[Freesurfer] incomplete forceps

2013-05-06 Thread Roschinski, Benjamin
Dear Freesurfer experts,

we have a problem with the forceps.
After the first trac-all we had a forcpes minor with a really unusually 
structure so we tried to fix it with an rerun of the trac-all.
The result was a forceps minor with a third thigh in the sagittal axis.
We did a second rerun and now the forceps minor normalized.
Our problem is that we don´t know if we should do more trac-all reruns by other 
patients with difficult tracula or how we should interpret this result.
Do you have any ideas to solve this?
The second problem is that we have many many  tracula results with incomplete 
forcepes minor or major.
We know that the forcepes are the most difficult tracts because of the 
curvature but do you have some ideas to fix that problem?

Kind regards
Benjamin


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Re: [Freesurfer] Probably activation due to vessels

2013-05-06 Thread Jörg Pfannmöller
Thanks for your help. It works fine if one uses 

preproc-sess -per-run -fwhm 5 -fsd bold -s sess01 ... .



On Fri, 19 Oct 2012 12:49:00 -0400
Douglas N Greve gr...@nmr.mgh.harvard.edu wrote:

 You'll have to run preproc like:
preproc-sess -per-session -fwhm 5 -fsd bold -s sess01
 In this case, you are just specifiying -per-session and not specifying 
 -mni305 or -surface
 
 When you run mkanalysis-sess, specify -native instead of -mni305 or 
 -surface, like:
 mkanalysis-sess -native -fwhm 5 ...
 
 doug
 
 
 
 On 10/19/2012 03:59 AM, Jörg Pfannmöller wrote:
  Hi Doug,
 
  the preprocessing is fine the quaility factor for the registration between 
  functional and anatomical is ~0.3. Have I to use feat to do the volume 
  analysis?
 
  Cheers pfannmoe
 
  On Thu, 18 Oct 2012 11:50:38 -0400
  Douglas N Grevegr...@nmr.mgh.harvard.edu  wrote:
 
  It is too hard to tell what is going on here from just this image. I
  would not immediately conclude that it is a vessel. Does the activation
  otherwise look ok? What about other contrasts? Is the registration
  accurate? When trying to debug these things, it often makes sense to
  analyze the data in the volume.
  doug
 
  On 10/17/2012 12:31 PM, Jörg Pfannmöller wrote:
  It is attached to this mail.
 
 
 
  On Tue, 16 Oct 2012 16:16:54 -0400
  Douglas N Grevegr...@nmr.mgh.harvard.edu   wrote:
 
  can you send a pic?
 
 
  On 10/16/2012 05:44 AM, Jörg Pfannmöller wrote:
  Hi Doug,
 
  the analysis is done on the cortex surface. The following commands are 
  used for the analysis of the functional activation in the right 
  hemisphere cortex:
 
  preproc-sess -s sessionID -fsd bold -nostc -surface fsaverage lhrh 
  -mni305 -fwhm 0 -per-run -nosmooth
 
  plot-twf-sess   -s sessionID -fsd bold -mc
 
  tkregister-sess -s sessionID -fsd bold -per-run -bbr-sum
 
  mkanalysis-sess -fsd bold -surface fsaverage rh -fwhm 0 -event-related 
  -paradigm stim.par -nconditions 1 -spmhrf 0 -TR 2 -refeventdur 10 
  -nskip 5 -polyfit 2 -analysis stim.sm0.rh -force
 
  mkcontrast-sess -analysis  stim.sm0.rh -contrast stim-li-v-base -a 1
 
  selxavg3-sess -s sessionID -analysis stim.sm0.rh -no-preproc
 
  tksurfer-sess -s sessionID -analysis stim.sm0.rh -c stim-li-v-base -tcl 
  ./label_01.tcl.
 
  Left hemisphere and sub-cortical analysis are also carried out. Results 
  are depicted on the flatted cortex surface in the primary somatosensory 
  cortex.
  This label is a combination of the freesurfer areas BA1, BA2, BA3a and 
  BA3b. The activation is masked to this label. An example of the line 
  like pattern
  is uploaded on your ftp server using my email (pfannmoelj ... 
  uni-greifswald.de, the at sign is replaced by dots) as the password. 
  There is a snaking
  line in the middle of the image which is a candidate for a vessel. In 
  other images the straight line like patterns or line like patterns with 
  gaps are
  found. Is there a way to analyze the data in a volume based stream 
  without differentiation between cortex and sub-cortical brain in which 
  the distance
  of the line like pattern relative to the gray substance is visible? 
  This could be used in order to classify between true activation and 
  vessel activation.
  We have epi data with spatial resolution of 2x2x4mm^3 (used to generate 
  attached image) and 1.5x1.5x2mm^3 which both show line like patterns. 
  Structural
  data are taken using the single echo freesurfer protocol for the flash 
  sequence, recommended for cortex. I hope those information are of help.
 
