Hello!
I'm encountering a problem with converting fMRI-Data from dicom- to
NIfTI-files (single file). The problem only occurs with data aquired on
Siemens Vision, data from Siemens Trio work just fine. The Siemens
ASCII header is missing (files have not been anonymized) and every
dicom-file
Many Thanks Doug. Will try that out.
Regards
Koushik
-Original Message-
From: freesurfer-boun...@nmr.mgh.harvard.edu
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Douglas N Greve
Sent: Monday, November 04, 2013 4:47 PM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re:
Hi everyone,
I run into an error when I try to do the tutorial on ROI group analysis. I
downloaded the tutorial set, but did not put it into
FREESURFER_HOME/subjects, because my computer doesn't allow it. I made my
own folder and copied everything in there. The error arises when I try to
map a
Also, quick question . . .
How exactly do you run a recon from scratch without nifti images? I’d always
delete the directory and restart with mri_convert -i …
Jon
On Nov 5, 2013, at 10:40 AM, Louis Nicholas Vinke vi...@nmr.mgh.harvard.edu
wrote:
Hi Jon,
I see the area you are talking
I think that the first option you provided is more along the lines of what
I'm looking for. Thanks
Corinna
On Mon, Nov 4, 2013 at 5:37 PM, Douglas N Greve
gr...@nmr.mgh.harvard.eduwrote:
Yes. As Bruce mentioned you can also use the program that creates the
wmparc (mri_aparc2aseg). You can
*fMRI postdoc*
At the Center for Mind/ Brain Sciences (CIMeC, www.unitn.it/en/cimec),
University of Trento, Italy, there will soon be an opening for a postdoc
position to work with Angelika Lingnau (
https://sites.google.com/site/angelikalingnau/) in collaboration with Carlo
Marzi, University
Hi,
Thank you very much, it works. I now however have another problem (sorry!).
I have run the command on test subject and want to display using tksurfer.
The file lh.pial_lgi has for sure been created, and i cd into correct
subjects directory however when I try tksurfer lh inflated -overlay
Are you in the 'surf' directory? If not, then do -overlay
$subject/surf/lh.pial_lgi
On 11/05/2013 11:26 AM, Linn Mittlestein wrote:
Hi,
Thank you very much, it works. I now however have another problem
(sorry!). I have run the command on test subject and want to display
using tksurfer. The
Hi
- Thank you for a fantastic piece of software :-)
- I have en one question:
- In the GUI-module QDEC, is it possible to adjust the GLM-model to account
for a pair-matched cohort? (diabetes vs non-diabetes - matched pairwise by
age, sex and bmi)
Kind regards
Christian, Denmark
Christian
Hi everyone,
I am very new to freesurfer/qdec. What I would like to do is examine the
results of a feat analysis in qdec and then perform further between-subject
analyses with behavioural data
(http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/FslFeatFreeSurfer). I've
run against problems
Dear Freesurfers,
I need to compare the cortical thickness values, obtained from a data set
of 32 healthy subjects, with some reference literature values of cortical
thickness.
I'd like to check the values of mean and standard deviation for each one of
the 32 cortical parcellations automatically
Hi All,
In a previous post Doug suggested two methods for generating voxel-wise
z-score maps, one using glmfit with one subject in one group and the second
using fscalc.fsl. Link to post:
https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2010-June/014673.html
I have tried both methods
Hi Anita,
I don't believe you have the complete path set to your SUBJECTS_DIR
environmental variable, unless Desktop is in your root dir which I doubt
is the case.
Easy way to set the variable:
cd /path/to/tutorial/data/
setenv SUBJECTS_DIR $PWD
Also, check you have fsaverage symlinked to
Hi Jon,
You can use the -clean flag, or you can just delete all the directories in
the subject's recon directory except the mri folder, and then delete
everything in the mri folder leaving the orig folder which contains the
001.mgz which is equivalent to the nifiti volume(s) initially passed
Hello,
I was wondering what output from the recon-all freesurfer scripts would be best
to make a grey matter only mask?
Thanks,
Emily
___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
you can do this
cd $SUBJECTS_DIR/subject/mri
mri_binarize --i aparc+aseg.mgz --gm --o gmmask.mgz
doug
On 11/05/2013 03:45 PM, ebell...@uwm.edu wrote:
Hello,
I was wondering what output from the recon-all freesurfer scripts would be
best to make a grey matter only mask?
