Thanks, Doug for the binary.
A quick follow-up: what does the sign in either mri_glmfit-sim/mri_fdr
indicate? When I open F.mgh, the values are only positive and p-values
obtained from them has sign of +/-. My understanding is + indicates where
mean_A>mean_B and vice versa.
If for example, I am
We use mris_anatomical_stats. Is that what you mean?
On 10/08/2016 05:33 AM, zhang yue wrote:
>
> Hello FreeSurfer Developers,
>
> I’m attempting to exact the result of ‘stats’filedir, such as file
> ‘lh.aparc.stats’, I want to know you guys how to do this work. Your
> kind reply would be
11 and 50
11 Left-Caudate122 186 220 0
50 Right-Caudate 122 186 220 0
On 10/11/2016 10:56 AM, Raney, Talia L. wrote:
> Hi,
> Is there any way in FSFAST to use caudate as a seed for connectivity
> analysis? I was checking to see if it
On 10/08/2016 02:43 AM, Anders Hougaard wrote:
> Dear Freesurfers,
>
> Please see the attached image.
> It shows inflated fsaverage surface with gamma.mgh overlaid.
> Gamma.mgh is from one contrast of a standard group analysis of
> cortical thickness (two groups A and B, two contrasts A>B and
On 10/10/2016 08:20 AM, Qi Ting wrote:
> Dear Freesurfer experts,
>
> I am trying to do the group analysis, before this I tried to smooth the data
> with the different smoothing kernel. However, when I checked the output dir,
> it turned out that data were smoothed with a larger smoothing
If all you want to do is fdr correction you can use this program:
https://gate.nmr.mgh.harvard.edu/safelinks/greve/mri_fdr
On 10/10/2016 07:31 PM, Mishra, Virendra wrote:
>
> Hi, FreeSurfer Users.
>
> I am comparing cortical thickness of 2 groups controlled for certain
> variables of no
Thank you, Doug.
Regards
Virendra
-Original Message-
From: freesurfer-boun...@nmr.mgh.harvard.edu
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Douglas N Greve
Sent: Wednesday, October 12, 2016 11:45 AM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer]
Try adding --projfrac 0.5
On 10/12/2016 11:29 AM, Crawford, Anna wrote:
> I did:
>
> mri_vol2surf --src
> /mnt/netScratch/crawforda/BrainStem/study11074/S2sdt/segfs/mri/aparc+asegRMnn.mgz
> --out
> /mnt/netScratch/crawforda/BrainStem/study11074/S2sdt/segfs/surf/lh.aparc+asegRMnnS.mgh
>
Hello Experts,
I have a question regarding the outputs to the longitudinal processing
stream.
I ran my two participant's scans through the Cross, then created a Base and
two longitudinal runs. I am primarily interested in looking at ventricular
change over time. Other than the aseg output
Dear FreeSurfers,
I've been trying to run a longitudinal cortical thickness analysis in
FreeSurfer but unfortunately, so far, it has not worked.
After preprocessing the data following the instructions from the tutorial,
I tried running:
*long_mris_slopes --qdec
I used:
--src
/mnt/netScratch/crawforda/BrainStem/study11074/S2sdt/segfs/mri/aparc+asegRMpostcent2.mgz
--out
/mnt/netScratch/crawforda/BrainStem/study11074/S2sdt/segfs/surf/lh.aparc+asegRMpostcent2S.mgh
--regheader segfs --hemi lh --surf white --out_type mgh
>From the help file online, it
Hello,
I am about to start my project on hippocampal subfield analysis and realise
that this function is highly improved in FS version 6.0. I have run my data in
FS 5.3 before this came to my knowledge, and I am now wondering when version
6.0 will be released to the public so I can run them
Dear Synne,
There will hopefully be a beta release of 6.0 some time soon, but it’s hard to
tell exactly when (please see recent messages on the list by Bruce Fischl and
Zeke Kaufman about this topic).
Cheers,
/Eugenio
Juan Eugenio Iglesias
ERC Senior Research Fellow
Translational Imaging Group
Dear all,
using mris_topo_fixer instead of mris_fix_topology also results in a
segmentation fault. The command line used was:
mris_topo_fixer -mgz -warning -seed 1234 lh
INFO: assuming .mgz format
setting seed for random number genererator to 1234
reading input surface /surf/lh.orig...
Before
Hi Hinke
mri_em_register, mri_ca_label, mri_ca_register and mri_ca_normalize all
take -lh and -rh commands to indicate that only one hemisphere exists. Try
including them and see if it fixes things (you should be able to use expert
options for this). We have only used it for ex vivo analysis
if the surfaces are fine probably not, but you will want to recreate the
stats tables
cheers
Bruce
On Tue, 11 Oct 2016, firet...@web.de wrote:
Dear experts
after editing aseg the Segmentations wiki says one:
" could recreate the final surfaces with the command:
recon-all
Dear Doug,
Thank you very much for your advice!
We get to extract results for the volumes from a ".curv file encoded ROI" using
your recommended command lines (mri_binarize and mri_segstats ), but
unfortunately the results are much smaller (around 3 times) than when we
extract total gray
Hi Synne
we are (hopefully!) in the final stages of alpha testing and will release
a beta soon
cheers
Bruce
On Wed, 12 Oct 2016, Synne Aanes wrote:
Hello,
I am about to start my project on hippocampal subfield analysis and realise
that this function is highly improved in FS version
that seems ok, as I think the default is nearest neighbor. Can you
visualize the volume you created and see if the incorrect labels are in
it?
