Dear Freesurfer-Experts,
I am trying to flip surface files (.mgh) from right to left.
I have read your instructions concerning xhemi and performed
registration to fsaverage_sym:
foreach subject (subjectlist)
surfreg --s $subject --t fsaverage_sym --lh
surfreg --s $subject --t fsaverage_sym -
Hi Freesurfer experts,
Qdec does not appear to allow me to automatically extract mean values for
significant clusters for each participant, so I have been doing this using
command line after running the original analysis in Qdec. However, I have
found that there are some differences in the signifi
Hi Freesurfers,
How can I perform seed based correlation analysis using PET images? In other
words how can I use the same approach of FSFAST, but by including PET images
instead of fmri images, to study the correlation between PET signal within a
seed mask ( e.g precentral gyrus ) and the whole
Just leave out that row (second case)
Best Martin
On Apr 13, 2016 8:30 AM, Mihaela Stefan wrote:Hi Martin!
Sorry to bug you but I have one more question. How do I create the Qdec table without the baseline for that subject? Do I leave the baseline time point out or I still enter it in the table?
Thanks, Doug.
When I do it, I get the following error: ERROR: must spec --sim
I am using FreeSurfer 5.3 in a Mac OS. I read in the wiki that mri_mcsim
got an atualization for Linux. Should I get that atualization for Mac Os?
Best,
Pedro.
On Wed, Apr 13, 2016 at 11:43 AM, Douglas Greve
wrote:
> T
Hi again,
in the paper, we used FreeSurfer 5.3 the process the data (recon-all), and then
run the hippocampal module on top of that. So, with a bit of trouble, you can
reproduce the results..
However, the 6.0 beta was taken down, so reproducing the results of the
recon-all stream would be hard
Hi Eugenio,
I understood this part that you mentioned but I didn't understand how is is
affected and what would be its consequences? Because I am referring to your
preprint paper that makes use of v6, so will the results/validity of that
paper also get affected by these differences. Because in my
Hi Tyson,
the hippocampal module shouldn't change between your beta and the FS6 release,
but the main recon-all stream will. Since the latter is used to initialize the
former, the results will be a bit different.
Cheers,
/Eugenio
Juan Eugenio Iglesias
Postdoctoral researcher BCBL
www.jeigl
what is your tksurfer command line? Can you send all the terminal output
from tksurfer? Does it work in freeview?
On 04/13/2016 11:20 AM, DeCross, Stephanie N. wrote:
> Hi,
>
> I’m trying to take an ROI in MNI152 volume space and make it into a
> cortical surface label, for visualization purpose
this is a known bug. Try this version instead
ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/mni152reg
On 04/13/2016 01:06 PM, Trisanna Sprung-Much wrote:
> Hi Doug
>
> So I tried running mni152reg and had the following error:
>
> mni152reg --s icbm-102_test
>
>
> setenv SUBJECTS_D
Hi Martin,
I am reposting this. Should we include the missing baseline in the qdec
table or leave it out?
Thanks!
Mihaela
On Wed, Apr 13, 2016 at 8:30 AM, Mihaela Stefan
wrote:
> Hi Martin!
> Sorry to bug you but I have one more question. How do I create the Qdec
> table without the baseline f
Just an aside: if you acquire oblique (e.g. AC/PC aligned), and don’t want
FS to rotate the volume back into the native scanner space as part of its
“conformation” step, you can edit the s/qform of the NIFTI header to
appear as a non-oblique acquisition. As Bruce noted, this isn’t a big
deal, alth
Hi FreeSurfers,
There is a research assistant position opening at the VA Boston Healthcare
System in neuroimaging and aging (job announcement is attached).
This would be a great position for someone who is interested in both the
technical aspects of MRI data processing/analysis as well as in
neuro
Hi,
I was wondering when would the new Freesurfer v6 beta be available? Also I
have been using the old beta for my hippocampal segmentation and I wanted
to know if this new beta will affect the results of that?
Thanks,
Tyson
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Do you have a .license file in your /Applications/freesurfer directory?
If so try making a copy of it and calling it license.txt and try again.
If that still doesnt work please email me your .license file TO MY
PERSONAL EMAIL ADDRESS, NOT THE FREESURFER LIST. Thanks.
-Zeke
On 04/13/2016 01:38
Hi list,
please see the error reported below. It occurs when I invoke tksurfer.Of note,
I have completed without problem fs-fast analysis without error.The .license
file is well placed and written.Thanks
Stefano
tksurfer fsaverage rh inflated -aparc -overlay
subj/rest/fc.ROI.surf.rh/ROI/sig.nii.
