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Dear FreeSurfer experts,
I try to explore the Gyrification Index of both hemispheres in a population.
For this I computed the LGI using the Freesurfer pipeline and used the command
suggested in previous mails:
mri_segstats --slabel subject lh $SUBJE
External Email - Use Caution
Dear FS experts,
We are currently exploring the Infant Freesurfer pipeline for surface based
analysis in our cohort. The generated surfaces seem reasonable, but now we are
wondering, how to proceed. To our understanding, by looking at the recon-all
//dmri/xfms/anatorig2diff.bbr.dat
--o /mri/dtifit_MD_registered.nii.gz
Thanks a lot
Celine
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The information in this e-mail is intended
Hi Anastasia and Tracula experts,
We are running a new set of tracula analysis from Bay 6 and are
wondering how do we define the number of echo spacing in the dmrirc
file. Is it a number that we get from the header of the field map
dicoms?
set echospacing = ...
Thanks a lot
Celine
--
Celine
the recon
directory, they are aligned althouth they don't have the same format (I am
always confused about that...)
Celine
>
> Oh, I see you do not have a recon for your high res volume. Could you try
> the below mri_vol2vol command with an additional -lta flag that has the
> t
Thank you Lilla for the suggestion.
You mean that I should run mri_cvs_register on the high res volume, is
that correct? In that case, how can I specify the input volume? I did not
find in the --help a way to specify manually the file to be registered,
just the subject id.
Thank you again
Celine
g freeview, they are not
registered (while the output of mri_cvs_register for that subject was
perfectly registered to the template).
Would you have an advice to help me on that?
Many thanks
Celine
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between 2 sections along one tract?
Thank you
Celine
--
Celine Louapre, MD-PhD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH
Building 149, Room 2301
13th Street
Charlestown, MA 02129
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sulci were already with a value of 0
in the WM.mgz, it can be helpful to change it to 1.
Thanks a lot for the tips (and also the visualization tip, super helpful :-)
Celine
> Hi Celine,
>
> I took a look at you data, and made some edits to the wm that help to push
> out the surfaces to
Hi everyone
I don't know if someone had the chance to look at the data we uploaded
for advice to edit the recons (see below).
Thank you so much
Celine
On Fri, 2015-01-16 at 11:43 -0500, Celine Louapre wrote:
> Thanks Bruce
> The aseg is correct, no ventricule labeled there (I was u
n
the left hemisphere was already present after autorecon2.
I have uploaded the recon directory there:
https://www.nmr.mgh.harvard.edu/facility/filedrop/showgroup/32464/1/2115a25100be43906c26359fbbd1ed08
Thank you again :-)
Celine
On Fri, 2015-01-16 at 11:03 -0500, Bruce Fischl wrote:
> H
ime I
couldn't have it work correctly. Would you have a clue to help me on that?
I can put the data in some folders if you want to take a look at the
entire volumes.
Thanks for your help
Celine
--
Celine Louapre, MD-PhD
Research Fellow at Massachusetts General Hospital
Department of Radi
way to work around, or should I just try to do it only
from non pvr glm analyses?
Celine
>
> X and C have different numbers of columns. What was your mri_glmfit
> command line? If you used a --pvr, then the pcc script will not work.
> doug
>
> On 09/22/2014 01:21 PM, Ce
fast_glm_pcc (line 28)
Xc = X*C';
And also I found this info in the script WARNING: X must have a column of
1s or both X and y must have been demeaned before the glm.
But I am not sure about what it means. Attached are Xg.dat and C.dat files.
Thanks again for your help
Celine
>
>
Indeed I ran mri_glmfit-sim. What file is the output of mri_segstat?
The cache.th13.abs.sig.ocn.annot contains the significant clusters it that
correct? So to get individual mean values from cluster 1 for example where
should I look?
Thanks!
Celine
>
> Have you run mri_glmfit-sim? It will
Celine
On 05/31/2012 06:09 AM, Knut J Bjuland wrote:
> Hi
>
> I am trying to calculate correlation coefficient using freesurfer GLM
> for associations between volumes and IQ. I found this ealier answar,
> but the matlab script but the link appear to be dead.
