[Freesurfer] correlation coefficient

2012-05-02 Thread Tetiana Dadakova
Dear FS experts,

I try to look at correlation between thickness and performance. I run
mri_glmfit (using performance as covariate) and mri_glmfit-sim. After
this I get some significant clusters.
I would like to ask if I could get a correlation coefficient for these
clusters, or/and a regression plot?

Thank you,
Tanja.
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Re: [Freesurfer] wm edits

2012-03-28 Thread Tetiana Dadakova
Hi Louis,

thank you very much for your reply.
The problem with our data is that wm is too dark sometimes to use
control points (intensity is too inhomogenious in some parts). That's
why we would like to have the opportunity to just draw the wm where
needed. But for some reason it doesn't correct the surfaces.

Best wishes,
Tanja.

On Tue, Mar 27, 2012 at 4:23 PM, Louis Nicholas Vinke
vi...@nmr.mgh.harvard.edu wrote:
 Hi Tanja,
 I would recommend you try using some control points.  Place one or two just
 inside the wm surface near that wm finger which is not being included, and
 then possibly one or two control points carefully placed along the wm finger
 on voxels with the highest intensity (in the middle it looks like).  Not
 sure what the other coronal slices look like, but you may want to do
 something similar on other slices.
 -Louis


 On Tue, 27 Mar 2012, Tetiana Dadakova wrote:

 Dear FS list,

 After recon-all -all we had some wm missing in temporal part of the
 brain (fig. wm_missing1). We edited wm.mgz and re-run recon-all
 -autorecon2 -autorecon3. After this, the wm.mgz looks as fig.
 wm_missing2, but the surfaces still look as fig. wm_missing1.
 What can be the reason that wm.mgz edits didn't affect the surfaces?

 Thank you,
 Tanja.



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Re: [Freesurfer] wm edits

2012-03-28 Thread Tetiana Dadakova
Hello Bruce. Thank you for your reply.

I am not sure why the wm is too dark. Our population is very stressed
(burnout) people vs controls, scanner GE Discovery MR750 3.0T, coil
8ch, we use BRAVO sequence with 1x1x1mm voxels.
Compared to the dataset I worked with before (from 1.5T scanner), here
wm is omitted much more often (and often control points do not work),
but also sometimes some brighter portions of gm are included as wm. I
think the problems can be caused by higher field inhomogeniety with
higher static magnetic field, but I am not sure.

Tanja.

On Wed, Mar 28, 2012 at 3:00 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 Hi Tanja

 why is the wm too dark? Can you tell us something about your data
 (population, coil, scanner, etc...)?

 cheers
 Bruce

 On Wed, 28 Mar 2012, Tetiana Dadakova wrote:

 Hi Louis,

 thank you very much for your reply.
 The problem with our data is that wm is too dark sometimes to use
 control points (intensity is too inhomogenious in some parts). That's
 why we would like to have the opportunity to just draw the wm where
 needed. But for some reason it doesn't correct the surfaces.

 Best wishes,
 Tanja.

 On Tue, Mar 27, 2012 at 4:23 PM, Louis Nicholas Vinke
 vi...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,
 I would recommend you try using some control points.  Place one or two
 just
 inside the wm surface near that wm finger which is not being included,
 and
 then possibly one or two control points carefully placed along the wm
 finger
 on voxels with the highest intensity (in the middle it looks like).  Not
 sure what the other coronal slices look like, but you may want to do
 something similar on other slices.
 -Louis


 On Tue, 27 Mar 2012, Tetiana Dadakova wrote:

 Dear FS list,

 After recon-all -all we had some wm missing in temporal part of the
 brain (fig. wm_missing1). We edited wm.mgz and re-run recon-all
 -autorecon2 -autorecon3. After this, the wm.mgz looks as fig.
 wm_missing2, but the surfaces still look as fig. wm_missing1.
 What can be the reason that wm.mgz edits didn't affect the surfaces?

 Thank you,
 Tanja.



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Re: [Freesurfer] wm edits

2012-03-28 Thread Tetiana Dadakova
Do you think 32ch coil would be better? We also have data with the
same scanner and same sequence, but 32ch coil. Although, visually,
32ch data is much more inhomogenious, especially in occipital part (it
is too bright). We were afraid that wm there would be hard to
distinguish from gm and that therefore the thickness would be too
underestimated, that is why we decided to use 8ch data.

Tanja.

On Wed, Mar 28, 2012 at 3:28 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 it may also be the 8 channel coil, which can make things hard, particularly
 near the vertex. Dielectric effects are usually still pretty modest at 3T
 although they are visible. I think control points would be your best bet.


 cheers
 Bruce


 On Wed, 28 Mar 2012, Tetiana Dadakova wrote:

 Hello Bruce. Thank you for your reply.

 I am not sure why the wm is too dark. Our population is very stressed
 (burnout) people vs controls, scanner GE Discovery MR750 3.0T, coil
 8ch, we use BRAVO sequence with 1x1x1mm voxels.
 Compared to the dataset I worked with before (from 1.5T scanner), here
 wm is omitted much more often (and often control points do not work),
 but also sometimes some brighter portions of gm are included as wm. I
 think the problems can be caused by higher field inhomogeniety with
 higher static magnetic field, but I am not sure.

 Tanja.

 On Wed, Mar 28, 2012 at 3:00 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:

 Hi Tanja

 why is the wm too dark? Can you tell us something about your data
 (population, coil, scanner, etc...)?

 cheers
 Bruce

 On Wed, 28 Mar 2012, Tetiana Dadakova wrote:

 Hi Louis,

 thank you very much for your reply.
 The problem with our data is that wm is too dark sometimes to use
 control points (intensity is too inhomogenious in some parts). That's
 why we would like to have the opportunity to just draw the wm where
 needed. But for some reason it doesn't correct the surfaces.

 Best wishes,
 Tanja.

 On Tue, Mar 27, 2012 at 4:23 PM, Louis Nicholas Vinke
 vi...@nmr.mgh.harvard.edu wrote:


 Hi Tanja,
 I would recommend you try using some control points.  Place one or two
 just
 inside the wm surface near that wm finger which is not being included,
 and
 then possibly one or two control points carefully placed along the wm
 finger
 on voxels with the highest intensity (in the middle it looks like).
  Not
 sure what the other coronal slices look like, but you may want to do
 something similar on other slices.
 -Louis


 On Tue, 27 Mar 2012, Tetiana Dadakova wrote:

 Dear FS list,

 After recon-all -all we had some wm missing in temporal part of the
 brain (fig. wm_missing1). We edited wm.mgz and re-run recon-all
 -autorecon2 -autorecon3. After this, the wm.mgz looks as fig.
 wm_missing2, but the surfaces still look as fig. wm_missing1.
 What can be the reason that wm.mgz edits didn't affect the surfaces?

 Thank you,
 Tanja.



 The information in this e-mail is intended only for the person to whom
 it
 is
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 e-mail
 contains patient information, please contact the Partners Compliance
 HelpLine at
 http://www.partners.org/complianceline . If the e-mail was sent to you
 in
 error
 but does not contain patient information, please contact the sender and
 properly
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Re: [Freesurfer] FS 5.1 control points problem

2012-03-08 Thread Tetiana Dadakova
Thank you, Sita, for your reply.

1. The skull strip was good, the cortex disappeared after we added cp.
I removed control points and put new ones that are surely in wm, now re-running.

2. I have one more question: I did previous analysis with FS5.0 on
1.5T data with non-isotropic voxels. Now for FS5.1 we use 3T images
with 1x1x1mm voxels. For previous analysis the error, when a part of
occipital cortex is excluded, appeared in around 1 per 40 cases. Now
with better data and newer version we have this problem in around 1
per 5 cases. The only idea I can think of is increased inhomogeniety
in field due to increased static field of scanner. Can it be true? Can
you suggest other possible reasons?

Thank you,
Tanja.

On Wed, Mar 7, 2012 at 4:29 PM, Sita Kakunoori s...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,

 Sorry if I missed something but was the cortex stripped off even
 before you made any edits. If so, it's probably skull strip error. Please
 refer to this wiki for instructions to correct the error.

 https://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/SkullStripFix

 But if part of the brain is missing only after you added control points
 and ran -autorecon2-cp -autorecon3, then please check if any of the
 control points were placed in GM or really close to GM.

 Sita.



 On Wed, 7 Mar 2012, Tetiana Dadakova wrote:

 Dear FS list,

 We started using FS 5.1 and encountered a problem with control points.
 After first recon-all some of the cortex (in occipital part) was
 missing, so we added control points and re-ran -autorecon2-cp
 -atorecon3.
 After that, the part of the brain with control points was removed from
 brainmask.mgz (Fig1).

 I never had this problem in 5.0, therefore I assume that something has
 been changed in 5.1 regarding cp. Could you please suggest what can be
 the problem and if it is described somewhere?

 Thank you,
 Tanja.

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Re: [Freesurfer] Number of entries error in trac-all

2012-02-17 Thread Tetiana Dadakova
Hi Fidel,

The bvecs/bvals files should have 3/1 columns respectively (as opposed
to 3/1 rows that yours have). Could you try if transposing the entries
in your files help?

