[Freesurfer] ERROR: QdecGlmDesign::Create: zero factors!

2014-08-18 Thread Minjeong Wang
Dear freesurfer user,


I'm new in this freesurfer and i want to analysis of the thickness of
two groups, dementia and normal.

I was trying to use qdec but when i pressed analyze button, there
was some message at the bottom, which is Error during design
creation.

At the same time, on the terminal, the following message came up.

ERROR: QdecGlmDesign::Create: zero factors! 


For details, See below.


Please let me know what the problem is.

Thanks.

*M.J. *


Reading /Applications/freesurfer/tktools/tkUtils.tcl

Using /Applications/freesurfer/lib/tcl/fsgdfPlot.tcl

Loading data table /Applications/freesurfer/subjects/qdec.table.dat...
Number of columns:  3
fsid column:1
Number of factors:  2
Number of subjects: 10
Reading discrete factor levels from config file
/Applications/freesurfer/subjects/diagnosis.levels
AD
Normal
done.

Data table /Applications/freesurfer/subjects/qdec.table.dat loaded.
Verifying subject data..Subject verification complete.
Input table: /Applications/freesurfer/subjects/qdec.table.dat
Subj#, SubjID, Data...
 1 a1002 AD 75.00
 2 a1003 AD 63.00
 3 a1009 AD 71.00
 4 a1015 AD 80.00
 5 a1019 AD 75.00
 6 n1004 Normal 72.00
 7 n1005 Normal 71.00
 8 n1006 Normal 57.00
 9 n1007 Normal 62.00
10 n1008 Normal 62.00
1  diagnosis  discrete 2
 1  AD
 2  Normal
2  age  continuous 0
 Continuous Factors: Mean:   StdDev:
  --- -   ---

  age68.800 7.361

Number of subjects:   10
Number of factors:2 (1 discrete, 1 continuous)
Number of classes:2
Number of regressors: 4


Data table loading completed successfully.
SUBJECTS_DIR is '/Applications/freesurfer/subjects'
ERROR: QdecGlmDesign::Create: zero factors!
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Re: [Freesurfer] Hippocampal Subfields missing nonPartialVolumeStatsRight.txt file

2014-08-18 Thread Eugenio Iglesias
Hi Yoon,
when you run the script  kvlQuantifyHippocampalSubfieldSegmentations.sh, it 
goes along the volumeStats_left.txt and volumeStats_right.txt to build a large 
table with all the volumes. The output files 
(nonPartialVolumeStatsLeft.txt/nonPartialVolumeStatsRight.txt) should be in 
your subjects directory  $subject.
Regarding the partial volume segmentation, it's not fully implemented / tested 
yet.
Cheers,
/Eugenio 

Juan Eugenio Iglesias
Postdoctoral researcher BCBL
www.jeiglesias.com
www.bcbl.eu

Legal disclaimer/Aviso legal/Lege-oharra: www.bcbl.eu/legal-disclaimer


- Original Message -
From: Yoonho Chung yoonho.ch...@yale.edu
To: freesurfer@nmr.mgh.harvard.edu
Sent: Friday, August 15, 2014 10:33:19 PM
Subject: [Freesurfer] Hippocampal Subfields missing 
nonPartialVolumeStatsRight.txt file

Hi,

I am running Hippocampal subfield processing stream and I think I got all the 
appropriate posterior_*.mgz files I need to get the stats, but I am not 
seeing  nonPartialVolumeStatsRight.txt anywhere as described in the wiki 
under $subjectsdir. What I am seeing is volumeStats_left.txt and 
volumeStats_right.txt files under the $subject/mri directory and one of the 
text files look like this.

volumeInVoxels:
Left-Hippocampus: 2616.97
left_presubiculum: 4050
left_CA1: 2880.55
left_CA2_3: 8120.59
left_fimbria: 212.439
left_subiculum: 5985.02
left_CA4_DG: 4459.07
left_hippocampal_fissure: 358.59
-

If I look at the end of the hippo-subfields.log file, it is saying it is 
skipping the partial volume segmentation (see below).

---
...
  Debug: Off
  Observers:
none
  Matrix:
-0.5 0 0
0 0 0.5
0 -0.5 0
  Offset: [41.7047, -40.8148, -4.10007]
  Center: [0, 0, 0]
  Translation: [41.7047, -40.8148, -4.10007]
  Inverse:
-2 0 0
0 0 -2
0 2 0
  Singular: 0
spacing: [0.5, 0.5, 0.5]
origin: [41.7047, -40.8148, -4.10007]
direction: -1 0 0
0 0 1
0 -1 0

done!
Skipping the partial volume segmentation part
---

Can please someone tell me what I am missing?
Also, what do I need to do to extract the values to a spreadsheet? Should I use 
asegstats2table? under '-help' it doesn't say which options it should be used 
to get the subfields.

Thank you so much for the help in advance.

