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Dear Freesurfer experts,
I would like to run surface based paired t test of PET data on surface. For
every subject I have visit pre treatment and post treatment. I tried to follow
the instructions here https://surfer.nmr.mgh.harvard.edu/fswiki/Paired
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Dear Freesurfer experts,
I have multiple PET volumetric images in MNI standard space. I can average (or
get the Tmean) of these images using fslmerge then fslmaths. I would like to do
something similar on surfaces images.
I registered the images from
this command to
fit PET data
mris_preproc --target fsaverage --hemi lh \
--meas thickness --out lh.paired-diff.thickness.mgh \
--fsgd pairs.fsgd --paired-diff
Thanks for any help!
John
‐‐‐ Original Message ‐‐‐
On Tuesday, November 20, 2018 6:34 PM, john Anderson
wrote:
> Dear Fr
how can I modify this command
> to fit PET data
>
> mris_preproc --target fsaverage --hemi lh \
>--meas thickness --out lh.paired-diff.thickness.mgh \
>--fsgd pairs.fsgd --paired-diff
>
> Thanks for any help!
> John
>
> ‐‐‐ Original Message ‐‐‐
> On
eproc with --help to get examples
On 12/06/2018 12:31 PM, john Anderson wrote:
>
> External Email - Use Caution
>
> Hi Dr Greve,
>> I tried to follow this web page
>> https://surfer.nmr.mgh.harvard.edu/fswiki/PairedAnalysis
>> This tutorial seems to be
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Dear experts,
I have three groups:
- pre treatment (baseline)
- post treatment (follow-up after 6 month of the baseline visit)
- healthy controls.
The three groups have PET data. I ran surface based paired t test between pre
and post treatment. The a
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Dear FS experts,
For visualization purposes, is there any way to show the cerebellum and brain
stem regions (similar to the attached figure), this figure was published used
CONN toolbox but I am not sure how they were able to map functional data in
b
with mris_smooth and load them into freeview.
Shouldn't be too hard.
cheers
Bruce
On Thu, 10 Jan 2019, john Anderson
wrote:
‐‐‐ Original Message ‐‐‐
On Thursday, January 10, 2019 7:40 AM, john Anderson
wrote:
> Dear FS experts,
> For visualization purposes, is there any
.mgs with fsaverage I believe. You can just
> tesselate that.
>
> cheers
> Bruce
> On Thu, 10 Jan 2019, john Anderson wrote:
>
> > External Email - Use Caution
> > Hi Dr Bruce, I highly appreciate your guidance.
> > I would like to load the cerebellum and brain
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Dear FS experts,
I resampled PET images for multiple subjects I used mri_vol2surfe to move these
images onto fsaverage, not I have for every subject lh.PET and rh.PET
How can I create the average of multiple surfaces. For example:
on the left hemisphe
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Dear FS experts,
I have a statistical map from the output of a surface based analysis in
subcortical regions. This statistical map shows significant difference between
the groups in the cerebellum cortex.
I reconstructed the cerebellar surfaces using
commands to improve the topology of these structures?
Your guidance is appreciated,
John
Sent with ProtonMail Secure Email.
‐‐‐ Original Message ‐‐‐
On Thursday, January 10, 2019 1:37 PM, john Anderson
wrote:
> Ah! great!! thank you so much for the great help!!
> Have a good day,
topologically correct.
>
> cheers
> Bruce
>
>
> On Tue, 22 Jan 2019, john Anderson wrote:
‐‐‐ Original Message ‐‐‐
On Tuesday, January 22, 2019 7:36 AM, john Anderson
wrote:
> Hi Dr Bruce,
> I applied your recommendations and I was able to create surfaces to the
&
n specific structural surfaces such as cerebellum
and brain stem?
Thanks
John
Can you be more specific about how mri_vol2surf failed? Eg, command line,
terminal output, reason you think it did not work
On 1/21/19 10:47 AM, john Anderson wrote:
>
> External Email - Use Cautio
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Hi Dr Greve,
I would like to correct surface based analyses of PET data for multiple
comparisons. I ran group comparisons in three spaces. left and right
hemispheres and subcortical.
I used the method --cache in mri_glmfit-sim to correct the analyses
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Dear FS experts,
I ran surface based PET analysis on subcortical regions. Then corrected the
results for multiple comparisons using the method --grf in the command
mri_glmfit-sim.
