Hi,
I am currently in the process of reconstructing my brains after edits.
However, the brains keep being reconstructed with large portions of brain
missing/cerebellum missing; ie they are much worse than before I edited
them. However, I am sure that I have only put control points in white
matter
Dear freesurfers.
I'm using freesurfer for two weeks. I'm currently trying to make a script
to get asegstats resultats for >100 patients.
I did this script in tcsh :
foreach filename (t1_)
asegstats2table --subjects ${filename} \
--segno 12 18 14\
--tablefile asegstats.txt
end
The p
On Sunday, December 02, 2012 23:56:38 Yaniv Kaufman wrote:
> Dear Freesurfer experts,
>
> I am trying to display DTI using freeview, however, every time I attempt to
> run freeview from the command line (I am using Ubuntu 12.4), I receive the
> following error:
>
> "freeview.bin: error whil
On Monday, December 03, 2012 13:46:11 charles laidi wrote:
> Dear freesurfers.
>
> I'm using freesurfer for two weeks. I'm currently trying to make a script
> to get asegstats resultats for >100 patients.
>
> I did this script in tcsh :
>
> foreach filename (t1_)
> asegstats2table --subj
Hello everyone,
I got grey matter/ white matter intensity ratio at each vertex across the
cortex. I would like to know the mean intensity ratio in one region (ex,
superior temporal gyrus).
Anyone knows how to get it?
Thanks in advance!
Li
___
Fre
Hi Cathy
What version are you running? If 5.1 you will need Nick's updated recon-all
Cheers
Bruce
On Dec 3, 2012, at 5:33 AM, Catherine Bois wrote:
> Hi,
>
> I am currently in the process of reconstructing my brains after edits.
> However, the brains keep being reconstructed with large port
Hi Octavian
it's hard to say. I would think you could get a bunch of it automatically
by looking for places that are significantly different between the two
timpoints, but that will depend on how well they register. You can
certainly do it manually in freeview.
cheers
Bruce
On Sun, 2 Dec 201
Hi Negar
perhaps Nick or PPJ can comment on how much a virtual box needs? In any
case, try increasing the ram and see what happens as the error message is
pretty clear. Also, if you can run "top" or something similar
(/usr/bin/free) to see how memory is actually available on the system that
w
Hi Li
save it as a .mgz volume and use mris_anatomical_stats with the
parcellation you want.
cheers
Bruce
On Mon, 3 Dec 2012, Kong, Li wrote:
Hello everyone,
I got grey matter/ white matter intensity ratio at each vertex across the
cortex. I would like to know the mean intensity rat
Dear Anastasia,
Thanks for the suggestions. The new control point didn't help. Therefore I
uploaded remaining images. It would be great if you could have a look
again.
All the best,
Arman
On Sat, Dec 1, 2012 at 1:45 AM, Anastasia Yendiki <
ayend...@nmr.mgh.harvard.edu> wrote:
>
> Hi Arman - On
Hi Bruce,
Thanks for your answer!
I tried mris_anatomical_stats command, but I met problems:
(1) I would like to get the mean intensity ratio of the superior temporal, so I
need a label of this region.
I first used mri_annotation2label to get lh.superiortemporal.label file.
(2) Then I used
Dear experts,
I am registering cortical labels from Talairach coordinates to my native
T1. For doing this, I have run the next script lines:
tkregister --targ brainmask.mgz --mov highres_brain.nii.gz --reg
T1FS2Highres.dat --regheader --noedit
mri_label2vol --annot rh.aparc.annot --temp highres
Dear FS team,
I would like to know if there is any options to get the
hippocampal subfield segmentation so I can get the volume for each segmentation
if I
was running only recon-all for all my subjects or I need to re-run recon-all
but with a
hippocampal subfield segmentation option this tim
Hi Antonella,
Just run recon-all with the flag "-hippo-subfields" but without the flag
"-all" (otherwise you'll be rerunning a lot of stuff you do not need to
rerun):
DO: recon-all -s bert -hippo-subfields
DON'T DO: recon-all -s bert -all -hippo-subfields
Kind regards,
/Eugenio
On Mon, 2012-12-03
I have not seen a lot of documentation on how to do this. I've attached two images of specific areas where I'd like to have the pial and main surfaces follow the actual surface of the brain. The aux volume OK in both of these cases. The empty space is segmented as white matter. In the past I have t
For the missing insula problem, try using a newer version of
mri_label2vol
ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/mri_label2vol
The 2nd problem is not so easy to fix. You might be better off using
aparc+aseg.mgz as input to mri_label2vol instead of
Hi Jon
those are probably due to topological defects, the fixing of which forces
the surfaces to enclose those spaces. See if you can find the source of
the defect - I think fixing it will remove these problems. You can verify
they are defects by looking at the filled.mgz. If the spaces aren't
Hi Li, they should not have been identical. The data under the
"ThickAvg" column should be the value you want. This and other columns
are mislabeled when thickness is not the actual input (eg, GrayVol is
meaningless). You might prefer to use mri_segstats, something like
mri_segstats --slabel s
I'm running FSv5.1.0 on RHEL6.
1) My goal is to run a glm-fit on White Matter aparc regions for a
"between group" surf-based analysis and evaluate spatial maps of significant
differences.
2) I noticed that fsaverage does not have a wmparc.mgz file, so I'm
currently working with bert
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