Cheers,
Yoon


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[Freesurfer] load_nifti.m - empty header

2014-08-18 Thread Nadine Schlichting
Dear Freesurfers,

I am struggling with a very basic step at the very beginning of my
processing pipeline.
This is what I've done: registered BOLD to anatomical data using
bbregister, results checked with tkregister2 - all seems fine. Then I want
to project BOLD data to the surfaces using mri_vol2surf - no error so far.
BUT when trying to load the mri_vol2surf output into matlab (load_nifti.m)
I get this error:

*??? Attempted to access hdr.dim(2); index out of bounds because
numel(hdr.dim)=0.*
*Error in == load_nifti_hdr at 121*
*if(hdr.dim(2)  0)*
*Error in == load_nifti at 80*
*hdr = load_nifti_hdr(niftifile);*

It seems that the hdr struct is completely empty.

Thanks in advance for any kind of help, have a nice week,

Nadine
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Re: [Freesurfer] Compatibility Tracula v.5.3 and recon v.5.2 longitudinal

2014-08-18 Thread Anastasia Yendiki

Hi Yoon - The update is here:
http://freesurfer.net/fswiki/Tracula#Updates

There will also be a new freesurfer release in the next couple of months, 
but I don't anticipate making more changes to longitudinal tracula before 
that, so this should be the same as in the future 5.4 version.

a.y

On Wed, 23 Jul 2014, Yoonho Chung wrote:

 Thank you for your input. Before we go ahead and reprocess our recon and DTI 
 data with FS v 5.3 we were wondering if you plan an update on the TRACULA DTI 
 longitudinal stream anytime soon.
 I think I saw somewhere in the email chain that this is likely to happen soon 
 with additional features and bug fixes. If so, I think it would be worth the 
 wait.

 Thank you!

 Yoon




 On May 22, 2014, at 5:37 PM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu 
 wrote:


 Hi Yoon - If you are getting an error from longitudinal tracula, do check 
 the tracula updates at the link that I gave you in my previous email.

 As for 5.2 recon-all, others can chime in here, but like I said it is not 
 recommended to use it. Sorry about that.

 a.y

 On Thu, 22 May 2014, Yoonho Chung wrote:

 Thanks for the quick response!

 If I already have all the T1 data processed using recon-all with FS v5.2, 
 do you think it is okay to switch the stream to FS v.5.3 and run Tracula? - 
 without having to do the recon-all again for the T1 data? It is because I 
 am also experiencing DTI longitudinal error due to the OS issue (according 
 to other threads). And if possible, I would like to avoid having to redo 
 all the recons if we have to switch it to v5.3.

 Thanks again!
 Yoon


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Re: [Freesurfer] Tracula : Path not entirely in the white matter

2014-08-18 Thread Anastasia Yendiki

Hi Emily - Yes, this is fine. I just meant that it shouldn't look like a 
single line.

a.y

On Thu, 24 Jul 2014, ebell...@uwm.edu wrote:

 Hi Anastasia,

 Just to be clear, is this what you mean by a more diffuse volumetric 
 distribution. Here is a snapshot of the right inferior longitudinal 
 fasiculous.

 I am just getting a better sense of what to look for in terms of bad vs. good 
 tracts.

 Emily

 - Original Message -
 From: Anastasia Yendiki ayend...@nmr.mgh.harvard.edu
 To: Freesurfer support list freesurfer@nmr.mgh.harvard.edu
 Sent: Wednesday, July 16, 2014 4:54:29 PM
 Subject: Re: [Freesurfer] Tracula : Path not entirely in the white matter


 Hi Emily - This is not necessarily a problem. To make sure, you can check
 the output path.pd.nii.gz file from that specific tract. If it got stuck
 somewhere (e.g., because the brain mask is missing a bit of brain that
 this tract should go through) then the path.pd.nii.gz will look like a
 single curve rather than a more diffuse volumetric distribution.

 Hope this helps,
 a.y

 On Wed, 16 Jul 2014, ebell...@uwm.edu wrote:

 Hello,

 I was looking at a trac-all log file to get my bearings on what is being 
 done and making sure things were done successfully,

 I did not get any errors for this subject but when I was looking at the 
 right uncinate fasciculus: It would say Path from initial control points 
 not entirely in the white matter and then it attempted to perturb control 
 points.

 I noticed that for this tract, it did not say that it did not say sucess 
 after how ever many control points. It just said that it reverted back to 
 the initial control points.

 Do I then need to be concerned about the validity of this particular tract 
 for this subject?

 Thanks,

 Emily
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Re: [Freesurfer] dmri_trk2trk issue

2014-08-18 Thread Anastasia Yendiki

Hi Tommi - The input reference volume (--inref) should be in the same 
space as the input .trk file, i.e., your individual's diffusion space. It 
seems that you're using the individual's T1 space instead?

a.y

On Fri, 25 Jul 2014, r...@nmr.mgh.harvard.edu wrote:

 Hi,

 I am attempting to morph deterministic tractography results (.trk file)
 from the individual diffusion space into the average brain
 cvs_avg35_inMNI152. However, something goes wrong, as the output trk file
 is greatly misplaced / strongly distorted / wrongly sized.

 The input file (dsi60.trk, a TrackVis trk file with an angle threshold of
 60 degrees) loads fine in Trackvis, as do the inref and outref volumes (in
 .nii format). The rigid body (.mat) and nonlinear (.m3z) registrations
 also appear ok. The mat file (or more precisely, the corresponding
 register.dat file) looked fine with tkregister2 and the latter was
 successfully used to morph the corresponding probabilistic tractography
 results from the individual diffusion space to cvs_avg35_inMNI152 (= the
 same transformation I am trying to do here).

