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It seems to work. Thanks a lot !
Jessica BOURGIN
Laboratoire de Psychologie et Neurocognition
CNRS UMR 5105
Université Savoie Mont Blanc (USMB)
BP 1104
73011 Chambery Cedex France
___
Freesurfer
Hi Heidi, I'm not sure I understand what you are trying to do. Can you
elaborate? What do you mean that you do not have statistical info any more? It
is unusual to smooth p-values. Probably you should apply smoothing before your
analysis
On 8/9/2019 2:46 PM, Jacobs, H (NP) wrote:
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Dear Freesurfer experts,
We had just reprocessed our subjects with the -long flag fr the
longitudinal processing, and when extracting volumes with asegstats2table I
have the following error:
WARN: SUBJ229_ses-1.long.SUBJ229_tmpl nmeasures = 63,
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Bruce,
Awesome! I'll try that!
Thanks,
Brendan
-Original Message-
From: freesurfer-boun...@nmr.mgh.harvard.edu
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Bruce Fischl
Sent: Friday, August 09, 2019 11:40 AM
To: Freesurfer
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Hi all,
I created an overlay surface map of my analyses (with pvalues in log10) using R.
Now I would like to smooth this map to extract clusters and I tried to use:
mri_surf2surf --prune --s fsaverage --hemi lh --fwhm 3 --sval lh_analyses.mgh
--tval
Hi Brendan
usually defects that are that big don't get corrected properly. I would
look at the wm.mgz and the lh.orig.nofix to understand what is causing the
large defects and correct them manually
cheers
Bruce
On Fri, 9 Aug 2019, Balken, Brendan wrote:
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Bruce,
Oh okay I understand now. This has been very enlightening! So, you think if I
let it keep running it will eventually correct the defects? And then I just
need to double check the result to make sure it corrected them properly? When I
got the
yes, because that is the total # of defects. The 29th or 30th isn't the
last one, just what it got stuck on. The #30 should look much bigger
though (you'll need to change the overlay thresholds)
On Fri, 9 Aug 2019,
Balken, Brendan wrote:
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Bruce,
I just
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Bruce,
I just imported lh.defect_labels as an overlay over the lh.inflated.nofix but
the values aren't 1-30 they're 0 - 160 roughly. I'm not sure why...
Thanks!
-Original Message-
From: freesurfer-boun...@nmr.mgh.harvard.edu
they are an overlay not a surface. Load the surface first then load them
as an overlay on top of it (e.g. the lh.inflated.nofix)
On Fri, 9 Aug 2019,
Balken, Brendan wrote:
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Bruce,
Thanks so much for the quick response! I don't know how to load the defect
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Bruce,
Thanks so much for the quick response! I don't know how to load the defect
labels. When I try to load them as a surface, I get an error. I'm doing this in
freeview gui. Also, I checked the cerebellum and it's not attached.
Thanks,
Brendan
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Sorry I did not see your reply (having issues getting notifications from
the freesurfer list). The error seemed to be an issue with the version I
was using, which wasn't reading the subject list correctly. Wanted to make
sure I posted a solution. Thank
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Hello,
I am running TRACULA on my data set and am having issues with one of my
subjects. For this subject, I get the following error.
INFO: input image orientation is LIS
INFO: input image determinant is 18.4229
rdc_new: Undefined variable.
Hi Brendan
the time to correct goes with the square of the size of the defect
(actually the convex hull of the defect) so it can take a very long time
for big ones. More importantly, if the defect is that large it may not be
corrected in the anatomically desired manner. You should take a look
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Hi!
I was wondering whether it is possible to do deconvolution of an fMRI time
series with FSFAST?
Specifically, I would like to get a deconvolved signal from a region of
interest to prepare predictors for a PPI analysis.
Additional considerations:
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