Hi Nick,
Thanks for the response. They are from a Philips machine though...
Niels
On 10/12/06, Nick Schmansky <[EMAIL PROTECTED]> wrote:
Niels,
Are they Siemens Dicom files? If so, try adding the flag -siemens_dicom
to mri_convert.
This wouldn't explain the difference in behavior between the
Niels,
Are they Siemens Dicom files? If so, try adding the flag -siemens_dicom
to mri_convert.
This wouldn't explain the difference in behavior between the 32bit and
64bit builds though. I have not personally encountered the message you
are seeing.
Nick
On Thu, 2006-10-12 at 16:40 -0400, Niel
Hi everyone,
My goal is to have the cortical segmentation in subject's native space
in analyze format volume images.
the series of commands i run are:
mri_extract_label aparc+aseg.mgz LABELNUM outVolume.mgz
mri_convert -rt nearest -rl rawavg.mgz outVolume.mgz outLabelSegmentation.img
the probl
Hi Nick,
It's working now!
Thanks!
Lei
Nick Schmansky
<[EMAIL PROTECTED]
rvard.edu>
Lei,
It looks like a bug in func2roi-sess. To fix it, open with a text
editor this file:
$FREESURFER_HOME/fsfast/bin/func2roi-sess
and delete the following line:
set V2R = ~greve/sg1/build/mri_vol2roi/mri_vol2roi
The line following it should read:
set V2R = mri_vol2roi
which is corre
Hi,
I am experiencing quite a strange problem. I have a set of DICOMs
that when I run the following on a 32bit machine, it works fine:
mri_convert 031G0110.101.dcm 001.mgz
When I run the exact same command (from within the same directory) on
the 64 bit machine, I get the following error:
"Curren
Dear all,
I am trying to overlay group-averaged data (FSL) on an averaged anatomical
brain (Freesurfer).
I did the following,
mri_vol2surf --src AVG.gfeat/cope1.feat/thresh_zstat1.img --src_type analyze
--srcreg register.dat --hemi lh --projfrac 0.5 --out
AVG.gfeat/cope1.feat/thresh_zstat1-lh.w -
Hi All,
I tried func2roi-sess with my data, it ran quickly and gave one message at
the end 'Unknow user: greve', but no other errer reports.
I checked the sessid directory and found it created the -roisef directory,
but no files in it.
I think there must be something wrong, associated with user?
An
Hi Bo,
you can use flags to mri_segment to change the intensity thresholds:
-wlo <>specify the min allowable value for white matter
-ghi <>specify the max allowable value for gray matter
-glo <>specify the min allowable value for gray matter
On Thu, 12 Oct 2006, Bo Shi wrote:
Good
I didn't want to clutter up one thread with two unrelated questions; Is
there a quick way to get a total count for wm/gm volume and subcortical
gray matter? AFAIK, the output is divided into a much finer structures...
Thanks!
___
Freesurfer mailin
Good morning!
I have a dataset whose white matter volume is a bit too aggressive and
I'd like to erode it a bit - is there a quick way to do this using
tkmedit or one of the command line tools?
Thanks,
Bo
___
Freesurfer mailing list
Freesurfer@nmr
oh, I take it back, you shouldn't have to conform at that stage. What
does the orig.mgz look like? It is 0-255, and the thing you want to avoid
is saturation of the intensities. It tries to put the bulk of the histogram
in the mid intensity range.
On Thu, 12 Oct 2006, Derin Cobia wrote:
I se
try specifying -conform also.
On Thu, 12 Oct 2006, Derin Cobia wrote:
I seem to be having some difficulty in converting my flash images into FS
format for processing. After using mri_convert my orig.mgz files become
excessively bright compared to the original analyze file, thus creating
poor au
I seem to be having some difficulty in converting my flash images into FS
format for processing. After using mri_convert my orig.mgz files become
excessively bright compared to the original analyze file, thus creating
poor autorecon1 output, etc. See the attached jpgs of before and after
shots.
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