Tanja.

On Fri, Feb 17, 2012 at 12:29 PM, Fidel falf...@hggm.es wrote:
 Dear all,

 I have tried to execute trac-all and I have found this error in the process
 (From the log):

  
 dtifit -k /X/subjects//S1/dmri/dwi.nii.gz -m
 /X/subjects//S1/dlabel/diff/aparc+aseg_mask.flt.nii.gz -r
 /X/subjects//S1/dmri/bvecs -b /X//S1/dmri/bvals -o
 /X/subjects//S1/dmri/dtifit

 Error: data and bvals/bvecs do not contain the same number of entries
  

 I have seen in the mailing list that it has happened before, but I have not
 found the solution.

 You can find the bvals and bvecs files attached. As far as I can see, they
 have the same number of rows, so... What is the problem?

 Thanks and best regards,

 Fidel.

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Re: [Freesurfer] TRACULA bvecs question

2012-02-15 Thread Tetiana Dadakova
Sorry for bothering you again,

I have another error now: Error: bvecs and bvals don't have the same
number of entries.
Visually my bval/bvec files seem ok to me. I can't find the problem.
I attach the files, could you please take a look on them?

Thank you very much,
Tanja.

On Tue, Feb 14, 2012 at 7:31 PM, Tetiana Dadakova tetian...@gmail.com wrote:
 I see, thank you :)


 On Tue, Feb 14, 2012 at 6:50 PM, Anastasia Yendiki
 ayend...@nmr.mgh.harvard.edu wrote:

 PS: The info on what you need to set it here:

 https://surfer.nmr.mgh.harvard.edu/fswiki/dmrirc

 # Number of low-b images
 # Must be specified if inputs are not DICOM
 # Default: Read from DICOM header
 #
 set nb0 = 10



 On Tue, 14 Feb 2012, Tetiana Dadakova wrote:

 Dear Priti, Anastasia,

 Thank you for your help, I created bvec and bval files and it went fine.
 But now I have another error in preprocessing step.
 I attach a log file. Could you please take a look at that?

 Thank you,
 Tanja.



 trac-preproc exited with ERRORS at Fri Feb 10 10:52:37 CET 2012




 On Fri, Feb 3, 2012 at 5:52 PM, Priti Srinivasan
 rspr...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,

 Can you check if the $dtroot/$subjectname/dmri/dwi_orig_flip.mghdti.bvecs
 was created at all? It looks like that may not have been created and
 that's why it can't find dwi_orig_flip.mghdti.bvecs. If your bvals and
 bvecs information is not encoded in the dicom header, then you can
 specify
 it explicitly in the dmrirc file.

 Please refer to the following page for instructions on how to specify
 your
 bvals and bvecs for tracula:

 http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/Tracula

 Hope this helps,
 Priti


 Hi Priti,

 I changed the dmrirc file to the one you sent, but unfortunately got
 the same error. I attach the log (although it is basically the same).
 Do you have any ideas what else can cause it?

 Thanks again,
 Tanja.

 On Fri, Feb 3, 2012 at 4:51 PM, Priti Srinivasan
 rspr...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,

 I think the problem may be due to the trailing slash you've included
 while
 specifying $dtroot, $SUBJECTS_DIR etc.


 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1/

 should be

 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1


 trac-all usually adds the '/' and since you're adding an extra '/',
 it's
 giving an error. I've edited your dmrirc file and removed those
 trailing
 slashes. Could you run this again and let us know if it solves the
 problem?

 Hope this is helpful,
 Priti





 Thank you Priti and Anastasia,

 Anastasia, just wanted to clarify, I meant
 $dtroot/$subjectname/dmri/bvecs, when I wrote /dmri/bvecs, sorry for
 this misunderstanding.

 I attach my configuration file and the command I use is  trac-all
 -prep -c /Applications/freesurfer/subjects/TRACULA/DTI/scripts/dmrirc

 .

 I also attach a picture of my file tree and a track-all.log file.

 Thank you for your time and help,
 Tanja.

 On Fri, Feb 3, 2012 at 2:21 AM, Anastasia Yendiki
 ayend...@nmr.mgh.harvard.edu wrote:


 Hi Tanja - The file is supposed to be created under
 $dtroot/$subjectname/dmri/bvecs. If it's trying to create it as
 /dmri/bvecs,
 this means that something wasn't defined correctly. What is the exact
 trac-all command line that you're using? And your configuration file
 if
 you're using one?

 a.y


 On Thu, 2 Feb 2012, Tetiana Dadakova wrote:

 Dear list,

 I try to run TRACULA pre-processing step and I get the following
 error: /dmri/bvecs: No such file or directory.

 I have a folder with reconstructed T1 data and a folder with raw
 dicom
 DTI data. When I start trac-all -prep, it creates directory /dmri/,
 but it doesn't create the bvecs file.
 Should I create it myself using dcm2nii or is it supposed to be
 created automatically?

 Thank you,
 Tanja.
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bval
Description: Binary data


bvec
Description: Binary data
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Re: [Freesurfer] TRACULA bvecs question

2012-02-14 Thread Tetiana Dadakova
Dear Priti, Anastasia,

Thank you for your help, I created bvec and bval files and it went fine.
But now I have another error in preprocessing step.
I attach a log file. Could you please take a look at that?

Thank you,
Tanja.



trac-preproc exited with ERRORS at Fri Feb 10 10:52:37 CET 2012




On Fri, Feb 3, 2012 at 5:52 PM, Priti Srinivasan
rspr...@nmr.mgh.harvard.edu wrote:
 Hi Tanja,

 Can you check if the $dtroot/$subjectname/dmri/dwi_orig_flip.mghdti.bvecs
 was created at all? It looks like that may not have been created and
 that's why it can't find dwi_orig_flip.mghdti.bvecs. If your bvals and
 bvecs information is not encoded in the dicom header, then you can specify
 it explicitly in the dmrirc file.

 Please refer to the following page for instructions on how to specify your
 bvals and bvecs for tracula:

 http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/Tracula

 Hope this helps,
 Priti


 Hi Priti,

 I changed the dmrirc file to the one you sent, but unfortunately got
 the same error. I attach the log (although it is basically the same).
 Do you have any ideas what else can cause it?

 Thanks again,
 Tanja.

 On Fri, Feb 3, 2012 at 4:51 PM, Priti Srinivasan
 rspr...@nmr.mgh.harvard.edu wrote:
 Hi Tanja,

 I think the problem may be due to the trailing slash you've included
 while
 specifying $dtroot, $SUBJECTS_DIR etc.


 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1/

 should be

 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1


 trac-all usually adds the '/' and since you're adding an extra '/', it's
 giving an error. I've edited your dmrirc file and removed those trailing
 slashes. Could you run this again and let us know if it solves the
 problem?

 Hope this is helpful,
 Priti





 Thank you Priti and Anastasia,

 Anastasia, just wanted to clarify, I meant
 $dtroot/$subjectname/dmri/bvecs, when I wrote /dmri/bvecs, sorry for
 this misunderstanding.

 I attach my configuration file and the command I use is  trac-all
 -prep -c /Applications/freesurfer/subjects/TRACULA/DTI/scripts/dmrirc
.
 I also attach a picture of my file tree and a track-all.log file.

 Thank you for your time and help,
 Tanja.

 On Fri, Feb 3, 2012 at 2:21 AM, Anastasia Yendiki
 ayend...@nmr.mgh.harvard.edu wrote:

 Hi Tanja - The file is supposed to be created under
 $dtroot/$subjectname/dmri/bvecs. If it's trying to create it as
 /dmri/bvecs,
 this means that something wasn't defined correctly. What is the exact
 trac-all command line that you're using? And your configuration file
 if
 you're using one?

 a.y


 On Thu, 2 Feb 2012, Tetiana Dadakova wrote:

 Dear list,

 I try to run TRACULA pre-processing step and I get the following
 error: /dmri/bvecs: No such file or directory.

 I have a folder with reconstructed T1 data and a folder with raw
 dicom
 DTI data. When I start trac-all -prep, it creates directory /dmri/,
 but it doesn't create the bvecs file.
 Should I create it myself using dcm2nii or is it supposed to be
 created automatically?

 Thank you,
 Tanja.
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 e-mail
 contains patient information, please contact the Partners Compliance
 HelpLine at
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 in
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 properly
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trac-all.log
Description: Binary data
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Re: [Freesurfer] TRACULA bvecs question

2012-02-14 Thread Tetiana Dadakova
I see, thank you :)


On Tue, Feb 14, 2012 at 6:50 PM, Anastasia Yendiki
ayend...@nmr.mgh.harvard.edu wrote:

 PS: The info on what you need to set it here:

 https://surfer.nmr.mgh.harvard.edu/fswiki/dmrirc

 # Number of low-b images
 # Must be specified if inputs are not DICOM
 # Default: Read from DICOM header
 #
 set nb0 = 10



 On Tue, 14 Feb 2012, Tetiana Dadakova wrote:

 Dear Priti, Anastasia,

 Thank you for your help, I created bvec and bval files and it went fine.
 But now I have another error in preprocessing step.
 I attach a log file. Could you please take a look at that?

