm05 --y
lh.paired-diff.thickness.sm05.mgh --fsgd
/cluster/roffman/users/fsgd/22_ActiveFolateAndPlacebo_PreAndPostPAIRED2_Structural.fsgd
--C /cluster/roffman/users/fsgd/Top_Minus_Bottom.mtx


Basically what we're wondering is if there's a way to do the same type of
paired within subjects analyses on the same data that will instead
generate volume thickness maps of the subcortical brain.
I hope this clarifies my question a bit better, and if anyone has any
ideas that'd be great!

Thanks,
Alex


 Hi Alex, do you want to do it on an ROI basis? If so, you can use
 asegstats2table to create a table of your subjects at the two time
 points, then import this table into SPSS. Or you can run the table
 through mri_glmfit to do the paired-t analysis.
 doug

 On 07/24/2012 01:56 PM, Alexandra Tanner wrote:
 Hi Doug,

 Yes, sorry about that! I realized after I'd sent the email to you that I
 should've sent the email to the freesurfer list as well.

 We were hoping to look at volume in subcortical regions of the brain --
 basal ganglia, hippocampus, amygdala, etc. Do know if there are commands
 to do the within subjects paired analysis this way? And if so, what they
 are?

 Thanks so much!
 Alex

 Hi Alexandra, what structure are you looking to analyze? Ie, the volume
 of what? The volume of cortex?
 doug
 ps. In the future, please post such questions to the freesurfer list as
 it gives others the opportunity to answer and to learn. thanks!

 On 07/23/2012 12:03 PM, Alexandra Tanner wrote:
 Hi Mr. Greve,

 My name is Alex Tanner, I'm the new CRC for Dr. Roffman in the Brain
 Genomics Lab. I had a question regarding conducting volume analyses.
 On
 the freesurfer wiki there are commands that show how to conduct Paired
 Analyses to look at average surface, and I was curious if it was
 possible
 to do a paired analysis looking at volume instead.
 Any information you have would be very helpful.

 Thanks so much!

 Best,

 Alexandra Tanner
 Clinical Research Coordinator
 Laboratory for Brain Genomics
 Division of Psychiatric Neuroimaging
 Massachusetts General Hospital
 149 13th Street
 Charlestown, MA 02129
 (p) 617.643.3215


 --
 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





 --
 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




___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
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The information in this e-mail is intended only for the person to whom it is
addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.