Hello,
I forgot to mention in my previous email that the system locale is in Swedish.
Can this be the reason?
Regards,Teodora
On Thursday, April 6, 2017, 1:07:56 PM GMT+2, teodora petrova
wrote:Hello,
I would like to correct my glm_fit results for multiple
Dear all,
I've been following the instructions for building a custom registration
template as written here (
http://surfer.nmr.mgh.harvard.edu/fswiki/SurfaceRegAndTemplates) and here (
https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2011-May/018345.html
).
I'm now at the mris_preproc
Dear FreeSurfer Developers,
I was trying to use the command recon-all -autorecon1 -subjid bert and got an
error.
When I checked I found the error was coming while executing the below command:
nu_correct -clobber ./tmp.mri_nu_correct.mni.7555/nu0.mnc
./tmp.mri_nu_correct.mni.7555/nu1.mnc
Dear all,
I am using Freesurfer 6.0 to run recon-all on 0.8 isotropic data. Whenever I
use the parallel flag I get this error.
dyld: lazy symbol binding failed: Symbol not found: ___emutls_get_address
Same subject without the parallel flag runs smoothly but of course takes much
longer. I have
Use
mri_binarize --i aseg.mgz --match 17 --binval -1 --o your.lefthippo.nii.gz
On 4/6/17 6:00 AM, Dilip Puri wrote:
Hi everyone,
I am working on Hippocampus segmentation using Neural Networks for
that I need labeled images of Hippocampus corresponding to original
images.
I am using
Hi list,
We're working on making a preprocessing stream that will be generally
accessible to different analysis streams, including FreeSurfer. One
component of this is sampling functional volumes to FreeSurfer meshes, and
I want to test this component by running a simple first-level GLM in
yes, those are the residuals
On 4/5/17 5:39 PM, std...@virgilio.it wrote:
Hi,
as you advise I have run selxavg3-sess with the -svres option.
I found a folder called "res" which contain "res-001.nii". Is it the
f.nii fully processed?
Thanks
Stefano
Messaggio originale
Da:
I got it from FSL in the $FSLDIR/data/standard, but it is distributed
with SPM as well
On 4/5/17 9:39 PM, Kevin Aquino wrote:
Hi Douglas,
I am wondering, where did you find the mini 152 T1 map? :)
Regarding this...
Would it be better to instead run recon-all on a higher-res MNI atlas?
and
I think this is a "language" problem in that it is converting the "1.3"
into "1,3" and then getting confused. I'm not sure how to fix it, but I
think it has to do with the LOCAL setting.
On 4/6/17 5:07 AM, teodora petrova wrote:
Hello,
I would like to correct my glm_fit results for multiple
It should save it in the current directory. But I don't think we write
out IMA files. Why not use nifti (nii or nii.gz)?
On 4/5/17 2:05 PM, Karan Vahi wrote:
Dear Freesurfers,
I am trying to implement the methods mentioned in this paper to deal
with partial volume effects when quantifying
It will be in the space that you analyzed it in. If you want the native
space, then use -native when running preproc-sess and mkanalysis
On 4/6/17 2:34 AM, std...@virgilio.it wrote:
Furthermore, the res-001.nii which is produce in produced in the res
folder in not the same dimension of f.nii.
The Mayo Clinic Departments of Neurology and Diagnostic Radiology in Rochester,
Minnesota are seeking applications for a fully-funded, two-year postdoctoral
Research Fellow position to begin in July of 2017. The Research Fellow
position will primarily work on developing advanced multi-modal
hi,
I've read through the list, and searched over the last few days, and can't
quite seem to find what I'm looking for. My first message wasn't clear at all
either (my apologies), it was one of those days where your brain ends up in a
bit of a fog.
I am trying to get a heat map style visual
Hi Chris
it's possible we never looked at -bigventricle in the long stage. What
was your recon-all command line?
cheers
Bruce
On Thu, 6 Apr 2017, Chris Adamson wrote:
It happens when I use -bigventricles.
From: freesurfer-boun...@nmr.mgh.harvard.edu
Hi Dilip
yes, freesurfer will do this for you, although the labels will be 17 for
left hippocampus and 53 for right.
cheers
Bruce
On Thu, 6 Apr 2017, Dilip Puri wrote:
> Hi everyone,
>
> I am working on Hippocampus segmentation using Neural Networks for that I
> need labeled images of
Hi Ilaria
do you have any reason to believe that it isn't just out of memory? If so,
there's not much to do other than get more RAM or use a different machine
cheers
Bruce
On Thu,
6 Apr 2017, Ilaria Sani wrote:
Dear All,
I’m trying to load a pretty big diffusion MRI dataset
is it a compressed nifti (nii.gz)? If so, try uncompressing it first
On 04/06/2017 02:53 PM, Ilaria Sani wrote:
> Hi Bruce,
>
> Not sure this answer your question...
