just visually. If we knew a way to automatically check it we would use
that to correct it :)
On Sat, 2 Jul 2016, Jasmin Alves wrote:
Hi Bruce,
Thank you for clarifying, this makes more sense, is there a way to check the
subcortical segmentation?
Thanks!
Jasmin
On Sat, Jul 2, 2016 at 7:28 PM
Hi Bruce,
Thank you for clarifying, this makes more sense, is there a way to check
the subcortical segmentation?
Thanks!
Jasmin
On Sat, Jul 2, 2016 at 7:28 PM, Bruce Fischl
wrote:
> Hi Jasmin
>
> the norm.mgz isn't a voxel labeling - it's an intensity volume. We
> typically check the aseg.mgz
Hi Jasmin
the norm.mgz isn't a voxel labeling - it's an intensity volume. We
typically check the aseg.mgz display *over* the norm.mgz to see if the
labels make sense w.r.t. the intensities.
cheers
Bruce
On Sat, 2 Jul 2016, Jasmin Alves
wrote:
Dear Freesurfer support,
I noticed in previous
Hi Richard,
Thanks anyway for taking a look. Despite a number of further tweaks to our cuda
libraries, we have made no further progress with this. Any chance you could
pass along your cuda binaries so that I can see whether they might just "work"?
Very curious.
-Derek
Dear Freesurfer support,
I noticed in previous threads, people have inquired about how to check the
quality of the aseg.mgz segmentation using the norm.mgz as a reference.
When I did this, there were several mislabeled regions according to the
norm.mgz ie. voxels labeled as white matter on the nor
Hi Lars,
I had the same problem. You can notice in your bvec file that there are some
unusual blank spaces sometimes. Try to look at each space between two numbers
and make sure it’s fine. You can also make sure about the number of entries by
running wc -w on each of your bvec or bval file.
Hop
how do you know it is the right hemi and not the left?
Also, we don't use or support tksurfer anymore. Try freeview instead
cheers
Bruce
On Sun,
3 Jul 2016,
李琬 wrote:
Dear all,
I've been trying to use "tksufer" to check the surface images according
to the instruction of "Inspectio
Hi Doug,
I ran cortical thickness analysis between two groups using Qdec and I want to correct the results for multiple comparison.
In Qdec there are two choices to correct the data for multiple comparison (FDR and montecarlo) . Which method do you recommend to correct the results of cortical
Yes, you can. If I remember correctly, you can goto view->configure
overlay, then find the item to specify that you want the labels under
the activation.
On 6/29/16 5:22 AM, Reza Rajimehr wrote:
Hi,
In Tksurfer, we want to show functional activity map and borders of
aparc on a surface. The
Dear all,
I've been trying to use "tksufer" to check the surface images according to
the instruction of "Inspection of Freesurfer Oupt".
I could get the images, but the direction is opposite.
Like if I typed "tksurfer fsaverage lh inflated ", but I got the right one.
W
Hi Clara,
If I am understanding your question correctly, you don't need to control
for brain volume when looking at thickness analyses.
See quote below from this link:
http://www.freesurfer.net/fswiki/eTIV
"Note that this correction is only useful in situations where the structure
scales with h
Hi Clara
I would use the stats from the long as they are most stable, and yes I
believe you should control for total volume when looking at surface area.
cheers
Bruce
On Thu, 30 Jun 2016, Clara
Kühn wrote:
Dear FreeSurfer experts,
I would like to look at longitudinal thickness data and
Dear FreeSurfer experts,
I would like to look at longitudinal thickness data and want to control for
total gray matter volume. Should I use that information from the CROSS before
anything has been registered and smoothed or from the LONG after they have been
registered to the BASE?
Also I was
Dear FreeSurfer experts,
I would like to look at longitudinal thickness data and want to control for
total gray matter volume. Should I use that information from the CROSS before
anything has been registered and smoothed or from the LONG after they have been
registered to the BASE?
Also I was w
Hi,
Trying to run trac-all -c dmric_file -prep, I get an error message stating
that there are different numbers of entries in the bval and bvec files. I
don't understand why, since both have the same number of rows (64).
OS = Ubuntu 14.04.4
Software: freesurfer-Linux-centos6_x86_64-stable-pub-v5
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