Re: [Freesurfer] Surface area measurement method

2013-06-10 Thread Andreas Berger
Hi,

basically, i would like to use the area measure for group analysis, but i'm 
not sure whether that's ok to do. my questions would be:

is it suitable for group analysis?

what should i cite if i do?

is surface area represented vertex-wise, with a vertex' adjacent face's area 
added and divided by 3?

What happens when resampling to the standard mesh:
The method assures that total area (or volume) is preserved when mapping 
between subjects
was that referring to the method described by Winkler or the default 
FreeSurfer way of doing it?


andreas


On Wednesday, June 05, 2013 23:22:46 Douglas N Greve wrote:
 Hi Andreas, it is not the same method but somewhat related. The method
 assures that total area (or volume) is preserved when mapping between
 subjects. How much detail do you need?
 doug
 
 On 06/04/2013 05:21 AM, Andreas Berger wrote:
  Hello FreeSurfers,
  
  after reading this [1] paper about measuring surface area, i realized i
  don't know what the default way of measuring surface area is in
  FreeSurfer. Is it similar to what's described in the paper? Could you
  point me to the right documentation or publication?
  Forgive me if i've overlooked it, i found something for thickness, but
  not for area. To clarify, i don't mean parcellation-based areas, i mean
  the measure that i find in /surf/hemi.area.
  
  
  thanks,
  regards,
  Andreas
  
  
  [1] Measuring and comparing brain cortical surface area and other areal
  quantities. Winkler AM, Sabuncu MR, Yeo BT, Fischl B, Greve DN, Kochunov
  P, Nichols TE, Blangero J, Glahn DC (2012). Neuroimage 61(4):1428-43
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[Freesurfer] OptSeq first time

2013-06-10 Thread fMRI
Hello all,

This is my first question in this list and it is about OptSeq2.

I am nee to this command. 

In brief, I wish to insert the following but Some of them I could not handle it:

My experiment has three conditions although I will later specify them as one 
condition:

Moving hand at three different target level ( say 10 20 30). Then I will model 
them as a one condition and enter the parametric response as a first order 
polynomial effects. 

My design will have two columns : main effect of moving hand and the 1 order.

My contrast will be like this [1 0; 0 1]

This is what I would like to optimize using OptSeq2:

Event design
1) ISI 6 seconds + or - 1.5 seconds ( I could not do this
2) TR 3
3) volumes 150
4) 45 hand movement; 15 at each target level   ( I could not do this )
5) each movement lasts for 3 seconds

I am not sure whether I should use null events or the Period between movement 
is enough.

Also my main aim is to optimize the best design in terms of detection.

Please any guide or help

Thanks


AS

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Re: [Freesurfer] tksurfer overlay scale bar background color

2013-06-10 Thread Bruce Fischl

you can change it to white via:

set scalebar_bright  255

cheers,
Bruce

On Mon, 10 Jun 2013, Jörg Pfannmöller wrote:


Dear FSexperts,

the overlay scale bar consists of a colored and a gray part. 
Unfortunately, the gray in the binary colored represetation of the brain 
curvature is exactly the same as in the overlay scale bar. Is it possible 
to change the color in the scale bar background to white?


Regards Joerg



On Fri, 31 May 2013 16:20:24 -0400 (EDT)
Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:


mri_normalize is a binary so you can't, just recon-all.

On Fri, 31 May 2013, Caspar M. Schwiedrzik wrote:


I only find flags for mri_normalize and mri_segment in recon-all, and I have
trouble reading the contents mri_normalize with a regular text editor.
caspar


2013/5/31 Bruce Fischl fis...@nmr.mgh.harvard.edu
  Hi Caspar

  it changes some parameters to the intensity normalization and
  segmentation to account for the lower SNR and increased CNR in
  the mprage. You'll need to look in the recon-all script for the
  details

  cheers
  Bruce


  On Thu, 30 May 2013, Caspar M. Schwiedrzik wrote:

Hi!
Is there more documentation on what settings the
mprage flag enables in
recon-all?
Specifically, I would be interested which individual
steps it affects and
what  the parameters are for each of the steps.
Thanks!
Caspar





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[Freesurfer] Coupling cortical and TRACULA results

2013-06-10 Thread stdp82
Hi list,
Thiebaut de Schotten et al., in an article on cortex (Monkey to human 
comparative anatomy of the frontal lobe association tracts reported that 
The superior longitudinal fasciculus has three distinct branches (Petrides and 
Pandya, 1984). In humans, the first branch of the superior longitudinal 
fasciculus (SLF I) connects to the superior parietal lobule and precuneus (BA 5 
and 7), to the superior frontal (BA 8, 9, 32) and perhaps to some anterior 
cingulate areas (BA 24). The second branch (SLF II) originatesin the anterior 
intraparietal sulcus and the angular gyrus (BA 39 and 40) and terminates in the 
posterior regions of the superior and middle frontal gyrus (BA 6, 8, 9). The 
third branch (SLF III) connects the intraparietal sulcus and inferior parietal 
lobule to the inferior frontal gyrus (BA 44, 45, 47)
By TRACULA output we have 2 output SLFp and SLFt.
Having also cortical results, I wonder if possible to know which are the seed 
and target areas of SLF p and SLFt or al least to know which is that branch 
that is described by SLFp output.
Thanks,

Stefano   ___
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Re: [Freesurfer] volume called 001.mgz

2013-06-10 Thread Douglas Greve

Hi Varghese, is Image1 a dicom file?
doug



On 6/10/13 10:09 AM, Varghese Chikku wrote:

Dear All,
I am   getting this   error  message on a scan.I deleted the created 
 subject folders and re-ran the command,but no luck.Any suggestions?

Thanks in advance,
CV

setting up environment for FreeSurfer/FS-FAST (and FSL)
FREESURFER_HOME   /usr/local/freesurfer
FSFAST_HOME   /usr/local/freesurfer/fsfast
FSF_OUTPUT_FORMAT nii.gz
SUBJECTS_DIR  /usr/local/freesurfer/subjects
MNI_DIR   /usr/local/freesurfer/mni
freesurfer@freesurfer-VirtualBox:~$ recon-all -i 
/home/freesurfer/Desktop/10035BL/T1pre/Image1 -autorecon-all -s 
10035BLFS

Subject Stamp: freesurfer-Linux-centos4_x86_64-stable-pub-v5.1.0
Current Stamp: freesurfer-Linux-centos4_x86_64-stable-pub-v5.1.0
INFO: SUBJECTS_DIR is /usr/local/freesurfer/subjects
Actual FREESURFER_HOME /usr/local/freesurfer
Linux freesurfer-VirtualBox 3.2.0-38-generic #61-Ubuntu SMP Tue Feb 19 
12:18:21 UTC 2013 x86_64 x86_64 x86_64 GNU/Linux

/usr/local/freesurfer/subjects/10035BLFS

 mri_convert /home/freesurfer/Desktop/10035BL/T1pre/Image1 
/usr/local/freesurfer/subjects/10035BLFS/mri/orig/001.mgz


mri_convert /home/freesurfer/Desktop/10035BL/T1pre/Image1 
/usr/local/freesurfer/subjects/10035BLFS/mri/orig/001.mgz
file not found or unknown file type for file 
/home/freesurfer/Desktop/10035BL/T1pre/Image1

#
#@# MotionCor Mon Jun 10 16:03:45 CEST 2013
ERROR: no run data found in 
/usr/local/freesurfer/subjects/10035BLFS/mri. Make sure to
have a volume called 001.mgz in 
 /usr/local/freesurfer/subjects/10035BLFS/mri/orig.