 Thank you,
 Tanja.



 trac-preproc exited with ERRORS at Fri Feb 10 10:52:37 CET 2012




 On Fri, Feb 3, 2012 at 5:52 PM, Priti Srinivasan
 rspr...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,

 Can you check if the $dtroot/$subjectname/dmri/dwi_orig_flip.mghdti.bvecs
 was created at all? It looks like that may not have been created and
 that's why it can't find dwi_orig_flip.mghdti.bvecs. If your bvals and
 bvecs information is not encoded in the dicom header, then you can
 specify
 it explicitly in the dmrirc file.

 Please refer to the following page for instructions on how to specify
 your
 bvals and bvecs for tracula:

 http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/Tracula

 Hope this helps,
 Priti


 Hi Priti,

 I changed the dmrirc file to the one you sent, but unfortunately got
 the same error. I attach the log (although it is basically the same).
 Do you have any ideas what else can cause it?

 Thanks again,
 Tanja.

 On Fri, Feb 3, 2012 at 4:51 PM, Priti Srinivasan
 rspr...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,

 I think the problem may be due to the trailing slash you've included
 while
 specifying $dtroot, $SUBJECTS_DIR etc.


 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1/

 should be

 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1


 trac-all usually adds the '/' and since you're adding an extra '/',
 it's
 giving an error. I've edited your dmrirc file and removed those
 trailing
 slashes. Could you run this again and let us know if it solves the
 problem?

 Hope this is helpful,
 Priti





 Thank you Priti and Anastasia,

 Anastasia, just wanted to clarify, I meant
 $dtroot/$subjectname/dmri/bvecs, when I wrote /dmri/bvecs, sorry for
 this misunderstanding.

 I attach my configuration file and the command I use is  trac-all
 -prep -c /Applications/freesurfer/subjects/TRACULA/DTI/scripts/dmrirc

 .

 I also attach a picture of my file tree and a track-all.log file.

 Thank you for your time and help,
 Tanja.

 On Fri, Feb 3, 2012 at 2:21 AM, Anastasia Yendiki
 ayend...@nmr.mgh.harvard.edu wrote:


 Hi Tanja - The file is supposed to be created under
 $dtroot/$subjectname/dmri/bvecs. If it's trying to create it as
 /dmri/bvecs,
 this means that something wasn't defined correctly. What is the exact
 trac-all command line that you're using? And your configuration file
 if
 you're using one?

 a.y


 On Thu, 2 Feb 2012, Tetiana Dadakova wrote:

 Dear list,

 I try to run TRACULA pre-processing step and I get the following
 error: /dmri/bvecs: No such file or directory.

 I have a folder with reconstructed T1 data and a folder with raw
 dicom
 DTI data. When I start trac-all -prep, it creates directory /dmri/,
 but it doesn't create the bvecs file.
 Should I create it myself using dcm2nii or is it supposed to be
 created automatically?

 Thank you,
 Tanja.
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Re: [Freesurfer] TRACULA bvecs question

2012-02-03 Thread Tetiana Dadakova
Hi Priti,

I changed the dmrirc file to the one you sent, but unfortunately got
the same error. I attach the log (although it is basically the same).
Do you have any ideas what else can cause it?

Thanks again,
Tanja.

On Fri, Feb 3, 2012 at 4:51 PM, Priti Srinivasan
rspr...@nmr.mgh.harvard.edu wrote:
 Hi Tanja,

 I think the problem may be due to the trailing slash you've included while
 specifying $dtroot, $SUBJECTS_DIR etc.


 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1/

 should be

 setenv SUBJECTS_DIR /Applications/freesurfer/subjects/TRACULA/T1


 trac-all usually adds the '/' and since you're adding an extra '/', it's
 giving an error. I've edited your dmrirc file and removed those trailing
 slashes. Could you run this again and let us know if it solves the
 problem?

 Hope this is helpful,
 Priti





 Thank you Priti and Anastasia,

 Anastasia, just wanted to clarify, I meant
 $dtroot/$subjectname/dmri/bvecs, when I wrote /dmri/bvecs, sorry for
 this misunderstanding.

 I attach my configuration file and the command I use is  trac-all
 -prep -c /Applications/freesurfer/subjects/TRACULA/DTI/scripts/dmrirc
.
 I also attach a picture of my file tree and a track-all.log file.

 Thank you for your time and help,
 Tanja.

 On Fri, Feb 3, 2012 at 2:21 AM, Anastasia Yendiki
 ayend...@nmr.mgh.harvard.edu wrote:

 Hi Tanja - The file is supposed to be created under
 $dtroot/$subjectname/dmri/bvecs. If it's trying to create it as
 /dmri/bvecs,
 this means that something wasn't defined correctly. What is the exact
 trac-all command line that you're using? And your configuration file if
 you're using one?

 a.y


 On Thu, 2 Feb 2012, Tetiana Dadakova wrote:

 Dear list,

 I try to run TRACULA pre-processing step and I get the following
 error: /dmri/bvecs: No such file or directory.

 I have a folder with reconstructed T1 data and a folder with raw dicom
 DTI data. When I start trac-all -prep, it creates directory /dmri/,
 but it doesn't create the bvecs file.
 Should I create it myself using dcm2nii or is it supposed to be
 created automatically?

 Thank you,
 Tanja.
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trac-all.log
Description: Binary data
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[Freesurfer] problem with visualizing hippo-subfields

2011-12-08 Thread Tetiana Dadakova
Dear FreeSurfer list,

I ran recon-all -bert -hippo-subfields, which finished without error.
Now I try to open it with freeview using:

cd $SUBJECTS_DIR/bert/mri
 freeview nu.mgz \
  -p-labels posterior_left_* posterior_Left-Hippocampus.mgz \
  -p-labels posterior_right_* posterior_Right-Hippocampus.mgz \
  -p-prefix posterior_ -p-lut $FREESURFER_HOME/FreeSurferColorLUT.txt

But get the following error: Failed to load posterior_left_CA1.mgz.
(posterior_left_CA1.mgz exists in bert/mri)
Do you have an idea why it goes wrong?

Thank you,
Tanja.
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Re: [Freesurfer] running recon-all after editing aseg.mgz

2011-11-25 Thread Tetiana Dadakova
Hi Maria,

Yes, you are editing aseg.mgz. After saving the segmentation, you should run
recon-all -s subject_name -autorecon2 -autorecon3.
If you also added some control points, then you should run
recon-all -s subject_name -autorecon2-cp -autorecon3

Best wishes,
Tanja.

On Fri, Nov 25, 2011 at 10:40 PM, Maria Jalbrzikowski
mjalbrzikow...@gmail.com wrote:

 Hi,

  I am a relatively new user of Freesurfer and have a couple questions.
 I have gone through the tutorials and I am now at the point where I check
 the segmentation.
 If I open my subject in tkemdit
 (tkmedit your_subject_name brainmask.mgz -surfs -aseg)  and use the edit the
 segmentation and then press save segmentation, I am editing the aseg.mgz
 file, correct?  After doing that, what parts of recon-all would I need to
 run again?
 Thanks,
 Maria
 --
 Maria Jalbrzikowski, M.A.
 University of California, Los Angeles


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[Freesurfer] control points didn't work

2011-11-21 Thread Tetiana Dadakova
Dear FreeSurfer list,

I was trying to edit wm surface by adding control points. After saving
them and re-running recon-all -autorecon2-cp -autorecon3, the control
points are still there, but wm is not edited (although cp worked in
other places for the same brain). The intensity there is around 95-98
depending on slice.
Could you please suggest what could go wrong?

Thank you,
Tanja.
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[Freesurfer] pial area surface - correcting for size of brain

2011-11-02 Thread Tetiana Dadakova
Dear FreeSurfer experts,

I have a question regarding pial area analysis.

What is commonly used as a nuisance variable to correct for brain size
difference between groups (e.g men vs women)? Can you suggest any
article where this is discussed or has been done?

Thank you,
Tanja.
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Re: [Freesurfer] pial area surface - correcting for size of brain

2011-11-02 Thread Tetiana Dadakova
Thank you Michael,

I was wondering about a nuisance specific to area analysis. I
understand using ICV or brain volume in volumetric analysis, but for
area analysis something like overall pial area seems more logical to
me. That is why I am curious if there is any literature about area
(surface) analysis in particular. Am I at the right track at all?

Best wishes,
Tanja.

On Wed, Nov 2, 2011 at 2:15 PM, Michael Harms mha...@conte.wustl.edu wrote:

 Typically one uses either a measure of brain volume or an estimate of
 intracranial volume -- the choice depends on whether or not you want to
 control for whole brain atrophy when making your interpretations, in
 which case you would use brain volume rather than ICV.  There have
 been numerous posts to the list on this issue, so try searching the
 archives.

