Dear All,
I wonder if you have experienced or there is any report on cortical
segmentation reliability in the mid-line structures of the brain, so one
should take them into consideration in running group differences with Qdec?
Best regards,
Amirhossein Manzouri
Hi Amirhossein
which structures do you mean? Like the ventricles? We usually mask those
regions out using the ?h.cortex.label. The surfaces should be "frozen" in
those regions in any case, meaning that the white and pial are in the same
location (and the thickness is 0)
cheers
Bruce
On Mo
Hi All,
I ran dt_recon and got the following error. Can someone suggest how to fix this
? I have attached the dwi-infodump.dat file for more information.
Thanks a lot for the help.
Best
Rito
#@#---
Fitting Tensors
Mon Aug 11 07:29:29 EDT 2014
cd /Users/iron/rito/V
Hi,
Does anyone have recommendations for good automated cortical segmentation
tools for brains with infarct (so some brain missing) or tumors? I am under
the impression that FreeSurfer is not reliable in these cases. If I am
incorrect, any pointers on how to use FreeSurfer in these cases would be
hi thank you marie. Ive tried this but it doesnt give me one single spreadsheet
for the value of each subjects lgi, just produces a file in each subjects stats
directory. How do I make a spreadsheet with everybody's lgi values in it?
Kind Wishes,
Melly
From: marie.sch...@unige.ch
To: freesurf
Hi Melly,
You can use aparcstats2table from the file you created:
aparcstats2table --subjects …. --hemi lh --meas thickness --parc aparc_lgi
--t summary_lgi.txt
Here you'll read the column "thickness" in the lh.aparc_lgi.stats file that you
have created with mri_anatomical_stats (i.e. corr
Question regarding reliability of midline cortical regions by Amir - it refers
to the cingulate cortex, the cuneus, precuneus.
Sincerely
Ivanka Savic M.D., PhD
> Professor of Neurology
> Karolinska Institute
> Dept of Women’s and Children’s Health
> and Neurology Clinic,Karolinska Hospital, Q2:07
Hi Rito.
It is not finding information about the gradient table that was used for
the acquisition. If you have that information you can use the below option
to manually include it
--b bvals bvecs
If you do not you could try using load_dicom in order to grab that
information.
Lilla
On Mon,
Just wanted to pose this question again to the Freesurfer community:
Can anyone provide any advice on how to justify using the V1, V2 labels in
FreeSurfer in clinical populations without also collecting functional
retinotopy data?
Thanks!
Krista
-- Forwarded message --
From: kris
It looks more likely that it is a problem with the skull stripping. If you
clone the brain voxels back in and rerun do things work?
> On Aug 11, 2014, at 4:11 PM, "Makaretz, Sara Johanna"
> wrote:
>
> I am having trouble getting a usable brainmask for one of my subjects -
> a screenshot of the
Hi Krista,
Please refer to the following publications from Geoff Aguirre's lab -
http://www.ncbi.nlm.nih.gov/pubmed/23041195
http://www.ncbi.nlm.nih.gov/pubmed/24676149
All templates are in fsaverage_sym space in .mgh format and are available for
download
https://cfn.upenn.edu/aguirre/wiki/pu
Katie,
Hi, is the SUBJECTS_DIR set to the proper directory? I see from the
output that it is set to:
SUBJECTS_DIR is
'/net/rc-fs-nfs/ifs/data/Shares/DMC-Sheridan2/projects/SAS/FreeSurfer/FS_5.3'
which seems to imply that it might be set to the location of your
freesurfer installation, and not t
Hi Nick,
Thanks for responding. We found a solution to the issue with the SUBJECTS_DIR
(which was pointing to the location of our data, not the FS installation).
This issue appeared after doing some software updates on our cluster (including
Ubuntu). Here is how we fixed it:
sudo mv /bin/sh
There's nothing even when the threshold is set to 0.
I just checked the preprocessing outputs. I can see normal-looking volumes
fmcpr.nii.gz
fmcpr.up.nii.gz
fmcpr.up.sm6.mni305.2mm.nii.gz
But there is nothing when I open fmcpr.up.sm6.fsaverage.lh.nii.gz or
fmcpr.up.sm6.fsaverage.rh.nii.gz
On
did you check the registration?
On 08/11/2014 03:53 PM, Jiahe Zhang wrote:
> There's nothing even when the threshold is set to 0.
>
> I just checked the preprocessing outputs. I can see normal-looking
> volumes
> fmcpr.nii.gz
> fmcpr.up.nii.gz
> fmcpr.up.sm6.mni305.2mm.nii.gz
>
> But there is not
I'm not sure how to check the registration. I see a register.dof6.dat being
produced for each run but I can't tell if it contains the correct
parameters. How can I tell if the registration was accurate?
On Mon, Aug 11, 2014 at 4:01 PM, Douglas N Greve
wrote:
> did you check the registration?
>
two ways:
1. run tkregister-sess to visually check them
2. look at the first value in register.dof6.dat.mincost. It is hard to
say what a threshold is for a good registration, but typical values are
about .5 or so. If it is .8 or more, it is probably a problem (and
probably the initialization i
Both looked fine. First value in .mincost is .45
On Mon, Aug 11, 2014 at 4:51 PM, Douglas N Greve
wrote:
> two ways:
>
> 1. run tkregister-sess to visually check them
> 2. look at the first value in register.dof6.dat.mincost. It is hard to
> say what a threshold is for a good registration, but
How did you look at fmcpr.up.sm6.fsaverage.lh.nii.gz? If you did not do
this, try it
tksurfer fsaverage lh inflated -ov fmcpr.up.sm6.fsaverage.lh.nii.gz -t
fmcpr.up.sm6.fsaverage.lh.nii.gz
This will bring up an overlay as well as a time course
On 08/11/2014 05:05 PM, Jiahe Zhang wrote:
> Both
Hi Nick,
We solved this.
Thanks for your help,
Kate
From: freesurfer-boun...@nmr.mgh.harvard.edu
[freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of McLaughlin, Katie
[katie.mclaugh...@childrens.harvard.edu]
Sent: Monday, August 11, 2014 3:42 PM
To: Fr
Hi all,
I have a simple doubt: I am updating my MAC OS X from Snow Leopard to Mavericks.
I am worried if FreeSurfer is going to run perfectly in the new OS X?
Thank you,
Carolina
___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://ma
Hi, Greg
I use to process my subjects with:
recon-all -s subjid -all -hippo-subfields
The -all flag makes the program run all the 3 stages (autorecon1,
autorecon2 and autorecon3) in sequence. Only after this it starts the
hippo-subfields stage. If you do not have any special reason to run each
au
Hi, all,
How to calculate the mean cortex thickness of fsaverage?
Thanks!
Wilder___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
The information in this e-mail is intended only for
Dear Freesurfers,
Has anyone accomplished analysis of longitudinal cortex changes in a
dataset with "flipped" hemispheres?
I am currently struggling with data from stroke patients, half of them
with lesions on the right, half of them on the left side of the brain.
What I am planning: flip all he
24 matches
Mail list logo