Thank you all for your suggestions.
I binarized my labels, used mri_concat --max, then re-binarize the volumes.
It worked great.
Thanks again,
Yuko Yotsumoto
On Jun 7, 2012, at 6:58 AM, Douglas Greve wrote:
It depends on how graceful you want to be with resolving the overlap.
One simple way
Thank you very much for your answer.
Are 10 000 iterations also used when I am running a Monte Carlo simulation
in qdec?
Thanks, Marie
2012/6/9 Douglas N Greve gr...@nmr.mgh.harvard.edu
they are two different correction schemes. If they gave the same answer,
then it would not make sense to
Thank you for your answer. Just one more question, is the fsaverage
already in MNI305 space? In this case, the RAS coordinates from
tksurfer/QDEC are already MNI?
Regards,
Yolanda
2012/6/7 Douglas N Greve gr...@nmr.mgh.harvard.edu
Here are instructions to go from a surface RAS to the mni305
Dear Freesurfer experts,
How could I overlay spmT.img maps from a VBM study on fsaverage? I would
like to convert the significant clusters into labels.
Thank you in advance,
Yolanda
___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
Hi Bruce,
Both are uploaded. FI137 is the missing brain from surfs and wm.mgz, and
OH120 is the cerebellum in -aseg. We're
running freesurfer-Linux-centos4_x86_64-stable-pub-v5.0.0.
thanks,
Nicole
On Fri, Jun 8, 2012 at 8:22 PM, Bruce Fischl fis...@nmr.mgh.harvard.eduwrote:
Hi Nicole
If you
yes, though I would probably do it outside of qdec as it can take a
while (hours or days)
On 06/12/2012 08:03 AM, Marie Schneider wrote:
Thank you very much for your answer.
Are 10 000 iterations also used when I am running a Monte Carlo
simulation in qdec?
Thanks, Marie
2012/6/9
yes
On 06/12/2012 08:17 AM, Yolanda Vives wrote:
Thank you for your answer. Just one more question, is the fsaverage
already in MNI305 space? In this case, the RAS coordinates from
tksurfer/QDEC are already MNI?
Regards,
Yolanda
2012/6/7 Douglas N Greve gr...@nmr.mgh.harvard.edu
This is not an easy thing to do because there is a non-linear transform
between them. One thing you can do is to run recon-all on the VBM
registration target. Or, you can average the transformed T1s together
and run recon-all on that.
doug
On 06/12/2012 09:22 AM, Yolanda Vives wrote:
Dear
Not sure. In principle no, but it might cause the brain to be
non-centered or out of the field of view. I would just run tkregister2
--fstal --s subject and get it more-or-less right (or at least check
that it is not out of the field of view).
doug
On 06/12/2012 09:32 AM, Yue, Xiaomin wrote:
Dear Dr. Bock,
I get the same error in FS 5.1.0 when running recon-all -s subject
-label_v1.
Did you find a solution?
Best regards,
Anders Hougaard, MD
Danish Headache Center
Dept. of Neurology
Glostrup Hospital
Copenhagen
Denmark
2011/11/11 Andrew Bock ab...@u.washington.edu
Hello,
I am
try symlinking the ?h.white surfaces to the ?h.smoothwm and see if that
solves your problem
cheers
Bruce
On Tue, 12 Jun 2012, Anders Hougaard wrote:
Dear Dr. Bock,
I get the same error in FS 5.1.0 when runningĀ recon-all -s subject
-label_v1.
Did you find a solution?
Best regards,
Anders
Akio,
the results of our dev tree will be different from the stable branch (as
we are continually incorporating improvements in the dev tree which
eventually make their way into the public stable release). The new
OpenMP code will also change the results, but we have found not
significant
Dear all,
How does the freesurfer calculate the ICV? By adding up all the cortical and
sub-cortical volumes including WM and GM and CSF? If so does it also include
cerebellum and brain stem?
Thanks
Ayaz
The information contained in this message and any attachments is intended only
for the
See http://www.freesurfer.net/fswiki/eTIV
On 06/12/2012 01:23 PM, Ayaz, Muhammad wrote:
Dear all,
How does the freesurfer calculate the ICV? By adding up all the
cortical and sub-cortical volumes including WM and GM and CSF? If so
does it also include cerebellum and brain stem?
Thanks
Hello experts,
I have the aparcstat files for corticla thickness. I would want to know is
there any information on how may I group these regions more broadly ex frontal
, temporal lobe areas.
Thanks
Rashmi.
This document may contain information covered under
Hey all-
This may be a simple question to answer, but in an analysis looking at say
cortical thickness between Group 1 and Group 2 with say 3 continues
variables (age, anxiety, IQ) there would be a contrast matrix of 1 -1 0 0 0
. How does free surfer correctly remove the effects of the continues
you might want to look into this:
http://surfer.nmr.mgh.harvard.edu/fswiki/CorticalParcellation
cheers
K
From: freesurfer-boun...@nmr.mgh.harvard.edu
[freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Rashmi Singh
[rsi...@laureateinstitute.org]
YOu can try grouping them into lobes by creating a new annotation with
mri_annotation2label --lobesStrict --subject subject --hemi lh
Then run mris_anatomical_stats using this annotation
doug
On 06/12/2012 02:34 PM, Rashmi Singh wrote:
Hello experts,
I have the aparcstat files for corticla
It includes them in the model as regressors, so, for example, the Group
1 mean (beta) is computed simultaneously with the slope. Think of a
bunch of dots that form a line. You fit it to y = x*m + y0. y0 is the
intercept (ie, expected y at x=0). In your case you have two y0's (one
for each
Hello Freesurfer experts,
How can I specify multiple contrasts for my thickness study with two
groups AA and BB, having different number of subjects in each group? My
variables are tract-wise FA values, age and IQ.
Thanks in advance,
Shantanu
--
Shantanu Ghosh, Ph.D.
Martinos Center for
Hello Freesurfer experts,
How can I specify multiple contrasts for my thickness study with two
groups AA and BB, having different number of subjects in each group? My
variables are tract-wise FA values, age and IQ.
Thanks in advance,
Shantanu
--
Shantanu Ghosh, Ph.D.
Martinos Center for
When I adjusted for the scale, the matrix is still ill-conditioned. It
looks like some of the columns are very similar to each other.
doug
On 06/12/2012 05:15 PM, mdkrue...@uwalumni.com wrote:
Hello-
I am trying to analyze the cortical thickness between two groups of
subjects Cl1 and CL2.
The FSGD file is incorrect. It has multiple subjects listed, and the
string after the subject name is not the name of a class (Tract1_FA is
not the same as Tract1). I would suggest working through the example on
the wiki tutorial and/or looking at the slides on group analysis.
doug
On
Here is the hack I use, taken from Krish's previous post. I hope this
helps:
cd $SUBJECTS_DIR
recon-all -s subject -label_v1
/usr/local/freesurfer4.5/freesurfer/bin/mris_spherical_average -osurf
v1.invivo.reg -n -o subject label rh.v1.invivo.label rh v1.invivo.reg
V1_average
24 matches
Mail list logo