 As for articles, you could start with the ones below.

 cheers,
 -MH


 1: Mathalon DH, Sullivan EV, Rawles JM, Pfefferbaum A. Correction for
 head size
 in brain-imaging measurements. Psychiatry Res. 1993 Jun;50(2):121-39. Erratum 
 in:
 Psychiatry Res 1994 Sep;55(3):179. PubMed PMID: 8378488.


 2: Arndt S, Cohen G, Alliger RJ, Swayze VW 2nd, Andreasen NC. Problems with 
 ratio
 and proportion measures of imaged cerebral structures. Psychiatry Res. 1991
 May;40(1):79-89. PubMed PMID: 1946842.


 3: O'Brien LM, Ziegler DA, Deutsch CK, Kennedy DN, Goldstein JM, Seidman LJ,
 Hodge S, Makris N, Caviness V, Frazier JA, Herbert MR. Adjustment for whole 
 brain
 and cranial size in volumetric brain studies: a review of common adjustment
 factors and statistical methods. Harv Rev Psychiatry. 2006 
 May-Jun;14(3):141-51.
 Review. PubMed PMID: 16787886.


 4: O'Brien LM, Ziegler DA, Deutsch CK, Frazier JA, Herbert MR, Locascio JJ.
 Statistical adjustments for brain size in volumetric neuroimaging studies: 
 some
 practical implications in methods. Psychiatry Res. 2011 Aug 30;193(2):113-22.
 PubMed PMID: 21684724.


 5: Sanfilipo MP, Benedict RH, Zivadinov R, Bakshi R. Correction for 
 intracranial
 volume in analysis of whole brain atrophy in multiple sclerosis: the 
 proportion
 vs. residual method. Neuroimage. 2004 Aug;22(4):1732-43. PubMed PMID: 
 15275929.


 On Wed, 2011-11-02 at 12:26 +0100, Tetiana Dadakova wrote:
 Dear FreeSurfer experts,

 I have a question regarding pial area analysis.

 What is commonly used as a nuisance variable to correct for brain size
 difference between groups (e.g men vs women)? Can you suggest any
 article where this is discussed or has been done?

 Thank you,
 Tanja.
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Re: [Freesurfer] pial area surface - correcting for size of brain

2011-11-02 Thread Tetiana Dadakova
Thank you very much Michael for an extensive answer.
I am doing analysis in QDEC, thank you for pointing that, I will check the list.

On Wed, Nov 2, 2011 at 2:52 PM, Michael Harms mha...@conte.wustl.edu wrote:

 Oops -- I missed that aspect of your question.  Yes, that would make
 sense, and is precisely what we did in a 2010 paper in Brit J Psychiatry
 (196:150-7).  Although the measures in that paper were not FS-based, we
 used appropriate global volume, area, and thickness measures to covary
 for each respective type of measure (see paper for details).

 As an aside, are you analyzing the area of parcellated regions, or are
 you doing a vertex-wise area analysis in QDEC.  If the latter, you
 should be aware that there are issues as to whether the vertex-wise area
 values are a meaningful, interpretable measure since the area of any
 given triangle of the mesh is more reflective of the mesh tesselation
 than an intrinsic property of that subject's brain (see previous posts
 regarding that as well).

 cheers,
 -MH


 On Wed, 2011-11-02 at 14:39 +0100, Tetiana Dadakova wrote:
 Thank you Michael,

 I was wondering about a nuisance specific to area analysis. I
 understand using ICV or brain volume in volumetric analysis, but for
 area analysis something like overall pial area seems more logical to
 me. That is why I am curious if there is any literature about area
 (surface) analysis in particular. Am I at the right track at all?

 Best wishes,
 Tanja.

 On Wed, Nov 2, 2011 at 2:15 PM, Michael Harms mha...@conte.wustl.edu wrote:
 
  Typically one uses either a measure of brain volume or an estimate of
  intracranial volume -- the choice depends on whether or not you want to
  control for whole brain atrophy when making your interpretations, in
  which case you would use brain volume rather than ICV.  There have
  been numerous posts to the list on this issue, so try searching the
  archives.
 
  As for articles, you could start with the ones below.
 
  cheers,
  -MH
 
 
  1: Mathalon DH, Sullivan EV, Rawles JM, Pfefferbaum A. Correction for
  head size
  in brain-imaging measurements. Psychiatry Res. 1993 Jun;50(2):121-39. 
  Erratum in:
  Psychiatry Res 1994 Sep;55(3):179. PubMed PMID: 8378488.
 
 
  2: Arndt S, Cohen G, Alliger RJ, Swayze VW 2nd, Andreasen NC. Problems 
  with ratio
  and proportion measures of imaged cerebral structures. Psychiatry Res. 1991
  May;40(1):79-89. PubMed PMID: 1946842.
 
 
  3: O'Brien LM, Ziegler DA, Deutsch CK, Kennedy DN, Goldstein JM, Seidman 
  LJ,
  Hodge S, Makris N, Caviness V, Frazier JA, Herbert MR. Adjustment for 
  whole brain
  and cranial size in volumetric brain studies: a review of common adjustment
  factors and statistical methods. Harv Rev Psychiatry. 2006 
  May-Jun;14(3):141-51.
  Review. PubMed PMID: 16787886.
 
 
  4: O'Brien LM, Ziegler DA, Deutsch CK, Frazier JA, Herbert MR, Locascio JJ.
  Statistical adjustments for brain size in volumetric neuroimaging studies: 
  some
  practical implications in methods. Psychiatry Res. 2011 Aug 
  30;193(2):113-22.
  PubMed PMID: 21684724.
 
 
  5: Sanfilipo MP, Benedict RH, Zivadinov R, Bakshi R. Correction for 
  intracranial
  volume in analysis of whole brain atrophy in multiple sclerosis: the 
  proportion
  vs. residual method. Neuroimage. 2004 Aug;22(4):1732-43. PubMed PMID: 
  15275929.
 
 
  On Wed, 2011-11-02 at 12:26 +0100, Tetiana Dadakova wrote:
  Dear FreeSurfer experts,
 
  I have a question regarding pial area analysis.
 
  What is commonly used as a nuisance variable to correct for brain size
  difference between groups (e.g men vs women)? Can you suggest any
  article where this is discussed or has been done?
 
  Thank you,
  Tanja.
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  The information in this e-mail is intended only for the person to whom it 
  is
  addressed. If you believe this e-mail was sent to you in error and the 
  e-mail
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  http://www.partners.org/complianceline . If the e-mail was sent to you in 
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Re: [Freesurfer] bug in surface-based area and volume

2011-10-05 Thread Tetiana Dadakova
Dear Doug,

Just wanted to ask you when approximately the fix will be ready? I
really looking forward to it, to be able to explain some results.

Thank you for your time and constant help,
Tanja.



On Fri, Aug 19, 2011 at 4:07 PM, Douglas N Greve
gr...@nmr.mgh.harvard.edu wrote:

 Hi Y'all, I recently found a bug in the way that FS converts
 surface-based area (eg, lh.area) and volume (eg, lh.volume) into
 standard space. I'm testing a fix now, but you should not use area or
 volume measures until I've posted the fix and you re-run either
 mris_preproc or qcache. The files themselves are fine, it is the way
 they are transfered to standard space that is the problem. You will not
 need to re-analyze any of your individual subject data. The volumes of
 the subcortical structures are unaffected by this problem. Global
 measures of cortical volume are also unaffected. I'll get back soon
 (next week) with the fix. Sorry for the inconvenience.

 doug






 --
 Douglas N. Greve, Ph.D.
 MGH-NMR Center
 gr...@nmr.mgh.harvard.edu
 Phone Number: 617-724-2358
 Fax: 617-726-7422

 Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
 FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html

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[Freesurfer] mean and stdev group-wise

2011-09-11 Thread Tetiana Dadakova
Dear list,

I would like to calculate mean and stdev of thickness group-wise.
Could you please give me a hint how to do it?

Thank you,
Tanja.
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[Freesurfer] two questions: asymmetry and controlling for global thickness abnormality

2011-09-05 Thread Tetiana Dadakova
Dear list,

I have two question:

1. Is it possible to do the asymmetry analysis in FS, I mean to
compare left and right hemispheres within one group?

2. Is it necessary to somehow control for global abnormality of
thickness while looking at regional abnormality, e.g. if one group has
thinner brain overall, but also thinner brain in some regions?
(Similar to dividing by total brain volume in volumetric analysis)

Thank you and best wishes,
Tanja.
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Re: [Freesurfer] two questions: asymmetry and controlling for global thickness abnormality

2011-09-05 Thread Tetiana Dadakova
Thank you Michael. I have more questions on this:

1. Is there a method to calculate if I have global difference in
thickness between groups?
2. How can I control for global thickness difference vertex-wise using
freesurfer?

Best wishes,
Tanja.


