Re: [Freesurfer] Label or Overlay of Surface files

2015-08-06 Thread Saeed Mahdizadeh Bakhshmand
And are they treated as label files (e.g. lh.aparc.annot ) in the label
directory? And how they can be added to the tksurfer snapshot procedure?

On Thu, Aug 6, 2015 at 4:04 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:

 no, the scalar overlays are stored separately (e.g. lh.curv, lh.sulc,
 etc...)

 On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:

 Hello,
 Is scalar overlay information embedded into surface file itself? When I
 open
 them in freeview they are loaded with color overlays (sulcus/gyrus), but
 when I load same models into 3D slicer or take a snapshot in tksurfer,
 they
 are plain gray.

 Thanks,
 Saeed


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Re: [Freesurfer] Label or Overlay of Surface files

2015-08-06 Thread Saeed Mahdizadeh Bakhshmand
I used it as this:
tksurfer subject hemisphere surface -snap  file name -overlay file name
And it adds a* gray scale* version of sulcus map to the plain gray, How can
I activate colors?

Thanks,
Saeed

On Thu, Aug 6, 2015 at 4:20 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:

 load them as curvature files

 cheers
 Bruce


 On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:

 And are they treated as label files (e.g. lh.aparc.annot ) in the label
 directory? And how they can be added to the tksurfer snapshot procedure?

 On Thu, Aug 6, 2015 at 4:04 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
 wrote:
   no, the scalar overlays are stored separately (e.g. lh.curv,
   lh.sulc, etc...)
   On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:

 Hello,
 Is scalar overlay information embedded into surface
 file itself? When I open
 them in freeview they are loaded with color overlays
 (sulcus/gyrus), but
 when I load same models into 3D slicer or take a
 snapshot in tksurfer, they
 are plain gray.

 Thanks,
 Saeed


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Re: [Freesurfer] (no subject)

2015-08-06 Thread Z K
Hello,

Thank you for the report. Can you please provide a simplified context of 
how this came about... meaning, does the crash ONLY occur when you alter 
the contents of a file? Does the crash ever occur during a normal recon?

Many files in freesurfer are read on a bite-wise basis and if the 
contents are changed manually than the slightest offset can cause 
anything from invalid values read into the data structure, to possible 
seg faults, and/or program crashing.

I could possibly investigate, but if you wish to have unstripped 
binaries I can provide that as well.

If you intend to pursue this further please contact my direct email 
address to prevent spamming the list on this detailed matter. Thanks.

-Zeke

On 08/06/2015 01:42 AM, Lionel zorzevic wrote:
 Hi,

 The recon pipeline outputed an apparently correct file, which happen to 
 confuse freesurfer reading functions.

 I attached a slightly-altered file named lh.data_crash which have the same 
 problem. The other file named lh.data_nocrash seems to be parsed fine, 
 despite differing by only 1 float-value somewhere in the middle of the data 
 section. Original file was lh.area

 The mri_info command outputs some meaningless values; and the mris_calc 
 command bails out.

 $ mri_info lh.data_crash

 WARNING: # of slices=-45 in header - assuming 124...
 Volume information for lh.data_crash
type: unknown
  dimensions: 3391 x 2677 x 124
 voxel sizes: -0., -0., -0.
type: SHORT (4)
 fov: 0.246
 dof: 0
  xstart: 548.5, xend: 5149214485235471024091229374082187264.0
  ystart: -0.0, yend: -0.0
  zstart: -1008284058362807724504196555655348224.0, zend: 0.0
  ...


 $ mri_info lh.data_nocrash
 Volume information for lh.data_nocrash
type: curv
  dimensions: 124254 x 1 x 1
 voxel sizes: 1., 1., 1.
type: FLOAT (3)
 fov: 124254.000
 dof: 0
  xstart: -62127.0, xend: 62127.0
  ystart: -0.5, yend: 0.5
  zstart: -0.5, zend: 0.0
  ...

 The difference between the two files are a single value change (4 bytes) at 
 offset 1095 (15+4*1095'th byte), although other alteration are possible which 
 avoid the crash too.

 This happens on Freesurfer version 5.3.0, and also 5.1.0, and 6-beta,
 on all arch i could test, which are RedHat 6.6 (64bits), Ubuntu 10.x 
 (32bits), and MacOSX 10.8 (64bits)

 Note: to preserve privacy, the original map values have been replaced by a 
 dummy 42.0 for most of the file, since i believe actual data is irrelevant 
 here.

 I couldn't track the problem further, as i only have (stripped) binaries here.



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Re: [Freesurfer] Label or Overlay of Surface files

2015-08-06 Thread Bruce Fischl
no, the scalar overlays are stored separately (e.g. lh.curv, lh.sulc, 
etc...)

On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:


Hello,
Is scalar overlay information embedded into surface file itself? When I open
them in freeview they are loaded with color overlays (sulcus/gyrus), but
when I load same models into 3D slicer or take a snapshot in tksurfer, they
are plain gray. 