  Sincerely yours
 
pfannmoe
 
 
  On Mon, 15 Oct 2012 17:52:04 -0400
  Douglas N Grevegr...@nmr.mgh.harvard.eduwrote:
 
  Hi Jorg, can you tell us a little more? A picture would be good. Also,
  describe how you have done your analysis (eg, on the surface or in the
  volume, how much smoothing).
  doug
 
  On 10/15/2012 11:01 AM, wrote:
  Dear Freesurfers,
 
  I computed the functional activation in a sensory task using 
  freesurfer's fsfast stream. In the cortex surface line like activated 
  regions are present. Their extension is much larger than the 
  extension of the expected regions. Therefore, I suppose that those 
  regions are due to vessels. Is there a possibility in freesurfer to 
  remove them. Ideally there would be something like a volume based 
  mode which does not sxclude the cortex. In this mode the vessels 
  couls be identified and removed. Any help is highly apprexiated.
 
  Respectfully yours
 
 pfannmoe
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  Freesurfer mailing list
  Freesurfer@nmr.mgh.harvard.edu
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  -- 
  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
 
  ___
  

Re: [Freesurfer] Probably activation due to vessels

2013-05-06 Thread Jörg Pfannmöller
Sorry, I have to cancel my last contribution. Another Problem crossed my way. 
If I have more than one run, only the first one is preprocessed if i use 
-per-session. What can I do about it?
If I use -per-run all runs are preprocessed, but selxavg3-sess tells me that it 
can not determine the file format of the fmc files. Actually those files are 
called fmcpr, if I use -per-run. How can do I have to proceed if there is more 
than one run?





On Mon, 6 May 2013 10:54:54 +0200
Jörg Pfannmöller pfannmo...@uni-greifswald.de wrote:

 Thanks for your help. It works fine if one uses 
 
 preproc-sess -per-run -fwhm 5 -fsd bold -s sess01 ... .
 
 
 
 On Fri, 19 Oct 2012 12:49:00 -0400
 Douglas N Greve gr...@nmr.mgh.harvard.edu wrote:
 
  You'll have to run preproc like:
 preproc-sess -per-session -fwhm 5 -fsd bold -s sess01
  In this case, you are just specifiying -per-session and not specifying 
  -mni305 or -surface
  
  When you run mkanalysis-sess, specify -native instead of -mni305 or 
  -surface, like:
  mkanalysis-sess -native -fwhm 5 ...
  
  doug
  
  
  
  On 10/19/2012 03:59 AM, Jörg Pfannmöller wrote:
   Hi Doug,
  
   the preprocessing is fine the quaility factor for the registration 
   between functional and anatomical is ~0.3. Have I to use feat to do the 
   volume analysis?
  
   Cheers pfannmoe
  
   On Thu, 18 Oct 2012 11:50:38 -0400
   Douglas N Grevegr...@nmr.mgh.harvard.edu  wrote:
  
   It is too hard to tell what is going on here from just this image. I
   would not immediately conclude that it is a vessel. Does the activation
   otherwise look ok? What about other contrasts? Is the registration
   accurate? When trying to debug these things, it often makes sense to
   analyze the data in the volume.
   doug
  
   On 10/17/2012 12:31 PM, Jörg Pfannmöller wrote:
   It is attached to this mail.
  
  
  
   On Tue, 16 Oct 2012 16:16:54 -0400
   Douglas N Grevegr...@nmr.mgh.harvard.edu   wrote:
  
   can you send a pic?
  
