[Freesurfer] Longitudinal TRACULA - Error in path reconstruction

2016-03-30 Thread Emad Ahmadi
Hi Anastasia,

I hope you’re enjoying your evening!

I’m doing longitudinal TRACULA analysis on two subjects, each having two time 
points. I have already taken the steps of longitudinal recon-all and trac-all 
-prep & -bedp.

Now I’m trying to do trac-all -path, but it gives me an error that I cannot 
recognize. I would greatly appreciate your help. I’ve attached the log files 
and the config file.

Thank you so much,
Emad


Emad Ahmadi, MD
---
Research Fellow in Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu


trc_.e11258806
Description: application/applefile


trc_.o11258806
Description: Binary data


trc_0001.e11258808
Description: application/applefile


trc_0001.o11258808
Description: Binary data
# FreeSurfer SUBJECTS_DIR
# T1 images and FreeSurfer segmentations are expected to be found here
#_
setenv SUBJECTS_DIR /cluster/guptagp/Emad/3LT/subjDir
setenv RAW_DATA /cluster/guptagp/Emad/3LT/rawData
#_

# Output directory where trac-all results will be saved
# Default: Same as SUBJECTS_DIR
#
#set dtroot = /path/to/tracts/of/ducks

# Subject IDs (one per time point per subject)
#_
set subjlist = ( 2a \
 2b \
 3a \
 3b )
#_

# Longitudinal base template subject IDs (one for each time point above)
#_
set baselist = ( 2tem \
 2tem \
 3tem \
 3tem )
#_

# In case you want to analyze only Huey and Louie
# Default: Run analysis on all time points and subjects
#
#set runlist = (1 2 5 6)

# Input diffusion DICOMs (file names relative to dcmroot)
# If original DICOMs don't exist, these can be in other image format
# but then the gradient table and b-value table must be specified (see below)
#_
set dcmroot = $RAW_DATA
set dcmlist = ( 2a/Diffusion/IM-0001-0001.dcm \
2b/Diffusion/IM-0001-0001.dcm \
3a/Diffusion/IM-0001-0001.dcm \
3b/Diffusion/IM-0003-0001.dcm )
#_

# Diffusion gradient tables (if there is a different one for each scan)
# Must be specified if inputs are not MGH DICOMs
# The tables must have either three columns, where each row is a gradient vector
# or three rows, where each column is a gradient vector
# There must be as many gradient vectors as volumes in the diffusion data set
# Default: Read from DICOM header
#_
set bveclist = (/cluster/guptagp/Emad/3LT/subjDir/codes/bvecXinv.txt \
/cluster/guptagp/Emad/3LT/subjDir/codes/bvecXinv.txt \
/cluster/guptagp/Emad/3LT/subjDir/codes/bvecXinv.txt \
/cluster/guptagp/Emad/3LT/subjDir/codes/bvecXinv.txt)
#_

# Diffusion gradient table (if using the same one for all scans)
# Must be specified if inputs are not MGH DICOMs
# The table must have either three columns, where each row is a gradient vector
# or three rows, where each column is a gradient vector
# There must be as many gradient vectors as volumes in the diffusion data set
# Default: Read from DICOM header
#_
#set bvecfile = /cluster/guptagp/Emad/3LT/subjDir/codes/bvecXinv.txt
#_

# Diffusion b-value table
# Must be specified if inputs are not MGH DICOMs
# There must be as many b-values as volumes in the diffusion data set
# Default: Read from DICOM header
#_
set bvalfile = /cluster/guptagp/Emad/3LT/subjDir/codes/bval.txt
#_

# Perform registration-based B0-inhomogeneity compensation?
# Default: 0 (no)
#
#set dob0 = 1

# Input B0 field map magnitude DICOMs (file names relative to dcmroot)
# Only used if dob0 = 1
# Default: None
#
#set b0mlist = ( huey/year1/fmag/XXX-1.dcm \
huey/year2/fmag/XXX-1.dcm \
dewey/year1/fmag/XXX-1.dcm \
dewey/year2/fmag/XXX-1.dcm \
louie/year1/fmag/XXX-1.dcm \
louie/year2/fmag/XXX-1.dcm )

# Input B0 field map phase DICOMs (file names relative to dcmroot)
# Only used if dob0 = 1
# Default: None
#
#set b0plist = ( huey/year1/fphas/XXX-1.dcm \
huey/year2/fphas/XXX-1.dcm \
dewey/year1/fphas/XXX-1.dcm \
dewey/year2/fphas/XXX-1.dcm \
louie/year1/fphas/XXX-1

[Freesurfer] Is the x-component of the b vectors extracted by mri_convert inverted?