Hi Kate
I don't think that will matter. Try running it through from the original
dicoms and see if things seem accurate. That isn't actually an artifact,
it just looks strange because of the slight angle of the view. My guess is
we will handle this fine
cheers
Bruce
On Wed, 13 Apr
2016, Ka
Hi Doug
So I tried running mni152reg and had the following error:
mni152reg --s icbm-102_test
setenv SUBJECTS_DIR /data-01/trisanna/freesurfer
cd /home/trisanna
/usr/local/freesurfer-5.3//bin/mni152reg --s icbm-102_test
fslregister --mov
/usr/share/fsl/5.0/data/standard/MNI152_T1_2mm_brain.ni
Hi all,
I'm trying to do FC connectivity analysis using the dorsalateral prefrontal
cortex as a seed. I checked the text file
$FREESURFER_HOME/average/colortable_desikan_killiany.txt and it looks like
DLPFC is not listed as a possible structure to do the FC analysis. I attempted
to use lh-prefr
I could be wrong, but the output in your email oscillates between
"/Users" and "Users" (Note the preceding forward slash). Im not sure if
thats just a copy/paste thing or directly related to your error.
-Zeke
On 04/12/2016 08:44 PM, Jasmin Alves wrote:
>
>
> So I have specified where the DTI fi
*Advanced Scientific Programming in Python*
a Summer School by the G-Node, and the Centre for Integrative Neuroscience
and Neurodynamics, School of Psychology and Clinical Language Sciences,
University of Reading, UK
Scientists spend more and more time writing, maintaining, and debugging
software
Hi,
I’m trying to take an ROI in MNI152 volume space and make it into a cortical
surface label, for visualization purposes.
With my input being the lh thresholded, binarized MNI152 nii.gz label (when I
visualize it, it looks as it should in fslview), I ran:
mri_vol2vol -- mov -- targ
$SUBJE
Dear Doug,
thank you very much for the support.
I am quite confused by this info about correcting of area of fsaverage
clusters. Could you please clarify to me the following:
How exactly the values of lh.area, lh.white.avg.area.mgh of fsaverage were
computed?
How the cluster area inside mri_s
Thank you!
- Ursprüngliche Mail -
Von: "Douglas Greve"
An: freesurfer@nmr.mgh.harvard.edu
Gesendet: Mittwoch, 13. April 2016 16:46:19
Betreff: Re: [Freesurfer] REPOST: Monte Carlo correction in QDEC
In most neuroimaging, people use p<.01 (sig threshold > 2). It is more
important to have
Looks like you are analyzing a table of data (ie, ROI analysis). In this
case you cannot use clusterwise correction because you cannot form
clusters of voxels when you don't have a voxel-wise analysis! You can do
a bonferroni or FDR correction. You can get an FDR program from here
ftp://surfer
In most neuroimaging, people use p<.01 (sig threshold > 2). It is more
important to have a more stringent threshold when using gaussian random
fields because the assumptions built into it. Since we use simulations
directly, we don't have problems with those assumptions and so I think
you can go
Try it without the --no-sim. The --no-sim was from before I stored the
cached data and you either had to run a simulation or not.
On 4/12/16 9:10 PM, Pedro Rosa wrote:
Dear list,
I want to limit my vertex-wise group analysis to a smaller spatial
region, then I ran my own Monte-Carlo simulation
Hi Clara,
You need to register and smooth again for only the first time point.
You could also open the full stack in Matlab, select the entries of your first time point and write it out again.
Best Martin
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Freesurfer@nmr.mgh.ha
Hi Doug,
One more question about feeding the -reg to mri_vol2surf, please.
I am specifying the registration .lta because I have made edits to it,
mri_vol2surf --src FS6_24551_MPRAGE_Neuro.nii/pet/pet2free_fsl.mgz --out
FS6_24551_MPRAGE_Neuro.nii/surf/lh.PETSurfce.mgh --projfrac 0.5 --hemi lh
--r
Dear FreeSurfer experts,
I'm trying to run a mri_glmfit on my first time point (out of 3). I ran the glm
with this:
mri_glmfit --table $SUBJECTS_DIR/aparcs_stats_sc1.txt --fsgd
$SUBJECTS_DIRfsgd_sc1.txt --C $SUBJECTS_DIR/group.mtx --surf 87kids_template lh
--cortex --glmdir $SUBJECTS_DIR/glm/l
Hi Doug,
thanks for your reply. It made things a lot clearer. I totally understand that
you're probably receiving more than one cry for help per day.
What would you say are the conventions for picking a threshold for analyses on
structural data?
Cheers, Clara
- Ursprüngliche Mail -
Hi Martin!
Sorry to bug you but I have one more question. How do I create the Qdec
table without the baseline for that subject? Do I leave the baseline time
point out or I still enter it in the table?
For example
fsid fsid-base years
Study1_Subj1_MRI0. Study1
Dear FreeSurfer experts
I have a question regarding the correct data analysis method for my study
design and could unfortunately not find an example of a similar analysis on
your mailing list or documentation on the wiki.
I have repeated structural MRI data from one group (within-subjects design)
Jasmin -
Check the DTI.nii.gz file using MRICRON and see if the images across the
gradients are OK. If the file is corrupt, then Tracula cannot read this.
best,
A
On Tue, Apr 12, 2016 at 8:44 PM, Jasmin Alves wrote:
>
>
> So I have specified where the DTI file is. I am not sure why Tracula
>
Dear FS experts,
I used the spatiotemporal LME to fit to my longitudinal data and performed some ad-hoc tests using the FDR2 correction.
May I know how can I extract the random slopes characterizing individual variability in rate of change of cortical thickness at the significant vertices,
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