If you have a second run of data call it 002.mgz, etc.
See also: http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/Conversion
Linux freesurfer-VirtualBox 3.2.0-38-generic #61-Ubuntu SMP Tue Feb 19 
12:18:21 UTC 2013 x86_64 x86_64 x86_64 GNU/Linux


recon-all -s 10035BLFS exited with ERRORS at Mon Jun 10 16:03:45 CEST 2013

For more details, see the log file 
/usr/local/freesurfer/subjects/10035BLFS/scripts/recon-all.log
To report a problem, see 
http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting


freesurfer@freesurfer-VirtualBox:~$



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Re: [Freesurfer] Coupling cortical and TRACULA results

2013-06-10 Thread Anastasia Yendiki


You can find the aparc+aseg mapped from T1 space to DWI space in the 
dlabel/diff directory. You can overlay it on the paths reconstructed from 
tracula to see which aparc+aseg labels the paths overlap with. The 
identities of the labels in the aparc+aseg are in 
$FREESURFER_HOME/FreeSurferColorLUT.txt.


On Mon, 10 Jun 2013, std...@virgilio.it wrote:


Hi list,
Thiebaut de Schotten et al., in an article on cortex (Monkey to human
comparative anatomy of the frontal lobe association tracts reported that 

The superior longitudinal fasciculus has three distinct branches (Petrides
and Pandya, 1984). 
In humans, the first branch of the superior longitudinal fasciculus (SLF I)
connects to the superior parietal lobule and precuneus (BA 5 and 7), to the
superior frontal (BA 8, 9, 32) and perhaps to some anterior cingulate areas
(BA 24). The second branch (SLF II) originatesin the anterior intraparietal
sulcus and the angular gyrus (BA 39 and 40) and terminates in the posterior
regions of the superior and middle frontal gyrus (BA 6, 8, 9). The third
branch (SLF III) connects the intraparietal sulcus and inferior parietal
lobule to the inferior frontal gyrus (BA 44, 45, 47)

By TRACULA output we have 2 output SLFp and SLFt.

Having also cortical results, I wonder if possible to know which are the
seed and target areas of SLF p and SLFt or al least to know which is that
branch that is described by SLFp output.

Thanks,


Stefano

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Re: [Freesurfer] Installation trouble on Macbook Air (no such file or directory)

2013-06-10 Thread zkaufman
Nate,

Try typing the following from the command window:

export FREESURFER_HOME=/Applications/freesurfer
source $FREESURFER_HOME/SetUpFreeSurfer.sh

Or, you can add these lines to your .bashrc file in your home directory by
using any text editor, or by typing the following in the command line:

echo export FREESURFER_HOME=/Applications/freesurfer  ~/.bashrc
echo source $FREESURFER_HOME/SetUpFreeSurfer.sh  ~/.bashrc

Once these lines are in your .bashrc file, freesurfer will load everytime
you open the terminal program.

-Zeke





 I am new to Unix and FreeSurfer, and I am having some trouble installing
 FreeSurfer on my Macbook Air (10.8). I've downloaded the .dmg file just
 fine, and when I start the installation steps, I'm instructed to add some
 lines to my .cshrc or .tcshrc files in my home directory. Can anyone point
 me to this file? Also, just below on the installation dialog, it says for
 sh or bash users:

 export FREESURFER_HOME=freesurfer_installation_directory/freesurfer
 source $FREESURFER_HOME/SetUpFreeSurfer.sh


 Can I use these instead of the first two lines of code? I tried to enter
 these bash lines one at a time into my terminal window. The first one
 (export) did not give me any errors but for the source one, I received
 the message:

 bash: /freesurfer/SetUpFreeSurfer.sh: No such file or directory.

 Any idea as to why I am getting this error? My apologies in advance for my
 lack of experience.

 Many thanks,
 Nate
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Re: [Freesurfer] volume called 001.mgz

2013-06-10 Thread Bruce Fischl

there are 2 ways to run FS:

1. Specify the input data with -i (usually one slice from a dicom series).
2. Create the subject directory and convert the input volumes to mgz 
volumes named subject/mri/orig/00[1234].mgz and run recon-all without -i.



sounds like you did 2 without the conversion. Easier to just do 1 in 
general and let recon-all create what it wants


cheers
Bruce

On Mon, 10 Jun 2013, Varghese Chikku wrote:


Dear All,I am   getting this   error  message on a scan.I deleted the created  
subject folders
and re-ran the command,but no luck.Any suggestions?
Thanks in advance,
CV

setting up environment for FreeSurfer/FS-FAST (and FSL)
FREESURFER_HOME   /usr/local/freesurfer
FSFAST_HOME       /usr/local/freesurfer/fsfast
FSF_OUTPUT_FORMAT nii.gz
SUBJECTS_DIR      /usr/local/freesurfer/subjects
MNI_DIR           /usr/local/freesurfer/mni
freesurfer@freesurfer-VirtualBox:~$ recon-all -i
/home/freesurfer/Desktop/10035BL/T1pre/Image1 -autorecon-all -s 10035BLFS
Subject Stamp: freesurfer-Linux-centos4_x86_64-stable-pub-v5.1.0
Current Stamp: freesurfer-Linux-centos4_x86_64-stable-pub-v5.1.0
INFO: SUBJECTS_DIR is /usr/local/freesurfer/subjects
Actual FREESURFER_HOME /usr/local/freesurfer
Linux freesurfer-VirtualBox 3.2.0-38-generic #61-Ubuntu SMP Tue Feb 19 12:18:21 
UTC 2013
x86_64 x86_64 x86_64 GNU/Linux
/usr/local/freesurfer/subjects/10035BLFS

 mri_convert /home/freesurfer/Desktop/10035BL/T1pre/Image1
/usr/local/freesurfer/subjects/10035BLFS/mri/orig/001.mgz 

mri_convert /home/freesurfer/Desktop/10035BL/T1pre/Image1
/usr/local/freesurfer/subjects/10035BLFS/mri/orig/001.mgz 
file not found or unknown file type for file 
/home/freesurfer/Desktop/10035BL/T1pre/Image1
#
#@# MotionCor Mon Jun 10 16:03:45 CEST 2013
ERROR: no run data found in /usr/local/freesurfer/subjects/10035BLFS/mri. Make 
sure to
have a volume called 001.mgz in  
/usr/local/freesurfer/subjects/10035BLFS/mri/orig.
If you have a second run of data call it 002.mgz, etc.
See also: http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/Conversion
Linux freesurfer-VirtualBox 3.2.0-38-generic #61-Ubuntu SMP Tue Feb 19 12:18:21 
UTC 2013
x86_64 x86_64 x86_64 GNU/Linux

recon-all -s 10035BLFS exited with ERRORS at Mon Jun 10 16:03:45 CEST 2013

For more details, see the log file
/usr/local/freesurfer/subjects/10035BLFS/scripts/recon-all.log
To report a problem, see http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting

freesurfer@freesurfer-VirtualBox:~$ 


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Re: [Freesurfer] autorecon3 error

2013-06-10 Thread Gabriel Gonzalez Escamilla
Dear Doug

Sorry for late answer.

I did open as:
tksurfer qsm1_17 lh inflated, and then File load surface  lh.sphere.reg
and
tksurfer qsm1_17 lh sphere.reg

Neither of them look bad, it looks very spherical, an has nothing strange to my 
eyes...
Any other ideas???

Best Regards
Gabriel



- Mensaje original -
De: Bruce Fischl fis...@nmr.mgh.harvard.edu
Fecha: Jueves, 6 de Junio de 2013, 6:16 pm
Asunto: Re: [Freesurfer] autorecon3 error
A: Gabriel Gonzalez Escamilla ggon...@upo.es
CC: freesurfer@nmr.mgh.harvard.edu

 Hi Gabriel
 
 seems like something is wrong with that surface file. Can you 
 load the lh.sphere.reg in tksurfer and see if it looks ok?
 Bruce
 
 
 On Thu, 6 Jun 2013, Gabriel Gonzalez Escamilla wrote:
 
 Dear Freesurfers
 
 I am running an autorecon3 to the same subject that Rafa sent 
 you (the name
 looks different but is exactly the same subject), with the 
 command to fix
 the ribbon.mgz the autorecon-2 has finished, so I continued with
 -autorecon3, but now is encountering the following error, this 
 time seems to
 be something with the seg.mgz.
 