 Any suggestions what I am doing wrong? For example, could this be related
 to inref/outref voxel sizes or coordinate systems?

 Just in case, I already tried using the inverse rigid registration
 (anat2diff.mat) and the FDT-generated files inside DSI.bedpostX/xfms
 (diff2str.mat and its inverse) but the results were in all cases very much
 wrong, just in different ways.

 FS 5.3 (nmr-std-env)
 on machine avml
 cd $SUBJECTS_DIR

 dmri_trk2trk \
 --in $SUBJECT/DSI/dsi60.trk \
 --out TMSDSIGA_19Jul14/${SUBJECT}inCVS35MNI152_dsi60.trk \
 --inref $SUBJECT/mri/norm.mgz \
 --outref $FREESURFER_HOME/subjects/cvs_avg35_inMNI152/mri/norm.mgz \
 --reg $SUBJECT/DSI/${SUBJECT}_diff2anat.mat \
 --regnl $SUBJECT/cvs_CVS35MNI152/final_CVSmorph_tocvs_avg35_inMNI152.m3z \

 reg (.mat) was computed as follows:
 bbregister --mov dsi_b0.nii --frame 0 --bold --s $SUBJECT --init-fsl --reg
 DSIregister.dat --fslmat ${SUBJECT}_anat2diff.mat

 I would be happy to copy the data to a location of your choosing if you
 would like to replicate the error. Thanks!

 Tommi

 ---
 Tommi Raij, MD, PhD
 MGH/MIT/HMS Athinoula A. Martinos Center for Biomedical Imaging
 Bldg 149, 13th St
 Charlestown, MA 02129
 U.S.A.
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Re: [Freesurfer] Diffusion analysis qs

2014-08-18 Thread Anastasia Yendiki


Hi Rotem - It's hard to tell without zooming into some key areas, like 
corpus callosum and cingulum for example. The colors look ok (red and 
green, respectively) but it's hard to see how the lines look.


a.y

On Mon, 28 Jul 2014, Rotem Saar wrote:


Dear Anastasia,

I followed your suggestion:

I calculated the FA maps in freesurfer using the script below (see last 
message): I
did it with both the rotated and the not rotated gradient table. The FA maps 
were
identical as u said.

BUT ! - when I used the rotated gradient table in FSL and tried to create the FA 

MD maps (as in the first step of tracula), I got the attached
results: http://tinypic.com/r/skzwqa/8

Does this map seems ok to u ? I think that something is wrong but can't specify
what.

I will appreciate your help here again:)



Hi Rotem - The FA values are actually invariant to a rotation of the
gradient vectors. You can test that yourself. If, however, you get
different FA maps with the different gradient tables, then something else
is going on and not a simple rotation.

a.y

On Wed, 23 Jul 2014, Rotem Saar wrote:

 Dear Anastasia  Michael,

 Thank u for your answers (I attached my last email and your answers at the
 end of this email.

 I still want to specify my question. If I only want to extract FA values
 using the following script (see script below), and I know that an angle was
 applied during the dMRI scans, should I use the rotated gradient matrix ?

 When I first analyzed 20 subjects with the gradient matrix that is published
 for a T3 Philips magnet (I also read the gradients from the dicom header -
 they were the same) I got reasonable results - but now I don't know what to
 think of them...


 source ~/Desktop/fs_script

 dt_recon --i /usr/local/freesurfer/subjects/Anatomy0207/DTI/I160.dcm --s
 Anatomy0207 --o /usr/local/freesurfer/subjects/Anatomy0207/DTI --b
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/bvals.bval
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/bvecs.bvec

 To check results, run:

 tkregister2 --mov /usr/local/freesurfer/subjects/Anatomy0207/DTI/lowb.nii
 --reg /usr/local/freesurfer/subjects/Anatomy0207/DTI/register.dat --surf

 tkregister2 --s fsaverage --surf white --reg
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/mask-tal.nii.reg --mov
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/mask-tal.nii

 tkregister2 --s fsaverage --surf white --reg
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa-tal.nii.reg --mov
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa-tal.nii

 freeview -v /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa.nii
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/adc.nii

 freeview 
-v/usr/local/freesurfer/subjects/Anatomy0207/mri/brain.mgz/usr/local/freesurfer/subje
cts/Anatomy0207/DTI/fa.nii:reg=register.dat:colo
 rmap=heat:heatscale=.2,.2,1

 tkmedit Anatomy0207?orig.mgz -aux brain.mgz -seg wmparc.mgz -reg
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/register.dat -overlay
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa.nii -fthresh 0.2 -fmax 1

 mri_vol2vol --mov /usr/local/freesurfer/subjects/Anatomy0207/DTI/lowb.nii \
 ??? --targ /usr/local/freesurfer/subjects/Anatomy0207/mri/wmparc.mgz
 \
 ??? --inv --interp nearest --o
 /usr/local/freesurfer/subjects/Anatomy0207/mri/wmparc2diff.mgz \
 ??? --reg
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/register.dat --no-save-reg