  
   On 10/16/2012 05:44 AM, Jörg Pfannmöller wrote:
   Hi Doug,
  
   the analysis is done on the cortex surface. The following commands 
   are used for the analysis of the functional activation in the right 
   hemisphere cortex:
  
   preproc-sess -s sessionID -fsd bold -nostc -surface fsaverage lhrh 
   -mni305 -fwhm 0 -per-run -nosmooth
  
   plot-twf-sess   -s sessionID -fsd bold -mc
  
   tkregister-sess -s sessionID -fsd bold -per-run -bbr-sum
  
   mkanalysis-sess -fsd bold -surface fsaverage rh -fwhm 0 
   -event-related -paradigm stim.par -nconditions 1 -spmhrf 0 -TR 2 
   -refeventdur 10 -nskip 5 -polyfit 2 -analysis stim.sm0.rh -force
  
   mkcontrast-sess -analysis  stim.sm0.rh -contrast stim-li-v-base -a 1
  
   selxavg3-sess -s sessionID -analysis stim.sm0.rh -no-preproc
  
   tksurfer-sess -s sessionID -analysis stim.sm0.rh -c stim-li-v-base 
   -tcl ./label_01.tcl.
  
   Left hemisphere and sub-cortical analysis are also carried out. 
   Results are depicted on the flatted cortex surface in the primary 
   somatosensory cortex.
   This label is a combination of the freesurfer areas BA1, BA2, BA3a 
   and BA3b. The activation is masked to this label. An example of the 
   line like pattern
   is uploaded on your ftp server using my email (pfannmoelj ... 
   uni-greifswald.de, the at sign is replaced by dots) as the password. 
   There is a snaking
   line in the middle of the image which is a candidate for a vessel. In 
   other images the straight line like patterns or line like patterns 
   with gaps are
   found. Is there a way to analyze the data in a volume based stream 
   without differentiation between cortex and sub-cortical brain in 
   which the distance
   of the line like pattern relative to the gray substance is visible? 
   This could be used in order to classify between true activation and 
   vessel activation.
   We have epi data with spatial resolution of 2x2x4mm^3 (used to 
   generate attached image) and 1.5x1.5x2mm^3 which both show line like 
   patterns. Structural
   data are taken using the single echo freesurfer protocol for the 
   flash sequence, recommended for cortex. I hope those information are 
   of help.
  
   Sincerely yours
  
 pfannmoe
  
  
   On Mon, 15 Oct 2012 17:52:04 -0400
   Douglas N Grevegr...@nmr.mgh.harvard.eduwrote:
  
   Hi Jorg, can you tell us a little more? A picture would be good. 
   Also,
   describe how you have done your analysis (eg, on the surface or in 
   the
   volume, how much smoothing).
   doug
  
   On 10/15/2012 11:01 AM, wrote:
   Dear Freesurfers,
  
   I computed the functional activation in a sensory task using 
   freesurfer's fsfast stream. In the cortex surface line like 
   activated regions are present. Their extension is much larger than 
   the extension of the expected regions. Therefore, I suppose that 
   those regions are due to vessels. Is there a possibility in 
   freesurfer to remove them. Ideally there would be something like a 
   

Re: [Freesurfer] Loading V5.2 on Virtualbox

2013-05-06 Thread zkauf...@nmr.mgh.harvard.edu
Hello Will,

Clicking the Terminal icon on the desktop will load Freesurfer. From 
that point on its just a matter of typing the appropriate commands.

-Zeke

On 05/04/2013 09:27 AM, will brown wrote:
 I am endeavouring to install FreeSurfer on a windows 8 PC. Virtualbox is
 installed along with the relevant FreeSurfer download, I have followed
 the installation instructions on the freesurfer wiki but when the
 virtualbox is running I do not see the XTerm shortcut that is shown on
 the last pane of the installation instructions
 https://surfer.nmr.mgh.harvard.edu/fswiki/Installation/FreeSurferVirtualImage,
 all I see is the attached screenshot. I have also downloaded the fast
 tutorial files (admittedly they were downloaded to the host machine
 other than virtualbox and I'm not sure how to move them to virtualbox if
 I need to do so). So, I believe I've got everything relevant downloaded,
 how do I now get FreeSurfer running? Any help would be greatly
 appreciated. Thanks, Will.


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The information in this e-mail is intended only for the person to whom it is
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contains patient information, please contact the Partners Compliance HelpLine at
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but does not contain patient information, please contact the sender and properly
dispose of the e-mail.



[Freesurfer] Gradient unwarp software / Siemens Verio scanner

2013-05-06 Thread Christian Thode Larsen
Hi,

I'm currently exploring gradient unwarping of data on a Siemens Trio
scanner (sonata coils) and a Siemens Verio scanner. I have got lists
with coil coefficients for both scanners.
According to the FS mail archives, you provide a binary for gradient
unwarping, but not any scanner tables (due to licensing), or the
conversion scripts mentioned
here:https://surfer.nmr.mgh.harvard.edu/fswiki/GradientUnwarping
https://surfer.nmr.mgh.harvard.edu/fswiki/GradientUnwarping.