>
> In matlab workspace, I am able to load data in two halves:
>
> H1=MRIread(half1)
> H2=MRIread(half2)
>
> And then concatenate
Thanks, I'll take a look at it and let you know how it goes.
Peter
From: freesurfer-boun...@nmr.mgh.harvard.edu
[freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of Douglas N Greve
[gr...@nmr.mgh.harvard.edu]
Sent: Thursday, April 06, 2017 1:00 PM
To:
You should be able to do it that way. When you run mkanalysis, specify
-funcstem fmcpr.sm0.fsaverage.lh.nii.gz, and then selxavg3-sess will
then use that file as input. If you want to smooth, then do that
explicitly and pass the smoothed file to mkanalysis
On 04/06/2017 12:35 PM, Christopher
1. The "..." means to include the other options needed for the command
to run. Looks like you figured it out. Using -f as you have is correct.
2. can you send the full terminal output?
On 04/06/2017 08:55 AM, Linda Zhang wrote:
> Dear all,
>
> I've been following the instructions for building
On 04/03/2017 01:45 PM, Veggeberg, Rosanna wrote:
> Hello,
> I am using QDEC to analyze cortical structural data and am looking for
> some clarification on some questions that have come up.
>
> 1. _Design tab_: In the "Measure" drop-down selection, I understand
> what we are getting when
Hi Bruce,
Not sure this answer your question...
In matlab workspace, I am able to load data in two halves:
H1=MRIread(half1)
H2=MRIread(half2)
And then concatenate the volumes
concatenate them var=cat(4,H1,H2).
So, somehow matlab can handle...
However, when those operations are embedded
that looks right. how different are the values?
On 04/05/2017 10:58 AM, Gullickson, James wrote:
> Hello all,
>
> I want to calculate a Ventricle-to-Brain ratio (VBR) as a measure of
> parenchymal atrophy using Freesurfer version 5.3.0. I have tried to go
> about this using the aseg.stats
what do you mean they do not differ in gender ratio? Just that the
relative number of M/F is the same in each group? If there is not a
significant interaction between gender and group, then you can usually
merge the genders.
On 04/05/2017 05:13 PM, Lim, Lena wrote:
>
> Dear Freesurfer
See if annotval2surfoverlay.m does what you want. It is in v6. If you
have v5.x, I can send you the mfile separtely
On 04/06/2017 01:00 PM, Senften, Peter wrote:
> hi,
>
> I've read through the list, and searched over the last few days, and can't
> quite seem to find what I'm looking for. My
can you send the full terminal output?
On 04/05/2017 04:02 PM, Taylor, Johnmark wrote:
> Hello,
>
> I am getting an odd bug on selxavg3-sess. I am getting the error message,
>
> *ERROR: cannot find [rest of file path]/fmc.sm0*
>
> I am indicating zero smoothing in mkanalysis-sess ("-fwhm 0"). I
these are good questions without good answers. It is hard to compare
surface-based vs volume-based. The surface-based may be smaller, but it
will only include gray matter whereas a volume-based sphere will be
bigger but will include WM and CSF. If you're voxel size is small, then
3mm radius
I guess you could average it over space (eg, over a cluster). Let me
know if you want instructions. Otherwise, I'm not sure what to say.
On 04/04/2017 06:49 AM, tom parker wrote:
> Hi Doug,
> Thanks! I realize now I didn't explain myself properly.
> I need one single R value for the correlation
Dear Freesurfer's experts,
I draw a specific region on fsaverage using QDEC, then I mapped this label
on each subject using mri_label2label. I looked at these registered labels
using freeview. Most of them are perfect but for some of them I would like
to correct the segmentation. I would like to
Thanks.The file could not be open by fslview.I presume that it is inflated.How
can I do to transform it?Stefano
Messaggio originale
Da: "Douglas Greve"
Data: 6-apr-2017 17.56
A:
Ogg: Re: [Freesurfer] R: R: Re: R: Re:
what is your label2label command line?
On 04/06/2017 04:52 PM, Arnaud Boré wrote:
> Dear Freesurfer's experts,
> I draw a specific region on fsaverage using QDEC, then I mapped this
> label on each subject using mri_label2label. I looked at these
> registered labels using freeview. Most of
Thanks, Doug.