Thanks,
Saeed

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[Freesurfer] FSFAST

2015-08-06 Thread sabin khadka
Hi all,If I understand correctly, preproc-sess command takes mid point of EPI 
image as reference and make template and calculate motion parameters. I could 
not figure if I could use different image as reference, is it possible?

Cheers,
Sabin Khadka___
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Re: [Freesurfer] Label or Overlay of Surface files

2015-08-06 Thread Bruce Fischl

load them as curvature files

cheers
Bruce

On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand 
wrote:



And are they treated as label files (e.g. lh.aparc.annot ) in the label
directory? And how they can be added to the tksurfer snapshot procedure?

On Thu, Aug 6, 2015 at 4:04 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:
  no, the scalar overlays are stored separately (e.g. lh.curv,
  lh.sulc, etc...)
  On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:

Hello,
Is scalar overlay information embedded into surface
file itself? When I open
them in freeview they are loaded with color overlays
(sulcus/gyrus), but
when I load same models into 3D slicer or take a
snapshot in tksurfer, they
are plain gray. 

Thanks,
Saeed


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Re: [Freesurfer] mkanalysis-sess, timewindow

2015-08-06 Thread Xiaomin Yue
The second number in the psdwin parameter is set as 40 in the flac_ev_parse.m 
for 'spmhrf', 'gamma', 'fslgamma'.  It seems that timewindow has no effect on 
hrf?   why is psdwin 40?

Thanks,
Xiaomin

From: yu...@hotmail.com
To: freesurfer@nmr.mgh.harvard.edu
Date: Thu, 6 Aug 2015 15:17:04 -0400
Subject: Re: [Freesurfer] mkanalysis-sess, timewindow




if it is useful,  i can upload the Xtmp.mat file.

thanks,
Xiaomin

 Date: Thu, 6 Aug 2015 10:36:50 -0400
 From: gr...@nmr.mgh.harvard.edu
 To: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] mkanalysis-sess, timewindow
 
 it would be helpful to have your mkanalysis-sess command
 
 On 08/05/2015 04:17 PM, Xiaomin Yue wrote:
  Hi,
 
  I set timewindow to 10 in the mkanalysis-sess.  When I loaded Xtmp.mat 
  in to maltlab, then plot(flac.ev(2).Xirf), the size of the 
  flac.ev(2).Xirf is 20 points, which is corrected because of psdwin is 
  [0 40 2].   Should the psdwin be [0 10 2]?  No matter what value I put 
  in to timewindow, the psdwin is alway [0 40 2].  Is it correct?  If 
  so, what aspect of design matrix does the timewidow have effect on?
 
  thanks very much for your help.
 
  Xiaomin
 
 
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Re: [Freesurfer] Label or Overlay of Surface files

2015-08-06 Thread Lee Tirrell

Hi Saeed,

You can run either of the following commands to overlay the ?h.sulc or ?h.curv 
file:


tksurfer subject hemisphere surface -snap  file name -sulc
tksurfer subject hemisphere surface -snap  file name -curv

Best,
Lee

On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:


I used it as this:tksurfer subject hemisphere surface -snap  file name -overlay 
file name
And it adds a gray scale version of sulcus map to the plain gray, How can I 
activate colors?

Thanks,
Saeed

On Thu, Aug 6, 2015 at 4:20 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:
  load them as curvature files

  cheers
  Bruce

  On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:

And are they treated as label files (e.g. lh.aparc.annot ) in the 
label
directory? And how they can be added to the tksurfer snapshot 
procedure?

On Thu, Aug 6, 2015 at 4:04 PM, Bruce Fischl 
fis...@nmr.mgh.harvard.edu
wrote:
      no, the scalar overlays are stored separately (e.g. lh.curv,
      lh.sulc, etc...)
      On Thu, 6 Aug 2015, Saeed Mahdizadeh Bakhshmand wrote:

            Hello,
            Is scalar overlay information embedded into surface
            file itself? When I open
            them in freeview they are loaded with color overlays
            (sulcus/gyrus), but
            when I load same models into 3D slicer or take a
            snapshot in tksurfer, they
            are plain gray. 

            Thanks,
            Saeed


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Re: [Freesurfer] Weird Freesurfer results

2015-08-06 Thread Brent Womble
Thanks, Dr. Fischl.

Original image and recon:
 + brainmask.mgz (1.27 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=agy57k1qjyh
 + lh.pial (4.33 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=1k79w4nsitw
 + lh.white (4.33 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=90gq0da66ar
 + rh.pial (4.29 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=afmeea5gzmq
 + rh.white (4.29 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=96jsu9l1wkx

Synthethic image and recon:
 + brainmask.mgz (1.27 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=96pjr5j7y9g
 + lh.pial (4.33 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=91u587oukvs
 + lh.white (4.33 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=7stlc9abt4k
 + rh.pial (4.32 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=66g81vebmo3
 + rh.white (4.32 MiB) 
http://gate.nmr.mgh.harvard.edu/filedrop2/?p=1kc9lmgx2dx

Area where we expect to see a change:
107  79  176

Areas where we found unexpected changes:
82  131  102
153  84  106
145  137  149
84  114  168
107  92  170

-Brent

On Thu, Aug 6, 2015 at 12:35 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:

 Hi Brent

 if you upload the subjects and point us at the specific locations you
 expect to see effects and the ones you don't we will take a look
 cheers
 Bruce


 On Thu, 6 Aug 2015, Brent Womble wrote:

 So I'm making changes to the intensity values in a specific area (a sphere
 or several slices, depending on the technique). I'm getting recons that
 are
 inconsistent in areas where the 2 images are exactly the same (far away
 from
 the changes I made). I can't figure out why.