With some googling, I have found this
version:https://code.google.com/p/gradunwarp/
https://code.google.com/p/gradunwarp/https://code.google.com/p/gradunwarp/

which seems to be the latest available version of the software
(originally written by Czanner). This package also provides the table
conversion scripts. The development appears to be stalled, however. I
have used this version for (what seems to be) successful gradient
unwarping of Siemens Trio data.


A couple of questions:

1)
Can you enlighten me as to the latest and 'most proper' version of the
software to use for gradient unwarping (bug fixes, scanner support)? Is
the binary in FS further developed than the google docs version, and if
so, have I somehow missed the table conversion scripts?

2)
At DRCMR (see below), we have a Siemens Verio scanner, as well as a list
with the associated gradient coil coefficients. As of now, it seems like
the correction software (public FS + google doc version) does not
support this scanner type. Is this something that could possibly  be
included? Or is a newer (possibly non-public) version available that
supports it already? We're aware that the scanner can perform correction
by itself, but as far as I know this is only in 3D, and also requires
you to do it immediately after the sequence.


Best Regards,
Christian Thode Larsen
PhD Student
Technical University of Denmark (DTU) / Danish Research Centre for
Magnetic Resonance (DRCMR)
Supervisor: Koen Van Leemput
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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
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but does not contain patient information, please contact the sender and properly
dispose of the e-mail.


Re: [Freesurfer] tip and tricks with patient with one big ventricle...

2013-05-06 Thread Nick Schmansky
Gonzalo,

Freeview will have a few small usability features to make it behave more
like tkmedit and tksurfer, but that update doesnt affect recon-all.

Nick


 Hi Nick:

   Ok... Tomorrow Sunday I will download and begin to test it...

   And which other new features has version 5.3.0 over 5.2.0 ?...

   Sincerely,


 Gonzalo Rojas Costa


 On Fri, May 3, 2013 at 5:46 PM, Nick Schmansky
 ni...@nmr.mgh.harvard.edu wrote:
 this link is here:

 ftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0-BETA/

 the centos6_x86_64 build is there now.  the others will appear as they
 finish their builds, which can take quite a bit of time... so check back
 every day or so

 n.

 --
 Gonzalo Rojas Costa
 Laboratory for Advanced Medical Image Processing
 Department of Radiology
 Clínica las Condes
 Lo Fontecilla 441, Las Condes, Santiago, Chile.
 Tel: 56-2-2105170
 Cel: 56-9-97771785
 www.clc.cl




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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
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dispose of the e-mail.



Re: [Freesurfer] The Asymmetry of surface area or thickness

2013-05-06 Thread Douglas N Greve
Follow the steps here:
http://surfer.nmr.mgh.harvard.edu/fswiki/Xhemi



On 05/06/2013 01:41 AM, xiangbo_2010 wrote:
 Dear experts

   I want to analysis the asymmetry of surface area or thickness, 
 what I do next? thanks!



 Bo Xiang




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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer

-- 
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: https://gate.nmr.mgh.harvard.edu/filedrop2
www.nmr.mgh.harvard.edu/facility/filedrop/index.html
Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/

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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
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Re: [Freesurfer] Probably activation due to vessels

2013-05-06 Thread Douglas N Greve

If you use -per-session, all of them should be processed. Why do you 
think they are not? Also, just saying something is not working is not 
very informative. Send command lines and terminal output of the error.
thanks!
doug

On 05/06/2013 05:46 AM, Jörg Pfannmöller wrote:
 Sorry, I have to cancel my last contribution. Another Problem crossed my way. 
 If I have more than one run, only the first one is preprocessed if i use 
 -per-session. What can I do about it?
 If I use -per-run all runs are preprocessed, but selxavg3-sess tells me that 
 it can not determine the file format of the fmc files. Actually those files 
 are called fmcpr, if I use -per-run. How can do I have to proceed if there is 
 more than one run?





 On Mon, 6 May 2013 10:54:54 +0200
 Jörg Pfannmöller pfannmo...@uni-greifswald.de wrote:

 Thanks for your help. It works fine if one uses

 preproc-sess -per-run -fwhm 5 -fsd bold -s sess01 ... .