2016-01-05 Thread Emad Ahmadi
Hi FreeSurfer Experts,

Happy New Year!

I am using mri_convert to extract b vectors (bvecs) from diffusion images 
obtained at Bay 4. Then I use TRACULA for reconstructing white-matter pathways. 
The shape of the reconstructed pathways are odd, so I checked if the extracted 
bvecs are correct. 

To check if the extracted bvecs are correct, I used Diffusion Toolkit together 
with the extracted bvecs to do deterministic tractography. Then I checked the 
shape of the extracted nerve fibers. I have put a slide deck in the following 
dropbox folder showing that the shape of the extracted nerve fibers don’t look 
right:

https://www.dropbox.com/s/1bt6on0rwm9url6/x_inversion.pptx?dl=0 
<https://www.dropbox.com/s/1bt6on0rwm9url6/x_inversion.pptx?dl=0>

Then I inverted the x-components of the extracted bvecs, and did the 
tractography again. This corrected the shape of the extracted nerve fibers (see 
the slide deck).

I additionally had a look at the extracted dtift_V1 vectors under the two 
conditions, i.e. before and after x-component inversion. The results showed the 
same thing: x inversion corrects the images.

I just wanted to see if others have had the same problem and confirm that I 
should invert the x-component of the bvecs extracted via mri_convert (I had the 
same experience with dcm2nii tool, where I had to invert the z-component of the 
extracted bvecs). 

I hope a wonderful new year for everyone!
Emad

Emad Ahmadi, MD
---
Research Fellow in Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu <mailto:e...@nmr.mgh.harvard.edu>___
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[Freesurfer] How can I convert Martinos Center dicoms to the dicom format that dcm2niix recognizes?

2015-10-30 Thread Emad Ahmadi
Hi Freesurfer experts,

I hope you’re all enjoying your day!

Working in Launchpad, I want to extract the bvals/bvecs from DTI dicoms 
obtained at Martinos Center. The dicoms have the following format:

MR1.3.12.2.1107.5.2.32.35006.2010052613553219211129919
MR1.3.12.2.1107.5.2.32.35006.2010052613553736471330196
MR1.3.12.2.1107.5.2.32.35006.201005261355429098330464
...

I receive error when I run dcm2niix (to extract the b values and b vectors): 

Command:
dcm2niix -f dti 

The error I receive:

Warning: output folder invalid 
MR1.3.12.2.1107.5.2.32.35006.2010052614044051320551992 will try 
Error: unable to find any DICOM images in 
Conversion required 0.00 seconds.

When I do the following steps to generate “treatable” dicoms, dcm2niix 
recognizes these dicoms:

1. copy Martinos Center dicoms to my local Mac
2. import dicoms into OsiriX
3. Export them as dicoms
4. copy the OsiriX-exported dicoms back to Launchpad
5. Run dcm2niix on the new dicoms

Since this copying back and forth takes a lot of time, I need a better way to 
convert the “crazy” Martinos Center dicoms into the “treatable” ones!

I would really appreciate your help.

Best,
Emad


Emad Ahmadi, MD
---
Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu

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Re: [Freesurfer] How can I convert Martinos Center dicoms to the dicom format that dcm2niix recognizes?

2015-10-30 Thread Emad Ahmadi
Hi,

Thank you for your quick response!

I have already copied the dicoms to my cluster space:

/cluster/guptagp/Emad/Epilepsy/temp/slices

and the permissions of this folder seem right to me:

drwxrwsr-x 2 emad guptagp 32768 Oct 30 10:30 slices

The permissions on the dicom files are the same:

-bash-4.1$ ls -l MR1.3.12.2.1107.5.2.32.35006.2009021913370421213012700

-rwxrwxr-x 1 emad guptagp 2219694 Oct 30 10:30 
MR1.3.12.2.1107.5.2.32.35006.2009021913370421213012700


Any thoughts?

