Hi Matthieu
I think 6.0 looks better overall, even in the beta that you have. The 5.3
segmentation looks like it is underestimating cerebellum and hippocampus to
me.
cheers
Bruce
On Tue, 15 Dec 2015, Matthieu Vanhoutte wrote:
> Dear FS's experts,
>
> I have tried the recon-all process on
1) what partial volume correction do you mean?
2) I'll leave this for Eugenio and Koen.
Bruce
On Tue, 15 Dec 2015, Matthieu
Vanhoutte wrote:
Hi Bruce,
All right then it's only a question of time ofr the new v6 release !
Meanwhile, is it possible and coherent :
1) to use the partial volume
Hi,
Just following up on my previous email (see below) as I have not yet heard
back. I also have another question regarding the lh.wm.mgh and rh.wm.mgh
generated by pctsurfcon. How do I view these as surface overlays on T1 brain
scans?
Thank you very much.
Hi Matthiew
we are still hoping to get an official v6 release out in the next month
or two, so it would be best to use that which I think will outperform
whatever beta you have and 5.3. If you can't wait you are probably better
off using 5.3 (although I think the v6 you have is more
On 12/15/2015 01:00 PM, Sabrina Yu wrote:
>
> Hi,
>
>
> Just following up on my previous email (see below) as I have not yet
> heard back. I also have another question regarding the lh.wm.mgh and
> rh.wm.mgh generated by pctsurfcon. How do I view these as surface
> overlays on T1 brain scans?
It is not subsegmented in 6.0 either:). When you run gtmseg, it will
create the new segmentation that include pons and a few other things
On 12/15/2015 12:56 PM, Matthieu Vanhoutte wrote:
> Dear Douglas,
>
> Please see below :
>
> 2015-12-15 18:37 GMT+01:00 Douglas N Greve
btw, we are still making changes to version 6 so don't assume that the
results from the beta will be consistent with the current beta distribution.
On 12/15/2015 12:22 PM, Bruce Fischl wrote:
> Hi Matthiew
>
> we are still hoping to get an official v6 release out in the next
> month or two, so
It seems problematic to me to use a nightly dev build for publication.
cheers,
-MH
--
Michael Harms, Ph.D.
---
Conte Center for the Neuroscience of Mental Disorders
Washington University School of Medicine
Department of
Hi Salvatore,
can you send
- the FS version you are using
- the recon-all command you called
- the recon-all.log file
thanks, Martin
On 12/15/2015 02:00 PM, salvatoreandrea...@libero.it wrote:
I have 4 Gb, but I tried with a more poweful machine in the hospital
and I got a similar error. I
I am trying to a brodmann mask using PALS B12 atlas in fsaverage. I used the
following command to create the volume from annotation file. I have two
questions associated with it.
mri_aparc2aseg --s my_subject --annot PALS_B12_Brodmann --o
PALS_B12_Brodmann_Mask.nii --annot-table
Not necessarily. It needs a good segmentation, so, to the extent that v6
has a better segmentation then v6 is better.
On 12/15/2015 02:57 PM, Matthieu Vanhoutte wrote:
>
> Thanks Douglas for the answer !
>
> But isn't PVC design for better working in terms of results with
> v6_beta than v5.3 ?
On 12/15/2015 04:46 AM, Matthieu Vanhoutte wrote:
> Dear experts,
>
> Could anyone answer to my questions below ?
>
> Thanks !
>
> Best regards,
> Matthieu
>
> 2015-12-10 10:10 GMT+01:00 Matthieu Vanhoutte
> >:
>
> Dear FS
Hi Doug - Yes, this is possible and indeed it is recommended to use the
latest version of tracula.
Best,
a.y
On Fri, 6 Nov 2015, Douglas Merkitch wrote:
Hello FreeSurfer experts,
We have a large dataset that was processed in FreeSurfer v 5.1 and we would
like to run tracula on the
Hi Henrik - There's no explicit parameter in the current version, but you
can run bedpostx the multi-exponential model yourself, and then let
tracula use the orientation estimates from that model (as long as the
output dir is called dmri.bedpostX, it'll read the files from there).