On Mon, Sep 5, 2011 at 7:42 PM, Michael Harms mha...@conte.wustl.edu wrote:

 Regarding #2: Yes, if you a have global difference in thickness between
 groups, then it is appropriate to control for that in the same manner that
 one frequently controls for total brain volume in volumetric analyses.

 cheers,
 -MH

 Dear list,

 I have two question:

 1. Is it possible to do the asymmetry analysis in FS, I mean to
 compare left and right hemispheres within one group?

 2. Is it necessary to somehow control for global abnormality of
 thickness while looking at regional abnormality, e.g. if one group has
 thinner brain overall, but also thinner brain in some regions?
 (Similar to dividing by total brain volume in volumetric analysis)

 Thank you and best wishes,
 Tanja.
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Re: [Freesurfer] what is thalamus-proper and clusters-table related question

2011-09-04 Thread Tetiana Dadakova
Thank you Doug,

One more question: what does the column Max mean in the table with
clusters' info?

Tanja.

On Fri, Sep 2, 2011 at 6:28 PM, Douglas N Greve
gr...@nmr.mgh.harvard.edu wrote:
 I'm not sure about #1, maybe BF can chime in.

 Tetiana Dadakova wrote:

 Dear FS list,

 1. What does a label Thalamus Proper include? Is it the same as thalamus?

 2. After correcting for multiple comparisons, I get a table of
 clusters. I have several questions regarding this table: What do the
 columns Max, CWPLow, and CWPHigh represent?

  1. CWP - cluster-wise pvalue. The pvalue of the cluster corrected for
    multiple comparisons
  2. CWPLow - lower 90% confidence limit of CWP based on binomial
 distribution
  3. CWPHi  - upper 90% confidence limit of CWP based on binomial
 distribution

 Regarding the NVtxs
 column: is it the number of vertexes in cluster?

 Yes

 What kind of information can I get from this value?

 It is not very informative so don't feel like you have to use it. It is good
 for assuring that the software is doing the right thing.

 If two clusters have different areas but the same number of vertexes, does
 it mean something?


 It means that the area of the component triangles that make up the vertices
 is different.

 doug

 Thank you very much for your help and for your time,
 Tanja.
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 MGH-NMR Center
 gr...@nmr.mgh.harvard.edu
 Phone Number: 617-724-2358 Fax: 617-726-7422

 Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
 FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html



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[Freesurfer] what is thalamus-proper and clusters-table related question

2011-09-02 Thread Tetiana Dadakova
Dear FS list,

1. What does a label Thalamus Proper include? Is it the same as thalamus?

2. After correcting for multiple comparisons, I get a table of
clusters. I have several questions regarding this table: What do the
columns Max, CWPLow, and CWPHigh represent? Regarding the NVtxs
column: is it the number of vertexes in cluster?  What kind of
information can I get from this value? If two clusters have different
areas but the same number of vertexes, does it mean something?

Thank you very much for your help and for your time,
Tanja.
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Re: [Freesurfer] pial and WM missing after reunning skullstrip

2011-08-22 Thread Tetiana Dadakova
Hi Julia,

After the skull strip was corrected, you should run:

recon-all -autorecon2 -autorecon3 -s Subject_name

this will create new surfaces based on new skull strip.

Tanja.

On Mon, Aug 22, 2011 at 6:47 AM, Julia Hill julia.h...@neura.edu.au wrote:

 Hi Bruce

 I am new to freesurfer and im having a few issues with a number of my
 scans.  The cerebellum and sections of the occipital lobe seems to be cut
 off on a number of subjects, so i went in and altered the skull stripping by
 increasing the watershed threshold to 35 and using -no-wsgcaatlas.  When i
 review the scans afterwards, the pial and WM surfaces haven't included the
 original missing sections of the scans.  How do i go back and include these
 missing sections?

 I have attached a screenshots.

 Thank you kindly

 Julia


  Julia Hill
 Research Assistant

 School of Psychiatry

 University of New South Wales

   Previously Prince of Wales Medical Research Institute

  www.NeuRA.edu.au http://neura.edu.au/
 Barker Street Randwick Sydney NSW 2031 Australia
 PO Box 1165 Randwick Sydney NSW 2031 Australia
 *T *+61 2 9399 1268



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Re: [Freesurfer] DOSS or DODS

2011-08-22 Thread Tetiana Dadakova
Hello Douglas,

I did as you suggested and I got the results, but I still have
difficulty understanding how exactly the choice of Design Matrix Type
influences the analysis, so I have several questions:

1. When I look at thickness difference between two groups and choose
age as nuisance parameter, doesn't it mean that calculation take into
account the difference in slopes already (as I correct for age)? So
therefore, when I also choose DODS or DOSS I do kind of double
correction (matrix type + nuisance), don't I?
2. When I choose e.g. DODS and do the analysis, can I see the slopes
(or the values of slopes) for two groups somehow? In which file this
output is?
3. Can you recommend me anything to read regarding mathematics of how
the analysis is done with either matrix type?
4. Just in case you know: how is this step implemented in SPM? It also
uses glm, but it doesn't ask for the DODS vs DOSS choice.

Thank you, I appreciate you time and help,
Tanja.



On Wed, Aug 17, 2011 at 6:19 PM, Tetiana Dadakova tetian...@gmail.com wrote:
 Thank you, Douglas.

 On Wed, Aug 17, 2011 at 5:48 PM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu wrote:

 Hi Tanja, you should use DODS and test for a difference between the age
 slopes of the groups (ie, an interaction between group and age). If there
 are no significant interactions, you should then use DOSS to test for the
 difference between thicknesses.
 doug

 Tetiana Dadakova wrote:

 Dear all,

 I have two groups of subjects, and I want to see a difference in
 thickness between them controlling for age.
 I couldn't find any information in the literature on how the subject's
 brains in my groups develop with age. Therefore I can't tell whether
 thickness as a function of age for both groups has the same slope or
 different.

 My question is if in this case I should use DODS?

 Thank you,
 Tanja.
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[Freesurfer] qdec: Measure: area vs area.pial

2011-08-19 Thread Tetiana Dadakova
Dear list,

In qdec in Measure option I can choose either area or area.pial.
What is the difference between them?

Thank you,
Tanja.
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Re: [Freesurfer] Error while loading qdec project file

2011-08-18 Thread Tetiana Dadakova
Dear Nick, dear all,

I am still having problem with loading the Project FIle.
When I save the Project File, one of the lines I get in the terminal window is:

cp: /Applications/freesurfer/subjects/qdec/*.levels: No such file or directory

I have several folders in /qdec, and a separate *.levels file in each
folder. Can it cause the problem?

Thank you,
Tanja.



On Wed, Jul 20, 2011 at 1:30 PM, Tetiana Dadakova tetian...@gmail.com wrote:
 Hi Nick,

 Unfortunately doesn't help. When I remove the folder
 qdec_project_archive from /tmp, and then try to Load Project File, a
 new qdec_project_archive is created, but it only contains those four
 folders/files that I mentioned in previous email. No qdec.table.dat.

 Is it the same qdec.table.dat that I use as Data Table just after starting 
 qdec?

 Thank you,
 Tanja.


 On Tue, Jul 12, 2011 at 11:00 PM, Nick Schmansky
 ni...@nmr.mgh.harvard.edu wrote:
 try deleting the directory qdec_project_archive:

 cd /tmp
 rm -Rf qdec_project_archive


 then run the Load Project command in Qdec.

 n.


 On Tue, 2011-07-12 at 19:10 +0200, Tetiana Dadakova wrote:
 When the Load Project is run, nothing is created in
 /tmp/qdec_project_archive, and then the error appears in terminal
 window.
 The only files/folders I have in /tmp/qdec_project_archive are:
 fsaverage, QdecProjectMetadata.txt, Untitled (this is the folder named
 as my project), Version.txt.

 Thank you,
 Tanja.


 On Mon, Jul 11, 2011 at 8:15 PM, Nick Schmansky
 ni...@nmr.mgh.harvard.edu wrote:
  what happens when the Load Project selection is run?
  when it is being saved, i expect it to exist in the tmp dir while it is
  being created, then it is deleted.  when it is loaded, it should extract
  it to that directory.
 
  n.
 
  On Thu, 2011-07-07 at 09:59 +0200, Tetiana Dadakova wrote:
  Hi Nick,
 
  I have Mac OS X 10.6.7.
  Now I found the tmp folder, and can explain in more details what happens:
  As I save the Project File, the qdec_project_archive/qdec.table.dat is
  created, but it exists in /tmp only for several seconds and then
  disappears.
  Have you heard about something like this before? Do you know what the
  problem can be?
 
  Thank you,
  Tanja.
 
 
  On Wed, Jul 6, 2011 at 10:03 PM, Nick Schmansky
  ni...@nmr.mgh.harvard.edu wrote:
   what is your operating system?  linux and mac typically have a /tmp 
   dir,
   unless you're running on a cluster?
  
   n.
  
   On Wed, 2011-07-06 at 15:46 +0200, Tetiana Dadakova wrote:
   Dear experts,
  
   When I try to load a saved Project File, I get an error:
  
   Loading data table /tmp/qdec_project_archive/qdec.table.dat...
   ERROR: could not open /tmp/qdec_project_archive/qdec.table.dat
   Error loading the project file.
  
   I do not have any /tmp subdirectory. Should it appear when I save the
   Project File? Should it be in /qdec directory?
  