 Where should I go from here?

 -Brent

 On Tue, Aug 4, 2015 at 2:08 PM, Brent Womble brentwom...@gmail.com
 wrote:
   Yes, I completely agree. In this project, I'm simulating 3
   possible changes: an expanded gyrus, a folded gyrus, and a
   denser gyrus (see poster here). The poster goes into more detail
   on the rationale for these 3 possible changes. I'm using these
   relatively focal changes because I'm modeling use-dependent
   structural neuroplasticity, not atrophy.
 I'm using a different method for the expanded/folded gyrus than the
 denser gyrus (see poster).
 The changes I make in the expanded/folded gyrus propagate through the
 entire slice. Here is a difference image from the center of the
 deformation:
 [IMAGE]


 ​Here is a difference image from a slice at the far end of the
 deformation (where the in-plane deformation is smallest):
 [IMAGE]


 ​I'm getting noisy results in all 3 datasets (in areas far away from
 the actual changes). I sent around the denser gyrus dataset first
 because it was simplest.

 On Tue, Aug 4, 2015 at 12:58 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:
   What you really want to simulate is an underlying
   geometric deformation (like atrophy) that gets propagated
   through an image formation model to create an atrophic
   image. I don't think multiplying the image intensities is
   a good model for what you want. Atrophy doesn't look like
   a uniform darkening of the gray matter.



   On Tue, 4 Aug 2015, Brent Womble wrote:


 Yes, I'm multiplying the image intensities by
 a scaling factor. Sorry if
 that wasn't clear.

 -Brent

 On Aug 4, 2015 12:09, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:
   Hi Brent

   a quick look and it seems that your
 answer is yes? You are
   multiplying the image intensities by
 some scale factor?
   Bruce


   On Tue, 4 Aug 2015, Brent Womble wrote:

 Yes. Here is the MATLAB script:

   for i = [1:20]

   %Load the original image and
 gray matter mask

   raw=load_nii([pwd,'/',
 num2str(i),
 '/pre.nii'])

   a=single(squeeze(raw.img));


   c1_raw=load_nii([pwd,'/',
 num2str(i),
 '/c1pre.nii']);

   c1=squeeze(c1_raw.img);

   %Mask is gray around edges.
 Threshold to make
 it binary

   c1(c10.1)=1;

   %Convert mask to logical

   c1=logical(c1);


   %%Generate a 3D gaussian
 kernel

   %Specify the origin, size,
 and intensity of
 the kernel

   k_origin=origins(i,:);
 %origins is an i by 3
 vector to store
   all coordinates

   k_size=20;


Re: [Freesurfer] how to obtain sulcal depth in a given region for a specific subject

2015-08-06 Thread Yang, Daniel
Thanks so much for your help!!

- Daniel

On 8/6/15, 3:06 PM, freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
Bruce Fischl freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
fis...@nmr.mgh.harvard.edu wrote:

ignore grayvol, the other two will be the mean and standard deviation of
the sulc

cheers
Bruce
On Thu, 6 Aug 2015, Yang, Daniel wrote:

 Hi Bruce,

 Thanks so much! From the output of mris_anatomical_stats, I can see that
 it affects the following three variables:

 GrayVol ThickAvg ThickStd

 When sulc is used instead of thickness, do you know what the meaning of
 these three variables is changed to?

 Many thanks,
 Daniel

 On 8/6/15, 1:35 PM, freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
 Bruce Fischl freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
 fis...@nmr.mgh.harvard.edu wrote:

 sure, you can use mris_anatomical_stats with the label (-l) and specify
 sulc instead of thickness on the command line
 Bruce
 On Thu, 6 Aug 2015, Yang,
 Daniel wrote:

 Dear FreeSurfer Experts,

 Is there a way to obtain sulcal depth in a given region (label) for a
 particular subject?

 Many thanks!
 Daniel


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[Freesurfer] Label or Overlay of Surface files

2015-08-06 Thread Saeed Mahdizadeh Bakhshmand
Hello,

Is scalar overlay information embedded into surface file itself? When I
open them in freeview they are loaded with color overlays (sulcus/gyrus),
but when I load same models into 3D slicer or take a snapshot in tksurfer,
they are plain gray.

