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Hi,
In freeview, is it possible to view a collection of labels with different
filled in colors, as well as their outlines?
So, a combination of the filled in and outline only modes?
Best,
Prad
-------- Forwarded Message --------
Subject: Innis Lab postdoc position 2022
Date: Thu, 8 Jul 2021 19:45:24 +0000
From: Innis, Robert (NIH/NIMH) [E] <innisr(a)mail.nih.gov>
To: Innis, Robert (NIH/NIMH) [E] <innisr(a)mail.nih.gov>
A postdoctoral position will be available in my lab starting in the
first half of 2022. Please forward the attached advertisement to anyone
who may be interested.
The two major goals are translational studies of neuroinflammation
(i.e., COX-1, COX-2, and TSPO) and indirect markers of cAMP signaling
(via PDE4B and PDE4D). The studies extend from transgenic mice to
monkeys and to patients, including those with depression or dementia.
Stay safe and many thanks,
Bob Innis
************************************
Robert B. Innis, MD, PhD
Chief, Molecular Imaging Branch
National Institute of Mental Health
10 Center Drive, MSC-1026
Bldg. 10, Rm. B1D43
Bethesda, MD 20892-1026
Tel: 301-594-1368
Fax: 301-480-3610
Email: robert.innis(a)nih.gov <mailto:robert.innis@nih.gov>
Branch Administrative Manager:Â Elizabeth Alzona
Tel:Â 301-594-1089
Email: alzonae(a)irp.nimh.nih.gov <mailto:alzonae@irp.nimh.nih.gov>
Molecular Imaging Branch
website<https://secure-web.cisco.com/1ArBJjYhVhrUft9gNOaLCuNtmSeJ1qPEnHkkGF7qzP9gVj…>
************************************
____________________________________
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External Email - Use Caution
Dear Freesurfer team,
It is my first time editing wm segmentation (white matter segmentation
errors + topological errors).
I wonder if there is a good tutorial on which I could rely.
Also, I have read there is an example of segmentation that comes with
FreeSurfer that is called Bert. I think it would be great to have it so I
can look at it as a good example.
Your help on this is very much appreciated
Kind regards,
Rosie
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Hi,
I am running Freesurfer on longitudinal datasets all obtained on 3T
scanners. Unfortunately, many of the MRIs were done on different
scanners, Phillips and GE.
Would longitudinal pipeline help reduced scanner variability or should I
process crossectionally each time point separately and normalize these time
points with eTIV?
Many thanks
AJ
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Dear Freesurfer team,
Following this link:
https://secure-web.cisco.com/1JQvIqqm3-q4IvkVi2SEZWuHP3qoo3qga0SfN71vLNIZ9q…
It says how to run segmentation of hippocampal subfields before running
recon-all but not once you already have recon-all -all run.
Any suggestions on how I can get the segmentation of hippocampal subfields
under this situation would be appreciated.
Kind regards,
Rosie
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Hello experts,
I am trying to calculate Hausdorff distance between two mri volumes for
cortical and subcortical structures across several subjects. I found a way
to calculate hausdorff distance for mri volumes using mri_hausdorff_dist
but it only seems to work if I specify one target label at a time.
My question is, so to calculate average hausdorff distance between two mri
volumes across several subjects should I first calculate hausdoff distance
between two mri volumes for each segmentation label for each subject and
then calculate the mean hausdorff distance for each segmentation label
across subjects?
Best,
Julia Shin
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Dear experts,
While visualizing my polar angle results using angle file, I almost don't get any interpretable results. However, if I show results with real+imag file, taken from the following link (http://secure-web.cisco.com/1JbJRUtZSYA97HQvtYOuYEBYhanfcOaUs2V4aEIfByy0FFh…) I have a clearer map.
Can you help me? Does it make sense to visualize with real and imag files layered on top of each other? Eccentricity results work fine with both of the visualization approach, what might be wrong it polar angle? I appreciate any cue.
Thanks in advance!
Beyza
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Dear Freesurfer team,
I am having the following error message when I try to run the stats table:
rosalia@rosalia-Lenovo-Y520-15IKBN ~/Desktop/CAN_RUTI/FREESURFER_CAN_RUTI $
asegstats2table --subjects sub-002_ses-BSL sub-003_ses-BSL sub-004_ses-BSL
sub-005_ses-BSL sub-006_ses-BSL sub-007_ses-BSL sub-009_ses-BSL --meas
volume --tablefile aseg_stats.txt
SUBJECTS_DIR : /home/rosalia/Desktop/CAN_RUTI
Parsing the .stats files
ERROR: Cannot find stats file
/home/rosalia/Desktop/CAN_RUTI/sub-002_ses-BSL/stats/aseg.stats
Use --skip flag to automatically skip bad or missing stats files
rosalia@rosalia-Lenovo-Y520-15IKBN ~/Desktop/CAN_RUTI/FREESURFER_CAN_RUTI $
The problem is that there is an actual aseg.stats in this directory where
it says it cannot find it.
Any idea why is this happening?
Kind regards,
Rosie
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Dear Experts,
I am running my polar angle and eccentricity following the freesurfer retinotopy analysis.
Saddly, i figured out that my eccentricity script has a shorter cycle compared to the polar angle (38sec vs 40sec pro cycle).
To bypass this error im splitting the analysis and i run the retinotopy separately on polar angle and eccentricity using two different folders and copying the polar angle as eccentricity ( same for eccentricity as polar angle) just in order to run selxavg3-sess.
Is this a legal step for the analysis?
Furthermore, im getting negative values for masked angles… is this indicating any specific problem?
Many thanks for your help!
Giorgio