I want to ask about differences in brain segmentation with freesurfer
version 5.2.0 and 6.0.0.
My dicom data have original size 0.375x0.375x0.75 mm and 600, 640, 224
voxels. If I process the data vith the version 5.2.0, freesurfer conformed
the data to 1 mm size and 256 voxels for all directions.
Hi all experts,
I am using freesurfer dev version for segmentation of hippocampus and
amydala. I have a doubt about it.
1. In FS 6.0, I can type '203-226' in freeview for viewing subfields of
hippocampus. In dev version, When I type 'freeview -v nu.mgz -v
lh.hippoAmygLabels-T1.v2x.FS60.mgz:c
A two-year postdoctoral fellowship in the Center for Observational and
Real-World Evidence (CORE) division at Merck, applying quantitative methods to
improve healthcare quality/outcomes and reduce cost:
https://taleo.msd.com/careersection/merck_external_career_section/jobdetail.ftl?job=POS00024
Hi all,
I read from the freesurfer discussion archives that when combining FSL FEAT
with freesurfer, one should definitely NOT do spatial smoothing in the
preprocessing when preparing to examine cortical data.
https://www.mail-archive.com/freesurfer@nmr.mgh.harvard.edu/msg11536.html
However I ca
Dear freesurfer experts,
I have tried the dev version of Segmentation of hippocampal subfields
and nuclei of the amygdala
for OSX el Capitan, downloaded today.
I did get an error message similar to a previous error I found on this
mailing list:
https://mail.nmr.mgh.harvard.edu/pipermail//freesurf
Hello Experts:
After running mri_glmfit sim, I got below clusters:
ClusterNo Max VtxMax Size(mm^2) MNIX MNIY MNIZCWPCWPLow
CWPHi NVtxsWghtVtx Annot
1 16.567 56197 13752.71-36.8 -15.5 55.0 0.00020 0.0
0.00040 30900 180209.80 precentral
Freesurfers,
I am trying to use a cortical label to label wm. I am using the following
command line:
mri_aparc2aseg --s $patient --annot 8V1 –labelwm
And most of the time in most subjects this works, however sometimes the output
file doesn’t label any wm with the 3000+N or 4000+N like it usuall
Hi – There are a few places in the config file where the variable
“$TUTORIAL_DATA” is referenced. Do you define that variable on your own before
your run trac-all? If not, you have to edit the config file and replace it
everywhere with the path to where you saved the tutorial data on your comput
Here is the configuration file. I think is the default by tutorial.
dmrirc.tutorial
Description: Binary data
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The information in th
Hi Danielle
if you send me the two input volumes (don't cc the list) I'll see if we
can replicate and fix this problem.
cheers
Bruce
On Wed, 31 Jan 2018, Cooke,Danielle (
BIDMC - Neurology ) wrote:
Hi Bruce,
This is the command and output on a CentOS 7 machine:
[dc155@pinto DANI]$ mri_con
Hello Dr. Greve,
Yes it exists. The output below was with debug option.
Best
Idil
From: freesurfer-boun...@nmr.mgh.harvard.edu
[freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of Douglas Greve
[gr...@nmr.mgh.harvard.edu]
Sent: Tuesday, January 30, 201
Hi Bruce,
This is the command and output on a CentOS 7 machine:
[dc155@pinto DANI]$ mri_convert 3062.nii.gz -rl MNI152_T1_2mm_brain.nii.gz
3062_MNI.nii.gz
mri_convert 3062.nii.gz -rl MNI152_T1_2mm_brain.nii.gz 3062_MNI.nii.gz
$Id: mri_convert.c,v 1.146.2.1 2007/11/30 23:18:44 greve Exp $
readin
Hi,
I want to clarify some aspects longitudinal TRACULA processing before
processing my data.
For example, I have 3 timepoints of data of the same participant:
sub101_01
sub101_02
sub101_03
All of these have structural and diffusion data (same scanner, same acquisition
parameters). I processe
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