Hi Freesurfers,
I want to create volume 6.25 X 6.25 X 7.5 in this position in scanner space ( x=48, y= 48, z=10)
I used the following command line to create the volume but I don't know how to choose it is position in scanner space.
mri_volsynth --dim 6.25 6.25 7.5 0 --o voxel.nii
I ha
,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent: Monday, August 31, 2015 at 11:30 AM
From: "Douglas Greve"
To: freesurfer@nmr.mgh.h
Thank you!
Actually when I run mri_volsynth --help
I can't find --revol. is it the same flag --res?
also what is the relationship between --dim and --volres?
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinma
Perfect!
Thank you very much for your help.
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent: Monday, August 31, 2015 at 4:30 PM
?)
3. If there is any atlas that can separate the outer and deep white matter then do the segmentation depending on this new atlas.
Thanks in advance for any suggestion,
John
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419
s and the outer white matter labels ?)
3. If there is any atlas that can separate the outer and deep white matter then running recon-all depending on this new atlas.
Thanks in advance for any suggestion.
John
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences
ce that can help. The number of the parcellate is very big and for the purposes of publication I need a reference to divide them.
Any help is highly appreciated.
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Bo
labels for one of my subjects.
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent: Monday, September 07, 2015 at 1:02 PM
From: &
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 4and the white matter volume generated by other methods like using fslstats19 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603
nii.gz -m >This command will output the mean FA for the probabilistic distribution map. How can I weight this FA value using the previous command line?
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Ha
separatly? Is there any tool in Freesurfer that can help? Thanks for any suggestion.
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Dear FS Experts,
Are there any tools in Freesurfer or Matlab scripts that can help to break down a 3D volume ( created using mri_volsynth) to a multiple equal sub volumes ( like the attached figure )
Thanks in a dvance for any suggestion!
John Anderson
Senior Research Associate
Psychological
ar subvolumes.
cheers
Bruce
On Wed, 8 Jun 2016, John Anderson wrote:
> Dear FS Experts,
> Are there any tools in Freesurfer or Matlab scripts that can help to break
> down a 3D volume ( created using mri_volsynth) to a multiple equal sub
> volumes ( like the attached figure )
> Than
g box, and (dx,dy,dz) is the extent of it (in
voxels)
On Wed, 8 Jun 2016, John
Anderson wrote:
> Hi Bruce,
> Thank you for the quick response. it is really highly appreciated!
> I have 3D mask in the form of nifti file and it has the shape of large
> square( the black big square in my
Hi FS experts,
I have T1 images with low quality (noise and artifacts). I am wondering if smoothing these images, before runing the command "Recon-all", can help to improve the segmentation and parcellation process for these images.
Thanks for any advice!
Bests,
John
___
any rules that I need to follow when I choose my method to correct the results for multiple comparison ( i.e FDR or montecarlo)
Thank you very much for any comment!
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207
montecarlo) . Which method do you recommend to correct the results of cortical thickness analysis? Are there any rules that I need to follow when I choose my method to correct the results for multiple comparison ( i.e FDR or montecarlo)
Thank you very much for any comment!
John Anderson
Senior
montecarlo) . Which method do you recommend to correct the results of cortical thickness analysis? Are there any rules that I need to follow when I choose my method to correct the results for multiple comparison ( i.e FDR or montecarlo)
Thank you very much for any comment!
John Anderson
Senior
thickness analysis? Are there any rules that I need to follow when I choose my method to correct the results for multiple comparison ( i.e FDR or montecarlo)
Thank you very much for any comment!
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College
R and mote carlo simulation? Does "empirical " means to follow the results that support the hypothesis?
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9
and the file ribbon.mgz the output of recon-all to create a a mask for global gray matter
Thank you for any advice!
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603
Hello, FS experts,
I am trying to use QA tool:
I ran the following command
recon_checker -snaps-only -s-file subjects.txt
The script output the following:
X11 connection rejected because of wrong authentication.
GLUT: Fatal Error in tkmedit.bin: could not open display: localhost:12.0
X1
Dear FS experts,
I want to know what is the output (volume or surface) of the following scripts.