   Thank you,
   Tanja.
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[Freesurfer] DOSS or DODS

2011-08-17 Thread Tetiana Dadakova
Dear all,

I have two groups of subjects, and I want to see a difference in
thickness between them controlling for age.
I couldn't find any information in the literature on how the subject's
brains in my groups develop with age. Therefore I can't tell whether
thickness as a function of age for both groups has the same slope or
different.

My question is if in this case I should use DODS?

Thank you,
Tanja.
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[Freesurfer] literature about multiple comparison correction

2011-07-21 Thread Tetiana Dadakova
Dear list,

Could you please recommend the literature about multiple comparisons
correction, especially about Monte-Carlo simulation.

Thank you,
Tanja.
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Re: [Freesurfer] Error while loading qdec project file

2011-07-20 Thread Tetiana Dadakova
Hi Nick,

Unfortunately doesn't help. When I remove the folder
qdec_project_archive from /tmp, and then try to Load Project File, a
new qdec_project_archive is created, but it only contains those four
folders/files that I mentioned in previous email. No qdec.table.dat.

Is it the same qdec.table.dat that I use as Data Table just after starting qdec?

Thank you,
Tanja.


On Tue, Jul 12, 2011 at 11:00 PM, Nick Schmansky
ni...@nmr.mgh.harvard.edu wrote:
 try deleting the directory qdec_project_archive:

 cd /tmp
 rm -Rf qdec_project_archive


 then run the Load Project command in Qdec.

 n.


 On Tue, 2011-07-12 at 19:10 +0200, Tetiana Dadakova wrote:
 When the Load Project is run, nothing is created in
 /tmp/qdec_project_archive, and then the error appears in terminal
 window.
 The only files/folders I have in /tmp/qdec_project_archive are:
 fsaverage, QdecProjectMetadata.txt, Untitled (this is the folder named
 as my project), Version.txt.

 Thank you,
 Tanja.


 On Mon, Jul 11, 2011 at 8:15 PM, Nick Schmansky
 ni...@nmr.mgh.harvard.edu wrote:
  what happens when the Load Project selection is run?
  when it is being saved, i expect it to exist in the tmp dir while it is
  being created, then it is deleted.  when it is loaded, it should extract
  it to that directory.
 
  n.
 
  On Thu, 2011-07-07 at 09:59 +0200, Tetiana Dadakova wrote:
  Hi Nick,
 
  I have Mac OS X 10.6.7.
  Now I found the tmp folder, and can explain in more details what happens:
  As I save the Project File, the qdec_project_archive/qdec.table.dat is
  created, but it exists in /tmp only for several seconds and then
  disappears.
  Have you heard about something like this before? Do you know what the
  problem can be?
 
  Thank you,
  Tanja.
 
 
  On Wed, Jul 6, 2011 at 10:03 PM, Nick Schmansky
  ni...@nmr.mgh.harvard.edu wrote:
   what is your operating system?  linux and mac typically have a /tmp dir,
   unless you're running on a cluster?
  
   n.
  
   On Wed, 2011-07-06 at 15:46 +0200, Tetiana Dadakova wrote:
   Dear experts,
  
   When I try to load a saved Project File, I get an error:
  
   Loading data table /tmp/qdec_project_archive/qdec.table.dat...
   ERROR: could not open /tmp/qdec_project_archive/qdec.table.dat
   Error loading the project file.
  
   I do not have any /tmp subdirectory. Should it appear when I save the
   Project File? Should it be in /qdec directory?
  
   Thank you,
   Tanja.
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Re: [Freesurfer] how can do ''mri_convert''quickly when there are too many subjects

2011-07-15 Thread Tetiana Dadakova
Hi Wang,

You can try

foreach s (subj1 subj2 etc)
mri_convert $s.nii $s.nii.gz
end

Hope it works,
Tanja.


2011/7/15 汪贵宏 wgh0...@126.com:
   Hi Bruce,

  In our research,if there are 100 subjects,how can I  process these data
 easily.For example,when I want to compare their thickness's difference,at
 first,I should do
  mri_convert  bert.nii bert.nii.gz,but when there are too many subjects,is
 there a way to do all of these 100 subjects at the same time?

  Many thanks,
  Wang



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Re: [Freesurfer] Error while loading qdec project file

2011-07-12 Thread Tetiana Dadakova
When the Load Project is run, nothing is created in
/tmp/qdec_project_archive, and then the error appears in terminal
window.
The only files/folders I have in /tmp/qdec_project_archive are:
fsaverage, QdecProjectMetadata.txt, Untitled (this is the folder named
as my project), Version.txt.

Thank you,
Tanja.


On Mon, Jul 11, 2011 at 8:15 PM, Nick Schmansky
ni...@nmr.mgh.harvard.edu wrote:
 what happens when the Load Project selection is run?
 when it is being saved, i expect it to exist in the tmp dir while it is
 being created, then it is deleted.  when it is loaded, it should extract
 it to that directory.

 n.

 On Thu, 2011-07-07 at 09:59 +0200, Tetiana Dadakova wrote:
 Hi Nick,

 I have Mac OS X 10.6.7.
 Now I found the tmp folder, and can explain in more details what happens:
 As I save the Project File, the qdec_project_archive/qdec.table.dat is
 created, but it exists in /tmp only for several seconds and then
 disappears.
 Have you heard about something like this before? Do you know what the
 problem can be?

 Thank you,
 Tanja.


 On Wed, Jul 6, 2011 at 10:03 PM, Nick Schmansky
 ni...@nmr.mgh.harvard.edu wrote:
  what is your operating system?  linux and mac typically have a /tmp dir,
  unless you're running on a cluster?
 
  n.
 
  On Wed, 2011-07-06 at 15:46 +0200, Tetiana Dadakova wrote:
  Dear experts,
 
  When I try to load a saved Project File, I get an error:
 
  Loading data table /tmp/qdec_project_archive/qdec.table.dat...
  ERROR: could not open /tmp/qdec_project_archive/qdec.table.dat
  Error loading the project file.
 
  I do not have any /tmp subdirectory. Should it appear when I save the
  Project File? Should it be in /qdec directory?
 
  Thank you,
  Tanja.
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  The information in this e-mail is intended only for the person to whom it 
  is
  addressed. If you believe this e-mail was sent to you in error and the 
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  contains patient information, please contact the Partners Compliance 
  HelpLine at
  http://www.partners.org/complianceline . If the e-mail was sent to you in 
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Re: [Freesurfer] Error while loading qdec project file

2011-07-07 Thread Tetiana Dadakova
Hi Nick,

I have Mac OS X 10.6.7.
Now I found the tmp folder, and can explain in more details what happens:
As I save the Project File, the qdec_project_archive/qdec.table.dat is
created, but it exists in /tmp only for several seconds and then
disappears.
Have you heard about something like this before? Do you know what the
problem can be?

Thank you,
Tanja.


On Wed, Jul 6, 2011 at 10:03 PM, Nick Schmansky
ni...@nmr.mgh.harvard.edu wrote:
 what is your operating system?  linux and mac typically have a /tmp dir,
 unless you're running on a cluster?

 n.

 On Wed, 2011-07-06 at 15:46 +0200, Tetiana Dadakova wrote:
 Dear experts,

 When I try to load a saved Project File, I get an error:

 Loading data table /tmp/qdec_project_archive/qdec.table.dat...
 ERROR: could not open /tmp/qdec_project_archive/qdec.table.dat
 Error loading the project file.

 I do not have any /tmp subdirectory. Should it appear when I save the
 Project File? Should it be in /qdec directory?

 Thank you,
 Tanja.
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 contains patient information, please contact the Partners Compliance HelpLine 
 at
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 error
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 properly
 dispose of the e-mail.



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[Freesurfer] having two freesurfer versions at one computer

2011-07-06 Thread Tetiana Dadakova
Dear list,

I would like to install both 5.0 and 5.1 versions on my computer. But
I am not sure how exactly I should proceed after downloading the 5.1
(5.0 is already installed).
For example, how should I set FREESURFER_HOME, can it be the same for
both versions? Also, can I have my 5.0 in /Applications/freesurfer and
5.1 in /Applications/freesurfer5.1/freesurfer ?

Thank you,
Tanja.
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[Freesurfer] Error while loading qdec project file

2011-07-06 Thread Tetiana Dadakova
Dear experts,

When I try to load a saved Project File, I get an error:

Loading data table /tmp/qdec_project_archive/qdec.table.dat...
ERROR: could not open /tmp/qdec_project_archive/qdec.table.dat
Error loading the project file.

I do not have any /tmp subdirectory. Should it appear when I save the
Project File? Should it be in /qdec directory?

Thank you,
Tanja.
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contains patient information, please contact the Partners Compliance HelpLine at
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Re: [Freesurfer] loading qdec.table.dat error

2011-05-23 Thread Tetiana Dadakova
Thank you Nick,

Now I have another error:

Loading data table
/Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat...
Number of columns:  384
fsid column:1
Number of factors:  383
Number of subjects: 0
ERROR: QdecDataTable::Load: number of subjects = 0
Error loading the data table.