 
 
 #-
 #@# Cortical Parc lh Thu Jun  6 17:01:26 CEST 2013
 /root/trabajo/freesurfer/subjects/qsm1_17/scripts
 
  mris_ca_label -l ../label/lh.cortex.label -aseg 
 ../mri/aseg.mgz -seed 1234
 qsm1_17 lh 
 ../surf/lh.sphere.reg/root/trabajo/freesurfer/average/lh.curvature.buckner40.filled.desikan_killiany.2010-03-25.gcs
  ../label/lh.aparc.annot
 
 setting seed for random number generator to 1234
 using ../mri/aseg.mgz aseg volume to correct midline
 $Id: mris_ca_label.c,v 1.35 2011/03/02 00:04:27 nicks Exp $
   $Id: mrisurf.c,v 1.693.2.2 2011/04/27 19:21:05 nicks Exp $
 f[113526]-v[1] = 539832625 - out of range!
 
 reading atlas 
 from/root/trabajo/freesurfer/average/lh.curvature.buckner40.filled.desikan_killiany.2010-03-25.gcs...
 reading color table from GCSA file
 average std = 1.0   using min determinant for regularization = 0.011
 0 singular and 384 ill-conditioned covariance matrices regularized
 Linux localhost.localdomain 2.6.9-34.ELsmp #1 SMP Thu Mar 9 
 06:23:23 GMT
 2006 x86_64 x86_64 x86_64 GNU/Linux
 
 recon-all -s qsm1_17 exited with ERRORS at Thu Jun  6 17:01:33 
 CEST 2013
 
 For more details, see the log file
 /root/trabajo/freesurfer/subjects/qsm1_17/scripts/recon-all.log
 To report a problem, see
 http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
 
 
 Any ideas how to fix this?
 
 Bests,
 Gabriel ___
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 The information in this e-mail is intended only for the person 
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 addressed. If you believe this e-mail was sent to you in error 
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 Compliance HelpLine at
 http://www.partners.org/complianceline . If the e-mail was sent 
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 sender and properly
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font size=3--br /PhD. student Gabriel 
González-Escamillabr /Laboratory of Functional Neurosciencebr /Department 
of Physiology, Anatomy, and Cell Biologybr /University Pablo de Olavidebr 
/Ctra. de Utrera, Km.1br /41013 - Sevillebr /- Spain -br /br /Email: 
ggon...@upo.esbr /http://www.upo.es/neuroaging/es//font


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Re: [Freesurfer] AR2 Error

2013-06-10 Thread Douglas N Greve

Copy this file to $FREESURFER_HOME/bin/mri_segstats
ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/mri_segstats.snowleopard

doug

On 06/07/2013 06:01 PM, Erin Browning wrote:

 The last thing I ran was

 recon-all -s freesurfer -autorecon2 -autorecon3

 Which still failed.

 We quality check after ar1, so we need to run ar1 separately from ar2 
 and 3.

 On Jun 7, 2013 4:53 PM, Douglas N Greve gr...@nmr.mgh.harvard.edu 
 mailto:gr...@nmr.mgh.harvard.edu wrote:


 you need to include the -autorecon3 flag simultaneously with the
 -autorecon1 and -autorecon2 flags.


 On 06/07/2013 05:45 PM, Erin Browning wrote:


 It fails before ar3 runs.

 On Jun 7, 2013 2:54 PM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu wrote:


 There is no indication in this log file that you ran
 autorecon3
 doug


 On 06/07/2013 02:51 PM, Erin Browning wrote:

 Here's the log. I ran mri_add_xform_to_header after it
 failed
 again last time and am currently rerunning AR2+3 on
 it, so you
 can probably ignore the latest modifications to it.

 http://gate.nmr.mgh.harvard.edu/filedrop2/?p=iowkgmv

 We're running Mac OSX 10.6.8.

 Thanks,
 Erin


 On Fri, Jun 7, 2013 at 12:22 PM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu wrote:

 Hmmm, I don't know. I think that something strange is
 happening.
 Can you
 send me the new recon-all.log file? Also, tell me what
 platform
 you are
 using and I'll send you a new version of mri_segstats

 doug



 On 06/07/2013 01:14 PM, Erin Browning wrote:
  Could it be that since we skip motioncor, we
 skip the
  mri_add_xform_to_header program as well? Should I be
 running that
  separately?
 
  Thanks,
  Erin Browning
 
 
  On Fri, Jun 7, 2013 at 11:54 AM, Erin Browning
 brown...@uwm.edu mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu mailto:brown...@uwm.edu
  mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu mailto:brown...@uwm.edu
 mailto:brown...@uwm.edu mailto:brown...@uwm.edu wrote:
 
  Hi Doug--
 
  Running:
 
  recon-all -s freesurfer -autorecon2 -autorecon3
 
  produced the same error. Could you send me
 the new
 version
 of the
  program?
 
  Thanks!
  Erin Browning
 
 
  On Thu, Jun 6, 2013 at 3:01 PM, Douglas N Greve
  gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu wrote:
 
 
  OK, this is a known problem when running
 recon-all with
  -autorecon1
  -autorecon2 but not autorecon3. If you
 run it with
  -autorecon3, then it
  

Re: [Freesurfer] surface stream steps

2013-06-10 Thread Douglas N Greve

The classification of WM probably takes the most. This includes a lot of 
things, the longest is the subcortical segmentation. See 
recon-all-status.log for a list of times of each operation.
doug

On 06/08/2013 03:05 PM, Joshua Lee wrote:
 Dear Freesurfers,

 From the Wiki Freesurfer surface stream follows something like:

  1. Affine registration to Tal.
  2. Bias correction and skull stripping
  3. Classify WM
  4. Cut hemisphere planes
  5. Tile WM surface
  6. Refine WM surface following GM-WM intensity gradients
  7. Nudge (nudge?) WM surface to follow the GM-CSF gradient to
 generate pial surface
  8. Labeling Data Set
  9. Stats

 May I ask which couple of these steps tend to be the most 
 computationally taxing/longest to complete?

 Also, I'm not sure I understand #7. Is the WM surface scaled in some 
 sense to approximate the GM-CSF boundary, or is this just a refinement 
 step like #6 of a surface that already approximates the GM-CSF boundary?

 Thanks, I've spent most of my time working with the sub-cortical stream.
 -
 Joshua


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Re: [Freesurfer] Surface area measurement method

2013-06-10 Thread Douglas N Greve

On 06/10/2013 02:18 AM, Andreas Berger wrote:
 Hi,

 basically, i would like to use the area measure for group analysis, but i'm
 not sure whether that's ok to do. my questions would be:

 is it suitable for group analysis?
yes

 what should i cite if i do?
We don't have a citation specifically for it. It is used by this paper, 
but it does not describe it in detail.
Greve, D. N., Van der Haegen, L., Cai, Q., Stufflebeam, S., Sabuncu, M. 
R., Fischl, B.,  Brysbaert, M. (2013). A Surface-based Analysis of 
Language Lateralization and Cortical Asymmetry. /Journal of cognitive 
neuroscience/, (Early Access), 1-16.

 is surface area represented vertex-wise, with a vertex' adjacent face's area
 added and divided by 3?
That is how the ?h.area file is created.