(The input is file.nii.gz which is a volumetric )
1. spmregister --s subj --mov file.nii.gz --reg reg.dat --o file_t1.mgh #is the output file (file_t1.mgh) is a volume or a surface
2. mris_prepr
Dear experts,
I ran surface based analysis using PET maps. As the following:
spmregister --s subj --mov pet.nii --reg reg.dat --out pet_t1.mgh
mris_preproc --target fsaverage --hemi lh --iv subj1/ubject1_pet.nii subject1/pet/pet_2_T1_register.dat . --projfrac 0.5 --out lh.mgh
mri_surf2sur
Hi FS experts,
I wanted to inquire if there are any tools in FS that can help to de-identify DICOMs?
Thank you for any comment
John
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https://mail.nmr.mgh.harvard.edu/mailman/listinfo/free
On 10/19/2016 05:09 PM, John Anderson wrote:
> Dear experts,
> I ran surface based analysis using PET maps. As the following:
> spmregister --s subj --mov pet.nii --reg reg.dat --out pet_t1.mgh
> mris_preproc --target fsaverage --hemi lh --iv subj1/ubject1_pet.nii subject1/pet/pet_2_
--cwpvalthresh .0166
All the bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent: Thursday, October 20, 2016 at 9:20 PM
From: "
y want to use permutation if your group analysis allows it.
On 10/23/16 10:25 AM, John Anderson wrote:
Thank you very much Doug,
The codes worked very well. I was using the wrong command to correct the data.
My command was
mri_glmfit-sim --glmdir subc.glmdir --cache 1.3 pos --cwp 0
than never:). But in the end, you probably want to use permutation if your group analysis allows it.
On 10/23/16 10:25 AM, John Anderson wrote:
Thank you very much Doug,
The codes worked very well. I was using the wrong command to correct the data.
My command was
mri_glmfit-sim --glmdir s
Dear Freesurfer experts,
I ran the following command on a T1 image
recon-all -subjid 089 -all -qcache
and I got the following error message:
talairach_afd -T 0.005 -xfm transforms/talairach.xfm
ERROR: talairach_afd: Talairach Transform: transforms/talairach.xfm ***FAILED*** (p=0.0344
I'm afraid that it
might left-right rev the volume. In either case, you can manually check
the tal reg to see if it looks ok.
On 11/11/2016 03:56 PM, John Anderson wrote:
> Thank you Doug,
> Attched are to snapshots
> #1 is for the original T1 ( i.e. as aquired) and this image wh
Dear Freesurfer experts,
I want to analyze DTI data using the command
dt_recon --i dwi.nii --b bvals bvecs --s subj1 --o /subj1
Under Fressurfer 5.3, the analysis fail showing this error message:
nifti1Read(): unsupported slice timing pattern 5 in /data/anaconda/mesgp/dtrecon3/subj1/dwi.nii
Thank you very much Doug. You are so awsome :)
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent: Monday, November 14, 2016 at 1
"John Anderson"
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] Fw: Re: surface based analysis for subcortical structures
Thank you very much Doug. You are so awsome :)
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College,
Dear FS experts,
I am working on surface based analysis using freesurfer. I want to inquire about the flag "projfrac" in the command "mris_preproc"
I ran voxel wise analysis including the same subjects. I found differnce between the groups in areas close to the corpus callosum. I want to get t
cortical GM. If you mean in GM near the CC, then the analysis is appropriate. The projfrac parameter sets the sampling location between the white and pial surfaces where 0.5 means half way.
On 1/10/17 8:07 AM, John Anderson wrote:
Dear FS experts,
I am working on surface based analysis using frees
PM
From: "Douglas N Greve"
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] surface based analysis (projfrac)
yes, that is correct. However, understand that there might only be a
difference of 1mm between those two locations, so it could easily be a
partial volume effect
On
d analysis (projfrac)
On 01/12/2017 05:20 PM, John Anderson wrote:
> Thank you very much Doug and thank you for briniging the issue of
> "partial volume effect " to my attention. Kindly, I have one last
> question.
> I found in wiki that the default values for projfrc value
Re: [Freesurfer] surface based analysis (projfrac)
What is the modality you are looking at?