We are in
Hi Bruce,
All right then it's only a question of time ofr the new v6 release !
Meanwhile, is it possible and coherent :
1) to use the partial volume correction provided in the v6 beta version of
FreeSurfer despite the fact that recon-all have been done for all subjects
with the v5.3 ?
2) to use
I mean that they may/will change between the current beta release and
the final release.
On 12/15/2015 02:51 PM, Matthieu Vanhoutte wrote:
>
> Sorry Douglas I didn't well understand what you mean. Did you mean
> that results from beta distribution aren't valuable ?
>
> Best regards,
>
>
Hi John - The values are weighted (multiplied) by the probability
distribution (path.pd.nii.gz) at the same voxel. So they are the expected
values, from a probabilistic standpoint. The distribution is thresholded
at 20% of its maximum by default (this is a parameter in dmri_pathstats).
Hi,
I am trying to show 3 aparc labels on the inflated surface, each in a different
color, let’s say lh.inferiortemporal, lh.middletemporal and lh.superiortemporal
.
I have 2 questions:
First I ran mris_annotation2label to extract the individual region aparc labels.
I can merge them into a
Dear Douglas,
Please see below :
2015-12-15 18:37 GMT+01:00 Douglas N Greve :
>
>
> On 12/15/2015 04:46 AM, Matthieu Vanhoutte wrote:
> > Dear experts,
> >
> > Could anyone answer to my questions below ?
> >
> > Thanks !
> >
> > Best regards,
> > Matthieu
> >
> >
Hi Bruce,
When the thickness/volume measure was compared between the results obtained
with recon-all with and without defaced T1 as input to recon-all, we obtained
20% errors (between them)
Example: 100*(Thalamus_left_volume_with_defaced_T1_to_recon-all MINUS
Hi Simon - You are correct, this was a bug specific only to running the
-stat part of trac-all with the CVS template. Your work-around was
correct. I've fixed the bug so that, as of the next version, the
configuration as shown in the sample config file should work with the
-stat part as
me too
On Tue, 15 Dec 2015, Harms, Michael wrote:
It seems problematic to me to use a nightly dev build for publication.
cheers,
-MH
--
Michael Harms, Ph.D.
---
Conte Center for the Neuroscience of Mental Disorders
Washington
I see. That is surprisingly large for whole structure volumes. We don't
have a lot of experience analyzing defaced volumes, so I would do recon-all
on the original data, then deface post-hoc. If you upload one subject where
you find a large (or the largest) difference, I'll take alook
On
Hi Ju - Are you using the same computer and are logged in in as the same
user when you create the directory manually and when you run trac-all?
It's hard to replicate this error. What the program does at that point is
run the system call
mkdir -p
Hi Deniz - It sounds like the reconstruction for this particular tract and
subject may have failed. You can try reinitializing it by using the reinit
variable in your configuration file (search reinit in the freesurfer email
list archives for previous posts on this). If you try that and the
Hi Ruth - It expects the output format of eddy_correct. It then computes
the transforms between consecutive frames from the transforms between each
frame and the reference frame.
Best,
a.y
On Sun, 29 Nov 2015, Ruth Carper wrote:
Hi,
I'm hoping to use the dmri_motion tool to quantify
Hi Doug - This post from the archives addresses the same error message.
Please check if this fixes it for you, too:
http://www.mail-archive.com/freesurfer%40nmr.mgh.harvard.edu/msg37920.html
Best,
a.y
On Mon, 9 Nov 2015, Douglas Merkitch wrote:
Hey D,
I also had the same error in the same
Hi Laura - It appears that you're using a different configuration file
than the one you attached. To use Laura.txt, you should pass it as the
argument to the "-c" option (instead of
/scratch/lm618/tutorial_data/diffusion_tutorial).