 On Fri, 19 Oct 2012 12:49:00 -0400
 Douglas N Greve gr...@nmr.mgh.harvard.edu wrote:

 You'll have to run preproc like:
 preproc-sess -per-session -fwhm 5 -fsd bold -s sess01
 In this case, you are just specifiying -per-session and not specifying
 -mni305 or -surface

 When you run mkanalysis-sess, specify -native instead of -mni305 or
 -surface, like:
 mkanalysis-sess -native -fwhm 5 ...

 doug



 On 10/19/2012 03:59 AM, Jörg Pfannmöller wrote:
 Hi Doug,

 the preprocessing is fine the quaility factor for the registration between 
 functional and anatomical is ~0.3. Have I to use feat to do the volume 
 analysis?

 Cheers pfannmoe

 On Thu, 18 Oct 2012 11:50:38 -0400
 Douglas N Grevegr...@nmr.mgh.harvard.edu  wrote:

 It is too hard to tell what is going on here from just this image. I
 would not immediately conclude that it is a vessel. Does the activation
 otherwise look ok? What about other contrasts? Is the registration
 accurate? When trying to debug these things, it often makes sense to
 analyze the data in the volume.
 doug

 On 10/17/2012 12:31 PM, Jörg Pfannmöller wrote:
 It is attached to this mail.



 On Tue, 16 Oct 2012 16:16:54 -0400
 Douglas N Grevegr...@nmr.mgh.harvard.edu   wrote:

 can you send a pic?


 On 10/16/2012 05:44 AM, Jörg Pfannmöller wrote:
 Hi Doug,

 the analysis is done on the cortex surface. The following commands are 
 used for the analysis of the functional activation in the right 
 hemisphere cortex:

 preproc-sess -s sessionID -fsd bold -nostc -surface fsaverage lhrh 
 -mni305 -fwhm 0 -per-run -nosmooth

 plot-twf-sess   -s sessionID -fsd bold -mc

 tkregister-sess -s sessionID -fsd bold -per-run -bbr-sum

 mkanalysis-sess -fsd bold -surface fsaverage rh -fwhm 0 -event-related 
 -paradigm stim.par -nconditions 1 -spmhrf 0 -TR 2 -refeventdur 10 
 -nskip 5 -polyfit 2 -analysis stim.sm0.rh -force

 mkcontrast-sess -analysis  stim.sm0.rh -contrast stim-li-v-base -a 1

 selxavg3-sess -s sessionID -analysis stim.sm0.rh -no-preproc

 tksurfer-sess -s sessionID -analysis stim.sm0.rh -c stim-li-v-base 
 -tcl ./label_01.tcl.

 Left hemisphere and sub-cortical analysis are also carried out. 
 Results are depicted on the flatted cortex surface in the primary 
 somatosensory cortex.
 This label is a combination of the freesurfer areas BA1, BA2, BA3a and 
 BA3b. The activation is masked to this label. An example of the line 
 like pattern
 is uploaded on your ftp server using my email (pfannmoelj ... 
 uni-greifswald.de, the at sign is replaced by dots) as the password. 
 There is a snaking
 line in the middle of the image which is a candidate for a vessel. In 
 other images the straight line like patterns or line like patterns 
 with gaps are
 found. Is there a way to analyze the data in a volume based stream 
 without differentiation between cortex and sub-cortical brain in which 
 the distance
 of the line like pattern relative to the gray substance is visible? 
 This could be used in order to classify between true activation and 
 vessel activation.
 We have epi data with spatial resolution of 2x2x4mm^3 (used to 
 generate attached image) and 1.5x1.5x2mm^3 which both show line like 
 patterns. Structural
 data are taken using the single echo freesurfer protocol for the flash 
 sequence, recommended for cortex. I hope those information are of help.

 Sincerely yours

pfannmoe


 On Mon, 15 Oct 2012 17:52:04 -0400
 Douglas N Grevegr...@nmr.mgh.harvard.eduwrote:

 Hi Jorg, can you tell us a little more? A picture would be good. Also,
 describe how you have done your analysis (eg, on the surface or in the
 volume, how much smoothing).
 doug

 On 10/15/2012 11:01 AM, wrote:
 Dear Freesurfers,

 I computed the functional activation in a sensory task using 
 freesurfer's fsfast stream. In the cortex surface line like 
 activated regions are present. Their extension is much larger than 
 the extension of the expected regions. Therefore, I suppose that 
 those regions are due to vessels. Is there a possibility in 
 freesurfer to remove them. 