 mri_vol2vol --mov /usr/local/freesurfer/subjects/Anatomy0207/DTI/lowb.nii \
 ??? --targ
 /usr/local/freesurfer/subjects/Anatomy0207/mri/aparc+aseg.mgz \
 ??? --inv --interp nearest --o
 /usr/local/freesurfer/subjects/Anatomy0207/mri/aparc+aseg2diff.mgz \
 ??? --reg
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/register.dat --no-save-reg

 freeview -v /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa.nii \
???/usr/local/freesurfer/subjects/Anatomy0207/mri/aparc+aseg2diff.mgz:color
map
 =lut


 mri_mask /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa.nii \
  /usr/local/freesurfer/subjects/Anatomy0207/mri/wmparc2diff.mgz \
  /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa-masked.mgz


 freeview 
-v/usr/local/freesurfer/subjects/Anatomy0207/DTI/fa-masked.mgz/usr/local/freesurfer/s
ubjects/Anatomy0207/mri/aparc+aseg2diff.mgz:colormap
 =lut

 mri_segstats --seg
 /usr/local/freesurfer/subjects/Anatomy0207/mri/wmparc2diff.mgz --ctab
 $FREESURFER_HOME/FreeSurferColorLUT.txt --i
 /usr/local/freesurfer/subjects/Anatomy0207/DTI/fa-masked.mgz --sum
 /usr/local/freesurfer/subjects/Anatomy0207/stats/all_stats_fa-masked


 It'd be nice if things were that simple, but!

 Although the pre-processing is done with FSL tools, tractography is done
 with locally written code. Some gradient sets may appear to work with FSL,
 but they won't work for us. For example, some dicom converters may perform
 a L-R flip as preparation for feeding the gradient vectors into FSL. We
 need the 

Re: [Freesurfer] trac-all -prep problem

2014-08-18 Thread Anastasia Yendiki

Hi Shantanu - It's stuck trying to initialize one of the tracts. You can 
check which tract it is, and then check the data to see if there's 
something wrong that would affect that particular tract (for example, if 
part of the brain that this tract goes through is cut off in the mask).

a.y

On Fri, 1 Aug 2014, Shantanu Ghosh wrote:

 Hi Freesurfer experts,

 I ran the command trac-all -prep -c dmrirc.txt

 on a bunch of subjects and all of them finished in ~90 minutes except one.
 This subject keeps on going into a seemingly endless loop. It has been
 running for almost 12 hours now. A section of the console output is
 reproduced below.

 What is the issue here, and how can this be solved?
 I am using the dev version on a Linux box.

 Thanks in advance for all help.
 Shantanu

 --
 SAMPLE CONSOLE OUTPUT
 --
 INFO: Distances between consecutive points in test subject's space are 11
 11 10 10 10
 WARN: Could not find satisfactory control point fit - try 1831
 Finding center streamline
 INFO: Step is 5 voxels
 WARN: Turning off deviation check for center streamline
 INFO: Step is 5 voxels
 WARN: Turning off FA check for center streamline
 INFO: Step is 5 voxels
 INFO: Length of center streamline is 91 voxels
 Selecting 6 points on center streamline
 INFO: Minimum allowable distance between dominant points is 9
 INFO: Minimum allowable curvature at a dominant point is 0.0283381
 INFO: Points where local peeks in curvature occur are
 106 105 67 (curv = 0.0284049)
 112 108 77 (curv = 0.0450985)
 115 108 98 (curv = 0.0526145)
 113 104 116 (curv = 0.0460477)
 107 103 128 (curv = 0.0759711)
 INFO: Intermediate dominant points are
 103 98 50
 112 108 77
 114 108 89
 115 108 98
 107 103 128
 105 106 145
 INFO: Final dominant points are
 103 98 50
 112 108 77
 114 108 89
 115 108 98
 107 103 128
 105 106 145
 WARN: Defaulting to equidistant dominant points
 WARN: Defaulting to equidistant control points
 INFO: Selected control points are
 103 98 50
 108 106 69
 114 108 89
 114 105 108
 108 103 126
 105 106 145
 INFO: Distances between consecutive points are 21 21 19 19 19
 INFO: Selected control points in test subject's space are
 80 62 23
 81 66 31
 84 68 40
 84 66 48
 82 64 56
 81 65 64
 INFO: Distances between consecutive points in test subject's space are 9
 10 8 8 8
 WARN: Could not find satisfactory control point fit - try 1832
 Finding center streamline
 INFO: Step is 5 voxels
 WARN: Turning off deviation check for center streamline
 INFO: Step is 5 voxels
 WARN: Turning off FA check for center streamline
 INFO: Step is 5 voxels





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Re: [Freesurfer] Tracula Missing Statistics

2014-08-18 Thread Anastasia Yendiki

Hi Emily - The weighted average is the most reliable in practice, and it 
is also the proper statistical definition of mean (expected) value. It 
weighs the value of FA etc at each voxel with the probability of the tract 
going through that voxel.