Thanks,
Saeed
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Re: [Freesurfer] Fwd: Inflated and Spherical Morphing --- Step by step surfaces

2015-08-06 Thread Saeed Mahdizadeh Bakhshmand
Ok, but how about the mophing process? Isn't inflated brain transformed to
the sphere directly? Is there a middle step that is hidden (e.g. inflatted
to the brain flat maps and spreading these maps over the sphere)? I want to
generate a contineous transformation video from WM to inflated and inflated
to a sphere.
On Aug 6, 2015 7:45 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:

 yes, because it is unfolding on the sphere to recover metric properties.
 -w 1 gives you every iteration. You will need to show curvature or you
 won't see anything

 On Thu, 6 Aug 2015, Saeed Mahdizadeh
 Bakhshmand wrote:

  Hello,
  What are your suggested values for w and n in mris_sphere? I set w to 5
 and
  all of the iterations are spheres!
 
  Thanks,
  Saeed
 
  On Wed, Aug 5, 2015 at 1:06 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
 
  wrote:
Hi Saeed
 
if you specify -w n to mris_inflate or mris_sphere it will
save snapshots
of the process every nth iteration
cheers
Bruce
 
 
On Wed, 5 Aug 2015,
Saeed Mahdizadeh Bakhshmand wrote:
 
 Hello,

 Since surface deformation from WM to inflated surface is a
gradual process,
 I assume that interim surfaces can also be saved and
visualized, as I have
 seen in the ppt of Analyzing the Individual Subject tutorial
session
 (slide #32). I am curious to know which command and options
can generate
 that type of gradual deformations from pial surface to
spherical surface, so
 that viewer can visually track region or points of interest?

 Best,

 Saeed



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Re: [Freesurfer] Fwd: Inflated and Spherical Morphing --- Step by step surfaces

2015-08-06 Thread Saeed Mahdizadeh Bakhshmand
Hello,

What are your suggested values for *w* and *n* in *mris_sphere*? I set *w*
to 5 and all of the iterations are spheres!

Thanks,
Saeed

On Wed, Aug 5, 2015 at 1:06 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:

 Hi Saeed

 if you specify -w n to mris_inflate or mris_sphere it will save snapshots
 of the process every nth iteration
 cheers
 Bruce


 On Wed, 5 Aug 2015,
 Saeed Mahdizadeh Bakhshmand wrote:

  Hello,
 
  Since surface deformation from WM to inflated surface is a gradual
 process,
  I assume that interim surfaces can also be saved and visualized, as I
 have
  seen in the ppt of Analyzing the Individual Subject tutorial session
  (slide #32). I am curious to know which command and options can generate
  that type of gradual deformations from pial surface to spherical
 surface, so
  that viewer can visually track region or points of interest?
 
  Best,
 
  Saeed
 
 
 
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[Freesurfer] Announcing PySurfer version 0.6

2015-08-06 Thread Michael Waskom
Hello everyone,

We are pleased to announce the 0.6 release of PySurfer
http://pysurfer.github.io/, a Python library for visualizing MRI and MEG
data.

Changes in this version include:

- Simplified the selection of parameters that customize the visualization
- Enhanced plotting of Freesurfer morphometry overlays (thickness,
curvature, etc.)
- Enhanced plotting of statistical overlays using contour maps
- Improved support for scripted animation of the brain visualization

See the release notes https://github.com/nipy/PySurfer/releases/tag/0.6
for more details about these changes.

For information on installation, documentation, and the example gallery,
you can visit our website (http://pysurfer.github.com/).

We hope you will find it useful in your research!

Michael Waskom, Eric Larson, Christian Brodbeck, and the rest of the Nipy
team
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Re: [Freesurfer] Fwd: Inflated and Spherical Morphing --- Step by step surfaces

2015-08-06 Thread Bruce Fischl
yes, because it is unfolding on the sphere to recover metric properties. 
-w 1 gives you every iteration. You will need to show curvature or you 
won't see anything

On Thu, 6 Aug 2015, Saeed Mahdizadeh 
Bakhshmand wrote:

 Hello,
 What are your suggested values for w and n in mris_sphere? I set w to 5 and
 all of the iterations are spheres!
 
 Thanks,
 Saeed
 
 On Wed, Aug 5, 2015 at 1:06 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
 wrote:
   Hi Saeed

   if you specify -w n to mris_inflate or mris_sphere it will
   save snapshots
   of the process every nth iteration
   cheers
   Bruce
 

   On Wed, 5 Aug 2015,
   Saeed Mahdizadeh Bakhshmand wrote:

Hello,
   
Since surface deformation from WM to inflated surface is a
   gradual process,
I assume that interim surfaces can also be saved and
   visualized, as I have
seen in the ppt of Analyzing the Individual Subject tutorial
   session
(slide #32). I am curious to know which command and options
   can generate
that type of gradual deformations from pial surface to
   spherical surface, so
that viewer can visually track region or points of interest?
   