There is no significant interaction and I merged the males and females within
each group, but the reviewer wants me to include gender as a covariate. Do we
always need to control for gender esp. when the group x gender is
insignificant? Will that be "over-controlled"?
Hi Douglas,
Thanks, good to know! That was the full terminal output after I ran
mris_preproc, though.
Cheers,
Linda
On Thu, 6 Apr 2017 at 22:07 Douglas N Greve
wrote:
> 1. The "..." means to include the other options needed for the command
> to run. Looks like you
probably so. It is up to you whether you want to fight the reviewer or not.
On 04/06/2017 05:08 PM, Lim, Lena wrote:
>
> Thanks, Doug.
>
>
> There is no significant interaction and I merged the males and females
> within each group, but the reviewer wants me to include gender as a
> covariate.
depends on your analysis but probably so
On 04/06/2017 05:26 PM, std...@virgilio.it wrote:
> Thanks.
> The file could not be open by fslview.
> I presume that it is inflated.
> How can I do to transform it?
> Stefano
>
> Messaggio originale
> Da: "Douglas Greve"
Doug,
Thanks for your reply.
Difference between the two TVV methods ranges between 1-6%
Difference between the two TBV methods ranges between 2-4%
Basically, my question is two-fold:
a) what is the most accurate representation of total ventricular volume
b) what is the most accurate
Hello Freesurfer Experts,
I want to compare the cortical thickness between the groups (HC & Patients),
and wanted to know where qdec shows this information. Once the design tab is
loaded, I am seeing the question in the analysis results – does the correlation
between thickness and Age differ
It happens when I use -bigventricles.
From: freesurfer-boun...@nmr.mgh.harvard.edu
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Chris Adamson
Sent: Thursday, 6 April 2017 12:27 PM
To: freesurfer@nmr.mgh.harvard.edu
Subject: [Freesurfer] long mri_ca_register error
Freesurfer
Dear Patricia,
this is I suppose the last issue concerning symbolic links, related with part
of code starting with following comment:
# if fsaverage is not in subjects dir, put it there
I think that the most straightforward solution of this issue is to manually
copy the fsaverage subject to
Hi Antonin,
I edited recon-all file, but another error was reported. This error
concerns symbolic links, too. Is there any way I could make it work on this
virtual machine? I coud try to substitute all ln commands with cp or
something like that.
Thanks.
Patricia
2017-04-04 13:43 GMT+02:00
Dear Freesurfer Experts,
As one of the new freesurfers, I really appreciate the excellent work of
authors as well as great support of users' forum.
A good guess of mine is that authors, e.g., Vasanth or Louis etc., are busy
updating QA tools after the FSv6 release since the QA Tools v1.2 was
Hi everyone,
I am working on Hippocampus segmentation using Neural Networks for that I
need labeled images of Hippocampus corresponding to original images.
I am using OASIS Dataset for this. I want to generate labeled images using
FREESURFER. Is there any way to label each 3D co-ordinate
Hello,
I would like to correct my glm_fit results for multiple comparisons. I am using
the following commands, similar to the one in the group analysis tutorial:
mri_glmfit-sim --glmdir lh.index.glmdir --cache 1.3 abs --cwp 0.05
--2spacesmri_glmfit-sim --glmdir lh.index.glmdir --cache
Just the standard pipeline.
recon-all -s cross1 -all -bigventricles
recon-all -base cross -tp cross1 ... -all -bigventricles
recon-all -long cross1 cross -all -bigventricles
-Original Message-
From: freesurfer-boun...@nmr.mgh.harvard.edu
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu]
Hi Doug,
Thanks for the tip. I can load the volume now!
I'm getting different types of errors when I proceed with my analyses though.
Can you help me to understand why it works when data are decompressed and in
what way data are different now.
Thanks a lot,
Ilaria
-Original Message-
Hi everyone,
when I used following command:
mri_binarize --i myfile.img --match 17 --binval -1 --o your.lefthippo.nii.gz
then I got output your.lefthippo.nii.gz file when I read this file using
FREEVIEW then it completly different from original mask.
Thanks
Dilip
On Thu, Apr 6, 2017 at
Furthermore, the res-001.nii which is produce in produced in the res folder in
not the same dimension of f.nii.I would do the whole FAST preprocessing on
f.nii., maintaining the same dimension and open it with FSL.ThanksStefano
Messaggio originale
Da: std...@virgilio.it
Data:
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