The cases that are missing stats may need to be rerun. I'm guessing that 
those will look like single curves if you view the path.pd.nii.gz volume. 
You can rerun them by using set reinit = 1 in the config file, and also 
specifying in the config file to run only the specific tract and specific 
subject. You'd have to rerun the -prior and -path steps only.

a.y

On Sun, 3 Aug 2014, Emily Louise Belleau wrote:


 
 Hello Tracula Experts,

 I noticed that for a few of my subjects, I am missing all Center statistics 
 for FA, MD etc. for certain tracts like the left uncinate fasciculus for 
 example.

 I am assuming this means that an optimal pathway was unable to be found?  I 
 do have the average and weighted statistics for these subjects. Should I 
 consider excluding these subjects or should I try analyzing them again with 
 different parameters?

 Additionally, I noticed that for a couple of my subjects, the Length Center 
 (length of the highest probability pathway) is unusually short compared to 
 the rest of the subjects? Is this a problem and do I consider excluding or 
 tweaking the parameters for these subjects?

 Also, do individuals usually report in publications just the average 
 statistics or are the weighted average or center statistics used?

 Attached are the stats of the problematic subjects. Any advice would be 
 greatly appreciated!

 Emily
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Re: [Freesurfer] DTI Statistics

2014-08-18 Thread Anastasia Yendiki


Weighted average recommended, see my previous email.


On Tue, 5 Aug 2014, Emily Louise Belleau wrote:




​Hello all,


I was just wondering if in publications/papers it is more common to report the
average FA statistics, the weighted average statistics, or the center statistics
(the average of the highest probability pathway).


These are the statistics provided by Tracula.


Thanks,


Emily


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Re: [Freesurfer] Steps for Longitudinal trac-all

2014-08-18 Thread Anastasia Yendiki

Hi Yoon - Sorry, the config file is necessary for anything that doesn't 
use default settings for trac-all, and that includes running it in 
longitudinal mode.

What kind of cluster do you have? I'm working on making running trac-all 
easier on clusters that are not currently supported, as part of the 5.4 
release.

a.y

On Tue, 12 Aug 2014, Chung, Yoonho wrote:

 Dear FS experts.

 I am trying run trac-all - the longitudinal version - on the cluster and not 
 by using the dmrirc file. I am looking at the 'trac-all -help' and also the 
 wiki, but I couldn't find a flag or option where I could specify the use of 
 unbiased-template (e.g. [subjectID-base]) and other steps that may be 
 necessary for the longitudinal analysis. Could someone please provide the 
 steps that is required for running the longitudinal stream using 'trac-all' ? 
 Thank you very much.

 Best,
 Yoon



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[Freesurfer] Cortical thickness via freesurfer

2014-08-18 Thread Laura Golz
Dear all.

I have a question concerning the estimation of cortical thickness in freesurfer.
My overall goal is the comparison of a patient and matched control group with 
VBM and cortical thickness.
My first try was the recon-all with masked MP2RAGE UNI-Images. Unfortunately it 
executed with error due to a not successfull skull-stripping
Secondly I was going to skull-strip in AFNI and feed the skull-stripped image 
to the recon-all, but unfortunately the skull-stripping in AFNI was better but 
not as good as hoped.

Next idea now is using the output of the VBM8 of SPM. Is it possible to use the 
segmented grey matter image from SPM in the recon-all to calculate overall 
cortical thickness and which steps of the recon-all are needed to be excluded 
for that? I am basically not interested in white matter...is it needed in the 
algorithm in general? The step 15 starts with the wm edits. So in case I am 
able to use only the segmented grey matter image from the VBM toolbox to avoid 
needing to skull-strip, I need to start with the step 21 (autorecon2-pial) of 
the recon-all? 

Or is there a possibility to improve the skull-stripping somehow? I tried 
lowering the threshold by adding the watershed trying to be more liberal, but 
it did not work as I was hoping...

Thank you all so much in advance!
Best Regards,
Laura 
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[Freesurfer] Checking in about FLAIR Registration Problem

2014-08-18 Thread Zamroziewicz, Marta Karolina
Good morning,

I wrote several weeks ago about a bbregister problem that we’ve encountered 
(I’ve attached the original email below). I’d like to check back in about the 
status of the patch that was being developed.

Thank you for your time and assistance!

Marta Zamroziewicz
MD/PhD Candidate
Decision Neuroscience Laboratory
University of Illinois Urbana-Champaign
mzam...@illinois.edumailto:mzam...@illinois.edu
815-980-3882

This email is related to the archived “bbregister and FLAIR” email chain posted 
by Kayle Sawyer on 5/23/2014 
(http://www.mail-archive.com/freesurfer%40nmr.mgh.harvard.edu/msg36117.html).

We have also been registering with FLAIR scans, and have run into a problem 
with approximately half of our subjects. Recon-all completes successfully but a 
bad registration step leaves our MPRAGE and FLAIR scans misaligned. I’ve 
attached two screenshots, the first of which shows a bad registration and the 
second of which shows a good registration.