Best,
Emad



> On Oct 30, 2015, at 10:43 AM, dgw <dgwake...@gmail.com> wrote:
> 
> Hi Emad,
> 
> The only problems, which I have run into is major weaknesses in dcm2nii:
> 1. You must have write permissions on the directory the files are 
> located in.
> 2. dcm2nii cannot work on symbolically linked files.
> 
> Therefore, first copy the files to your own analysis workspace: e.g. 
> /cluster//
> then run dcm2nii.
> With that I have no problems.
> 
> hth
> d
> 
> On 10/30/15 10:28 AM, Emad Ahmadi wrote:
>> Hi Freesurfer experts,
>> 
>> I hope you’re all enjoying your day!
>> 
>> Working in Launchpad, I want to extract the bvals/bvecs from DTI dicoms
>> obtained at Martinos Center. The dicoms have the following format:
>> 
>> MR1.3.12.2.1107.5.2.32.35006.2010052613553219211129919
>> MR1.3.12.2.1107.5.2.32.35006.2010052613553736471330196
>> MR1.3.12.2.1107.5.2.32.35006.201005261355429098330464
>> ...
>> 
>> I receive error when I run dcm2niix (to extract the b values and b
>> vectors):
>> 
>> Command:
>> dcm2niix -f dti 
>> 
>> The error I receive:
>> 
>> Warning: output folder invalid
>> MR1.3.12.2.1107.5.2.32.35006.2010052614044051320551992 will try
>> Error: unable to find any DICOM images in
>> Conversion required 0.00 seconds.
>> 
>> When I do the following steps to generate “treatable” dicoms, dcm2niix
>> recognizes these dicoms:
>> 
>> 1. copy Martinos Center dicoms to my local Mac
>> 2. import dicoms into OsiriX
>> 3. Export them as dicoms
>> 4. copy the OsiriX-exported dicoms back to Launchpad
>> 5. Run dcm2niix on the new dicoms
>> 
>> Since this copying back and forth takes a lot of time, I need a better
>> way to convert the “crazy” Martinos Center dicoms into the “treatable” ones!
>> 
>> I would really appreciate your help.
>> 
>> Best,
>> Emad
>> 
>> 
>> Emad Ahmadi, MD
>> ---
>> Research Fellow
>> Department of Radiology
>> Massachusetts General Hospital
>> Harvard Medical School
>> 
>> 25 New Chardon Street, Suite 400
>> Boston, MA 02114
>> Tel: 617 726 5237
>> Email: e...@nmr.mgh.harvard.edu <mailto:e...@nmr.mgh.harvard.edu> 
>> <mailto:e...@nmr.mgh.harvard.edu <mailto:e...@nmr.mgh.harvard.edu>>

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[Freesurfer] Free surfer dev env doesn't extract bvals/bvecs

2015-10-30 Thread Emad Ahmadi
Hi Freesurfers,I’m using the dev env on Launchpad to analyze DTI dicoms using TRACULA.It cannot extract the bvecs from the dicom header since it gives me the following error:ERROR: Must specify input table of gradient vectorsI’ve attached the TRACULA configuration file (dmrirc3.txt) and the log file. I would appreciate your help!Best,Emad
Emad Ahmadi, MD---Research FellowDepartment of RadiologyMassachusetts General HospitalHarvard Medical School25 New Chardon Street, Suite 400Boston, MA 02114Tel: 617 726 5237Email: e...@nmr.mgh.harvard.edu

# FreeSurfer SUBJECTS_DIR
# T1 images and FreeSurfer segmentations are expected to be found here
#_
setenv SUBJECTS_DIR /cluster/guptagp/Emad/Epilepsy/subjDir
setenv RAW_DATA /cluster/guptagp/Emad/Epilepsy/rawData
#_

# Output directory where trac-all results will be saved
# Default: Same as SUBJECTS_DIR
#
#set dtroot = /path/to/tracts/of/ducks

# Subject IDs
#_
set subjlist = (310)
#_

# In case you want to analyze only Huey and Louie
# Default: Run analysis on all subjects
#
#set runlist = (1 3)

# Input diffusion DICOMs (file names relative to dcmroot)
# If original DICOMs don't exist, these can be in other image format
# but then bvecfile and bvalfile must be specified (see below)
#_
set dcmroot = $RAW_DATA
set dcmlist = 
(310/DIFFUSION_high_res/slices/MR1.3.12.2.1107.5.2.32.35006.2009020220092419345382942)
#_