On 01/13/2017 02:08 PM, John Anderson wrote:
> Thank you very much Doug,
> Kindly, do you suggest me any steps to avoid patial volume effects in
> surface based analyses ?
> Best,
> John
> *Se
@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] surface based analysis (projfrac)
These differences are hard to track down because they are so subtle.
You may want to use our PET module, which includes PVC
http://surfer.nmr.mgh.harvard.edu/fswiki/PetSurfer
On 01/13/2017 03:10 PM, John Anderson wrot
words the number of distinct tracts that pass through the manually constructed sets of ROIs) ?
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603
Dear experts,
I want to run recon-all on a stripped brains ( T1 images after applying bet tool).
Do I need to add any flags to the command recon -all -all subjid
Bests,
John
___
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Freesurfer@nmr.mgh.harvard.edu
https
Dear Experts,
Is there any tool in Freesurfer that can help to evaluate the SNR for T1 MPRAGE images directly ( i.e script). If not knidly can any help me to figure out the best way to dao it.
I highly appreciate your help!
Bests,
John Anderson
Senior Research Associate
Psychological and
Dear Jürgen
This really helps!
I highly appreciate your input on this.
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent
ted by the binary "mri_cnr"?
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
Sent: Monday, October 19, 2015 at 8:36 AM
From
Hi All,
Thank you very much for your comments!
Is it advisable to include SNR as a covariate when we use Qdec to run the final statistics on volumetrics, surfaces and cortical thickness?
Does it make sence ?
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences
ality of the image is fine. Also calculating the SNR, CNR want help a lot!
any suggestions?
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646
Dear FS experts,
I want to inquire if there is any script in Freesurfer that can help to calculate the head circumference from MPRAGE ?
Thanks for any advice!
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman
Dear FS experts,
I want to inquire if there is any tool or method in Freesurfer that can help to calculate the head circumference from MPRAGE ?
Thanks for any advice!
Bests,
John
___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
htt
Hi Doug and Bruce,
Kindly, I have question regarding the difference between voxel based ( VBM/ FSL pipeline) and surface based analysis ( Freesurfer ).
I have two groups of subjects Group A and Group B
I ran morphometric analysis in Freesurfer ( recon-all then manual edits) to check the differenc
differnt? (i.e In norm.mgz the voxel dimentions are equal while in orig.mgz it is not)?
3. Is it correct if I convert norm.mgz to "nii" file and use it as a "T1" for further processing?
bests,
John Anderson
___
Freesurfer
3.5 I use reversed matrix to move the mask to FA map.
The problem in this approach is the voxel dimentions ( between the mask and the T1). Can I use norm.mgz ( which has the same voxel dimentions of the mask ) istead of T1 to do the previous steps?
Bests,
John Anderson
Senior
freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] recon-all
On 11/5/15 8:37 AM, John Anderson wrote:
Thanks a lot Doug!
Kindly ...
1. What do you mean by intensity normalized?
Removing non-biological intensity fluctuations such as darkening/brightening from multiple head coil
correction for multiple comparisons is cluster-based. Each cluster
gets a single number. In the display, all the vertices get that same number.
On 12/18/2015 03:17 PM, John Anderson wrote:
> Hi Freesurfer experts,
> I am using Qdec in Freesurfer 5.3 to do some cortical thickness
> comp
andard variance
(so take the square root)
On 12/21/2015 02:08 PM, John Anderson wrote:
> Thanks you very much Doug,
> Please one more question. Is there any way in Qdec to get the stamdard
> error (SE) ?
> Bests,
> John
> *Sent:* Monday, December 21, 2015 at 11:
nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] Qdec visualization
it helps to see the error msg, but my guess is that you need to specify
an mgh file, not a txt file. This will give you the voxel-wise stderr,
not a standard error for the cluster (which does not make sense)
On 12/21/2015 02:38 PM, John An
upport!
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Moore Hall, Hinman Box 6207, Hanover, NH 03755
Phone: +1 (603) 646-9834
Fax: +1 (603) 646-1419
___
Freesurfer mailing list
Freesurfer
h esame order of the groups in qdec tables?