 What happens when resampling to the standard mesh:
 The method assures that total area (or volume) is preserved when mapping
 between subjects
 was that referring to the method described by Winkler or the default
 FreeSurfer way of doing it?
No, his way is more elaborate and probably much better but harder to 
implement and slower. The currently implemented version effectively 
preserves area over any given patch when mapping to fsaverage. I don't 
know what the size of the patch is but is probably on the order of 5mm 
(probably smaller).
doug


 andreas


 On Wednesday, June 05, 2013 23:22:46 Douglas N Greve wrote:
 Hi Andreas, it is not the same method but somewhat related. The method
 assures that total area (or volume) is preserved when mapping between
 subjects. How much detail do you need?
 doug

 On 06/04/2013 05:21 AM, Andreas Berger wrote:
 Hello FreeSurfers,

 after reading this [1] paper about measuring surface area, i realized i
 don't know what the default way of measuring surface area is in
 FreeSurfer. Is it similar to what's described in the paper? Could you
 point me to the right documentation or publication?
 Forgive me if i've overlooked it, i found something for thickness, but
 not for area. To clarify, i don't mean parcellation-based areas, i mean
 the measure that i find in /surf/hemi.area.


 thanks,
 regards,
 Andreas


 [1] Measuring and comparing brain cortical surface area and other areal
 quantities. Winkler AM, Sabuncu MR, Yeo BT, Fischl B, Greve DN, Kochunov
 P, Nichols TE, Blangero J, Glahn DC (2012). Neuroimage 61(4):1428-43
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Re: [Freesurfer] OptSeq first time

2013-06-10 Thread Douglas N Greve
Hi, can you at least come up with an optseq2 command line that I could 
then help you with? There are lots of examples on the web page. You 
should be able to get to a point where you have an error.
thanks
doug


On 06/10/2013 05:14 AM, fMRI wrote:
 Hello all,

 This is my first question in this list and it is about OptSeq2.

 I am nee to this command.

 In brief, I wish to insert the following but Some of them I could not handle 
 it:

 My experiment has three conditions although I will later specify them as one 
 condition:

 Moving hand at three different target level ( say 10 20 30). Then I will 
 model them as a one condition and enter the parametric response as a first 
 order polynomial effects.

 My design will have two columns : main effect of moving hand and the 1 order.

 My contrast will be like this [1 0; 0 1]

 This is what I would like to optimize using OptSeq2:

 Event design
 1) ISI 6 seconds + or - 1.5 seconds ( I could not do this
 2) TR 3
 3) volumes 150
 4) 45 hand movement; 15 at each target level   ( I could not do this )
 5) each movement lasts for 3 seconds

 I am not sure whether I should use null events or the Period between movement 
 is enough.

 Also my main aim is to optimize the best design in terms of detection.

 Please any guide or help

 Thanks


 AS

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[Freesurfer] HypoIntense Lesions

2013-06-10 Thread Fotiadis, Panagiotis
Hi FreeSurfer Community,

I was wondering whether there is an automatic tool that outlines the 
hypointense lesions in a SWI scan.

Thank you,
Panos
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Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Bruce Fischl
Hi Panos

sorry, forgot to respond to this. We have tools for labeling 
hyper-intense T2/hypo-intense T1. Not sure about the hypointense SWI. It 
might work on those if you also had a good T1 and some training data. Doug 
might know

cheers
Bruce


On Mon, 10 Jun 2013, Fotiadis, Panagiotis 
wrote:

 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
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Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Douglas N Greve
Hi Panos, not in an SWI scan. The aseg.stats file created by recon-all 
will give you WM hypointensities based on the T1.
doug

On 06/10/2013 11:50 AM, Fotiadis, Panagiotis wrote:
 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
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Re: [Freesurfer] white matter volume per lobe...

2013-06-10 Thread Douglas N Greve
Hi Gonzalo, the segmentation that you are seeing is paired with the 
insula parcellation.
doug


On 05/30/2013 04:36 PM, Gonzalo Rojas Costa wrote:
 Hi Doug:

The command is:

   mri_aparc2aseg --s OAS1_0001_MR1 --labelwm --hypo-as-wm --rip-unknown
 --volmask --o mri/lobulitos.mgz --annot lobulos --wmparc-dmax 200

 and the terminal output is:

 mri_aparc2aseg --s OAS1_0001_MR1 --labelwm --hypo-as-wm --rip-unknown
 --volmask --o mri/lobulitos_2.mgz --annot lobulos --wmparc-dmax 200

 SUBJECTS_DIR /usr/local/freesurfer/subjects
 subject OAS1_0001_MR1
 outvol mri/lobulitos_2.mgz
 useribbon 0
 baseoffset 0
 labeling wm
 labeling hypo-intensities as wm
 dmaxctx 200.00
 RipUnknown 1

 Reading lh white surface
   /usr/local/freesurfer/subjects/OAS1_0001_MR1/surf/lh.white

 Reading lh pial surface
   /usr/local/freesurfer/subjects/OAS1_0001_MR1/surf/lh.pial

 Loading lh annotations from
 /usr/local/freesurfer/subjects/OAS1_0001_MR1/label/lh.lobulos.annot
 reading colortable from annotation file...
 colortable with 8 entries read (originally none)

 Reading rh white surface
   /usr/local/freesurfer/subjects/OAS1_0001_MR1/surf/rh.white

 Reading rh pial surface
   /usr/local/freesurfer/subjects/OAS1_0001_MR1/surf/rh.pial

 Loading rh annotations from
 /usr/local/freesurfer/subjects/OAS1_0001_MR1/label/rh.lobulos.annot
 reading colortable from annotation file...
 colortable with 8 entries read (originally none)
 Have color table for lh white annotation
 Have color table for rh white annotation
 Loading ribbon segmentation from
 /usr/local/freesurfer/subjects/OAS1_0001_MR1/mri/ribbon.mgz
 Loading filled from 
 /usr/local/freesurfer/subjects/OAS1_0001_MR1/mri/filled.mgz
 Ripping vertices labeled as unkown
 Ripped 7659 vertices from left hemi
 Ripped 7544 vertices from right hemi

 Building hash of lh white

 Building hash of lh pial

 Building hash of rh white

 Building hash of rh pial

 Loading aseg from /usr/local/freesurfer/subjects/OAS1_0001_MR1/mri/aseg.mgz
 ASeg Vox2RAS: ---
 -1.000   0.000   0.000   128.000;
   0.000   0.000   1.000  -128.000;
   0.000  -1.000   0.000   128.000;
   0.000   0.000   0.000   1.000;
 -

 Labeling Slice
0   1   2   3   4   5   6   7   8   9  10  11  12  13  14  15  16  17  18  
 19
   20  21  22  23  24  25  26  27  28  29  30  31  32  33  34  35  36  37  38  
 39
   40  41  42  43  44  45  46  47  48  49  50  51  52  53  54  55  56  57  58  
 59
   60  61  62  63  64  65  66  67  68  69  70  71  72  73  74  75  76  77  78  
 79
   80  81  82  83  84  85  86  87  88  89  90  91  92  93  94  95  96  97  98  
 99
 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 
 119
 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 
 139
 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 
 159
 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 
 179
 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 
 199
 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 
 219
 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 
 239
 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 nctx = 688931
 Used brute-force search on 139 voxels
 Fixing Parahip LH WM
Found 0 clusters
 Fixing Parahip RH WM
Found 0 clusters
 Writing output aseg to mri/lobulitos_2.mgz

Sincerely,


 Gonzalo Rojas Costa


 On Thu, May 30, 2013 at 4:10 PM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu wrote:
 can you send me your full command line as well as the terminal output?

 On 05/30/2013 02:26 PM, Gonzalo Rojas Costa wrote:
 Hi Doug:

 But, in the mri_aparc2aseg command, I test with the --wmparc-dmax
 200 option... I put that big value to test it, but I got the image
 that I sent you...