Per your previous suggestion, we ran bbregister using the following flag:

bbregister --s SLOTS007 --mov flair.mgz --init-header --reg reg.test.dat
--t2 --lta reg.test.lta

This did result in a good registration, and we are hoping to incorporate this 
into our processing pipeline to ensure that we can use the FLAIR for refining 
the pill surface. The problem that we’ve run into is that we aren’t sure at 
which point this bbregister step occurs within the recon-all process flow. We 
were thinking there are a couple of possibilities:

1. manually create the transformation matrix for the FLAIR using the command 
mentioned above, and then re-run whichever steps necessary in recon-all to 
include this manually created xform;

2. apply the manually created xform to the mri/orig/FLAIRraw.mgz image to 
create a new, properly aligned mri/FLAIR.mgz, and then re-run recon-all with 
whatever steps/flags we need to include this FLAIR image to refine the pial 
surface.

Unfortunately we're not exactly sure which flags to include in recon-all in 
order to most efficiently re-process our data with the manually created FLAIR 
transformation, and we were hoping you might offer some advice on this point. 
Please let me know if I can provide any additional information.




[cid:795E512B-0727-4B3D-8B43-17BE1640FBD8@beckman.uiuc.edu][cid:9003C1C6-AA59-46E3-BF4A-0CEE22C57030@beckman.uiuc.edu]







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[Freesurfer] None region label number (color) not in FreeSurferColorLUT.txt

2014-08-18 Thread Axelson, Eric D
I am trying to make a custom label color scheme and wanted to change the None. 
Region but the FreeSurferColorLUT.txt only lists the unknown region (0) rather 
than None.  I replaced the unknown region label name with None. to no avail 
like this.  Is the None. region a different label number and color code?

  0  None.   120 120 120   0
  1  bankssts120 120 120   0
  2  caudalanteriorcingulate 120 120 120   0
  3  caudalmiddlefrontal 120 120 120   0
  4  corpuscallosum  120 120 120   0
  5  cuneus  120 120 120   0
  6  entorhinal  120 120 120   0
  7  fusiform120 120 120   0
  8  inferiorparietal120 120 120   0
  9  inferiortemporal120 120 120   0
10  isthmuscingulate120 120 120   0
11  lateraloccipital120 120 120   0
12  lateralorbitofrontal120 120 120   0
13  lingual 120 120 120   0
14  medialorbitofrontal 120 120 120   0
15  middletemporal  120 120 120   0
16  parahippocampal 120 120 120   0
17  paracentral 120 120 120   0
18  parsopercularis 120 120 120   0
19  parsorbitalis   120 120 120   0
20  parstriangularis120 120 120   0
21  pericalcarine   255 0   0 0
22  postcentral 120 120 120   0
23  posteriorcingulate  120 120 120   0
24  precentral  255 192 203   0
25  precuneus   120 120 120   0
26  rostralanteriorcingulate120 120 120   0
27  rostralmiddlefrontal255 99 710
28  superiorfrontal 120 120 120   0
29  superiorparietal240 128 128   0
30  superiortemporal120 120 120   0
31  supramarginal   120 120 120   0
32  frontalpole 120 120 120   0
33  temporalpole120 120 120   0
34  transversetemporal  255 69   00
35  insula  120 120 120   0

Eric Axelson
Research Specialist
Department of Psychiatry
Iowa Neuroimaging 
Consortiumhttp://www.medicine.uiowa.edu/iowaneuroimagingconsortium/
University of Iowa
319-384-9206
eric-axel...@uiowa.edumailto:eric-axel...@uiowa.edu




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[Freesurfer] mismatch between FWHM data in fwhm.dat specified smoothing kernel

2014-08-18 Thread Vy Dinh
Dear Surfers,

While running a mri_glmfit-sim (monte carlo simulation) for roi analyses
generated using mri_glmfit, I encountered the following error code:

ERROR: cannot find
/Applications/MRI/freesurfer_5.30_x86_64/average/mult-comp-cor/fsaverage/lh/cortex/fwhm31/abs/th13/mc-z.csd

I checked the fwh.dat file within my glm/ directories and realize that
there is a discrepancy between the fwhm I set for the analyses and the fwhm
in this file (which explains why I encountered the error above.)

Can someone explain why there is a large discrepancy for these roi analyses
(which is specified using the --label option)? What kinds of things can I
do to run the monte carlo simulation appropriately?

Thank you,
Vy Dinh
MD Candidate, Class of 2017
University of Wisconsin School of Medicine and Public Health
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Re: [Freesurfer] mismatch between FWHM data in fwhm.dat specified smoothing kernel

2014-08-18 Thread Douglas Greve


The fwhm.dat is computed from your data and reflects all the spatial 
correlation in your data, not just the smoothing you imposed. It is 
usually the case  that there is some inherent smoothness and so the 
total smoothness is more than what you apply. This may be due to an 
outlier or just that some areas don't fit the GLM that well (which will 
create correlation). It could be that one or more subjects have a global 
thickness  that tends to be less than the rest of the subjects. Some 
modalities (eg, gyrification) also tend to have very high inherent 
spatial correlation.


doug



On 8/18/14 11:42 AM, Vy Dinh wrote:

Dear Surfers,

While running a mri_glmfit-sim (monte carlo simulation) for roi 
analyses generated using mri_glmfit, I encountered the following error 
code:


ERROR: cannot find 
/Applications/MRI/freesurfer_5.30_x86_64/average/mult-comp-cor/fsaverage/lh/cortex/fwhm31/abs/th13/mc-z.csd



I checked the fwh.dat file within my glm/ directories and realize that 
there is a discrepancy between the fwhm I set for the analyses and the 
fwhm in this file (which explains why I encountered the error above.)