# Diffusion gradient tables (if there is a different one for each scan)
# Must be specified if inputs are not MGH DICOMs
# The tables must have either three columns, where each row is a gradient vector
# or three rows, where each column is a gradient vector
# There must be as many gradient vectors as volumes in the diffusion data set
# Default: Read from DICOM header
#
#set bveclist = ()

# Diffusion gradient table (if using the same one for all scans)
# Must be specified if inputs are not MGH DICOMs
# The table must have either three columns, where each row is a gradient vector
# or three rows, where each column is a gradient vector
# There must be as many gradient vectors as volumes in the diffusion data set
# Default: Read from DICOM header
#
#set bvecfile = /path/to/bvecs.txt

# Diffusion b-value table
# Must be specified if inputs are not MGH DICOMs
# There must be as many b-values as volumes in the diffusion data set
# Default: Read from DICOM header
#
#set bvalfile = /path/to/bvals.txt

# Perform registration-based B0-inhomogeneity compensation?
# Default: 0 (no)
#
#set dob0 = 1

# Input B0 field map magnitude DICOMs (file names relative to dcmroot)
# Only used if dob0 = 1
# Default: None
#
#set b0mlist = (huey/fmag/XXX-1.dcm dewey/fmag/XXX-1.dcm louie/fmag/XXX-1.dcm)

# Input B0 field map phase DICOMs (file names relative to dcmroot)
# Only used if dob0 = 1
# Default: None
#
#set b0plist = (huey/fphas/XXX-1.dcm dewey/fphas/XXX-1.dcm 
louie/fphas/XXX-1.dcm)

# Echo spacing for field mapping sequence (from sequence printout)
# Only used if dob0 = 1
# Default: None
#
#set echospacing = 0.7

# Perform registration-based eddy-current compensation?
# Default: 1 (yes)
#
#set doeddy = 1

# Rotate diffusion gradient vectors to match eddy-current compensation?
# Only used if doeddy = 1
# Default: 1 (yes)
#
#set dorotbvecs = 1

# Fractional intensity threshold for BET mask extraction from low-b images
# This mask is used only if usemaskanat = 0
# Default: 0.3
#
#set thrbet = 0.5

# Perform diffusion-to-T1 registration by flirt?
# Default: 0 (no)
#
set doregflt = 1

# Perform diffusion-to-T1 registration by bbregister?
# Default: 1 (yes)
#
set doregbbr = 0

# Perform registration of T1 to MNI template?
# Default: 1 (yes)
#
#set doregmni = 1

# MNI template
# Only used if doregmni = 1
# Default: $FSLDIR/data/standard/MNI152_T1_1mm_brain.nii.gz
#
#set mnitemp = /path/to/mni_template.nii.gz

# Perform registration of T1 to CVS template?
# Default: 0 (no)
#
#set doregcvs = 0

# CVS template subject ID
# Only used if doregcvs = 1
# Default: cvs_avg35
#
#set cvstemp = donald

# Parent directory of the CVS template subject
# Only used if doregcvs = 1
# Default: $FREESURFER_HOME/subjects
#
#set cvstempdir = /path/to/cvs/atlases/of/ducks

# Use brain mask extracted from T1 image instead of low-b diffusion image?
# Has no effect if there is no T1 data
# Default: 1 (yes)
#
#set usemaskanat = 1

# Paths to reconstruct
# Default: All paths in the atlas
#
#set pathlist = ( lh.cst_AS rh.cst_AS \
 lh.unc_AS rh.unc_AS \
 lh.ilf_AS rh.ilf_AS \
 fmajor_PP fminor_PP \
 lh.atr_PP rh.atr_PP \
 lh.ccg_PP rh.ccg_PP \
 lh.cab_PP rh.cab_PP

[Freesurfer] Recon-all error

2015-06-29 Thread Emad Ahmadi
Hi,I keep getting an error when I run recon-all and can’t figure out what is wrong. I would really appreciate your help. I’ve attached the log file.Thank you so much,Emad
Emad Ahmadi, MD---Research FellowDepartment of RadiologyMassachusetts General HospitalHarvard Medical School25 New Chardon Street, Suite 400Boston, MA 02114Tel: 617 726 5237Email:e...@nmr.mgh.harvard.edu



recon-all.log
Description: Binary data
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Re: [Freesurfer] Trac-all error

2015-03-16 Thread Emad Ahmadi
Thank you so much, Zeke! That helped a lot.