4. The BW in this command was chosen 0.7 and the default is 0.6 how can I choose this number correctly?
Thanks for your support!
Bests,
John Anderson
Senior Research Associate
Psychological and Brain Sciences Dept.
Dartmouth College, 419 Mo
Dear Freesurfer experts,
I want to inquire if there is any tool in Freesurfer that can help to convert the p files ( raw data generated by GE scanner ) to DICOMs
Thanks for any advice!
Bests,
John
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Freesurfer@nmr.m
Hi Experts,
I have statistical map in MNI space and I want to view it using tksurfer how can i transform this map to a surface ?
Bests,
John
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Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/list
stical map in MNI to surface
If it is in mni152 space, then you can run recon-all on the mni152 T1
map, then use mri_vol2surf with --regheader to map the volume tothe
surface, then use tksurfer or freeview to view the resulting map
On 01/08/2016 12:49 PM, John Anderson wrote:
> Hi Expe
upport list"
Subject: Re: [Freesurfer] transform statistical map in MNI to surface
you wouldn't run it on the stats map - you would run it on the
T1-weighted MNI152 volume
On Fri, 8 Jan 2016, John Anderson wrote:
> Thanks you Doug,
> Kindly how can I run recon-all on the statistica
Dear experts,
I am wondering if there is any way to divide the cortical thickness parcellates in the atlas "?h.aparc.annot" by lobe. I highly appreciate any suggestion.
Bests,
John
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Freesurfer@nmr.mgh.harvard.edu
https://
cortical thickness by lobe?
Sent: Wednesday, January 13, 2016 at 12:41 PM
From: "Douglas N Greve"
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] Cortical thickness parcellates
Try mris_divide_parcellation
On 01/13/2016 12:18 PM, John Anderson wrote:
> Dear ex
Dear Dr Martin,
I have longitudinal database for subjects scanned multiple times. I want to study the changes in cortical thickness over time. I prepared my longitudinal table ( column#1 fsid column#2 fsid-base column#3 group column#4 bilateral motor cortex thickness column#5 time (years) column#
Dear experts,
I wanted to register T1 mprage image to the standard space MNI152. The output of FLIRT at dof 12 is not effective. How can I get better results using bbregister? What are the commands that I need to use ?
thanks for any help!
John
__
1 image (NOT your map), then use
mri_vol2surf to map the stats map onto the resulting surfaces. Note that
this won't give you great results as a bunch of your clusters will
probably not be near the cortical surface (since in general subjects
cortices don't align well in MNI 152)
cheers
B
Hi Dr Martin,
I have two groups of patients and one group of controls.
The patients scanned multiple times but the number of time points is different between the subjects.
The controls have only one time point.
I aim to :
1. I wanted to study the changes in cortical thickness over time in e
t, Martin
On Jan 28, 2016, at 12:23 PM, John Anderson <j.ander...@publicist.com> wrote:
Hi Dr Martin,
I have two groups of patients and one group of controls.
The patients scanned multiple times but the number of time points is different between the subjects.
The controls have
ditional co-variates in your LME model.
Best, Martin
On Jan 28, 2016, at 1:12 PM, John Anderson <j.ander...@publicist.com> wrote:
Thanks a lot D martin for your quick answer.
Regarding my patients I have two groups but the subject in every group have differnt time points. i.e Gr
Dear FS experts,
I am using Qdec to study the differnce in cortical thicnkess between two groups.
Qdec is running a GLM analysis. This will output a statistical map (sig.mgh) for the differnce between the groups in cortical thicnkess.
How can I extract the numbers of cortical thickness for every
freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] Qdec-statistical map
not sure what you mean. the statistical map will have a single value,
not a value for each subject
On 03/03/2016 12:31 PM, John Anderson wrote:
> Dear FS experts,
> I am using Qdec to study the differnce in cortical thicnke
a row for each
frame in y.mgh (ie, each subject) and a column for each cluster
On 03/03/2016 12:43 PM, John Anderson wrote:
> Hi Doug,
> How can I use this statistical map ( e.g. as a mask) to calculate the
> mean cortical thickness only in the areas of significant differnce
> betw
Hi FS experts,
I am trying to run OSGM analysis between two groups using mri_glmfit as follow :
mri_glmfit --y lh_10mm.mgh --fsgd fsgd.dat --glmdir lh_10mm --surf fsaverage lh --osgm
it keep returning as:
ERROR: DOF = 0
my FSGD is as follow
GroupDescriptorFile 1
Title OSGM
Class group1
Hi FS experts,
How can ai do surface based analysis on FA maps.