Although there are just 3 columns and 126 subjects.Maybe I do
something wrong when creating the file, therefore here are my steps:
1. Create table it in MS Excel, save it as tab-delimited qdec.table.txt
2. Open qdec.table.txt and end one carriage return in the end to
prevent problem described above
3. change .txt into .dat

Am I doing something wrong?

Thanks,
Tanja.


On Sat, May 21, 2011 at 6:09 PM, Nick Schmansky
ni...@nmr.mgh.harvard.edu wrote:
 I think you might need to add an extra carriage return at the end of the
 last line.  in other words, your cursor should go an empty line at the
 bottom of the file.

 n.



 On Sat, 2011-05-21 at 14:34 +0200, Tetiana Dadakova wrote:
 Dear list,

 I am trying to load qdec.table.dat file using qdec, and get the following 
 error:

 Loading data table
 /Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat...
 QdecDataTable::Load: will attempt to open as Mac text file...
 Number of columns:  3
 fsid column:        1
 Number of factors:  2
 Number of subjects: 126
 ERROR: QdecDataTable::Load: problem parsing file
 /Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat
 This line did not appear to end with a newline:
 PAT_ViOl        25      pat
 Error loading the data table.

 This is the last line in the file and therefore there is no new line after 
 it.
 What can cause this error?

 Thank you,
 Tanja.
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Re: [Freesurfer] loading qdec.table.dat error

2011-05-23 Thread Tetiana Dadakova
Ok, now everything works. I just opened the file in terminal using
pico and saved it.

On Mon, May 23, 2011 at 9:43 AM, Tetiana Dadakova tetian...@gmail.com wrote:
 Thank you Nick,

 Now I have another error:

 Loading data table
 /Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat...
 Number of columns:  384
 fsid column:        1
 Number of factors:  383
 Number of subjects: 0
 ERROR: QdecDataTable::Load: number of subjects = 0
 Error loading the data table.

 Although there are just 3 columns and 126 subjects.Maybe I do
 something wrong when creating the file, therefore here are my steps:
 1. Create table it in MS Excel, save it as tab-delimited qdec.table.txt
 2. Open qdec.table.txt and end one carriage return in the end to
 prevent problem described above
 3. change .txt into .dat

 Am I doing something wrong?

 Thanks,
 Tanja.


 On Sat, May 21, 2011 at 6:09 PM, Nick Schmansky
 ni...@nmr.mgh.harvard.edu wrote:
 I think you might need to add an extra carriage return at the end of the
 last line.  in other words, your cursor should go an empty line at the
 bottom of the file.

 n.



 On Sat, 2011-05-21 at 14:34 +0200, Tetiana Dadakova wrote:
 Dear list,

 I am trying to load qdec.table.dat file using qdec, and get the following 
 error:

 Loading data table
 /Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat...
 QdecDataTable::Load: will attempt to open as Mac text file...
 Number of columns:  3
 fsid column:        1
 Number of factors:  2
 Number of subjects: 126
 ERROR: QdecDataTable::Load: problem parsing file
 /Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat
 This line did not appear to end with a newline:
 PAT_ViOl        25      pat
 Error loading the data table.

 This is the last line in the file and therefore there is no new line after 
 it.
 What can cause this error?

 Thank you,
 Tanja.
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[Freesurfer] loading qdec.table.dat error

2011-05-21 Thread Tetiana Dadakova
Dear list,

I am trying to load qdec.table.dat file using qdec, and get the following error:

Loading data table
/Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat...
QdecDataTable::Load: will attempt to open as Mac text file...
Number of columns:  3
fsid column:1
Number of factors:  2
Number of subjects: 126
ERROR: QdecDataTable::Load: problem parsing file
/Applications/freesurfer/subjects/group_analysis/qdec/qdec.table.dat
This line did not appear to end with a newline:
PAT_ViOl25  pat
Error loading the data table.

This is the last line in the file and therefore there is no new line after it.
What can cause this error?

Thank you,
Tanja.
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Re: [Freesurfer] How to proceed after manual edit of segmentation

2011-05-05 Thread Tetiana Dadakova
Thank you Bruce,

So if I want to edit both cortex and subcortical structures, should
the steps be the following:

1. edit wm.mgz
2. recon-all -autorecon2-wm -subjid
3. edit subcortical structures
4. recon-all -autorecon2 -autorecon3 -subjid ?

Best wishes,
Tanja.

On Thu, May 5, 2011 at 2:40 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:
 Hi Tanja

 yes, there is really no visible extreme capsule white matter, I guess
 because it is so thin. If you are trying to fix the surfaces you will want
 to edit the wm.mgz though, not the aseg.mgz.

 cheers
 Bruce

 On Thu, 5 May 2011, Tetiana Dadakova wrote:

 Dear Bruce,

 For some of my subjects the segmentation of putamen sticks to the
 cortex (please look at attached image before.jpg). Therefore, I do
 some manual corrections that affect the cortex (please look at
 attached image after.jpg).

 How should I proceed after this kind of manual correction?

 Thank you,
 Tanja.

 On Wed, Mar 30, 2011 at 3:31 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:

 Hi Tanja
 unless the editing would change the cortex, you don't need to worry about
 it

 Bruce
 On Wed, 30 Mar 2011, Tetiana Dadakova wrote:

 Dear FreeSurfer list,

 I am making some manual correction to subcortical structures using
 Edit Segmentation Tool.
 And my question is: how should I proceed after saving aseg.mgz? Should
 I re-run autorecon2 with some options?

 Thank you,
 Tanja.
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Re: [Freesurfer] inflated surface

2011-04-30 Thread Tetiana Dadakova
Dear Bruce, Allison,

Thank you for your answer.

In tkmedit the surfaces look good.
Can this concavity mean that sulci are deeper in this region as
compared to neighboring regions? I am not sure I understand how to
interpret the inflated surface, therefore I cannot control if it is
correct.

Best wishes,
Tanja.

On Fri, Apr 29, 2011 at 8:05 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 I agree, sometimes this happens in the inflated surface and I don't think
 it's cause for concern

 Bruce
 On Fri, 29 Apr 2011, Allison Stevens wrote:

 When you look at the case in tkmedit, in that same area, do you see an
 error? Looking at your snapshot, it looks like it could be normal.

 On Apr 26, 2011, at 8:45 AM, Tetiana Dadakova tetian...@gmail.com wrote:

 Dear FreeSurfer list,

 When I look at inflated surface of my subjects (healthy males and
 females), almost all of them have a concavity in the posterior part of
 the brain (the arrow in attached image).
 It doesn't look correct to me. What can cause this problem?

 Thank you,
 Tanja.
 tksurfer.tiff
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[Freesurfer] Non-linear Volumetric Registration

2011-04-17 Thread Tetiana Dadakova
Dear list,

Could you please recommend me the literature on non-linear volumetric
registration used in FS?
Also, is there a possibility to view talairach.m3z file?

Thank you,
Tanja.
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[Freesurfer] ?h.aparc.stats file question

2011-04-14 Thread Tetiana Dadakova
Dear list,

I was trying to find the values of volumes for different cortical
regions. What I found is the 4th column (called GrayVol) in
?h.aparc.stats file.
Although, the values don't really seem to be what I look for, as
values are too small (e.g. 0.5 mm^3 for cuneus).

Could you please guide me where I should look for these values, or
probably how should I interpret the values in ?h.aparc.stats file.

Thank you,
Tanja.
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Re: [Freesurfer] ?h.aparc.stats file question

2011-04-14 Thread Tetiana Dadakova
Thank you Doug,

I was looking at the wrong column.

Best wishes,
Tanja.

On Thu, Apr 14, 2011 at 5:18 PM, Douglas N Greve
gr...@nmr.mgh.harvard.edu wrote:
 Hi Tanja, the GrayVol is the number that you should be looking at. Are you
 sure you're looking at the right column? It should be the 4th col (including
 the structure name). Eg:

 cuneus                                   1722   1127   2145  1.835 0.411
 0.160     0.072       45     5.1

 this one has:
 NumVert 1722 SurfArea 1127 GrayVol 2145
 ThickAvg 1.835

 doug





 Tetiana Dadakova wrote:

 Dear list,

 I was trying to find the values of volumes for different cortical
 regions. What I found is the 4th column (called GrayVol) in
 ?h.aparc.stats file.
 Although, the values don't really seem to be what I look for, as
 values are too small (e.g. 0.5 mm^3 for cuneus).

 Could you please guide me where I should look for these values, or
 probably how should I interpret the values in ?h.aparc.stats file.

 Thank you,
 Tanja.
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 gr...@nmr.mgh.harvard.edu
 Phone Number: 617-724-2358 Fax: 617-726-7422

 Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
 FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html



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[Freesurfer] N3 for improving cerebellum segmentation

2011-04-05 Thread Tetiana Dadakova
Dear list,

I have a question regarding intensity non-uniformity correction using
N3 (as in Boyes et al, 2008).
Does anyone have experience of using it for improving cerebellum
segmentation, specifically distinguishing between white and grey
matter in cerebellum?
If yes, what are the best values for the options: -distance and -iterations?