 Sincerely,


 Gonzalo Rojas Costa
 --
 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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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
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Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Fotiadis, Panagiotis
Hi Doug and Bruce,

Don't worry about it! Actually, Bruce, tools for labeling hypo-intense T1 would 
work great as well. Do you know where I could look for them?
In addition, Doug besides the WM hypointensities in the aseg.stats is there 
something that shows the number of lesions, instead of the volume (or the 
volume that corresponds to each lesion)?

Thanks for your help,
Panos

From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
Sent: Monday, June 10, 2013 11:52 AM
To: Fotiadis, Panagiotis
Cc: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] HypoIntense Lesions

Hi Panos

sorry, forgot to respond to this. We have tools for labeling
hyper-intense T2/hypo-intense T1. Not sure about the hypointense SWI. It
might work on those if you also had a good T1 and some training data. Doug
might know

cheers
Bruce


On Mon, 10 Jun 2013, Fotiadis, Panagiotis
wrote:

 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
 ___
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 Freesurfer@nmr.mgh.harvard.edu
 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer




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Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Douglas N Greve

On 06/10/2013 12:12 PM, Fotiadis, Panagiotis wrote:
 Hi Doug and Bruce,

 Don't worry about it! Actually, Bruce, tools for labeling hypo-intense T1 
 would work great as well. Do you know where I could look for them?
This is already done in recon-all (aseg.mgz and aseg.stats)
 In addition, Doug besides the WM hypointensities in the aseg.stats is there 
 something that shows the number of lesions, instead of the volume (or the 
 volume that corresponds to each lesion)?
That is not output by default, but you can get it relatively easily in 
two steps:
mri_binarize --i aseg.mgz --o wmhypo.mgz --match 77  -- This 
creates a binary image
Then run mri_volcluster with --in wmhypo.mgz --thmin .5. The number and 
volume of each lesion will be in the summary file
doug

 Thanks for your help,
 Panos
 
 From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
 Sent: Monday, June 10, 2013 11:52 AM
 To: Fotiadis, Panagiotis
 Cc: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] HypoIntense Lesions

 Hi Panos

 sorry, forgot to respond to this. We have tools for labeling
 hyper-intense T2/hypo-intense T1. Not sure about the hypointense SWI. It
 might work on those if you also had a good T1 and some training data. Doug
 might know

 cheers
 Bruce


 On Mon, 10 Jun 2013, Fotiadis, Panagiotis
 wrote:

 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
 ___
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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer



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gr...@nmr.mgh.harvard.edu
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Fax: 617-726-7422

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Re: [Freesurfer] OptSeq first time

2013-06-10 Thread A a
Correction

This is the lats code :

 optseq2 --ntp 140 --tr 3 --psdwin 6 15 3 --ev ev20 3 20 --ev ev40 3 20
--ev ev60 3 20 --nkeep 3 --o OptSeq_TRIALS/trial_squ --nsearch 1

So The duration is 3 seconds for each and each repeat it 20 times. What I
need is to change/add the ISI to be 7 + or - 1.5 seconds.

Any help please ?

Another point is about the psdwin, I am not sure what exactly it
represents. I saw your slides but I thought this should also change the
ISI,. Can you comment on it please ?

Thanks

AS



On Mon, Jun 10, 2013 at 5:49 PM, fMRI fmri2...@gmail.com wrote:

 Dear Prof Douglas,

 Thanks for your response.

 I managed to do the following:

 optseq2  --ntp 140 --tr 3 --padwin 0 12 3 --ev ev15 --ev ev30 --ev ev45
 --nkeep 3 --o trial --nsearch 1

 Now what I really want to do is to make the ISI 7 seconds + or - 1.5
 seconds. I am not sure how I should use the percentage option if this is
 what I should change plus the ISI time?

 I hope this clarifies it more

 Regards,

 AS

 On 10 Jun 2013, at 16:21, Douglas N Greve gr...@nmr.mgh.harvard.edu
 wrote:

  Hi, can you at least come up with an optseq2 command line that I could
  then help you with? There are lots of examples on the web page. You
  should be able to get to a point where you have an error.
  thanks
  doug
 
 
  On 06/10/2013 05:14 AM, fMRI wrote:
  Hello all,
 
  This is my first question in this list and it is about OptSeq2.
 
  I am nee to this command.
 
  In brief, I wish to insert the following but Some of them I could not
 handle it:
 
  My experiment has three conditions although I will later specify them
 as one condition:
 
  Moving hand at three different target level ( say 10 20 30). Then I
 will model them as a one condition and enter the parametric response as a
 first order polynomial effects.
 
  My design will have two columns : main effect of moving hand and the 1
 order.
 
  My contrast will be like this [1 0; 0 1]
 
  This is what I would like to optimize using OptSeq2:
 
  Event design
  1) ISI 6 seconds + or - 1.5 seconds ( I could not do this
  2) TR 3
  3) volumes 150
  4) 45 hand movement; 15 at each target level   ( I could not do this )
  5) each movement lasts for 3 seconds
 
  I am not sure whether I should use null events or the Period between
 movement is enough.
 
  Also my main aim is to optimize the best design in terms of detection.
 
  Please any guide or help
 
  Thanks
 
 
  AS
 
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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
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  www.nmr.mgh.harvard.edu/facility/filedrop/index.html
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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.
 

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[Freesurfer] Hippocampal subfields intensity

2013-06-10 Thread Marcos Martins da Silva
Hi, Freesurfer Experts

After usual processing with recon-all -all we get the aseg.stats file
with several data including intensity values like:
normMean normStdDev
normMin normMax normRange
Left-Hippocampus  77.8939 7.574846.
105.59.

How could I get similar results for each hippocampal subfield, assuming
I also generated all posterior*.mgz files corresponding to each
subfield?
I guess I should first binarize each of the subfields file with a
threshold=127 to map all the pertinent voxels, and then use these files
as masks over nu.mgz and calculate the intensities values. But I do not
know the best way to accomplish this after the binarize step.

Thank you in advance for any help.

Marcos
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Re: [Freesurfer] Hippocampal subfields intensity

2013-06-10 Thread Juan Eugenio Iglesias
Hi Marcos,
the right way of doing this is using the soft posteriors to compute the
mean and variance, rather than thresholding at p=0.5. For instance, if
you wanted to compute the mean and variance of the intensitites of the
subiculum, you would do something like this:
mean=sum(Ps.*NU)/sum(Ps);
variance=sum(Ps.*(NU-mean).^2)/sum(Ps);
(where Ps is the posterior of the subiculum)
Cheers,
/Eugenio



On Mon, 2013-06-10 at 15:12 -0300, Marcos Martins da Silva wrote:
 Hi, Freesurfer Experts
 
 After usual processing with recon-all -all we get the aseg.stats file
 with several data including intensity values like:
 normMean normStdDev
 normMin normMax normRange
 Left-Hippocampus  77.8939 7.574846.
 105.59.
 
 How could I get similar results for each hippocampal subfield,
 assuming I also generated all posterior*.mgz files corresponding to
 each subfield?
 I guess I should first binarize each of the subfields file with a
 threshold=127 to map all the pertinent voxels, and then use these
 files as masks over nu.mgz and calculate the intensities values. But I
 do not know the best way to accomplish this after the binarize step.
 
 Thank you in advance for any help.
 
 Marcos 
 ___
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 Freesurfer@nmr.mgh.harvard.edu
 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer

-- 
Juan Eugenio Iglesias, PhD
http://www.jeiglesias.com
igles...@nmr.mgh.harvard.edu
Athinoula A. Martinos Center for Biomedical Imaging
149 Thirteenth Street, Suite 2301
Charlestown, Massachusetts 2129
U.S.A.



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[Freesurfer] How to measure the surface dimension in a mask image after mri_glmfit?

2013-06-10 Thread Glen Lee
Dear freesurfer users

I'm wondering if there is any way of figuring out the surface size within a
mask image (mask.mgh)
which is generated after running a group-level GLM analysis (2nd RFX) using
mri_glmfit.