In other wods:
I have 20 subjects( two groups 10/10) and FA map for every subject. How can I dtufy the differnce between the groups in FA on surface?
Best,
John
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Freesurfer mailing l
Hi experts,
I am trying to correct the results of groups analysis using mri_glmfit-sim
the command is :
mri_glmfit-sim --glmdir lh_10mm --cache 3 pos --cwpvalthresh .0166
I receive the follwoing error :
ERROR: cannot find /usr/local/freesurfer/stable6/average/mult-comp-cor/fsaverage/lh/cort
Hi FS experts,
I am trying to correct the results of groups analysis using mri_glmfit-sim
the command is :
mri_glmfit-sim --glmdir lh_10mm --cache 3 pos --cwpvalthresh .0166
I receive the follwoing error :
ERROR: cannot find /usr/local/freesurfer/stable6/average/mult-comp-cor/
Hi Doug,
I ran voxel based analysis in FSL to check the differnce in PET signal between two groups. The results are totally differnt than surface based analysis in Freesurfer. I this real or I am doing something wrong? I tried to do the same but using FA maps and also I got totally differnt resul
Hi Experts,
What is the meaning of this error as an output of the command mri_glmfit
Found 0 voxels in mask
ERROR: no voxels found in the mask
make sure at least one voxel has a non-zero value for each input
in other words what are therrors that can lead to such like error message
cluster is covering most of the brain, including precentral gyrus. The precentral gyrus ROI in the table file indicates that is where the peak of the cluster is and does not mean that the cluster is confined to that ROI
On 3/16/16 9:43 AM, John Anderson wrote:
Dear experts,
I am running into
Hi FS experts,
I am trying to use the folowing command:
mri_fwhm --i lh.mgh --auto-mask 0.2 --sum lh.fwhm5.sum --fwhm 5 --o lh_5mm.mgh
I keep receiving an error message as follow:
voxelvolume 1 mm3
Computing mask, relative threshold = 0.2, gmean = 0.501858, absthresh = 0.100372
Search re
Hi Dr Martin
I want to study the change in cortical thickness overtime in one group of subjects.
I have only one group of subjects who scanned multiple times ( two time points and more)
I followed the pipeline exactly as in wiki.
I want to inquire about X in this case . Is it supposed to be 1
03/21/2016 12:40 PM, John Anderson wrote:
Hi Dr Martin
I want to study the change in cortical thickness overtime in one group of subjects.
I have only one group of subjects who scanned multiple times ( two time points and more)
I followed the pipeline exactly as in wiki.
I want to inquire abo
Dear experts,
I want to use the atlas V1 to calculate PET signal for Brodman areas. How can I create this atlas in the form of “aseg.mgz” or ”wmparc.mgz” ( i.e all the BAs in one file) to feed it in the command “mri-segstat”?
Bests,
John
___
Freesur
uot;
Subject: Re: [Freesurfer] V1 Atlas ( brodman maps)
Hi John
recon-all should create lh.BA.annot and rh.BA.annot parcellations that
contain all the Brodmann areas we know how to label
cheers
Bruce
On Thu, 12 May 2016, John Anderson wrote:
> Dear experts,
> I want to use the atlas V
Dear Experts,
I want to calculate PET signal within each Brodman map! I will give an example: If I want to caclulate PET singal for every parcellate and segment in the brain I do the following:
bbregister --t1 --mov T1_MPRAGE.nii.gz --init-fsl --reg t1.reg.dat --s SUBJID
mri_vol2vo
Hello Freesurfers,
I am working on a PET surface based analysis between two groups. I did the following:
1. I concatentaed the PET images using the command "mris_preproce" and I got the file (lh.mgh) for left hemisphere and (rh.mgh) for right hemisphere.
