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Hello Experts,
I am wondering if any of you are aware of any commands of optseq for a mixed
design? We are specifically not sure how to specify block duration. It seems
like optseq is designed for event related design according to the help page,
but
Cool. Thanks again!
Panagiotis Fotiadis
Senior Imaging Research Technologist
J. P. Kistler Stroke Research Center, Department of Neurology
Massachusetts General Hospital, Boston, MA
T: (617) 643-3869
From: freesurfer-boun...@nmr.mgh.harvard.edu
on behalf of Bruc
as I said, I don't think I would trust the ex vivo thicknesses. Definitely
not in an absolute sense
On Mon, 30 Jul 2018,
Fotiadis, Panagiotis wrote:
Hi Bruce,
Thanks, that is actually really helpful.
Also, I realized I misspoke earlier when I was talking about the cortical
thickness rang
Hi Bruce,
Thanks, that is actually really helpful.
Also, I realized I misspoke earlier when I was talking about the cortical
thickness range. The 3.7-3.9 mm range that I mentioned was referring to global
cortical thickness across (not within) the different brains I have processed.
The range o
Hi Panos
I think you can trust the white surface (more or less), it's the pial
that is tougher. So you might sample say 1mm out from the white and not
use the pial at all
cheers
Bruce
On Mon, 30 Jul 2018, Fotiadis, Panagiotis wrote:
Hi Bruce,
Thanks for your prompt response! I see, in tha
Hi Bruce,
Thanks for your prompt response! I see, in that case I will disregard cortical
thickness for now. I was also interested in measuring the average signal
intensities of the gray and white matter in those ex vivo brains. Do you think
it would be prudent to use the resulting surfaces fro
Hi Panos
I wouldn't trust the thickness from the ex vivo pipeline, and in any case
those number are way to narrow a range. The normal cortex thickness ranges
from about 1.5mm to 4 or 4.5mm. Getting reasonable thickness from ex vivo
data is high on our to-do list
cheers
Bruce
On Mon, 30 Jul
Hi Bruce and Doug,
I have processed a few ex vivo brains with the help of the ex vivo freesurfer
pipeline (outlined in https://surfer.nmr.mgh.harvard.edu/fswiki/ExvivoRecon),
and have extracted their cortical thickness. So far the range of the cortical
thicknesses have been approximately betwe
Yes, that should work. You can create a mask by breaking the annotation
into labels (mri_annotation2label), then converting the label into a
binary mask (mri_label2label with --mask option), then mri_binarize --i
lh.thickness --mask youmask.mgh --o lh.thickness.masked.mgh
On 07/30/2018 01:47 A
Hi Siti
it is more or less the same protocol, but I exepect there are some
differences as for example neuromorphometrics used differentt (probably
better) visualization and editing tools. We rebuild the atlas for every
release to account for changes in registration, normalization, etc
We
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Hello.
I manually edited the brainmask.mgz file for three subjects. This was done to
prevent the pial surface from extending into non-cortical areas, in particular
the soft-tissue near the brain stem, and some cerebellar areas. Usually this
type of
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Hello,
I’m working on a comparison of atlas and segmentation methods. One of the atlas
sets I’m using is the subset of Neuromorphometrics data from the MICCAI 2012
Grand Challenge and Workshop on Multi-Atlas Labeling. From what I understand,
the “ge
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Dear Eugenio
Thank you for your help.
As I need to segment the nuclei of amygdala, I'll try to download the
development version.
Thanks!!
Jinyoung
2018-07-30 17:39 GMT+09:00 Iglesias Gonzalez, Eugenio
:
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>
> D
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Dear Jin,
6.0 does not segment the nuclei of the amygdala; you can ignore that line,
assuming the code runs to completion (I am assuming it does?)
If you want to segment the nuclei of the amygdala, you’ll have to download the
development version:
http
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Dear Jinyoung,
Can you please send us the log, or at least the last few lines before the error?
Also, which exact version are you using? 6.0 or dev?
Cheers,
/Eugenio
--
Juan Eugenio Iglesias
ERC Senior Research Fellow
Centre for Medical Image Computing
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