Re: [Freesurfer] question about glm setup

2013-05-06 Thread Subhabrata Chaudhury
Hello Dr. Greve,

Thank you for your reply. I have set up the qdec.

I have gender as the discrete factor and age and clinical score as continuous 
factors. 

In order to look at the relationship between clinical score and whole brain 
cortical thickness while accounting for age and gender effects, do I select 
score as the continuous factor and age as the nuisance factor or should it be 
the other way round ? 

Thanking you in anticipation,
Subha
- Original Message -
From: Douglas Greve
Sent: 05/05/13 11:53 PM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] question about glm setup

Hi Subha, yes, you can. You will need to create a table in the format with QDEC 
expects. Have you looked at the tutorial?

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

doug

On 5/4/13 11:31 AM, Subhabrata Chaudhury wrote:
Hi, 

I am new to freesurfer. I have run reconall on 50 AD subjects. I have also run 
recon-all -qcache.

So I have the following -

1) Whole brain thickness map for each AD subject
2) age of each subject
3) gender of each subject
4) clinical score of each subject

I DO NOT have control subjects. 

I want to run a glm to investigate whether if there is a relation between the 
clinical score for each subject and their cortical thickness while accounting 
for age, gender and whole brain average thickness. 

Can I use qdec for this ? 

This is my first time doing this sort of analysis, so I will be grateful if I 
can get some step-by-step help. 

Thank you very much

Subha

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[Freesurfer] R: Re: version 5.3 coming out soon

2013-05-06 Thread stdp82
Hi Bruce, 
thank for new 5.3.
I'm finishing tracula analyis with 5.2 (I only have a subject that give me some 
problem). Do you advice me to cancel my analysis and re-run it by new version 
5.3? Is the results obtained with version 5.2 reliable?
Thank you very much,

Stefano



Messaggio originale
Da: fis...@nmr.mgh.harvard.edu
Data: 4-mag-2013 14.55
A: lukas.sch...@ukb.uni-bonn.de
Cc: freesurfer@nmr.mgh.harvard.edu
Ogg: Re: [Freesurfer] version 5.3 coming out soon

Hi Luke

Nick will post a command line you can run that should take about 2 
hours/dataset. Rerunning shouldn't be necessary. Sorry for the trouble, I 
really, really wish we had more engineering resources.

Bruce


On Sat, 4 May 2013, 
lukas.sch...@ukb.uni-bonn.de wrote:

 
 Hi Bruce,
 
 Thanks a lot for the info. Would it mean we have to completely reprocess the
 data processed with 5.2? Or at which point of the preprocessing pipeline we
 should step in to fix the problems of 5.2...? I just have finished to
 process about 200 data sets with 5.2...
 
 Best wishes,
 
 Luke
 
 Am 03.05.2013 um 02:58 schrieb Bruce Fischl fis...@nmr.mgh.harvard.edu:
 
  Hi All,
 
  We have recently uncovered problems with version 5.2. Based on these
  problems, we are recommending that people stop using 5.2, mainly in
  regards to usage of the surface data.  A new version, 5.3, will be
  released within two weeks, and a beta version for each platform will be
  available within a couple days.
 
  There were two main problems that were uncovered. First, a change was made
  that was only meant to affect the white surface placement in
  high-resolution data sets, but unfortunately is being applied to all data
  sets. This causes the white surface to contract a small amount. This
 causes
  the surface area to be smaller and cortex to be measured as thicker
  relative to version 5.1. Visually, the surfaces do not necessarily look
  less accurate, but we feel that the systematic differences with previous
  versions are ill-advised without a clear reason for the change.
 
  Second, a change made to the placement of the pial surface in order to
  improve the positioning based on T2/FLAIR that caused it to extend too far
  in some data sets during the T1-based pial surface deformation. This
  unfortunately became the default behavior, which was not intended. None of
  the dozens of test data sets we ran displayed this problem. The behavior
  was reported by other users which led us to the bug.
 
  In general, we rigorously test each version. However, our systematic
  comparison of a new version with previous versions which would have caught
  these problems was conducted prior to these changes. We are now tightening
  and regimenting our testing procedures to ensure this doesnt happen again.
  Note that there are no problems with the volumetric segmentation (aseg)
  in version 5.2.
 