Best,
Emad

 On Mar 10, 2015, at 11:43 PM, zkauf...@nmr.mgh.harvard.edu wrote:
 
 Hello Emad,
 
 The download page states that OSX versions of freesurfer require the user
 to download and install XQuartz onto their machine. I have updated the
 download page so it is a little more clear.
 https://surfer.nmr.mgh.harvard.edu/fswiki/Download 
 https://surfer.nmr.mgh.harvard.edu/fswiki/Download
 
 Also, the dev version of freesurfer is in a high degree of flux right now.
 We are undergoing compiler upgrades and other various changes to the
 build. This means I would expect the nightly builds to be unstable for the
 next couple days.
 
 But installing XQuartz should resolve the issue you experienced below.
 
 -Zeke
 
 
 
 Hello Anastasia,
 
 I’m using the nightly-built version for Mac OS Lion; I double checked it
 by the command freesurfer -ver and got this response:
 
 You are running this version of FreeSurfer:
 
  freesurfer-Darwin-lion-dev-20150227
 
 I’m using this version on Mac OS X Yosemite. I tried to re-download a
 nightly built version, but it didn’t let me (presumably because it’s
 workshop time). Please let me know how I should proceed.
 
 Yours,
 Emad
 
 On Mar 6, 2015, at 7:11 PM, Anastasia Yendiki
 ayend...@nmr.mgh.harvard.edu mailto:ayend...@nmr.mgh.harvard.edu wrote:
 
 
 Hi Emad - The error is:
 dyld: Library not loaded: /usr/X11/lib/libGLU.1.dylib
 
 Does the freesurfer build that you're using match the computer that
 you're running it on?
 
 a.y
 
 On Wed, 4 Mar 2015, Emad Ahmadi wrote:
 
 Hello Freesurfers!
 
 I’m trying to use tracheal -prep, and I’m getting an error. Would
 you please help me with figuring out where the problem is? The log file
 is attached.
 
 Thank you very much,
 Emad
 
 
 
 Emad Ahmadi, MD
 ---
 Research Fellow
 Department of Radiology
 Massachusetts General Hospital
 Harvard Medical School
 
 25 New Chardon Street, Suite 400
 Boston, MA 02114
 Tel: 617 726 5237
 Email: e...@nmr.mgh.harvard.edu
 
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[Freesurfer] TRACHEAL error

2015-03-04 Thread Emad Ahmadi
Hello Freesurfers!I’m trying to use tracheal -prep, and I’m getting an error. Would you please help me with figuring out where the problem is? The log file is attached.Thank you very much,EmadEmad Ahmadi, MD---Research FellowDepartment of RadiologyMassachusetts General HospitalHarvard Medical School25 New Chardon Street, Suite 400Boston, MA 02114Tel: 617 726 5237Email:e...@nmr.mgh.harvard.edu



trac-all.log
Description: Binary data
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Re: [Freesurfer] TRACHEAL error

2015-03-04 Thread Emad Ahmadi
* I’m trying to use trac-all

 On Mar 4, 2015, at 4:42 PM, Emad Ahmadi e...@nmr.mgh.harvard.edu wrote:
 
 Hello Freesurfers!
 
 I’m trying to use tracheal -prep, and I’m getting an error. Would you please 
 help me with figuring out where the problem is? The log file is attached.
 
 Thank you very much,
 Emad
 
 
 
 Emad Ahmadi, MD
 ---
 Research Fellow
 Department of Radiology
 Massachusetts General Hospital
 Harvard Medical School
 
 25 New Chardon Street, Suite 400
 Boston, MA 02114
 Tel: 617 726 5237
 Email: e...@nmr.mgh.harvard.edu mailto:e...@nmr.mgh.harvard.edu
 
 trac-all.log
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Re: [Freesurfer] Recon-all error

2014-07-08 Thread Emad Ahmadi
Thank you very much, Bruce! I ran it again and this time, it didn’t give me 
error.