I can visualize the output of multiple comparisons (i.e. the file
gr
n if it is the entire cerebellum as FS commands generally
require a hemisphere.
The run mri_vol2surf specifying --hemi lh --surf cerebellum
On 1/23/19 10:04 AM, john Anderson wrote:
>
> External Email - Use Caution
>
> Dear FS experts,
> I ran surface based PET analys
send the full terminal output?
On 1/24/19 4:56 PM, john Anderson wrote:
>
> External Email - Use Caution
>
> Hi Dr Greve, I appreciate your guidance very much.
>
> I followed your suggestion. I put lh.cerebellum in fsaverage and I ran
> mri_vol2surf.
> as follow
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Hi FS experts,
I would like to inquire about the command "dtrecon" in Freesurfer.
Is this command able to process multishell diffusion data? if not would you
recommend any method?
Thanks in advance
John___
F
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hi FS experts.
I would like to inquire about the command mri_ convert
I use this command to convert fMRI and PET 4D volumes from dicom format to
nifti.
Are there any flags that can be used in mri_convert command line to enable it
to extract a text fi
much!
John
you mean you want the acquisition times to do kinetic modeling? I don't have
anything to do that. Also, you should check to see whether your PET has
intensity scaling imbedded in the dicom as the v6 mri_convert does not handle
this properly.
On 2/20/19 11:44 AM, john
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Hi Dr Greve,
I would like to use petsurfet to do kinetic modeling (KM), the pipeline is
straightforward and easy to use. Thank you so much! I would appreciate any
clarifications relevant to my questions bellow:
1) I understand that the flag "--km-ref"
.ctab. Is there any way to let
--km-ref know that I want to do whole brain normalization without feeding a
very long list of numbers?
Thank you so much for help
John
On 2/22/19 7:58 AM, john Anderson wrote:
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Hi Dr Greve,
I would like to use petsurfet to d
this flag
represent regions of high binding affinity in patients or healthy controls or
it doesn't matter just regions known to have high binding. For example some
tracers show regions of high binding affinity on healthy scans as well as
patients scans.
On 2/22/19 11:43 AM, john
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Dear FS experts,
I would like to move PET image to MNI152. What is the correct command to do so.
I tried
mri_vol2vol --mov PET.nii.gz --s subjID --targ
$SUBJECTS_DIR/subjID/mri/orig.mga --regheader --o PET_T1.nii.gz
mni152reg --s subjID
then
mri_vol2
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Dear Freesurfer experts,
I processed DTI data using dt_recon, and I want to register FA images to
the standard MNI152 space. However, after running the command
mri_synthmorph fa.nii.gz template.nii.gz -o fa_in_MNI.nii.gz,
the registration is not accura
; Cheers,
> Malte
>
>
> From: freesurfer-boun...@nmr.mgh.harvard.edu <
> freesurfer-boun...@nmr.mgh.harvard.edu> on behalf of John Anderson <
> jb19790...@gmail.com>
> Sent: Friday, September 1, 2023 12:45
> To: Freesurfer sup
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assuming that all preprocessing steps, fsgd file and contrasts are correct,
the choice between doss and dods could explain some of the variability
you're seeing in your results. Consider running both models and possibly
additional validation to see whic
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- FreeSurfer 5.3 QA Tools
https://secure-web.cisco.com/1xhhgMhrQlSBmGkb8NMn06KLlNRaz3DnQ7vzdZdQzrqjoeDsU5-gpo8VaUCxtX79W2O5j9rC87MnVFoBXzpHmSrCDzkZXGGR7I_PmSZlic0yw_BJBu2NDNAuQxkdpXtMPVHqiMbinZ5ak8HWwws2ZWPYgfTlbVjDSje40bRgu0R5XIZ3hox3WQjltQwACheB5Jq32
3A*2F*2Fwww.yahoo.com__;JSUl!!NZvER7FxgEiBAiR_!q-NbuKT23td_9o4DVH6jwPBlnCTPblT-heTmAHOlh6z6ucR3zZIfrZ4zbIojHZWpC28OyCiJjDFgI-IJC6-Qp_YtDOe9CqExedn8dmq0OW4$>*
+98 914 526 9298
On Saturday, October 14, 2023 at 03:29:11 PM GM
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Dear FreeSurfer experts, I would like to know if there is a command in
FreeSurfer that can help me measure the distance (in voxels or mm) between
a lesion mask and the closest voxels in the ribbon after applying recon-all
to T1 images. Thanks for your a
appreciate your suggestions.