  We realize that this will cause a substantial inconvenience for users. We
  have isolated and fixed the problems and have run two rounds of alpha
  testing and have one more to go, after which we will release a beta
 version
  in a couple of days to anyone that wants it.
 
  sorry for the problems.
 
  Bruce
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 is
  addressed. If you believe this e-mail was sent to you in error and the
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 HelpLine at
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 properly
  dispose of the e-mail.
 
 
 
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[Freesurfer] Open Brain Mapping at the 1st HBM Hackathon

2013-05-06 Thread Nolan Nichols
 Sent on behalf of Thomas Grabowski, OHBM 2013, LOC Chair:


Open Brain Mapping at the 1st HBM Hackathon: Open Brain Mapping in the Cloud

**

OHBM 2013 is only six weeks away, bringing the brain mapping community to
Seattle, a city at the forefront of open neuroscience and information
technology.  The Local Organizing Committee, the Allen Institute for Brain
Science, and Amazon Web Services are excited for the opportunity to
highlight these aspects of our field in the HBM
Hackathonhttp://humanbrainmapping.org/hackathon,
a meeting-long event integrated with and running parallel to the activity
in the poster and exhibition space.

 Our goals are to accelerate the development of a critical mass of
cloud-based data, analytic, and computational resources for human brain
mapping, and to provide OHBM attendees with access to and knowledge about
them.

The event is being supported by a broad spectrum of partners from the open
neuroimaging community, making it possible to allow an unprecedented degree
of access to key resources in the field, including the Allen Human Brain
Atlas, the first data release of the Human Connectome Project, the NITRC
Computational Environment, and more.  Experts from the Allen Institute,
Amazon Web Services, Human Connectome Project, NITRC, INCF, LONI, NDAR,
BIRN, and others will bring their expertise on-venue.

Register for the HBM Hackathon http://humanbrainmapping.org/hackathon to
participate in a contest organized around three challenges, to tinker less
formally, or just to be open to open neuroscience.  You’ll also receive
$100 in free AWS credits to make use of cloud computing technologies.



The contest is organized around three Challenges:

**

Challenge 1. Best imaging and gene expression relationship discovered via
integration of imaging data with the Allen Human Brain Atlas.

**

Challenge 2.  Best cortical neural systems relationship or visualization
based on integration of resting state fMRI data with other HBM Hackathon
accessible datasets.

**

Challenge 3.  To be announced the week of the meeting and pursued
completely on site.

*See the list of datasets http://ohbm-seattle.github.io/datasets*

**

Winning entries in each category receive:


*

   -

   An invitation to submit project to Frontiers in Brain Imaging Methods
   with Open Access Publication Fees waived (must undergo standard peer
   review)
   -

   Amazon Kindle Fire and/or Paperwhite (limit 3 per team)
   -

   AWS hosts AMI and/or data resulting from the hackathon free of charge
   -

   Free GitHub Membership with private repositories (Challenge 1: one year
   silver, Challenge 2: 1 year bronze, Challenge 3: six months bronze)

*
**

To learn more, visit the HBM Hackathon Blog
http://ohbm-seattle.github.io/or join the discussion
group http://www.linkedin.com/groups/HBM-Hackathon-4957800.

And be sure to register at: humanbrainmapping.org/hackathon
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Re: [Freesurfer] Pial surface errors

2013-05-06 Thread Bruce Fischl
Hi Valeria

what version are you running? It's hard to tell from a single slice, but 
what is the white-matter appearing stuff that is outside the white matter 
surface? I think that is what's messing stuff up. If you want to upload the 
data subject one of us will take a look (that is, upload the entire subject 
directory)

cheers
Bruce


On Mon, 6 May 2013, Contarino Valeria wrote:

 
 Dear Freesurfers,
 
 I usually get very satisfying results but in my last analysis I noticed some 
 errors in a few subjects' pial
 surface (see attached example image). I really don't get how it failed in 
 that way.
 What I know I can surely do is to manually modify the WM and run again the 
 autorecon command.
 
 Could someone kindly advice me on how to avoid/solve the problem in a less 
 time-consuming way?
 Thank you.
 
 Regards,
 
 Valeria Elisa Contarino, MEng
 Neuroradiology Department
 IRCCS Foundation Neurological Institute C.Besta
 Via Celoria 11,
 20133 Milano, Italy
 ph: +39 02 23942472
 
 
 
 
 
 
 
 
 
 
 

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[Freesurfer] DTI metrics along the whole tract?