Yours,
Emad

On Jul 7, 2014, at 12:30 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:

 hmmm, hard to say. Is it possible that you ran out of memory? Maybe something 
 else was running on the machine? Try rerunning and see if it is ok, and also 
 monitor memory usage. It died right in the middle of mri_ca_label which I 
 can't remember seeing before
 
 
 On Mon, 7 Jul 2014, Emad Ahmadi wrote:
 
 Hello FreeSurfers,
 
 Wish you a great summer time!
 
 I’m running recon-all on DICOM images of a healthy control, and it's giving 
 me an error. I have attached the log file; I’m running FreeSurfer on a Mac 
 computer and the version I’m using is: freesurfer-Darwin-lion-dev-20140701.
 
 I would really appreciate your help.
 
 Best,
 Emad
 
 
 Emad Ahmadi, MD
 ---
 Postdoc Research Fellow
 Department of Radiology
 Massachusetts General Hospital
 Harvard Medical School
 
 25 New Chardon Street, Suite 400
 Boston, MA 02114
 Tel: 617 726 5237
 Email: e...@nmr.mgh.harvard.edu
 
 
 
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[Freesurfer] Dura correction using MEMPRAGE vs bandwidth-matched FLAIR

2014-06-11 Thread Emad Ahmadi
Hi,We are at the start of a study on TBI, in which we’re obtaining MEMPRAGE and T2-SPACE-FLAIR images (the images are obtained in Lunder 6 scanner, and I wonder if I can find T1  FLAIR matched sequences for morphormetry on that scanner). The pixel size of the MEMPRAGE sequence is 1mm isotropic, while the one for T2-SPACE-FLAIR is 0.5 x 0.5 x 1mm; they’re not bandwidth matched either (I’ve attached the details of the sequences we’re using). I just wanted to know if we should make changes to our T2-SPACE-FLAIR sequence and match it with the MEMPRAGE sequence to feed the FLAIR images into recon-all for dura correction, or if we should leave the T2-SPACE-FLAIR sequence as it is and use the four echoes of MEMPRAGE for dura correction (I mean, is dura correction using different echoes of MEMPRAGE as good as feeding FLAIR images into recon-all?)Thank you very much,Emad
Emad Ahmadi, MD---Postdoc Research FellowDepartment of RadiologyMassachusetts General HospitalHarvard Medical School25 New Chardon Street, Suite 400Boston, MA 02114Tel: 617 726 5237Email: e...@nmr.mgh.harvard.edu


   SIEMENS MAGNETOM Skyra syngo MR D13
-
  \\USER\RESEARCH\Gupta_Research\Main Sequences\MEMPRAGE_IPAT3
  TA:4:28  PAT:3  Voxel size:1.0×1.0×1.0 mm Rel. SNR:1.00   :tfl_me  
-
Properties
 Prio Recon  Off 
 Load to viewer  On 
 Inline movieOff 
 Auto store images   On 
 Load to stamp segments  Off 
 Load images to graphic segments Off 
 Auto open inline displayOff 
 Wait for user to start  On 
 Start measurements  single 
Routine
 Nr. of slab groups  1 
 Slabs   1 
 Dist. factor50 %
 PositionIsocenter 
 Orientation Sagittal 
 Phase enc. dir. A  P 
 AutoAlign   --- 
 Phase oversampling  0 %
 Slice oversampling  0.0 %
 FoV read256 mm
 FoV phase   100.0 %
 Slice thickness 1.00 mm
 TR  2530.0 ms
 TE 11.69 ms
 Averages1 
 Concatenations  1 
 Filter  Prescan Normalize 
 Coil elements   HEA;HEP 
Contrast
 Magn. preparation   Non-sel. IR 
 TI  1100 ms
 Flip angle  7.0 deg
 Fat suppr.  None 
 Water suppr.None 
 Averaging mode  Long term 
 Measurements1 
 Reconstruction  Magn./Phase 
 Multiple series Each measurement 
Resolution
 Base resolution 256 
 Phase resolution100 %
 Phase partial Fourier   Off 
 Interpolation   Off 
 PAT modeGRAPPA 
 Accel. factor PE3 
 Ref. lines PE   32 
 Reference scan mode Integrated 
 Image FilterOff 
 Distortion Corr.Off 
 Accel. factor 3D1 
 Unfiltered images   Off 
 Prescan Normalize   On 
 Normalize   Off 
 B1 filter   Off 
 Raw filter  Off 
 Elliptical filter   Off 
 Slice resolution100 %
 Slice partial Fourier   Off 
Geometry
 Nr. of slab groups  1 
 Slabs   1 
 Dist. factor50 %
 PositionIsocenter 
 Phase enc. dir. A  P 
 Phase oversampling  0 %
 Slice oversampling  0.0 %
 Slices per slab 176 
 Multi-slice modeSingle shot 
 Series  Interleaved 
 Nr. of sat. regions 0 
 Position mode