Cerebellum is very important for our study, therefore I am looking for
ways of how to make the segmentation as good as possible.

Thank you for your time and help,
Tanja.
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[Freesurfer] How to proceed after manual edit of segmentation

2011-03-30 Thread Tetiana Dadakova
Dear FreeSurfer list,

I am making some manual correction to subcortical structures using
Edit Segmentation Tool.
And my question is: how should I proceed after saving aseg.mgz? Should
I re-run autorecon2 with some options?

Thank you,
Tanja.
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[Freesurfer] open .gca file

2011-03-09 Thread Tetiana Dadakova
Dear FreeSurfer list,

I try to open RB_all_2008-03-26.gca by typing

mri_convert RB_all_2008-03-26.gca  -nth 0 means.mgz

and get an error:

mri_convert RB_all_2008-03-26.gca -nth 0 means.mgz
$Id: mri_convert.c,v 1.166.2.2 2010/08/10 19:11:50 greve Exp $
reading from RB_all_2008-03-26.gca...
reading frame 0 of gca
TR=0.00, TE=0.00, TI=0.00, flip angle=0.00
i_ras = (-1, 0, 0)
j_ras = (0, 0, -1)
k_ras = (0, 1, 0)
writing to means.mgz...
mghWrite(means.mgz, -1): could not open file
ERROR: failure writing means.mgz

Could you please tell me what can be wrong?

Thank you,
Tanja.
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Re: [Freesurfer] fixing hippocampus segmentation

2011-02-23 Thread Tetiana Dadakova
Dear Bruce,

The problem is that the volumes I get for hippocampus are much larger
than they should be (like 5000 mm^3 for healthy female). Same is for
some other structures.

Best wishes,
Tanja.


On Wed, Feb 23, 2011 at 3:08 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 Hi Tetiana,

 I think what you're seeing are just the consequences of a voxel-based
 segmentation. The borders have to be voxelated. Note that much of this will
 be corrected in the volume calculation that performs a partial-volume
 correction.

 cheers
 Bruce

 On Wed, 23 Feb 2011, Tetiana Dadakova wrote:

 Dear Bruce, dear all,

 I attach several images to show where I would like to manually
 interfere into segmentation process.

 img1: Hippocampus' volume covers part of amygdala and parahippocampal
 area. The intensity in these non-hippocampal regions are between
 75-95.

 img2: Segmentation of brain stem (problem point are shown by arrows).
 This problem repeats more or less for every subject.

 img3: Edges of thalamus are too pixelated. I mean, shouldn't the
 line be smoother? Can this cause overestimation of thalamus' volume?

 Manual correction (drawing) of all the mis-segmented parts would take
 a lot of time, so I would like to find out other way of controlling
 the segmentation process. (Something like putting control points
 would be perfect).

 Thank you,
 Tanja.


 On Mon, Feb 21, 2011 at 2:56 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:

 Hi Tanja,
 Can you send us an image? Is parahippocampal white matter significantly
 darker than 110?
 Bruce



 On Feb 21, 2011, at 6:41 AM, Tetiana Dadakova tetian...@gmail.com
 wrote:

 Dear Freesurfer users,

 For some of my subjects Freesurfer strongly overestimates hippocampus'
 volume. Is there any way to fix the segmentation of hippocampus by
 e.g. adding some control points (like for white matter here
 http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/ControlPoints)?

 Thank you,
 Tanja.
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Re: [Freesurfer] volume of CSF for hemispheres

2011-02-21 Thread Tetiana Dadakova
Hello Bruce,

Could you please give me a link to this coordinate tutorial. I don't
think I can find it.

Thank you,
Tanja.


On Wed, Feb 16, 2011 at 5:28 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 Hi Tanja,

 I think Doug just put up a coordinate tutorial. For each voxel in the aseg
 label you are interested, compute it's tal coords and if the x is negative
 assign it to one pool and if it is positive assign it to the other

 cheers
 Bruce


 On Wed, 16 Feb 2011, Tetiana Dadakova wrote:

 Thank you, Bruce.

 Could you recommend me any tutorial on this? Or probably can you just
 mention some steps or commands, where I should insert coordinates?

 Tanja.


 On Wed, Feb 16, 2011 at 3:15 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:

 Hi Tanja

 we don't do this by default, but I guess you could use the Talairach x
 coordinate to try to differentiate.

 cheers
 Bruce
 On Wed, 16 Feb 2011, Tetiana Dadakova wrote:

 Dear list,

 I would like to calculate CSF volume separately for left and right
 hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
 ventricles as a whole.
 Is there any possibility to get volume values for right/left parts of
 3rd, 4th and 5th ventricles?

 Thank you,
 Tanja.
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[Freesurfer] fixing hippocampus segmentation

2011-02-21 Thread Tetiana Dadakova
Dear Freesurfer users,

For some of my subjects Freesurfer strongly overestimates hippocampus'
volume. Is there any way to fix the segmentation of hippocampus by
e.g. adding some control points (like for white matter here
http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/ControlPoints)?

Thank you,
Tanja.
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[Freesurfer] volume of CSF for hemispheres

2011-02-16 Thread Tetiana Dadakova
Dear list,

I would like to calculate CSF volume separately for left and right
hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
ventricles as a whole.
Is there any possibility to get volume values for right/left parts of
3rd, 4th and 5th ventricles?

Thank you,
Tanja.
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Re: [Freesurfer] volume of CSF for hemispheres

2011-02-16 Thread Tetiana Dadakova
Thank you, Bruce.

Could you recommend me any tutorial on this? Or probably can you just
mention some steps or commands, where I should insert coordinates?

Tanja.


On Wed, Feb 16, 2011 at 3:15 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 Hi Tanja

 we don't do this by default, but I guess you could use the Talairach x
 coordinate to try to differentiate.

 cheers
 Bruce
 On Wed, 16 Feb 2011, Tetiana Dadakova wrote:

 Dear list,

 I would like to calculate CSF volume separately for left and right
 hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
 ventricles as a whole.
 Is there any possibility to get volume values for right/left parts of
 3rd, 4th and 5th ventricles?

 Thank you,
 Tanja.
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[Freesurfer] Three starting questions

2011-02-08 Thread Tetiana Dadakova
Dear FreeSurfer community,

You were very helpful for my last question, thank you.

Now I have three basic questions.

1. I would like to check the segmentation by loading T1.mgz and
aseg.mgz as an -aux volume, so that I can switch between them. How can
I do this? (tkmedit subject T1.mgz -aux aseg.mgz gives some king of
black and white segmentation instead of colorful one).

2. When I press View - View configuration, I have three options there
(Single view, Multiple orientations, and Mosaic). How can I view just
3 orientations or 2 (e.g. sagittal and transverse)?

3. Do MacOS users have problems with mouse? When I try to edit
segmentation or surfaces with Edit Tools, my mouse doesn't seem to
work. I mean, when I click on the pixel with any of three buttons,
nothing changes. I saw similar problem on the mailing list, but there
was no answer.

Thank you for your time,
Tanja.
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Re: [Freesurfer] Segmentation problems

2011-02-02 Thread Tetiana Dadakova
Dear Bruce and all,

I am trying to fix the scull strip, as it affects ?h.white/?h.pial
surfaces. I used -wsthresh with preflooding height of down to 1. It
didn't really help much. Therefore, I have two question:

1. Regarding mri_gcut: should I use the default intensity of 110 for
white matter mask? How much it is acceptable to change the -T
parameter (threshold to value of WM intensity), which default value is
0.36?

2. Regarding manual removing of some voxels: the 'Edit Voxels' tool
doesn't seem to work on MacOS. Even though I have a 3-button mouse,
when I try click (or click and drag) with any mouse button, nothing
happens. What can be wrong?

Thank you,
Tetiana.


On Mon, Jan 31, 2011 at 2:00 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 Hi Tetiana,

 do you mean the bit of skull left over that is misclassified? I wouldn't
 worry about it unless it causes the ?h.white/?h.pial surfaces to be
 inaccurate. In general we use the surface-based measures to estimate
 gray/white morphometry and the aseg for everything else. It is a minor skull
 strip failure and you could either fix it by manually erasing it from the
 brainmask.mgz or trying to mess with the watershed/gcut.

 cheers
 Bruce


 On Mon, 31 Jan 2011, Tetiana Dadakova wrote:

 Dear FreeSurfer users,

 I run a recon-all -all for one of my subjects. When I check the
 segmentation, it looks incorrect (see attached picture).
 What can be the problem? At which step can I change something? Should
 I do manual correction?

 Thank you,
 Tetiana.



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[Freesurfer] Testing installation, recon-all problem

2011-01-19 Thread Tetiana Dadakova
Dear Freesurfer users,

I installed Freesurfer and now I am trying to test the installation.
When I type recon-all -s bert -all, I get an error

ERROR: you do not have write permission to
/Applications/freesurfer/subjects/bert

But actually I do have write permission to this folder. Do you have
any idea what can be wrong? Or what else should I check regarding
installation to understand where this problem comes from?

Thank you for your time,
Tetiana.
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The information in this e-mail is intended only for the person to whom it is
addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.