As I'm thinking, this may be:
  number of vertex by dimension of one vertex (1mm).

But I could be wrong and let me know if anyone knows the solution.

-Glen

fyi) the group analysis was performed in freesurfer sym space.
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Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Fotiadis, Panagiotis
Hi Doug,

Thanks for your response, it was really helpful. In addition to the previous 
comments, I have some subjects that have a hematoma that is not shown in the 
aseg.mgz file, and hence is not shown as a hypointense cluster after doing the 
analysis provided below. Do you know if there is any other way to extract 
information (such as outlining it and/or acquiring its volume) about something 
like?

Thanks again,
Panos

From: freesurfer-boun...@nmr.mgh.harvard.edu 
[freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of Douglas N Greve 
[gr...@nmr.mgh.harvard.edu]
Sent: Monday, June 10, 2013 12:18 PM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] HypoIntense Lesions

On 06/10/2013 12:12 PM, Fotiadis, Panagiotis wrote:
 Hi Doug and Bruce,

 Don't worry about it! Actually, Bruce, tools for labeling hypo-intense T1 
 would work great as well. Do you know where I could look for them?
This is already done in recon-all (aseg.mgz and aseg.stats)
 In addition, Doug besides the WM hypointensities in the aseg.stats is there 
 something that shows the number of lesions, instead of the volume (or the 
 volume that corresponds to each lesion)?
That is not output by default, but you can get it relatively easily in
two steps:
mri_binarize --i aseg.mgz --o wmhypo.mgz --match 77  -- This
creates a binary image
Then run mri_volcluster with --in wmhypo.mgz --thmin .5. The number and
volume of each lesion will be in the summary file
doug

 Thanks for your help,
 Panos
 
 From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
 Sent: Monday, June 10, 2013 11:52 AM
 To: Fotiadis, Panagiotis
 Cc: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] HypoIntense Lesions

 Hi Panos

 sorry, forgot to respond to this. We have tools for labeling
 hyper-intense T2/hypo-intense T1. Not sure about the hypointense SWI. It
 might work on those if you also had a good T1 and some training data. Doug
 might know

 cheers
 Bruce


 On Mon, 10 Jun 2013, Fotiadis, Panagiotis
 wrote:

 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
 ___
 Freesurfer mailing list
 Freesurfer@nmr.mgh.harvard.edu
 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer



 ___
 Freesurfer mailing list
 Freesurfer@nmr.mgh.harvard.edu
 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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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.



Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Douglas N Greve
Hi Panos, I don't know an automatic way to do it. You could label it by 
hand on tkmedit or freeview.
doug


On 06/10/2013 03:31 PM, Fotiadis, Panagiotis wrote:
 Hi Doug,

 Thanks for your response, it was really helpful. In addition to the previous 
 comments, I have some subjects that have a hematoma that is not shown in the 
 aseg.mgz file, and hence is not shown as a hypointense cluster after doing 
 the analysis provided below. Do you know if there is any other way to extract 
 information (such as outlining it and/or acquiring its volume) about 
 something like?

 Thanks again,
 Panos
 
 From: freesurfer-boun...@nmr.mgh.harvard.edu 
 [freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of Douglas N Greve 
 [gr...@nmr.mgh.harvard.edu]
 Sent: Monday, June 10, 2013 12:18 PM
 To: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] HypoIntense Lesions

 On 06/10/2013 12:12 PM, Fotiadis, Panagiotis wrote:
 Hi Doug and Bruce,

 Don't worry about it! Actually, Bruce, tools for labeling hypo-intense T1 
 would work great as well. Do you know where I could look for them?
 This is already done in recon-all (aseg.mgz and aseg.stats)
 In addition, Doug besides the WM hypointensities in the aseg.stats is there 
 something that shows the number of lesions, instead of the volume (or the 
 volume that corresponds to each lesion)?
 That is not output by default, but you can get it relatively easily in
 two steps:
 mri_binarize --i aseg.mgz --o wmhypo.mgz --match 77  -- This
 creates a binary image
 Then run mri_volcluster with --in wmhypo.mgz --thmin .5. The number and
 volume of each lesion will be in the summary file
 doug
 Thanks for your help,
 Panos
 
 From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
 Sent: Monday, June 10, 2013 11:52 AM
 To: Fotiadis, Panagiotis
 Cc: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] HypoIntense Lesions

 Hi Panos

 sorry, forgot to respond to this. We have tools for labeling
 hyper-intense T2/hypo-intense T1. Not sure about the hypointense SWI. It
 might work on those if you also had a good T1 and some training data. Doug
 might know

 cheers
 Bruce


 On Mon, 10 Jun 2013, Fotiadis, Panagiotis
 wrote:

 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
 ___
 Freesurfer mailing list
 Freesurfer@nmr.mgh.harvard.edu
 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer



 ___
 Freesurfer mailing list
 Freesurfer@nmr.mgh.harvard.edu
 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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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer

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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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contains patient information, please contact the Partners Compliance HelpLine at
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Re: [Freesurfer] Set Up question

2013-06-10 Thread Douglas N Greve
Hi David, it is not a problem if you're not going to run FS-FAST. If it 
bugs you, you can
setenv NO_FSFAST 1
in your cshrc file prior to sourcing the FS env

doug




On 06/10/2013 03:35 PM, David Dalton wrote:
 Hello FreeSurfer experts,

 I recently downloaded and installed FreeSurfer on my Mac computer, but 
 I have a few questions about the startup.

 1. When I run FreeSurfer, I get the following.  I know the Wiki says 
 to ignore the warning, and FreeSurfer does run normally after this, 
 but I wanted to be sure it really was not a problem.

 [SiriasBook:/] csirias% setenv FREESURFER_HOME Applications/freesurfer/
 [SiriasBook:/] csirias% source Applications/freesurfer/SetUpFreeSurfer.csh
  freesurfer-Darwin-lion-stable-pub-v5.3.0 
 Setting up environment for FreeSurfer/FS-FAST (and FSL)
 FREESURFER_HOME   Applications/freesurfer/
 FSFAST_HOME   Applications/freesurfer//fsfast
 FSF_OUTPUT_FORMAT nii.gz
 SUBJECTS_DIR  Applications/freesurfer//subjects

 WARNING: The /Users/csirias/matlab/startup.m file does not appear to be
  configured correctly. You may not be able
  to run the FS-FAST programs
 Try adding the following lines to /Users/csirias/matlab/startup.m
 -cut-
 fshome = getenv('FREESURFER_HOME');
 fsmatlab = sprintf('%s/matlab',fshome);
 if (exist(fsmatlab) == 7)
 path(path,fsmatlab);
 end
 clear fshome fsmatlab;
 fsfasthome = getenv('FSFAST_HOME');
 fsfasttoolbox = sprintf('%s/toolbox',fsfasthome);
 if (exist(fsfasttoolbox) == 7)
 path(path,fsfasttoolbox);
 end
 clear fsfasthome fsfasttoolbox;
 -cut-

 MNI_DIR   Applications/freesurfer//mni
 [SiriasBook:/] csirias%


 2. When I type in 'freeview' to the command line, I get several other 
 messages as the program opens.  I am not sure if they are a problem, 
 but here they are. I seem to be able to run freeview despite these 
 messages, but some others have told me that these messages do not 
 appear on their computers, so I am wondering why they appear.

 [SiriasBook:/] csirias% freeview
 2013-06-10 12:22:57.739 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.740 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.754 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.755 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.768 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.769 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.781 Freeview[1200:303] invalid drawable
 2013-06-10 12:22:57.782 Freeview[1200:303] invalid drawable

 3. And my last question. How do I run FreeSurfer automatically when I 
 open the terminal window? I would like to just type 'freeview' into 
 the command line to have the program run, but I currently have to type

 setenv FREESURFER_HOME Applications/freesurfer/

 followed by

 source Applications/freesurfer/SetUpFreeSurfer.csh

 in order for the program to run.