[Freesurfer] Unpacking Problem

2014-06-04 Thread Emad Ahmadi
Hello,I’m trying to unpack and run recon-all on a set of MEMPRAGE images we’ve obtained in Lunder 6 scanner (Siemens Skyra), but recon-all is giving me errors. I’ve attached for the scan.info file (outputted by unpacksdcmdir), the unpack.config file that I used to unpack the MEMPRAGE images, and the recon-all.log file containing the error that recon-all command gives me. I’m running recon-all on in MEMPRAGE3 folder containing MEMPRAGE_IPAT3 RMS images. Please let me know if I have to provide any further info about this problem.Thank you very much for your help,EmadEmad Ahmadi, MD---Postdoc Research FellowDepartment of RadiologyMassachusetts General HospitalHarvard Medical School25 New Chardon Street, Suite 400Boston, MA 02114Tel: 617 726 5237Email: e...@nmr.mgh.harvard.edu

scan.info
Description: Binary data


unpack.config
Description: Binary data


recon-all.log
Description: Binary data
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[Freesurfer] Applying a precomputed transform matrix to an image in free surfer

2014-04-23 Thread Emad Ahmadi
Hello, 

I’m having a volume (e.g. dtifit_FA.nii.gz) and a transform matrix (e.g. 
diff2anatorig.bbr.mat), and I want to apply the transform matrix to the image 
and generate a transformed image. This is a general question I’m having, but in 
this particular case, I want to apply the transform matrix (from diffusion 
space to the anatomical space generated by TRACULA) to the FA map to generate a 
transformed FA map that can be overlaid on the anatomical images.

I wonder if I have to use mri_vol2vol command for doing this, and I don’t know 
how to provide it with appropriate flags. I’m already having the transform 
matrix generated by TRACULA (and I don’t want to change it; I just want to 
apply it to the image!). My crude guess would be something like this:

mri_vol2vol --mov address of dtifit_FA.nii.gz --o address of 
transformed_dtifit_FA.nii.gz --reg diff2anatorig.bbr.mat

Please let me know how I should run this command. 

Thank you very much,
Emad

P.S. I know that for this particular example, I can use the anatomical images 
in dlabel/diff, but the point for me is to learn how to apply a transform 
matrix to an image and generate a transformed image in freesurfer

Emad Ahmadi, MD
---
Postdoc Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu___
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[Freesurfer] How to define a new label for aparc+aseg.mgz in FreeView

2014-03-03 Thread Emad Ahmadi
Hello,

I want to define a new label in aparc+aseg.mgz (to mark certain brainstem 
structures); I would appreciate it if you help me with how I have to do it.

Lots of thanks,
Emad



Emad Ahmadi, MD
---
Postdoc Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu



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Re: [Freesurfer] How to define a new label for aparc+aseg.mgz in FreeView

2014-03-03 Thread Emad Ahmadi
 Hi Bruce,
 
 Thank you for your response. I just want to draw manually the region of the 
 new label on the images of few subjects.
 
 What I am about to do is to define a new label for the trigeminal nerve 
 sensory nucleus (just roughly as the region that the nerve enters the 
 brainstem); I just need to label it manually for all subjects.
 
