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Hola Miguel Ángel,
First, you need to run the T1 through recon-all normally, as you have already
done. Next, you run the subfield module with the highres T2 as input - no
recon-all on the T2 required, as it's used in a different way.
Cheers
Eugenio
S
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Thanks for your reply Eugenio.
You have mentioned like "No recon-all on the T2 required, as it's used in a
different way". May I know the actual purpose of using T2 images for
reconstruction process. Why we should not T2 images as input for recon-all
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Sorry if I didn’t explain myself properly.
T2 scans of the whole head can be used by recon-all to improve the segmentation
of the pial surface, but: a) They are not required (you can use the T1 alone);
and b) Cannot be run through recon-all independe
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Hi,
What would be the command for hippocampal subfields using only the T2
images?
This?
recon-all -s -hippocampal-subfields-T2
I tried but obtained the following error
pcpb3846:~ lab1-rmn$ recon-all -s /Applications/freesurfer/subjects/4235
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Hi,
Sorry for coming back to this, but I'm still confused about the issue of
having unbalanced classes. I thought that I could not remove the class
as you suggested since this would mean that the contrast positive and
negative values would no longer
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It depends on the version, but yes, in 6.0 it’d be that command.
The file name of the additional scan should be an existing nii/nii.gz/mgz file,
though (right now you just have “T2”).
Cheers,
/E
--
Juan Eugenio Iglesias
ERC Senior Research Fellow
Tran
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Hi Eugenio,
In my error free surfer say that cannot find the file, It´s necessary put
the additional scan in a specific folder? I have this organization in the
free surfer subjects directory
4235_T2 (main folder)
mri (subfolder)
orig (sub
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recon-all –sd /Applications/freesurfer/subjects -s 4235_T2
-hippocampal-subfields-T2
/Applications/freesurfer/subjects/4235_T2/mri/orig/T2.mgz T2_3D_SAG
--
Juan Eugenio Iglesias
ERC Senior Research Fellow
Translational Imaging Group
Universi
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Hi all,
I’m having some trouble getting an an accurate registration between an
individual functional volume and MNI152 space. Presently, I’m using the
commands:
bbregister --s MNI152_FS --mov volumeInFunctional --reg
mniDir/filename2mni.lta --init
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Martin,
Thanks for the feedback. Given our data set (1mm^3 timepoint1 and 0.8mm^3
timepoint 2), what would be the best way to salvage this data and look for
longitudinal changes? Would it be possible to upsample/downsample the
images so that they are t
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The freeview flag "annot_outline=1" is great for viewing results for
significant clusters from mri_glmfit-sim. Is there a way to make the
outlines thicker?
With the default thickness, the outlines are difficult to make out in a
multipanel figure. (The
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Hi Doug,
funcVol is an individual functional resting state scan. We are doing some
clustering analyses and trying to visually compare the clustering across
subjects (I would be a bit sketched out trying to quantify the overlap between
subjects due t
Hi Kayle,
There is no such option. I'll put it on my list for future improvement.
Best,
Ruopeng
On 05/04/2018 01:09 PM, Kayle Sawyer wrote:
The freeview flag "annot_outline=1" is great for viewing results for
significant clusters from mri_glmfit-sim. Is there a way to make the
outlines thick
Hello,
I just wanted to follow up on this again. Is there any way to transform
functional data (already in T1 space) to tal space directly? Something like
passing an identity registration matrix to mri_vol2vol or another command that
would apply the tal transform without a registration?
If n
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Hi Freesurfer developers,
After having executed the recon-all in several subjects I tried to export
all measures of the Destrieux atlas (area, volume, curvind, foldind,
gauscurv, meancurv, thickness and thicknesstd) but I got an error because
in some
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