 Thank you so much for any help you can give!  Like I said, the program 
 appears to run normally despite the messages, but I just want to know 
 why they are appearing. The last question is more of a convenience issue.

 Thanks,
 David




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 Freesurfer mailing list
 Freesurfer@nmr.mgh.harvard.edu
 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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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.



[Freesurfer] Neuroinformatics Database (NIDB) 4.2.0 released

2013-06-10 Thread Greg Book
This is an announcement that Neuroinformatics Database version 4.2.0 has
been released. This version includes many performance enhancements and new
features. There is also a demo server available with some sample MR data
and the ABIDE dataset hosted for users who want to test the database
without needing to install it locally.

General features:
* store any binary or text data, including MR (any dicom modality), EEG,
SNP, video, audio, images, etc.
* store assessment/clinical measure values (DSM code, etc, only values, not
full assessments)
* real-time QC for MR data, with values stored in the database
* automatic pipeline processing of any image data, with results stored in
the database
* query and retrieve any of the above data and dump to local/remote FTP,
NFS share, or export in NiDB format
* additionally: DICOM receiver, store family pedigree information, store MR
behavioral data, download stats, reports

New features:
* sharing of imaging data between NiDB instances, while maintaining
anonymity and eliminating subject duplication
* improved pipelines: testing mechanism for new pipelines, creating/editing
scripts, and second level pipelines
* query performance improved on pipeline results: 4.4 million result values
retrieved in 107 seconds.
* methods for creating new back-end NiDB modules

Download version 4.2.0 in .tar.gz format or VirtualBox VM:
http://nidb.sourceforge.net. We'll be presenting at HBM in Seattle next
week, so stop by! NiDB is developed by and with support from the Olin
Neuropsychiatry Research Center at Hartford Hospital/Institute of Living.
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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.


Re: [Freesurfer] HypoIntense Lesions

2013-06-10 Thread Fotiadis, Panagiotis
Great, thank you!

Panos 

From: freesurfer-boun...@nmr.mgh.harvard.edu 
[freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of Douglas N Greve 
[gr...@nmr.mgh.harvard.edu]
Sent: Monday, June 10, 2013 3:40 PM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] HypoIntense Lesions

Hi Panos, I don't know an automatic way to do it. You could label it by
hand on tkmedit or freeview.
doug


On 06/10/2013 03:31 PM, Fotiadis, Panagiotis wrote:
 Hi Doug,

 Thanks for your response, it was really helpful. In addition to the previous 
 comments, I have some subjects that have a hematoma that is not shown in the 
 aseg.mgz file, and hence is not shown as a hypointense cluster after doing 
 the analysis provided below. Do you know if there is any other way to extract 
 information (such as outlining it and/or acquiring its volume) about 
 something like?

 Thanks again,
 Panos
 
 From: freesurfer-boun...@nmr.mgh.harvard.edu 
 [freesurfer-boun...@nmr.mgh.harvard.edu] on behalf of Douglas N Greve 
 [gr...@nmr.mgh.harvard.edu]
 Sent: Monday, June 10, 2013 12:18 PM
 To: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] HypoIntense Lesions

 On 06/10/2013 12:12 PM, Fotiadis, Panagiotis wrote:
 Hi Doug and Bruce,

 Don't worry about it! Actually, Bruce, tools for labeling hypo-intense T1 
 would work great as well. Do you know where I could look for them?
 This is already done in recon-all (aseg.mgz and aseg.stats)
 In addition, Doug besides the WM hypointensities in the aseg.stats is there 
 something that shows the number of lesions, instead of the volume (or the 
 volume that corresponds to each lesion)?
 That is not output by default, but you can get it relatively easily in
 two steps:
 mri_binarize --i aseg.mgz --o wmhypo.mgz --match 77  -- This
 creates a binary image
 Then run mri_volcluster with --in wmhypo.mgz --thmin .5. The number and
 volume of each lesion will be in the summary file
 doug
 Thanks for your help,
 Panos
 
 From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
 Sent: Monday, June 10, 2013 11:52 AM
 To: Fotiadis, Panagiotis
 Cc: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] HypoIntense Lesions

 Hi Panos

 sorry, forgot to respond to this. We have tools for labeling
 hyper-intense T2/hypo-intense T1. Not sure about the hypointense SWI. It
 might work on those if you also had a good T1 and some training data. Doug
 might know

 cheers
 Bruce


 On Mon, 10 Jun 2013, Fotiadis, Panagiotis
 wrote:

 Hi FreeSurfer Community,

 I was wondering whether there is an automatic tool that outlines the 
 hypointense lesions in a SWI scan.

 Thank you,
 Panos
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Re: [Freesurfer] How to measure the surface dimension in a mask image after mri_glmfit?

2013-06-10 Thread Glen Lee
Thanks Doug!

I just tried, but I got an error:
mri_segstats --seg mask.mgh --id 1 --i
/fMRI/2D/freesurfer/fsaverage_sym/surf/lh.area --o sum.dat
ERROR: Option --o unknown

I don't see --o option when I looked up mri_segstats --help either. FYI,
I'm using v5.1.
Any idea?



On Mon, Jun 10, 2013 at 3:39 PM, Douglas N Greve
gr...@nmr.mgh.harvard.eduwrote:


 Hi Glen, you can use

 mri_segstats --seg mask.mgh --id 1 --i
 $SUBJECTS_DIR/fsaverage_sym/surf/lh.area --o sum.dat

 doug


 On 06/10/2013 03:17 PM, Glen Lee wrote:
  Dear freesurfer users
 
  I'm wondering if there is any way of figuring out the surface size
  within a mask image (mask.mgh)
  which is generated after running a group-level GLM analysis (2nd RFX)
  using mri_glmfit.
 
  As I'm thinking, this may be:
number of vertex by dimension of one vertex (1mm).
 
  But I could be wrong and let me know if anyone knows the solution.
 
  -Glen
 
  fyi) the group analysis was performed in freesurfer sym space.
 
 
 
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 MGH-NMR Center
 gr...@nmr.mgh.harvard.edu
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 Fax: 617-726-7422

 Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
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Re: [Freesurfer] Hippocampal subfields intensity

2013-06-10 Thread Juan Eugenio Iglesias
Hi Marcos,
1. your fix of MRIread.m is great. I forgot of this bug; we should
totally take care of it.
2. a problem is that nu.mgz (or norm.mgz) and the posteriors are in
difference voxel space. So, you need to resample norm.mgz to the space
of the subfields. To do so, you can use mri_convert with the option -rl
(reslice like):
mri_convert norm.mgz norm_resampled.mgz -rl posterior_subiculum.mgz 
3. Now you can do:
A=MRIread('norm.mgz');
data=A.vol(:);
B=MRIread('posterior_subiculum.mgz');
post=double(B.vol(:));
mean=sum(data.*post)/sum(post);
variance=sum((data-mean).^2.*post)/sum(post);
Cheers,
/Eugenio

On Mon, 2013-06-10 at 17:17 -0300, Marcos Martins da Silva wrote:
 Hi, Eugenio
 TY for your fast help. I understood you were suggesting to compute
 that on MatLab and I tried this:
 
 NU=MRIread('nu.mgz')### that runs ok
 Ps=MRIread('posterior_left_subiculum.mgz')  ### it fails with the
 following message 
 WARNING: error reading MR params
 Attempted to access mr_parms(1); index out of bounds because
 numel(mr_parms)=0.
 