2. I smoothed "lh.mgh and rh.mgh) using
. You'll have to
build your own. here are the instructions:
http://surfer.nmr.mgh.harvard.edu/fswiki/BuildYourOwnMonteCarlo
On 01/26/2017 01:09 PM, John Anderson wrote:
> Hello Freesurfers,
> I am working on a PET surface based analysis between two groups. I did
> the following:
> 1.
Hi FS experts,
I want to register T1 image to its freesurfer space (i.e. wmparc.mgz) using the command
bbregister --t1 --mov T1.nii --init-fsl --reg t1.reg.dat --s subj
do I need to apply brain extraction tools before this step or bb register can accept non-brain extracted images?
Best,
e. I guess it might make the initialization less robust, not sure, but
I expect it works pretty well without doing brain extraction
cheers
Bruce
On Fri, 10 Feb 2017, John Anderson wrote:
> Hi FS experts,
> I want to register T1 image to its freesurfer space (i.e. wmparc.mgz) using
> th
volume. I guess it might make the initialization less robust, not sure, but
I expect it works pretty well without doing brain extraction
cheers
Bruce
On Fri, 10 Feb 2017, John Anderson wrote:
> Hi FS experts,
> I want to register T1 image to its freesurfer space (i.e. wmparc.mgz) using
>
Dear Freesurfer experts,
I have used the following commandline to generate the final statistics in my
analysis:
mri_segstats --seg aseg.mgz --ctab-default --i suvr.nii --mask mask.nii --sum
stats.dat
The final output of this command is (attached). Depedning on the anatomical
location of the ma
Dear Freesurfer experts,
I see that the tool "mri_coreg" has been implemented recently in Free Surfer 6
and I really wanted to know what are the differences between the registration
tools "bbregister", " spmregister" and "mri_coreg"! Kindly:
1. Are these tools similar? if not what are the differe
. bbregister uses the BBR cost function and is preferred
for all MRI. For registration to MNI space, we usually use mni152reg (a wrapper
around fsl's flirt)
On 2/25/17 8:49 AM, John Anderson wrote:
Dear Freesurfer experts,
I see that the tool "mri_coreg" has been implemen
Dear experts:
I have nifti file with 96 slices. I want to re-slice it to form nifti file with
200 slice. Are there any tools in Freesurfer that can help to achieve this?
Many thanks for any suggestion
John___
Freesurfer mailing list
Freesurfer@nmr.mgh.
Hi Freesurfer experts,
I followed "dt_recon" pipeline
https://surfer.nmr.mgh.harvard.edu/fswiki/dt_recon to analyze DTI data. The
analysis ran smoothly without any issues.
I want to inquire waht is the correct method to move "fa-tal.nii" to MNI152_2mm
Is this command correct"?
mri_vol2vol --mov f
Dear Dhaval,
when your recon-all finishs the process you will get images 256^3 and 1mm
isootropic.
The you can simply follow the instructions mentioned here
https://surfer.nmr.mgh.harvard.edu/fswiki/FsAnat-to-NativeAnat to send your
images back to native space.
All the best,
John
>
> On Mon,
Dear Freesurfer experts,
I highly appreciate if anybody clarify how Freesurfer calculate cortical
thickness and gray matter volume.
If the cortical thickness of e.g. precentral gurus is measured as the closest
distance from the gray-white boundary to the gray-CSF boundray at each vertex
on the t
17 11:04 AM
UTC Time: April 12, 2017 3:04 PM
From: seman...@nyspi.columbia.edu
To: John Anderson , freesurfer@nmr.mgh.harvard.edu
Hi John,
Yes understanding how freesurfer deals with edits can be a bit confusing. I
have a lot of experience doing edits to the wm.mgz and brainmask.mgz for
Dear Freesurfer experts,
I know how to do cortical thickness group analysis using Freesurfer, also I
know how to use Qdec to compare groups regarding gray matter volume
differences, cortical thickness, curvatures, area,... etc.
I am wondering if there is any way in Freesurfer to study the differe
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