Can someone explain why there is a large discrepancy for these roi 
analyses (which is specified using the --label option)? What kinds of 
things can I do to run the monte carlo simulation appropriately?


Thank you,
Vy Dinh
MD Candidate, Class of 2017
University of Wisconsin School of Medicine and Public Health


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[Freesurfer] FreeSurfer platform/performance questions

2014-08-18 Thread Lazarevich, Alexander
Hello FreeSurfer mailing list,

First off, I am not a scientist and I have no experience running FreeSurfer. I 
have installed it, and seen it run, but that's it.

I work for the IT department in the Beckman Institute, part of the University 
of Illinois. We support a computer lab here called the Visualization 
Laboratory - aka Vislab. 
(http://itg.beckman.illinois.edu/visualization_laboratory/) The Vislab lab has 
dozens of very nice workstations in it. (16 x 3GHz Xeon cores, 128GB of mem, 
NVIDIA Quadro K6000 video, etc.) In short, the Vislab supports research which 
needs high end computing. (less power than supercomputers, but much better than 
normal desktops and much easier to access/use than supercomputers) The Vislab 
has hundreds of active users, students, faculty, postdocs, etc., all of whom do 
some kind of scientific research.

One of the packages we have recently installed upon request is FreeSurfer. We 
have installed 
freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gzftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz
 on our Red Hat Enterprise Linux 6 workstations, as well as on our Windows 7 
Enterprise 64bit workstations. We have also installed Oracle's VirtualBox on a 
Windows 7 Enterprise 64bit machine, and run the VM 
freesurfer-Virtualbox-linux-x86-stable-pub-v5.3-full.vdi.gzftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Virtualbox-linux-x86-stable-pub-v5.3-full.vdi.gz
 inside that virtual environment.

The researchers who requested FreeSurfer are all part of the same group, and 
they are trying to complete a very large research project which requires 
FreeSurfer to process large amounts of data. They have normally been running 
FreeSurfer on the VM in the XUbuntu VirtualBox environment on their own average 
desktop PC's. However, they are concerned about their processing time with 
FreeSurfer, so they are hoping to take advantage of the Vislab computing 
resources to decrease the processing time in FreeSurfer.

We are running into the following problems/concerns:


1)  The FreeSurfer VM (Xubuntu) that runs in VirtualBox is a 32bit host. Is 
there a 64bit VM available? That 32bit host can only access 4GB of memory, 
whereas they would like to be able to access more of the workstations 128GB of 
memory.

2)  The users have expressed concern about switching platforms to Red Hat 
Enterprise Linux6 with the FreeSurfer 
freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gzftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz
 installed.  They have told us that FreeSurfer on XUbuntu might give different 
results than if it were run on Red Hat Enterprise Linux 6, given the same 
dataset. They are concerned about switching platforms in the middle of the 
research study, and that it might contaminate results. Is this possible? Or 
should the same version of FreeSurfer provide the same results, even with a 
different platform?

3)  Does anyone else on this list run very large FreeSurfer processes on 
high end 64bit computers? If a high-end processing method works well for you, I 
would love to hear about it so I can share it with the researchers here.

Thanks for your time!

Alex Lazarevich
5321 Beckman Institute - 217-244-1565
Information Technology Services - 
http://its.beckman.illinois.eduhttp://its.beckman.illinois.edu/
Beckman Institute - http://beckman.illinois.eduhttp://beckman.illinois.edu/
University of Illinois - http://illinois.eduhttp://illinois.edu/


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Re: [Freesurfer] FreeSurfer platform/performance questions

2014-08-18 Thread Lazarevich, Alexander
Nevermind question 2, I was just shown this from the FreeSurfer website:

Important Note! When processing a group of subjects for your study, it is 
essential to process all your subjects with the same version of freesurfer, on 
the same OS platform and vendor, and for safety, even the same version of the 
OS. While we continue to work to ensure that results match across platforms 
(for instance the 32b and 64b CentOS 4 builds should produce identical 
results), there are none-the-less system-level libraries that are OS dependent. 
An exception to this rule is that you may view and edit files across any 
platform or version, and run some post-processing tools (outside the recon-all 
stream) if you check with us first (for instance you may run the longitudinal 
processing with newer versions).

But I'm still hoping for some advice on question 1 and 3.

Thanks!

Alex

From: freesurfer-boun...@nmr.mgh.harvard.edu 
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Lazarevich, 
Alexander
Sent: Monday, August 18, 2014 11:08 AM
To: freesurfer@nmr.mgh.harvard.edu
Cc: Taylor, Marc D
Subject: [Freesurfer] FreeSurfer platform/performance questions

Hello FreeSurfer mailing list,

First off, I am not a scientist and I have no experience running FreeSurfer. I 
have installed it, and seen it run, but that's it.