2013-05-06 Thread celine
Hi Tracula team
I am using tracula to study the corticospinal tract in a patient
population. I am wondering if there would be a way to have the different
DTI metrics from the whole tract at different depth/portion of the tracts.
Something like the information given by the pathstats.byvoxel.txt file,
but for the whole width of the tract?
If not, do you see a way to sample the value of the diffusion metrics on a
certain tract starting from the cortex (like with projfrac or projdist
with the WM surface)?
Thanks very much for your help
Celine



-- 
Celine Louapre, MD
Research Fellow at Massachusetts General Hospital
Department of Radiology, MGH

Building 149, Room 2301
13th Street
Charlestown, MA  02129
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[Freesurfer] BBregister issue during autorecon3 with T2pial option (5.2.0 with updated beta binaries)

2013-05-06 Thread Todd Thompson
Hi, all. I'm trying to refine my pial surfaces with a T2 (or, in this
case, t2*) image and I'm running into an error inside bbregister/fslregister.

I'm running the command:
recon-all -s gf04 -3T  -autorecon3 -T2pial -T2
/mindhive/gablab/fluid/Analysis/Nipype/flash/gf04/tissue_parameters/T2star.mgz

and the recon process makes it to the point of
#@# Refine Pial Surfs w/ T2/FLAIR

when it runs:
bbregister --s gf04 --mov
/mindhive/gablab/fluid/Data/gf04/mri/orig/T2raw.mgz --lta
/mindhive/gablab/fluid/Data/gf04/mri/transforms/T2raw.lta --init-fsl
--T2

bbregister does some initial processing, then calls fslregister, like so:
fslregister --s gf04 --mov
/mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/template.nii
--reg 
/mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/reg.init.dat
--niters 1 --maxangle 90 --nobetmov --tmp
/mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/fslregister
--dof 6 --fsvol brainmask

which immediately crashes with:
/mindhive/gablab/fluid/Data/gf04
mri_convert ERROR: could not determine file for
/mindhive/gablab/fluid/Data/gf04/mri/ERROR:
/mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/fslregister/refvol.fslregister.nii

And so on.

running the fslregister command manually and changing brainmask to
brainmask.mgz seems to fix the problem (after manually
creating/filling the appropriate tmp directory, of course).

Any thoughts?

Thanks!
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Re: [Freesurfer] BBregister issue during autorecon3 with T2pial option (5.2.0 with updated beta binaries)

2013-05-06 Thread Douglas Greve

Newer version of linux changed the way cshell behaves which causes 
bbregister to crash in some instances.

Get a new version from here:
ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/bbregister

doug


On 5/6/13 8:10 PM, Todd Thompson wrote:
 Hi, all. I'm trying to refine my pial surfaces with a T2 (or, in this
 case, t2*) image and I'm running into an error inside bbregister/fslregister.

 I'm running the command:
 recon-all -s gf04 -3T  -autorecon3 -T2pial -T2
 /mindhive/gablab/fluid/Analysis/Nipype/flash/gf04/tissue_parameters/T2star.mgz

 and the recon process makes it to the point of
 #@# Refine Pial Surfs w/ T2/FLAIR

 when it runs:
 bbregister --s gf04 --mov
 /mindhive/gablab/fluid/Data/gf04/mri/orig/T2raw.mgz --lta
 /mindhive/gablab/fluid/Data/gf04/mri/transforms/T2raw.lta --init-fsl
 --T2

 bbregister does some initial processing, then calls fslregister, like so:
 fslregister --s gf04 --mov
 /mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/template.nii
 --reg 
 /mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/reg.init.dat
 --niters 1 --maxangle 90 --nobetmov --tmp
 /mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/fslregister
 --dof 6 --fsvol brainmask

 which immediately crashes with:
 /mindhive/gablab/fluid/Data/gf04
 mri_convert ERROR: could not determine file for
 /mindhive/gablab/fluid/Data/gf04/mri/ERROR:
 /mindhive/gablab/fluid/Data/gf04/mri/transforms/tmp.bbregister.23921/fslregister/refvol.fslregister.nii

 And so on.

 running the fslregister command manually and changing brainmask to
 brainmask.mgz seems to fix the problem (after manually
 creating/filling the appropriate tmp directory, of course).

 Any thoughts?

 Thanks!
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