Thanks,
Emily
Hi Freesurfer team
We are sampling diffusion images below the WM surface , and would like to
visualize with tkmedit or freeview the surface itself to see if it is
appropriate to our analysis (not the surface overlay, but the surface as a
line like the one that are on the surfs directory). I
Hi,
I have fMRI data which has been co-registered with the FS reconstruction
using bbregister. I would like to extract the voxel time series for
the voxels in the subcortical labels from the aseg subcortical
segmentation. I know that mri_segstats can be used with the --avgwf
option to extract
No sorry, you'll have to use the command line stream rather than QDEC
(ie, mris_preproc, mri_surf2surf to smooth, and mri_glmfit). See the
FSGD examples on our wiki for how to do the paired analysis
doug
On 11/05/2013 12:07 PM, christian buhl wrote:
Hi
- Thank you for a fantastic piece
no, sorry, you'll have to do it with matlab. You can do something like
mri_vol2vol --mov func.nii --reg register.dat --fstarg --o func.anat.nii
aseg = MRIread('aseg.mgz');
indroi = find(aseg.vol == 17); % 17 = left hippo
func = MRIread('func.anat.nii');
funcmat = fast_vol2mat(func);
funcroi =
hi martin,
if you had one region you can use mri_segstats to extract for each voxel in
that roi, but not for multiple rois.
here is a snippet i use for timecourses in each roi.
https://github.com/nipy/nipype/blob/master/examples/rsfmri_preprocessing.py#L219
cheers,
satra
On Tue, Nov 5, 2013
Hi Doug,
Thanks for your reply. I will do it in Python then ;). Is there a table
somewhere with a list of values used for each label (17 = left hippo etc.)?
Martin
On 11/05/13 17:32, Douglas N Greve wrote:
no, sorry, you'll have to do it with matlab. You can do something like
mri_vol2vol
Hi Celine
we usually use mris_expand with a negative number to grow the surface
inwards. Something like
mris_expand lh.white -1 lh.interior
would move the surfaces inwards by 1mm everywhere and save it in a file
name lh.initerior. You could then visualize that in freeview or tkmedit as
Thanks Satra, very helpful.
On 11/05/13 17:34, Satrajit Ghosh wrote:
hi martin,
if you had one region you can use mri_segstats to extract for each voxel
in that roi, but not for multiple rois.
here is a snippet i use for timecourses in each roi.
$FREESURFER_HOME/FreeSurferColorLUT.txt
On 11/05/2013 05:42 PM, Martin Luessi wrote:
Hi Doug,
Thanks for your reply. I will do it in Python then ;). Is there a
table somewhere with a list of values used for each label (17 = left
hippo etc.)?
Martin
On 11/05/13 17:32, Douglas N Greve
I am a bit stumped. Can you check that cache.th20.pos.sig.ocn.mgh and
concat_output.nii.gz? I'm sure they most be. If so, send both to me on
our file drop.
doug
On 11/04/2013 07:00 PM, Michael Waskom wrote:
Hi Doug,
I'm running into a strange seg fault when trying to use mri_segstats
Is reg-feat2anat in your path? It should be in
$FREESURFER_HOME/bin/reg-feat2anat
doug
On 11/05/2013 12:15 PM, Christophe de Bezenac wrote:
Hi everyone,
I am very new to freesurfer/qdec. What I would like to do is examine the
results of a feat analysis in qdec and then perform further
Can you send your command lines for both aparc+aseg and aseg?
doug
ps. Please remember to post to the list and not to me personally. Thanks!
On 11/05/2013 12:45 PM, Roderick McColl wrote:
Actually does not display properly at least not in freeview.
Slices are also upside down.
Also the
When you say that you are getting very different results, what are you
comparing exactly? I can't tell what your mri_glmfit command is because
it is embedded in a script with lots of variables. Have mercy on me and
just give me a simple command line that I don't have to struggle with:)
doug
Sure, no problem.
Run from within the folder $SUBJECTS/fsaverage/mri :-
mri_vol2vol --targ $FSLDIR/data/standard/MNI152_T1_1mm.nii.gz --mov aseg.mgz
--reg transforms/reg.mni152.1mm.dat --o aseg_mni152.nii.gz
mri_vol2vol --targ $FSLDIR/data/standard/MNI152_T1_1mm.nii.gz --mov
aparc+aseg.mgz
Hi Bruce,
The ROIs all on different subjects, but we've been able to put them all
onto an average surface that we made using make_average_surface (using
mri_label2label as explained in my previous email). We were hoping that now
that they're all on a common average subject that we could some how
Dear Drs. Bruce and Doug
Thanks for the valuable comments.
Discrepancy between FS and VBM lies in putamen and hippocampus.
Would you please briefly comment regarding segmentation method of above
structures in FS?
I'm just wondering whether segmentation of grey matter in FS is largely
different
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