>
> http:/
Hi
I just find out how to launch the command, it is in the terminal where
tksurfer is running, after the % sign. (I didn't understand what the tcl
window was meaning)
Best
Celine
> Hi
> I am sorry if my question is really basic, but I am choosing the seeds for
> fsfast resting stat
vertex number on fsaverage surface, so that I can build the
corresponding label that I could use for the fcseed-sess command.
I found this previous email, and there seem to be a command to do that but
I don't know how to launch this command select_talairach_point
Thank you very much
C
Best
Celine
--
Celine Louapre, MD-PhD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH
Building 149, Room 2301
13th Street
Charlestown, MA 02129
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oh yes I see, I have renamed the dpath/${TRACT[$num_tract]} directories to
have a backup, so the name is not correct anymore. Actually I didn't need
to do that, I can just set a different name for the outputs
pathpathstats.byvoxel.txt and pathstats.overall.txt
Thanks
Celine
>
> Hi Ce
TS_3T[$subj]}/dpath/fmajor_PP_avg33_mni_bbr
ERROR: fio_pushd:
${PATH_3T}${SUBJECTS_3T[$subj]}/dpath/fmajor_PP_avg33_mni_bbr
ERROR: must specify at least one type of output
Would you have some idea about that?
Thank you very much
Celine
>
> Hi Celine - That's an interesting question.
from whom the 2
spaces are really different, it is easier to figure out about
registration). So anatorig2diff means diffusion space to anat space?
Thanks a lot
Celine
>
> I concur. If this is the lowb.nii.gz from trac-all and brainmask.mgz from
> recon-all, they will be in their respecti
e
DTI images, then my sampling is probably wrong too?
The tracts are correctly displayed on the native DTI images, but if I want
to display them on the anat space then it is not correct.
Thanks for your help
Celine
--
Celine Louapre, MD-PhD
Research Fellow at Massachusetts General Hospital
Departme
't
it?
>
>
>
> doug
>
>
>
>
>
> On 2/17/14 10:41 PM, Celine Louapre wrote:
>> The lesion_vol2vol volume is still not correctly overlapping the DTI.
>>
>> The only command that didn't give me registration issue is mri_convert
>> wh
olate and then binarize the mask was one possible option). I can
show you the results tomorrow if you prefer
Celine
>
> what does it look like if you run
>
> tkmedit -f lowb.nii.gz -ov lesion_WM_vol2vol.nii.gz -fminmax .5 1
>
>
>
> On 2/17/14 10:00 PM, Celine Louapre wrote
freeview
maybe? or actually all the volumes are already on the recons space so
maybe I should not use any registration matrix?
Celine
>
> oops, sorry! That command looks like it is correct. Can you say more
> about what is going wrong? How are you determining that something is
> going w
threshold
parameter but it does not solve the problem of the registration file?
also mri_convert
And eventually I also saw this command:
mri_mask but I guess that the mask volume needs to be in the same
dimension as the diffusion space?
Thanks a lot
Best
Celine
--
Celine Louapre, MD-PhD
Research
lesion_WM_vol2vol.nii.gz in freeview, the voxel sieze
is the same as the DTI images, but the lesions are not at the same place.
That is why I thought I had picked the wrong registration file...?
Celine
>
> Hi Celine - If the lesion mask is already in the space of the freesurfer
> recon, you ca
t the registration file to
use.
And eventually I also saw this command:
mri_mask but I guess that the mask volume needs to be in the same
dimension than the diffusion space?
Thanks a lot in advance for your help
Best
Celine
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in the formula, I would not be able to
calculate the motion factor for this parameter because median, upper and
lower quartile are all 0, is that correct (it would make (x-0/0-0))?
Thanks for your help
Celine
> Hi Anastasia and freesurfer experts,
> I am trying to get DTI values along the tra
exclusion of the lesion? (I guess
the last step of trac-all -path could be applied to DTI maps that were
masked by the lesions?)
I would like to keep the advantage of having the DTI weighted metrics in
particular.
Thanks a lot for your help!