Best,
   
Saeed
   
   
   
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Re: [Freesurfer] Fornix Segmentation

2015-08-06 Thread Bruce Fischl
Hi Maryam

try specifying -f on the mri_cc command line (as the first option)

cheers
Bruce
On Thu, 6 
Aug 2015, Syeda Maryam wrote:

 Hi everyone,
 
 So I've been going through the list trying to see if someone has encountered
 the same problem as me with regards to segmentation of the fornix but have
 not found a solution as yet. I'm a grad student and still relatively new to
 freesurfer. My research group is using freesurfer to segment and visualize
 white matter tracts in data obtained from the ADNI database. We are
 primarily working with the subcortical segmentation in the aseg volume. My
 current issue is that I am unable to find the labels for the fornix in the
 aseg volume; they seem to only be located in the wm volume generated by
 freesurfer. When I try to run mri_cc on my aseg, the corpus callosum and
 fornix segmentation are output together and I'm unable to analyze them
 separately. I'd really like all the labels I require to be contained in a
 single volume rather than multiple ones as that will make my job a lot
 easier.
 Is there something I'm missing? Is there a way of extracting the fornix and
 corpus callosum, and indeed, all white matter tracts from the same volume?
 Any help will be highly appreciated!
 
 Thanks in advance,
 Maryam
 
 

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Re: [Freesurfer] how to obtain sulcal depth in a given region for a specific subject

2015-08-06 Thread Bruce Fischl
sure, you can use mris_anatomical_stats with the label (-l) and specify 
sulc instead of thickness on the command line
Bruce
On Thu, 6 Aug 2015, Yang, 
Daniel wrote:

 Dear FreeSurfer Experts,
 
 Is there a way to obtain sulcal depth in a given region (label) for a
 particular subject?
 
 Many thanks!
 Daniel
 

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Re: [Freesurfer] Fornix Segmentation

2015-08-06 Thread Syeda Maryam
Yes, I was able to locate that file. Thank again! Don't know how I managed to 
miss it the first time!
Regards,Maryam
 


 On Thursday, August 6, 2015 1:35 PM, Bruce Fischl 
fis...@nmr.mgh.harvard.edu wrote:
   

 does it not say writing fornix to mri/fornix.mgz and write out a 
separate file?

The other thing you could consider is using tracula for this, which I think 
will work even in the absence of diffusion data.

cheers
Bruce


On Thu, 6 Aug 2015, Syeda Maryam wrote:

 Hi Bruce,
 
 Thanks so much for getting back to me on this! Yes, I have tried mri_cc with
 -f and I am able to view part of the fornix along with the corpus callosum
 when I call up the appropriate labels. However, I don't seem to be able to
 visualize the two structures separately. Is it possible to separate the two?
 Thanks in advance!
 
 Regards,
 Maryam
 
 
 
 On Thursday, August 6, 2015 1:22 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:
 
 
 Hi Maryam
 
 try specifying -f on the mri_cc command line (as the first option)
 
 cheers
 Bruce
 On Thu, 6
 Aug 2015, Syeda Maryam wrote:
 
  Hi everyone,
 
  So I've been going through the list trying to see if someone has
 encountered
  the same problem as me with regards to segmentation of the fornix but have
  not found a solution as yet. I'm a grad student and still relatively new
 to
  freesurfer. My research group is using freesurfer to segment and visualize
  white matter tracts in data obtained from the ADNI database. We are
  primarily working with the subcortical segmentation in the aseg volume. My
  current issue is that I am unable to find the labels for the fornix in the
  aseg volume; they seem to only be located in the wm volume generated by
  freesurfer. When I try to run mri_cc on my aseg, the corpus callosum and
  fornix segmentation are output together and I'm unable to analyze them
  separately. I'd really like all the labels I require to be contained in a
  single volume rather than multiple ones as that will make my job a lot
  easier.
  Is there something I'm missing? Is there a way of extracting the fornix
 and
  corpus callosum, and indeed, all white matter tracts from the same volume?
  Any help will be highly appreciated!
 
  Thanks in advance,
  Maryam
 
 
 
 
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Re: [Freesurfer] Fornix Segmentation

2015-08-06 Thread Syeda Maryam
Hi Bruce,
Thanks so much for getting back to me on this! Yes, I have tried mri_cc with -f 
and I am able to view part of the fornix along with the corpus callosum when I 
call up the appropriate labels. However, I don't seem to be able to visualize 
the two structures separately. Is it possible to separate the two? Thanks in 
advance!
Regards,Maryam
 


 On Thursday, August 6, 2015 1:22 PM, Bruce Fischl 
fis...@nmr.mgh.harvard.edu wrote:
   

 Hi Maryam

try specifying -f on the mri_cc command line (as the first option)

cheers
Bruce
On Thu, 6 
Aug 2015, Syeda Maryam wrote:

 Hi everyone,
 
 So I've been going through the list trying to see if someone has encountered
 the same problem as me with regards to segmentation of the fornix but have
 not found a solution as yet. I'm a grad student and still relatively new to
 freesurfer. My research group is using freesurfer to segment and visualize
 white matter tracts in data obtained from the ADNI database. We are
 primarily working with the subcortical segmentation in the aseg volume. My
 current issue is that I am unable to find the labels for the fornix in the
 aseg volume; they seem to only be located in the wm volume generated by
 freesurfer. When I try to run mri_cc on my aseg, the corpus callosum and
 fornix segmentation are output together and I'm unable to analyze them
 separately. I'd really like all the labels I require to be contained in a
 single volume rather than multiple ones as that will make my job a lot
 easier.
 Is there something I'm missing? Is there a way of extracting the fornix and
 corpus callosum, and indeed, all white matter tracts from the same volume?
 Any help will be highly appreciated!
 