Best,
a.y
On Sun, 8 Nov 2015, L. Moreno-Lopez wrote:
> Dear
Hi Amanda - These are probability distributions, so this has to do with
how you threshold them. When you use the -tv option in freeview to open
the merged file with all tracts, each of them is thresholded at 20% of its
maximum. When you open one of them as a plain volume, freeview doesn't do
Hi Noa - If you're still having this issue, please send the complete
trac-all.log file and your configuration file. It's impossible to guess
what goes wrong without seeing the full output.
Best,
a.y
On Fri, 30 Oct 2015, Golan, Noa wrote:
> Hi,
> I am currently analyzing DTI data and I am
Hi John - This is a probabilistic tractography method, so it draws samples
from the probability distribution of the particular tract, and then adds
up these sample streamlines to estimate the probability distribution. The
number that you see is the number of sample streamlines. It's a
Sorry Douglas I didn't well understand what you mean. Did you mean that
results from beta distribution aren't valuable ?
Best regards,
Matthieu
Le 15 déc. 2015 19:24, "Douglas N Greve" a
écrit :
> btw, we are still making changes to version 6 so don't assume that the
Thanks Douglas for the answer !
But isn't PVC design for better working in terms of results with v6_beta
than v5.3 ?
Best regards,
Matthieu
Le 15 déc. 2015 19:02, "Douglas N Greve" a
écrit :
> It is not subsegmented in 6.0 either:). When you run gtmseg, it will
>
Dear experts,
Could anyone answer to my questions below ?
Thanks !
Best regards,
Matthieu
2015-12-10 10:10 GMT+01:00 Matthieu Vanhoutte :
> Dear FS experts,
>
> 1) First Is it possible to use the partial volume correction provided in
> the v6 beta version of
Hi - how much memory do you have on your machine?
On Mon, Dec 14, 2015 at 10:54 AM, salvatoreandrea...@libero.it <
salvatoreandrea...@libero.it> wrote:
> Hi Freesurfer experts!
>
> I tried to run recon-all base for a longitudinal analysis on my data. But
> I get the following error:
>
>
>
>
Dear FS's experts,
I have tried the recon-all process on one subject with both FS v5.3 and
v6_beta.
Although subcortical structures seems to be better segmented in v6_beta, I
find that v6_beta over-segmented some other structures as cerebellum,
hippocampus, ...
I will attached in the FileDrop
Hello -
I am having a similar error to this post from 2011:
https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2011-July/019290.html
...but as far as I can tell, no answer was given to this post. Perhaps
I am just not seeing it?
I am taking some contrasts that I computed in volume space for
Your surfaces are out-of-synch. This is usually caused by recon-all
crashing or only running autorecon2 but not autorecon3
On 12/15/2015 05:31 PM, Ed Vessel wrote:
> Hello -
>
> I am having a similar error to this post from 2011:
>
On 12/15/2015 03:19 PM, Woo, Jonghye wrote:
> I am trying to a brodmann mask using PALS B12 atlas in fsaverage. I used the
> following command to create the volume from annotation file. I have two
> questions associated with it.
> mri_aparc2aseg --s my_subject --annot PALS_B12_Brodmann --o
>
Hi Freesurfer Mailing List,
I have just completed a GLM analysis with monte carlo correction and now
have my "cache.th13.abs.sig.cluster.mgh" files showing the significant
clusters for a specific contrast. I would now like to get mean cortical
thickness values for these ROIs in another
Follow the same procedures that you used to get the input (--y) to
mri_glmfit, then run
mri_segstats --seg cache.th13.abs.sig.cluster.mgh --i y.new.mgh
--excludeid 0 --avgwf avg.thickness.dat
The avg.thickness.dat will be a file with a row for each subject and a
column for each cluster
doug
Dear Doug,
I’ve got the table from this command: mis_info lh.PALS_B12_Brodmann.annot &
mis_info rh.PALS_B12_Brodmann.annot
(https://surfer.nmr.mgh.harvard.edu/fswiki/PALS_B12)
Thanks,
Jonghye
On Dec 15, 2015, at 6:23 PM, Douglas N Greve
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