Dear Doug,
Thanks very much for your prompt response. I tried what you suggested
and the sig map looks fine now, that's probably the best that we can
get for the sig map, because of the limitation of the MATLAB I guess.
But for the t map, the values are still not correct for those voxels
that
Hi everyone,
In our lab we use different versions of FreeSurfer on different computers.
Since we share computers with other labs some updates are out of our control.
We'd like to edit scans in FreeSurfer V4.5 and V5.1 and thereafter run recon
-all in V5.0.
Is it important to use the same
Hi Lara,
The biggest consideration is that someone editing data run with v4.5 will
probably have a lot more edits to do than if the same case was run with
5.0 or 5.1. It's probably best to rerun with 5.0 before editing if that's
the version that you are going to work with. For your longitudinal
Hi Antonella,
Thank you very much for your answer and your help. I followed all the
recommended steps (I introduced a white matter mask that will ensure that I am
only
considering diffusion values in the white matter and then also I did corrected
for multiple comparison running
Actually, you are right! Most of the non-gray matter structures in the
medial wall are zeroed out, but the part that goes through the hippo and
amygdala are non-zero. As Mike points out, this is going to be a very
small portion of the total cortical volume, but we'll find a way to
remove it.
Hi Antonella,
I am doing a DTI group analysis study more exactly I am interested to see any
changes in the FA values within two groups: controls versus patients (children
with epilepsy). I introduced a white matter mask that will ensure that I am
only considering diffusion values
in the
The t is computed as the signed square root of the F (not Fsig) volume:
t.vol = sqrt(Fvol.vol) .* sign(ces.vol);
The Fvol (and do t) is not computed from the sig (the other way around).
Are you sure that the t-value does not look right in those areas?
doug
Qi Zhu wrote:
Dear Doug,
Thanks
Hi Martijn, sorry for the delay. Your contrast matrices look correct.
The differences between demeaning and not demeaning is somewhat
expected. When you do not demean, you are testing whether there is a
difference between groups at age=0 (ie, birth). When you demean, you are
testing for a
Yes, seems weird. The image that I attached to you in the first mail
is actually a t map, so the t value in those areas are also zero.
And according to what I read from fast_selxavg3.m, the t value is
actually calculated from the fsig, which is: t.vol =
sqrt(fsig.vol).*sign(ces.vol), and fsig.vol
Yes that is correct. That was fixed with version 5.1 so current
distributions do the right thing.
doug
Qi Zhu wrote:
Yes, seems weird. The image that I attached to you in the first mail
is actually a t map, so the t value in those areas are also zero.
And according to what I read from
Dear Surfer,
I was trying to project a DTI FA image onto the T1 WM surface (for
now), and eventually into the fsaverage as in a recent paper: Phillips
OR, Nuechterlein KH, Asarnow RF, Clark KA, Cabeen R, Yang Y, et al.
Mapping corticocortical structural integrity in schizophrenia and
effects of
Hi Freesurfers,
We are trying to do a resting-state functional connectivity analysis using
freesurfer. Instead of using the aparc+aseg segmentations as seeds, we
would like to use a subject-specific surface labels that we have defined
apriori.
In the fcseed-config step, we then don't have a
Hi Lingqiang, convert your .label file to a volume using mri_label2vol
for each subject, something like
cd $SUBJECTS_DIR/$subject/mri
mri_label2vol --label lh.yourlabel.label --temp orig.mgz --regheader
orig.mgz --subject $subject --hemi lh --proj frac 0 1 .1 --o yourlabel.mgz
When you run
Hi Minjie,
You'll want to give tksurfer the name of one of the regular surfaces
(e.g., inflated, pial, etc.) as the third positional argument and then view
your FA file as an overlay ( -overlay rh.fa.vol2surf2.w ). The former
gives the surface geometry information (where the vertices are and
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