 Best,
 Emad
 
 
 
 On Mar 3, 2014, at 11:32 AM, Bruce Fischl fis...@nmr.mgh.harvard.edu wrote:
 
 Hi Emad
 
 do you mean draw one manually or add it so it is automatically labeled in 
 new subjects? If the latter it requires manually labeling a training set and 
 rebuilding a classifer, etc..., so it is far from trivial
 
 cheers
 Bruce
 
 
 On Mon, 3 Mar 2014, Emad Ahmadi wrote:
 
 Hello,
 I want to define a new label in aparc+aseg.mgz (to mark certain brainstem
 structures); I would appreciate it if you help me with how I have to do it.
 Lots of thanks,
 Emad
 Emad Ahmadi, MD
 ---
 Postdoc Research Fellow
 Department of Radiology
 Massachusetts General Hospital
 Harvard Medical School
 25 New Chardon Street, Suite 400
 Boston, MA 02114
 Tel: 617 726 5237
 Email: e...@nmr.mgh.harvard.edu
 
 
 
 

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[Freesurfer] How to clone from T1 to brainmask in freeview to amend a bad skull strip

2014-02-28 Thread Emad Ahmadi
Hi!

I want to know how to clone from T1.mgz to brainmask.mgz in freeview (to amend 
a skullstript that has removed too much). I couldn’t find the tool in freeview. 

Thank you very much,
Emad


Emad Ahmadi, MD
---
Postdoc Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu



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[Freesurfer] Recon-all error

2014-01-31 Thread Emad Ahmadi
Hello,

I am using recon-all, and it gives me error and exits and I cannot
understand why. I would appreciate it if you give me a clue why it's not
working.

I've written a piece of script (recon.bash attached) to be copied to the
subject's folder, and when run it should automatically go through the
analysis pipeline, but it gives me the error and exits.


Thank you very much,
Emad


Emad Ahmadi, MD

Postdoc Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu



recon-all.log
Description: Binary data


recon.bash
Description: Binary data
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[Freesurfer] recon-all error

2014-01-06 Thread Emad Ahmadi
Hello  Happy New Year!

I'm running recon-all for one subject on MGH clusters (ERISone), and it
exits with error. I would appreciate it if you help me figure out what the
problem is. The log file is attached.

All the best throughout 2014!
Emad


Emad Ahmadi, MD

Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu



recon-all.log
Description: Binary data


recon1job.bash
Description: Binary data
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[Freesurfer] Recon-all exits with errors for a patient with TBI

2013-12-23 Thread Emad Ahmadi
Hello,

I'm analyzing some images of patients with TBI. There's one of them having
abnormalities in T1 images (skull fracture, epidural/intracranial
hemorrhage, shifts) that can trouble image registration; when I run
recon-all for this patient, it exits with errors. I wonder if it has
anything to do with the abnormalities troubling the registration of
T1 images. I've attached the log file, and some axial sections of the T1
images can be viewed here:

https://drive.google.com/folderview?id=0B4AFmHFjy_bsbkotd2QyZjZ6dW8usp=sharing

Thank you and Merry Christmas!

Emad

recon-all.log
Description: Binary data
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[Freesurfer] Generating list of subjects: a tcsh scripting problem

2013-12-16 Thread Emad Ahmadi
Hello,

I am having a tcsh scripting problem for generating a text file containing
the list of subjects, and I would appreciate any help. I've explained my
problem here:

http://stackoverflow.com/q/20617206/2769441

All the best,
Emad
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[Freesurfer] Do these bvec and bval files match?

2013-12-10 Thread Emad Ahmadi
Hello,

I'm using TRACULA to analyze images obtained by a non-Siemens scanner, and
I'm using dcm2niigui app to generate bvec and bval files from DICOMs.

My question is whether or not the attached bvec and bval files match,
because the 0 bval is the first entry while the 0,0,0 bvec is somewhere
in the middle. If they don't, how should I generate the correct bval/bvec
files from dicoms?

Lots of thanks,
Emad

bval
Description: Binary data


bvec
Description: Binary data
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[Freesurfer] Is there anyway to define multiple processing cores for FreeSurfer to speed up its commands?

2013-11-07 Thread Emad Ahmadi
Hello,

I'm using FreeSurfer on a 6-core Mac Pro machine. It takes quite a bit for
commands like recon-all to complete, while I've noticed that my CPU and
memory resources are mostly idle.

I just wanted to know if there's anyway to define multiple cores for
FreeSurfer (something like matlabpool in matlab parallel computing
toolbox).

Thank you,
Emad


Emad Ahmadi, MD

Research Fellow
Department of Radiology
Massachusetts General Hospital
Harvard Medical School

25 New Chardon Street, Suite 400
Boston, MA 02114
Tel: 617 726 5237
Email: e...@nmr.mgh.harvard.edu



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