Thank you
John
On Mon, Nov 20, 2023 at 7:13 AM John Anderson wrote:
> Dear FreeSurfer experts, I would like to know if there is a command in
> FreeSurfer that can help me measure the distance (in voxels or mm) between
> a lesion mask and the closest voxels in t
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Dear experts,
this is the first time I have used Freesurfer. I am a clinician and I don't
have previous experience. I followed wiki instructions. I have a group of
T1 images. I need cortical thickness and cortical gray matter volume
measurements . I ran
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Dear Freesurfer,
I have a volumetric atlas in nifti format. I can open this atlas in
freeview. Using the Lookup Table>FreesurferColorLUT, I can see how
every label has a specific color. When I move the mouse cursor over an area
of this atlas. I can see
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You might consider the command wm-anat-snr to compute SNR
On Thu, Feb 9, 2023 at 10:38 AM Kumar, Avnish
wrote:
> You could also use these:
>
>1. For CNR you can use the mri_cnr tool:
>
> mri_cnr [options]
>
> For example:
>
> mri_cnr $SUBJECTS_
qrt(gray_var), sqrt(csf_var)
>
> label : read hemisphere labels from and
>
> -u, -?, -help : print usage information and quit
>
> -version : print software version information and quit.
>
> On Thu, Feb 9, 2023 at 3:46 PM John Anderson wrote:
>
>> Exte
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Dear Freesurfer community,
Please forgive me for the basic nature of my question.
I was wondering whether there is an argument that can be included in
mri_segstats to display the results in cubic centimeters (cm^3) instead of
cubic millimeters (mm^3). t
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Dear Freesurfer,
I have ASL DICOM data from a Siemens scanner in mosaic format.
For each subject, there are 64 DICOM files, which consist of both tags and
controls.
I would like to convert each individual DICOM into a separate NIfTI file or
a single 4D
rt those DICOMs? It will use dcm2niix to
> convert.
>
>
>
> Best,
>
>
>
> Yujing
>
>
>
> *From:* freesurfer-boun...@nmr.mgh.harvard.edu <
> freesurfer-boun...@nmr.mgh.harvard.edu> *On Behalf Of *John Anderson
> *Sent:* Wednesday, March 15, 2023
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Dear Dr Doug Greeve,
For each participant in my dataset, I have 8 mosaic volumes with 36 slices
each. I am trying to convert the DICOM files to Nifti format using the
mri_convert command in FreeSurfer version 7.3.2. However, the conversion
process fails
e a NIfTI image with multiple volumes as expected by using the
mri_convert command with the --nslices-override argument, but I'm not sure
if I'm using it correctly.
On Mon, Mar 27, 2023 at 11:19 AM Douglas N. Greve
wrote:
> Can you try it with --dcm2niix ?
>
> On
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Hello Freesurfer,
Currently, I am using the Petsurfer manual, which is easily understandable
and clear. Nonetheless, I have a question regarding the "mri_glmfit" step.
As far as I know, this command is used to correct data for multiple
comparisons among
rect for multiple comparisons. For ROI-based
> analyses, you can use bonferroni or FDR. For maps you can use
> mri_glmfit-sim.
>
> On 4/4/2023 4:53 PM, John Anderson wrote:
>
> External Email - Use Caution
> Hello Freesurfer,
> Currently, I am using the Petsurf
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Dear experts,
I have been using the mri_normalize in FSv7.3.2 to standardize the
intensity of FLAIR images , and I've observed that increasing the sigma
parameter up to 25 is effective in improving the quality of the normalized
images for noisy datasets
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Dear experts,
I have been using the mri_normalize in FSv7.3.2 to standardize the
intensity of FLAIR images , and I've observed that increasing the sigma
parameter up to 25 is effective in improving the quality of the normalized
images for noisy datasets
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Let's say the red spot is overlay.nii.gz
1) convert aparc+aseg from mgz to nii.gz using:
mri_convert aparc+aseg.mgz aparc+aseg.nii.gz
2) create mask between overlay and the atlas using fslmaths:
fslmaths aparc+aseg.nii.gz -mas overlay.nii.gz overlay_ove
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