Celine
--
Celine Louapre, MD-PhD,
Research Fellow at
Oh so we don't report the significance itself? because for example if we
have a small cluster but highly significant, does the cluster-wise
correction p value take it into account? (compared to a large cluster but
with lower significance). I may not have completely got this.
Thanks Doug
C
?
Thanks for advices
Celine
--
Celine Louapre, MD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH
Building 149, Room 2301
13th Street
Charlestown, MA 02129
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Celine
> Yes thanks so much, it worked very fine
> Celine
>
>>
>> In that case, I think you will want to change the design at each voxel
>> based on which subjects are present. I have not tried to do this with
>> pvr, but there is no reason it should not work. To d
Yes thanks so much, it worked very fine
Celine
>
> In that case, I think you will want to change the design at each voxel
> based on which subjects are present. I have not tried to do this with
> pvr, but there is no reason it should not work. To do this, create a
> binary volume
--pune flag, but I am not sure if it is the one to use.
Thanks
Celine
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depth?
And the 2nd question would be: is the contrast correct to test the
correlation between the 2 surfaces at each vertex?
Thanks a lot for your help
Celine
PS: here is the terminal output:
gdfReadHeader: reading ms_age_gender.fsgd
INFO: DeMeanFlag keyword not found, DeMeaning will NOT be d
couldn't find how to
do it but maybe I didn't choose the correct keywords in the archives!
Thanks so much for you help!
CĂ©line
--
Celine Louapre, MD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH
Building 149, Room 2301
13th Street
Charlestown,
Thank you.
For the contrast, if I don't enter any other regressor, then it will be 1 -1?
Celine
> Hi Celine, use mri_glmfit with the --pvr option (pvr = per-vertex
> regressor)
> doug
>
>
> On 10/30/2013 10:20 AM, cel...@nmr.mgh.harvard.edu wrote:
>> Hi freesurfer tea
region level? From what I understood, when we use glmfit, the regressors
that we can put are single values like age, group, cognitive testing etc,
but maybe not an entire surface?
Thanks a lot
Best,
Celine
--
Celine Louapre, MD
Research Fellow at Massachusetts General Hospital
Department of
obtain an ROI that
is consistent among subjects or is is possible that I would get a very
thin CST in some subjects, or a very wide cst for example?
Thanks for your help
Celine
--
Celine Louapre, MD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH
Building 149, Room
Hi Bruce
The aseg is correctly labeled as regards right and left GM cortex, but
definitely some voxels are belonging to both hemisphere. The filled.mgz is
fine too. Should we delete from aseg the voxels that are at the border
between the lh and rh?
Thanks
Celine
> Hi Celine
>
> is
ggest?
> Thanks
> Celine
>
> --
> Celine Louapre, MD
> Research Fellow at Massachusetts General Hospital
> Department of Radiology, MGH
>
> Building 149, Room 2301
> 13th Street
> Charlestown, MA 02129
> ___
> Freesurfer
Hi Freesurfer team
I am wondering if there would be a way to improve surfaces on the medial
wall, not for the measurement of cortical thickness, but also for laminar
analysis in the cortex. We would need them to be accurate even for the
medial wall. What would you suggest?
Thanks
Celine
aking a weighted metrics would be
possible in order to remove values that are a bit far from the highest
probability of the tract.
Thanks a lot!
Celine
>
> Hi Celine - Since 5.2, there are 2 types of measures in the
> pathstats.byvoxel.txt file: The value at every point along the trajector
your help.
Celine
--
Celine Louapre, MD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH
Building 149, Room 2301
13th Street
Charlestown, MA 02129
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Hi again
I am sorry I found out that I needed to delete this file IsRunning.trac
and then it works again.
Sorry for the inconvenience
Best
Celine
> Hi Freesurfer team
> I am very new with tracula so my problem might be very obvious.
>
> I previously run trac-all -prep on a patient a
file,
but for the whole width of the tract?
If not, do you see a way to sample the value of the diffusion metrics on a
certain tract starting from the cortex (like with projfrac or projdist
with the WM surface)?
Thanks very much for your help
Celine
--
Celine Louapre, MD
Research Fellow at
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