I work for the IT department in the Beckman Institute, part of the University 
of Illinois. We support a computer lab here called the Visualization 
Laboratory - aka Vislab. 
(http://itg.beckman.illinois.edu/visualization_laboratory/) The Vislab lab has 
dozens of very nice workstations in it. (16 x 3GHz Xeon cores, 128GB of mem, 
NVIDIA Quadro K6000 video, etc.) In short, the Vislab supports research which 
needs high end computing. (less power than supercomputers, but much better than 
normal desktops and much easier to access/use than supercomputers) The Vislab 
has hundreds of active users, students, faculty, postdocs, etc., all of whom do 
some kind of scientific research.

One of the packages we have recently installed upon request is FreeSurfer. We 
have installed 
freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gzftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz
 on our Red Hat Enterprise Linux 6 workstations, as well as on our Windows 7 
Enterprise 64bit workstations. We have also installed Oracle's VirtualBox on a 
Windows 7 Enterprise 64bit machine, and run the VM 
freesurfer-Virtualbox-linux-x86-stable-pub-v5.3-full.vdi.gzftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Virtualbox-linux-x86-stable-pub-v5.3-full.vdi.gz
 inside that virtual environment.

The researchers who requested FreeSurfer are all part of the same group, and 
they are trying to complete a very large research project which requires 
FreeSurfer to process large amounts of data. They have normally been running 
FreeSurfer on the VM in the XUbuntu VirtualBox environment on their own average 
desktop PC's. However, they are concerned about their processing time with 
FreeSurfer, so they are hoping to take advantage of the Vislab computing 
resources to decrease the processing time in FreeSurfer.

We are running into the following problems/concerns:


1)  The FreeSurfer VM (Xubuntu) that runs in VirtualBox is a 32bit host. Is 
there a 64bit VM available? That 32bit host can only access 4GB of memory, 
whereas they would like to be able to access more of the workstations 128GB of 
memory.

2)  The users have expressed concern about switching platforms to Red Hat 
Enterprise Linux6 with the FreeSurfer 
freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gzftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz
 installed.  They have told us that FreeSurfer on XUbuntu might give different 
results than if it were run on Red Hat Enterprise Linux 6, given the same 
dataset. They are concerned about switching platforms in the middle of the 
research study, and that it might contaminate results. Is this possible? Or 
should the same version of FreeSurfer provide the same results, even with a 
different platform?

3)  Does anyone else on this list run very large FreeSurfer processes on 
high end 64bit computers? If a high-end processing method works well for you, I 
would love to hear about it so I can share it with the researchers here.

Thanks for your time!

Alex Lazarevich
5321 Beckman Institute - 217-244-1565
Information Technology Services - 
http://its.beckman.illinois.eduhttp://its.beckman.illinois.edu/
Beckman Institute - http://beckman.illinois.eduhttp://beckman.illinois.edu/
University of Illinois - http://illinois.eduhttp://illinois.edu/


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[Freesurfer] download link broken?

2014-08-18 Thread Wynn Legon
Hi,
Trying to download freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz
ftp://surfer.nmr.mgh.harvard.edu/pub/dist/freesurfer/5.3.0/freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz.
Link gives 550 error and terminal error is:
No such directory 'pub/dist/freesurfer/5.3.0'

Please advise
-- 

Wynn Legon  PhD
Assistant Professor
Department of Physical Medicine and Rehabilitation
School of Medicine
University of Minnesota
R398 - 426 Church St. E
Minneapolis, MN 55455
USA

Ph. (612) 626-1183
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Re: [Freesurfer] download link broken?

2014-08-18 Thread Anastasia Yendiki


Hi Wynn - There is a scheduled outage of the Martinos Center storage 
cluster today and tomorrow.


a.y

On Mon, 18 Aug 2014, Wynn Legon wrote:



Hi,Trying to
download freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0.tar.gz. Link
gives 550 error and terminal error is:
No such directory 'pub/dist/freesurfer/5.3.0'

Please advise
--
---
-Wynn Legon
 PhD
Assistant Professor
Department of Physical Medicine and Rehabilitation
School of Medicine
University of Minnesota
R398 - 426 Church St. E
Minneapolis, MN 55455
USA

Ph. (612) 626-1183

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[Freesurfer] no improvement for recon-all result after edits

2014-08-18 Thread Jidan Zhong
Hi Freesurfer experts,

I was doing some manual editing on our subjects which are patients with
lesions. I managed to correct most of them, however, 4 subjects have the
same problem that I can't fix no matter what edits I tried.

So, the 4 subjects, they all have the same problem, which is: frontal part
of superior temporal gyrus region is not segmented as white matter, thus
they are just missing from the final surfaces and final segmentations.
But when just do eye check, there is nothing wrong with this part, even the
intensity looks the same of other white matter parts.Its just cut suddenly.

When I went back to those subjects, first I tried with control points. - It
didnt help.

I confirmed that white matter is present connected to the main brain white
matter volume. -- I reran from recon-all autorecon2-wm, didnt help.

Then I checked the aseg.mgz, that part is segmented as white matter
correctly.  I even modified the aseg.mgz (although not suggested), it still
didn't work

It is just weird that the surface was just cut from the middle of STG.

So, is there any other way I can tell FreeSurfer that this is really STG
and please keep it?

Thanks!!
-- 
Regards,

Jidan
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