Hi Doug,
What is your preferred citation for FsFast (used for resting-state)? I
couldn't really find a clear answer in the Zotero library or mail
archives.
Thanks and happy holidays!
Linda
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https:
ously going
from a template to dicoms is not that easy.
I'd appreciate any tips!
--
Linda Douw, Ph.D.
Branco Weiss fellow
Department of Radiology
Athinoula A. Martinos Center for Biomedical Imaging
Massachusetts General Hospital
Harvard Medical School
149 13th Street
Charlestown
Hi experts,
I have a bunch of custom-made labels (from the ConnectomeMapper software)
that I want to put into a single annotation file. Therefore, I create a
color-lookup table and use mris_label2annot as follows:
mris_label2annot --s fsaveragec --h lh --ctab lh_laus500_clut_new.txt --a
laus500_f
I'd be happy to check it out.
Thanks so much,
--
Linda Douw, Ph.D.
Research fellow
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The information in this e-mail is intended o
ct) that do not have any
voxels in your parcellation. Eg, #82:
>
> 8282 ic4.tri_vertex_82 0
>
> So the problem appears to be with mris_make_face_parcellation, not with
mri_segstats.
> doug
>
>
> On 09/10/2012 10:56 AM, Linda Douw wrote:
>> Hi Doug,
>> Outpu
mri_segstats
> To: freesurfer@nmr.mgh.harvard.edu
> Message-ID: <5025264e.3030...@nmr.mgh.harvard.edu>
> Content-Type: text/plain; charset=ISO-8859-1; format=flowed
>
> what are your command lines?
> doug
>
> On 08/09/2012 01:21 PM, Linda Douw wrote:
>> Dear Freesurfers,
e for height (1, usually 256) in volume structure
I should probably use mri_vol2vol first, but which target volume should I
then use? Or is there something else I'm doing wrong?
Thanks for your help!
--
Linda Douw, Ph.D.
Research fellow
Department of Radiology
Athinoula A. Martinos
me reason. Am I
missing something?
Thanks,
--
Linda Douw, Ph.D.
Research fellow
Department of Radiology
Athinoula A. Martinos Center for Biomedical Imaging
Massachusetts General Hospital
Harvard Medical School
149 13th Street
Charlestown, MA 02129
___
on.
>
> cheers
> Bruce
>
>
> On Thu, 19 Apr 2012, Linda Douw wrote:
>
>> Hi all,
>>
>> I would like to make a fine-grained surface parcellation from aparc -
>> let's say 500 labels, and I would like the labels to be more or less
>> isometric.
ay to get a different result?
Thanks!
--
Linda Douw, Ph.D.
Research fellow
Department of Radiology
Athinoula A. Martinos Center for Biomedical Imaging
Massachusetts General Hospital
Harvard Medical School
149 13th Street
Charlestown, MA 02129
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Frees
ation, but
you need the coordinates of the labels for that. In my case, I've made my
own parcellation by using mris_divide_parcellation, so then I would have
to know where to find the coordinates (I don't).
And do you think this is the most efficient method?
Thanks!
--
L
Hi all,
I have nifti files containing the surface-projected time series data of a
subject (obtained using procsurffast), both lh and rh. These time series
are projected onto fsaverage5, and are 3414 x 1 x 3 time points, where
3414*3 = 10242 are the number of vertices for each hemisphere.
Now, I wo
hinal label define in the
> aparc+aseg since it fills in the ribbon:
> mri_binarize --i aparc+aseg.mgz --match 1006 --o lh_entorhinal.nii.gz
> 1006 comes from $FREESURFER_HOME/FreeSurferColorLUT.txt
>
> doug
>
>
>
>
> Linda Douw wrote:
>> Hi Doug,
>> Thanks f
cmd:
> mri_vol2vol --targ lh_entorhinal.nii.gz --mov MNI152_T1_2mm.brain.nii.gz
> --o lh_entorhinal_MNI.nii.gz --reg
> $FREESURFER_HOME/average/mni152.register.dat --inv
>
> doug
>
> Linda Douw wrote:
>> Hi all,
>>
>> I am trying to transform some labels from the apa
But here the entorhinal was also in the wrong place.
Do you know how to fix this?
Thanks,
--
Linda Douw, PhD.
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