 Error in MRIread (line 100)
   tr = mr_parms(1);
 
 I solved creating a little customized nMRIread.m with the following
 changes:
 
 if numel(mr_parms)  0
 tr = mr_parms(1);
 flip_angle = mr_parms(2);
 te = mr_parms(3);
 ti = mr_parms(4);
   else
 mr_parms(1) = 0;
 mr_parms(2) = 0;
 mr_parms(3) = 0;
 mr_parms(4) = 0;
 tr = mr_parms(1);
 flip_angle = mr_parms(2);
 te = mr_parms(3);
 ti = mr_parms(4);
   end
   
 With those changes I assigned 0 to mr-parms elements so it runs
 without errors
 But whe I tried the following line I copy and pasted from your
 message:
mean=sum(Ps.*NU)/sum(Ps);  ### I got the following error
 Undefined function 'times' for input arguments of type 'struct'.
 
 Any help?
 Cheers, Marcos
 
 PS: I promised I will post the final solution to list. But I guess it
 is more didactic if these little problems are solved before.
 TY, again.
 Em Seg, 2013-06-10 às 14:19 -0400, Juan Eugenio Iglesias escreveu: 
  Hi Marcos,
  the right way of doing this is using the soft posteriors to compute the
  mean and variance, rather than thresholding at p=0.5. For instance, if
  you wanted to compute the mean and variance of the intensitites of the
  subiculum, you would do something like this:
  mean=sum(Ps.*NU)/sum(Ps);
  variance=sum(Ps.*(NU-mean).^2)/sum(Ps);
  (where Ps is the posterior of the subiculum)
  Cheers,
  /Eugenio
  
  
  
  On Mon, 2013-06-10 at 15:12 -0300, Marcos Martins da Silva wrote:
   Hi, Freesurfer Experts
   
   After usual processing with recon-all -all we get the aseg.stats file
   with several data including intensity values like:
   normMean normStdDev
   normMin normMax normRange
   Left-Hippocampus  77.8939 7.574846.
   105.59.
   
   How could I get similar results for each hippocampal subfield,
   assuming I also generated all posterior*.mgz files corresponding to
   each subfield?
   I guess I should first binarize each of the subfields file with a
   threshold=127 to map all the pertinent voxels, and then use these
   files as masks over nu.mgz and calculate the intensities values. But I
   do not know the best way to accomplish this after the binarize step.
   
   Thank you in advance for any help.
   
   Marcos 
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igles...@nmr.mgh.harvard.edu
Athinoula A. Martinos Center for Biomedical Imaging
149 Thirteenth Street, Suite 2301
Charlestown, Massachusetts 2129
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Re: [Freesurfer] Fwd: problem about file format

2013-06-10 Thread huang bs
Thanks.

I now find that, when I copy (or cut) the re-con folder from SUBJECTS_DIR
to the shared folder (with XP), it seems that no changes happen - the file
format remains the same.

But if I restart the Xubuntu, and copy (or cut) this re-con folder from
shared folder back to SUBJECTS_DIR, then the file format automatically
changes and the re-con results can not be recognized. This is quite odd...

I have to move the re-con results to the shared folder because in the
Xubuntu FSV5.1.0 virtual hard disk the space is only 10G. So to me now, if
I can expand the disk to, say for example, 50G, then at least I don't need
to move the re-con results but just save them in SUBJECTS_DIR, and so the
file formats will not change.

On 7 June 2013 20:38, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:

 I meant for you to cat them and put them in the text of the email.
 Something is badly wrong with them. They should be simple text files with a
 4x3 matrix and a couple of header lines. Not sure what happened but you
 will need to delete them and regenerat them

 cheers
 Bruce

 On Fri, 7 Jun 2013, huang bs wrote:

  Seems that I can not post the attachements...

 -- Forwarded message --
 From: huang bs huan...@gmail.com
 Date: 5 June 2013 22:51
 Subject: Re: [Freesurfer] problem about file format
 To: Bruce Fischl fis...@nmr.mgh.harvard.edu
 Cc: freesurfer@nmr.mgh.harvard.edu


 Dear Bruce,

 Yes, sure. I printed the screens and showed you two cases. One can be
 recognized, the other one can not. Please find attached for the six
 figures. I also attached the files talairach.xfm and
 talairach.auto.xfm for the subject linziyi.

 One more question: how to extend the hard disk space in Xubuntu,
 especially in the folder /home/virtualuser/freesurfer/**subjects ? If
 possible, I don't want to move the data to the shared folder and then
 face such problem.

 Sorry I am quite new to Linux so some questions may be quite stupid.

 Thank you very much!

 On 05/06/2013, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:
  no, I haven't seen that before. Can you cat
  /home/virtualuser/freesurfer/**subjects/linziyi/mri/**
 transforms/talairach.xfm
 
  and send us the contents?
 
  Bruce
  On
  Wed, 5 Jun 2013, huang bs wrote:
 
  Hi All,
 
  Sorry to take up your time.
 
  My freesurfer now can not recognize the re-con files (such as the .mgz
  files, or .xfm files, etc).
  For example, I run this command to check the talairach transform:
  tkregister2 --mgz --s linziyi --fstal --surf orig
  The terminal then reports:
  ERROR:
 
 /home/virtualuser/freesurfer/**subjects/linziyi/mri/**
 transforms/talairach.xfm
  does not start as 'MNI Transform File
  This file talairach.xfm does exist. But under Xubuntu, this
  talairach.auto.xfm file has a different icon and appears as executable
  file. That's quite strange because I did not make such change to it.
 
  These files did work when I just finished the re-con. But afer the
 re-con,
  I
  moved them from the freesurfer subjects folder to the shared folder
  (shard
  with XP), because the freesurfer subjects folder has a limited space.
  After
  a few days, I moved them back to the subjects folder for doing the
  statistical analysis, and then I have such problem. Even under the
 shared
  folder, the files can not be read either.
 
  For the cases I just re-con, since they are not moved to elsewhere,
  everything seems OK.
 
  Have you guys had such problem before and how to fix it? Thanks!
 
  --
  Best Regards,
 
  B Huang
 
 
 
 
 
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 it
  is
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 --
 Best Regards,

 Bingsheng Huang
 Postdoctoral Research Fellow
 Diagnostic Radiology, The University of Hong Kong



 --
 Best Regards,

 Bingsheng Huang
 Postdoctoral Research Fellow
 Diagnostic Radiology, The University of Hong Kong




-- 
Best Regards,

Bingsheng Huang
Postdoctoral Research Fellow
Diagnostic Radiology, The University of Hong Kong
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Re: [Freesurfer] How to measure the surface dimension in a mask image after mri_glmfit?

2013-06-10 Thread Douglas Greve

It's --sum for this, not --o
doug

On 6/10/13 4:44 PM, Glen Lee wrote:

Thanks Doug!

I just tried, but I got an error:
mri_segstats --seg mask.mgh --id 1 --i 
/fMRI/2D/freesurfer/fsaverage_sym/surf/lh.area --o sum.dat

ERROR: Option --o unknown

I don't see --o option when I looked up mri_segstats --help either. 
FYI, I'm using v5.1.

Any idea?



On Mon, Jun 10, 2013 at 3:39 PM, Douglas N Greve 
gr...@nmr.mgh.harvard.edu mailto:gr...@nmr.mgh.harvard.edu wrote:



Hi Glen, you can use

mri_segstats --seg mask.mgh --id 1 --i
$SUBJECTS_DIR/fsaverage_sym/surf/lh.area --o sum.dat

doug


On 06/10/2013 03:17 PM, Glen Lee wrote:
 Dear freesurfer users

 I'm wondering if there is any way of figuring out the surface size
 within a mask image (mask.mgh)
 which is generated after running a group-level GLM analysis (2nd
RFX)
 using mri_glmfit.

 As I'm thinking, this may be:
   number of vertex by dimension of one vertex (1mm).

 But I could be wrong and let me know if anyone knows the solution.

 -Glen

 fyi) the group analysis was performed in freesurfer sym space.



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MGH-NMR Center
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Fax: 617-726-7422 tel:617-726-7422

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