Also you shouldn’t be using the HCP 7T fMRI data at this time. See the message
about this on the list.
Peace,
Matt.
From:
>
on behalf of Timothy Coalson >
Date: Friday,
Most of the released HCP data are on a 32k mesh. You can find the Yeo
parcellation on the 32k mesh here: https://balsa.wustl.edu/study/show/WG33
Peace,
Matt.
From:
>
on behalf of David Hartman
I would recommend that both images are 0.8mm isotropic, though there is no
matrix size requirement (they just both need to cover the whole brain). Why do
you want to use differing resolutions?
You can download my percolation here: https://balsa.wustl.edu/file/show/3VLx
Peace,
Matt.
From:
As for the 59k vertices you mentioned, I'm guessing you were looking at a
cifti file that contains both hemispheres, and excludes the medial wall -
if so, this actually uses surfaces with 32k vertices. Unfortunately, our
1.6mm 7T data was processed with a mesh that happens to use 59k-vertex
Hi David,
With 59k vertices, it sounds like you are using the versions of the HCP
individual data that was preprocessed at 1.6mm resolution for use with the 7T
data contained in the "Structural Preprocessed for 7T (1.6mm/59k mesh)" package
in ConnectomeDB. The 3T "Structural Preprocessed"
Dear HCP users,
I'm trying to use the multi-model parcellation (MMP) data. I have the label
names for the 180 parcellations, and also their location map available at
https://balsa.wustl.edu/78X3. But cannot find out the full name or meaning
of each name (e.g., what does p32pr mean). Can someone
Hi,
*Background:*
Regarding the parcellation of the cortex into functional networks (“The
organization of the human cerebral cortex estimated by intrinsic functional
connectivity,” Yeo et al.) Yeo breaks up the cortex into 7 networks.
However, his cortical data has 163842 vertices, while the
What banding artifact are you referring to? Could you post a picture to a
sharing site?
thx
--
Michael Harms, Ph.D.
---
Conte Center for the Neuroscience of Mental Disorders
Washington University School of Medicine
Department of
Dear David,
Thank you very much for your response. A colleague has forwarded the
mail to me. I have no idea why I am not receiving your mails, I seem to
be receiving all the other [HCP-Users] mail. I will check my settings.
Thanks once again and regards,
Claude
>
>
> Forwarded
It is better for finding brain areas, but that bias correction will also remove
low spatial frequency differences across subjects that you might be interested
in (see Glasser et al 2013 Neuroimage for how it works).
The protocol looks fine, though TI=1000 would be better from the perspective of
I'm using Myelin_BC as I thought it would be more accurate due to bias
correction. I will recalculate with the normal myelin maps.
Can you please tell me why MyelinMaps are better for the stats than
MyelinMaps_BC? And do I understand correctly that our acquisition protocol
is okay?
Thanks a lot!
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