 Thanks in advance,
 Maryam
 
 

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[Freesurfer] Changing Color Labels

2015-08-06 Thread Owais Syed
Hi freesurfer experts!

Sorry if this is a basic question, but I have a manual parcellations for
the cortex of the temporal lobe. The problem is that since my voxel size is
0.38, 0.38, 0.38, I converted it to 1 mm voxel size (which I did using
mri_convert -c) so that I can compare it to, but the color labels are all
mixed up.

Is there a way to make all the color labels into one single color label
without manual editing each one? I need to be able to use
mri_compute_overlap to compare the parcellations, and they won't work
unless they are equal voxel size.

Thank you and best,
Owais
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Re: [Freesurfer] mkanalysis-sess, timewindow

2015-08-06 Thread Xiaomin Yue
if it is useful,  i can upload the Xtmp.mat file.

thanks,
Xiaomin

 Date: Thu, 6 Aug 2015 10:36:50 -0400
 From: gr...@nmr.mgh.harvard.edu
 To: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] mkanalysis-sess, timewindow
 
 it would be helpful to have your mkanalysis-sess command
 
 On 08/05/2015 04:17 PM, Xiaomin Yue wrote:
  Hi,
 
  I set timewindow to 10 in the mkanalysis-sess.  When I loaded Xtmp.mat 
  in to maltlab, then plot(flac.ev(2).Xirf), the size of the 
  flac.ev(2).Xirf is 20 points, which is corrected because of psdwin is 
  [0 40 2].   Should the psdwin be [0 10 2]?  No matter what value I put 
  in to timewindow, the psdwin is alway [0 40 2].  Is it correct?  If 
  so, what aspect of design matrix does the timewidow have effect on?
 
  thanks very much for your help.
 
  Xiaomin
 
 
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 gr...@nmr.mgh.harvard.edu
 Phone Number: 617-724-2358
 Fax: 617-726-7422
 
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[Freesurfer] how to obtain sulcal depth in a given region for a specific subject

2015-08-06 Thread Yang, Daniel
Dear FreeSurfer Experts,

Is there a way to obtain sulcal depth in a given region (label) for a 
particular subject?

Many thanks!
Daniel
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Re: [Freesurfer] wm parcellation freesurfer

2015-08-06 Thread Owais Syed
That was it! (and yes, we were trying to have freesurfer do an
autoparcellation for higher resolution MRI, but the full reconstruction
unfortunately keeps failing on processes like skull strip). But for now, we
will use the 1 mm reconstruction. Thank you for the help!

Owais

On Mon, Aug 3, 2015 at 12:58 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:

 Hi Owais

 are your voxels really .36mm isotropic? That is extremely high resolution
 and very very rare (and hard!) if you are getting whole-brain coverage. You
 can use -cm in recon-all (conform to min) to keep the resolution, but
 everything will take way longer and use way more memory. I would check to
 see what the true resolution of your data is first though.

 cheers
 Bruce



 On Mon, 3 Aug 2015, Owais Syed wrote:

 Thanks for the reply, I think I misspoke though. My original T1 MRI has a
 voxel size of 0.36, 0.36, 0.36. But when I am looking through the files
 created via recon -all (specifically wmparc.mgz, although present in other
 files as well), I noticed that the voxel size is a bit larger (about 1,
 1,
 1).
 Is there a way to edit the voxel size to match the MRI during recon -all?

 Also how would I do that specifically for just creating wmparc.mgz from
 the
 original T1 MRI? If it is possible to do so that would be nice, otherwise
 I
 will probably try to run the entire recon -all with the new voxel size.

 Thanks,
 Owais

 On Wed, Jul 29, 2015 at 11:25 AM, Bruce Fischl 
 fis...@nmr.mgh.harvard.edu
 wrote:
   Hi Owais

   do you mean the wmparc.mgz or the aparc+aseg.mgz? You can use
   mris_divide_parcellation or mris_make_face_parcellation to
   subdivide or
   make an isotropic finer scale one if you want. I believe that
   you can then
   create a new aparc+aseg from one of those and then the wmparc
   from that to
   get a finer one
   cheers
   Bruce


   On Tue, 28 Jul 2015,
   Owais Syed wrote:

Hi,
Is it possible to increase the number of parcellations when
   making the aparc+aseg
file? I have a high resolution MRI, and one parcellation will
   match every three
slides, but I want a better match overall.
   
Thanks,
   
Owais
   
   
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Re: [Freesurfer] how to obtain sulcal depth in a given region for a specific subject

2015-08-06 Thread Bruce Fischl
ignore grayvol, the other two will be the mean and standard deviation of 
the sulc

cheers
Bruce
On Thu, 6 Aug 2015, Yang, Daniel wrote:

 Hi Bruce,

 Thanks so much! From the output of mris_anatomical_stats, I can see that
 it affects the following three variables:

 GrayVol ThickAvg ThickStd

 When sulc is used instead of thickness, do you know what the meaning of
 these three variables is changed to?