On Wed, 12 Oct 2016, Crawford, Anna wrote:
> I used:
>
> --src
>
Hi Falk
you are almost certainly running into a problem with some MAX number of
defects/faces or something. If you upload the subject dir I'll fix it
cheers
Bruce
On
Wed, 12 Oct 2016, Falk Lüsebrink wrote:
Dear all,
using mris_topo_fixer instead of mris_fix_topology also results in a
Dear all,
I’m having troubles getting a good Freesurfer output from a hemispherectomised
brain using recon-all. I was wondering whether there’s someone that has
experience with running Freesurfer on such an unusual brain?
The first couple of issues I bumped into were failures regarding the
The problem appears to be that the PET or the MRI (or both) have
incorrect voxel sizes (about 15%). You need to fix the problem. You can
get a decent registration using something like
mri_coreg --mov BS7_PET.lps.nii.gz --s 207118_FS_Filedrop --reg
dof9.wb.lta --dof 9 --no-ref-mask --ref
That seems to have worked and the regions are solid now.
Thank you!
Anna
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: Wednesday, October 12, 2016
Dear Douglas and Trisanna,
Thank you very much for your explanations.
I just would like to be sure of what I am doing since there is no example
on the wiki as complex as mine.
If I have the following classes :
Diagnosis : Patient or Control
Gender : Male or Female
Site : Site1 or Site2 or
On 10/11/2016 11:41 AM, kinson li wrote:
> /Hello, /
> /
> /
> /Question 1: I would like to conduct an Unpaired T-test group
> analysis, I have two group of people, Group A8 age is 8 and Group A9
> age is 9, and I to test the/ change in thickness with age. But I am
> little confusion about
The sign depends on how you set up the contrast. If you are using an
FSGD file and have two classes A and B and a contrast [+1 -1], then
positive indicates A>B. The F.mgh is the map of F values which are
unsigned. The gamma.mgh file will have the contrast values themselves
including sign. The
Thank you for that clarification,Doug.
VM
On Oct 12, 2016 12:09 PM, "Douglas N Greve"
wrote:
> The sign depends on how you set up the contrast. If you are using an
> FSGD file and have two classes A and B and a contrast [+1 -1], then
> positive indicates A>B. The
Hello All,
Quick question, I ran recon-all with the qcache option and after converting
the ?.thickness.fsaverage.mgh to an ascii text file via mri_convert I am
noticing some vertices have 0mm thickness and it varies, for example, one
subject had 53 vertices labeled as zeros while another had over
Thank you for your diagnosis Douglas. How could I get the voxel sizes right
from input nifti pet and mri data ?
Best regards,
Matthieu
Le 12 oct. 2016 10:05 PM, "Douglas N Greve" a
écrit :
> The problem appears to be that the PET or the MRI (or both) have
> incorrect
you need to go back to the source data. At some point someone set or
changed the voxel size to the wrong thing. This can sometimes happen in
PET as reconstruction into volumes is not all that standardizeed
On 10/12/2016 06:12 PM, Matthieu Vanhoutte wrote:
>
> Thank you for your diagnosis
Hello Freesurfer Experts,
I am using Freeview to visualize cortical thickness with the command
freeview -v mri/T1.mgz \ -f surf/lh.pial:overlay=lh.thickness
While the cortical thickness overlay is visible in the 3-Dimensional
display, I was wondering if it was possible to also view the cortical
Hi Sancgeetha
you can use mri_surf2vol to sample the thickness into the volume if you
want. The thickness file itself does not contain any topological
information - that is stored in the surface files (e.g. lh.pial)
cheers
Bruce
On Wed, 12
Oct 2016, Sancgeetha Kulaseharan wrote:
Hello
That is surface-based smoothing. the voxel size differences create
differences in volume-based smoothing (a partial volume effect). I don't
know of a good way to simulate volume-based PVC. This cannot be done in qdec
On 10/06/2016 06:36 PM, Martin Juneja wrote:
> Dear Dr. Greve,
>
> Thanks a
Hmmm, I don't know what could be going on. Can you send the command line
and all terminal output?
On 10/06/2016 10:37 PM, Trisanna Sprung-Much wrote:
> Hi Doug
>
> So the pixel values are 0 and 1 *in the original .mnc*. It seems that
> after performing mri_vol2surf they become 0 and 255, and
try this binary
https://gate.nmr.mgh.harvard.edu/safelinks/greve/mri_fdr
On 10/07/2016 04:11 PM, neuroimage analyst wrote:
>
> Hi,
>
> I was wondering if there is a way to perform fdr correction using
> command line in freesurfer without using matlab as mri_glmfit-sim only
> does bonferroni
Excellent, thanks!
2016-10-12 20:27 GMT+02:00 Douglas N Greve :
>
>
> On 10/08/2016 02:43 AM, Anders Hougaard wrote:
> > Dear Freesurfers,
> >
> > Please see the attached image.
> > It shows inflated fsaverage surface with gamma.mgh overlaid.
> > Gamma.mgh is from one
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