 Many thanks,
 Daniel

 On 8/6/15, 1:35 PM, freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
 Bruce Fischl freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
 fis...@nmr.mgh.harvard.edu wrote:

 sure, you can use mris_anatomical_stats with the label (-l) and specify
 sulc instead of thickness on the command line
 Bruce
 On Thu, 6 Aug 2015, Yang,
 Daniel wrote:

 Dear FreeSurfer Experts,

 Is there a way to obtain sulcal depth in a given region (label) for a
 particular subject?

 Many thanks!
 Daniel


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Re: [Freesurfer] Changing Color Labels

2015-08-06 Thread Douglas N Greve
use nearest neighbor interpolation. Also, probabaly better to use 
mri_label2vol instead

On 08/06/2015 02:17 PM, Owais Syed wrote:
 Hi freesurfer experts!

 Sorry if this is a basic question, but I have a manual parcellations 
 for the cortex of the temporal lobe. The problem is that since my 
 voxel size is 0.38, 0.38, 0.38, I converted it to 1 mm voxel size 
 (which I did using mri_convert -c) so that I can compare it to, but 
 the color labels are all mixed up.

 Is there a way to make all the color labels into one single color 
 label without manual editing each one? I need to be able to use 
 mri_compute_overlap to compare the parcellations, and they won't work 
 unless they are equal voxel size.

 Thank you and best,
 Owais


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Re: [Freesurfer] how to obtain sulcal depth in a given region for a specific subject

2015-08-06 Thread Yang, Daniel
Hi Bruce,

Thanks so much! From the output of mris_anatomical_stats, I can see that
it affects the following three variables:

GrayVol ThickAvg ThickStd

When sulc is used instead of thickness, do you know what the meaning of
these three variables is changed to?

Many thanks,
Daniel

On 8/6/15, 1:35 PM, freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
Bruce Fischl freesurfer-boun...@nmr.mgh.harvard.edu on behalf of
fis...@nmr.mgh.harvard.edu wrote:

sure, you can use mris_anatomical_stats with the label (-l) and specify
sulc instead of thickness on the command line
Bruce
On Thu, 6 Aug 2015, Yang,
Daniel wrote:

 Dear FreeSurfer Experts,
 
 Is there a way to obtain sulcal depth in a given region (label) for a
 particular subject?
 
 Many thanks!
 Daniel
 

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Re: [Freesurfer] mkanalysis-sess, timewindow

2015-08-06 Thread Xiaomin Yue
Hi, Doug,

Thanks for your response.  Here is my command:  mkanalysis-sess -fsd bold 
-paradigm xy_mky_category_eye_weights.par -event-related -refeventdur 1 
-timewindow 10 -TER 2 -no-inorm -delay 0 -polyfit 3 -gammafit 0 8 -gammaexp 0.3 
-nuisreg mcprextreg 3 -nuisreg eye_movTR_xy 2 -nuisreg fsl_DAVRS 1 -TR 2. 
-ncondition 940 -funcstem f.mc.perrun.so.nativespace.nii -abcbins 3 -analysis 
perrun_eye_weights_eyeMovTRxy_tpe_fslmotoutlier -per-run -native -force 
-tpexclude xy_eye_tpe -runlistfile xyrunlist

After running selxavg3-sess, I loaded Xtmp.mat into matlab.  The psdwin under 
flac.ev(2) is [0 40 2].  I also tried to change the timewindow to 20 in the 
mkanalysis-sess, the psdwin is still [0 40 2].  If I changed the TER to 0.5 , 
the psdwin is [0 40 0.5] no matter timewindow is 10 or 20.  

Thanks for looking into this,
Xiaomin

 Date: Thu, 6 Aug 2015 10:36:50 -0400
 From: gr...@nmr.mgh.harvard.edu
 To: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] mkanalysis-sess, timewindow
 
 it would be helpful to have your mkanalysis-sess command
 
 On 08/05/2015 04:17 PM, Xiaomin Yue wrote:
  Hi,
 
  I set timewindow to 10 in the mkanalysis-sess.  When I loaded Xtmp.mat 
  in to maltlab, then plot(flac.ev(2).Xirf), the size of the 
  flac.ev(2).Xirf is 20 points, which is corrected because of psdwin is 
  [0 40 2].   Should the psdwin be [0 10 2]?  No matter what value I put 
  in to timewindow, the psdwin is alway [0 40 2].  Is it correct?  If 
  so, what aspect of design matrix does the timewidow have effect on?
 
  thanks very much for your help.
 
  Xiaomin
 
 
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Re: [Freesurfer] ID-swapping freesurfer data?

2015-08-06 Thread Douglas N Greve
We don't have tools to explicitly change those strings. You can read 
them into matlab as Bruce suggests. You can also convert them to nifti 
and then back to mgz.

On 08/05/2015 05:07 PM, Nate Vack wrote:
 Thanks!

 One complication I'm seeing is that when I uncompress, say, an .mgz 
 file, the old subject number is still embedded in some text near the 
 end of the file*. Since we want to change these ID numbers for 
 de-identification purposes, we'd need to change them there, too.

 Is there a way to either strip those things or edit them?

 Thanks!
 -Nate

 * For example:

 P/studies/STUDY/DATA/mri/processed/freesurfer/IDENTIFIER/mri/transforms/talairach.xfm
 UNKNOWN
 @AutoAlign   0.00   0.00   0.00   0.00 0.00   
 0.00   0.00   0.00   0.00 0.00   0.00   
 0.00   0.00   0.00 0.00   0.00
 mri_convert 
 /studies/STUDY/DATA/mri/processed/IDENTIFIER/anat/T1High_native1.nii 
 /studies/STUDY/DATA/mri/processed/freesurfer/IDENTIFIER/mri/orig/001.mgz 
 ProgramVersion: $Name: stable5 $  TimeStamp: 2014/08/25-21:51:59-GMT 
  BuildTimeStamp: May 13 2013 16:24:28  CVS: $Id: mri_convert.c,v 
 1.179.2.7 2012/09/05 21:55:16 mreuter Exp $  User: USER  Machine: 
 MACHINE  Platform: Linux  PlatformVersion: 2.6.32-431.20.3.el6.x86_64 
  CompilerName: GCC  CompilerVersion: 40400
 mri_convert 
 /studies/STUDY/DATA/mri/processed/freesurfer/IDENTIFIER/mri/rawavg.mgz 
 /studies/STUDY/DATA/mri/processed/freesurfer/IDENTIFIER/mri/orig.mgz 
 --conform ProgramVersion: $Name: stable5 $  TimeStamp: 
 2014/08/25-21:54:39-GMT  BuildTimeStamp: May 13 2013 16:24:28  CVS: 
 $Id: mri_convert.c,v 1.179.2.7 2012/09/05 21:55:16 mreuter Exp $ 
  User: USER  Machine: MACHINE  Platform: Linux  PlatformVersion: 
 2.6.32-431.20.3.el6.x86_64  CompilerName: GCC  CompilerVersion: 40400

 On Mon, Aug 3, 2015 at 12:03 PM Douglas N Greve 
 gr...@nmr.mgh.harvard.edu mailto:gr...@nmr.mgh.harvard.edu wrote:

 I think that should work without problem.

 On 08/03/2015 12:51 PM, Nate Vack wrote:
  Hi all,
 
  We're looking to change the ID system we're using for some
 freesurfer
  data. Will doing do be as simple as renaming our single-subject data
  directories and restarting analysis from that point, or would we
 need
  to do something more complicated?
 
  Many thanks,
  -Nate
 
 
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Re: [Freesurfer] mri_convert IMA to MGZ

2015-08-06 Thread Douglas N Greve


On 08/05/2015 04:24 PM, Borzello, Mia wrote:
 Hi freesurfers,

 I want to localize electrode locations from a NHP CT scan, am i able 
 to do that with tkmedit without coregistering first? I don't need all 
 the parcellations of a specific atlas, just the RAS coordinates.
Yes

 Also, the CT images are IMA files. Is there a way to convert from IMA 
 to MGZ, something like:
 mri_convert -i first_ct_dicom.dcm -o ct.mgz
That should work

 I tried this and it created a file but i want to make sure i didn't 
 need to make any specifications in the command.

 Thanks,
 m


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Re: [Freesurfer] mkanalysis-sess, timewindow

2015-08-06 Thread Douglas N Greve
it would be helpful to have your mkanalysis-sess command

On 08/05/2015 04:17 PM, Xiaomin Yue wrote:
 Hi,

 I set timewindow to 10 in the mkanalysis-sess.  When I loaded Xtmp.mat 
 in to maltlab, then plot(flac.ev(2).Xirf), the size of the 
 flac.ev(2).Xirf is 20 points, which is corrected because of psdwin is 
 [0 40 2].   Should the psdwin be [0 10 2]?  No matter what value I put 
 in to timewindow, the psdwin is alway [0 40 2].  Is it correct?  If 
 so, what aspect of design matrix does the timewidow have effect on?

 thanks very much for your help.

 Xiaomin


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[Freesurfer] Fornix Segmentation

2015-08-06 Thread Syeda Maryam
Hi everyone,

So I've been going through the list trying to see if someone has encountered 
the same problem as me with regards to segmentation of the fornix but have not 
found a solution as yet. I'm a grad student and still relatively new to 
freesurfer. My research group is using freesurfer to segment and visualize 
white matter tracts in data obtained from the ADNI database. We are primarily 
working with the subcortical segmentation in the aseg volume. My current issue 
is that I am unable to find the labels for the fornix in the aseg volume; they 
seem to only be located in the wm volume generated by freesurfer. When I try to 
run mri_cc on my aseg, the corpus callosum and fornix segmentation are output 
together and I'm unable to analyze them separately. I'd really like all the 
labels I require to be contained in a single volume rather than multiple ones 
as that will make my job a lot easier. Is there something I'm missing? Is there 
a way of extracting the fornix and corpus callosum, and indeed, all white 
matter tracts from the same volume? Any help will be highly appreciated!

Thanks in advance,
Maryam
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