[Freesurfer] Segmentation using Free Surfer.

2014-02-12 Thread Saurabh Thakur
Hello Free surfer Expert,

I have started working on Free surfer. Now i m facing two issues such as :

1. I m trying to use contour ...

but it is working as per guidance in website given.

https://surfer.nmr.mgh.harvard.edu/fswiki/FreeviewGuide/FreeviewTools/VoxelEdit

   Under heading of Contour Drawcan any tell me pre requisite to draw
contour.

   I have loaded T1 image and then made new volumeafter tat ctrl+alt+
left clicknot working...?

 Can any one help me with contour function, how to use in details.


2. I wanted to do segmentation of image into WM,GM and CSF.

Please suggest what the best way/ Algorithm to so get MRI image
segmentation using Freesurfer.



Thanks in advance.


cheers
Saurabh Thakur,
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[Freesurfer] Can -min_border_white and -min_gray_at_white_border be edited for single subject in a large group of subjects?

2014-02-12 Thread Erik Lindberg
Dear Freesufers,

I am trying to understand what happens if I go in and edit the numbers for
-min_border_white  -min_gray_at_white_border  in a single subjects in a
large group.

Generally we aim to set everything identical when running a group of
subjects in FS.  I went in and had a look at the recon-all log file and I
can see that the numbers for -min_border_white
 -min_gray_at_white_border  different for different subjects.

Thus - what will happened if I go and edit the -min_border_white
 -min_gray_at_white_border numbers for  a single subjects in a large bach
 will I still be able compare cortical thickness with subjects that I
did not edit?

Or is it necessary to keep the number identical for all subjects when
editing the min_border_white  -min_gray_at_white_border
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Re: [Freesurfer] Number of pixel count

2014-02-12 Thread Bruce Fischl

Hi Saurabh

we don't measure sulcal CSF as it's really not visible on only a T1. The 
other measures should all be in the files in the stats directory - no 
need to measure it yourself.


cheers
Bruce

On Wed, 12 Feb 2014, Saurabh Thakur wrote:


Hello Free surfer Expert ,
 
I am kooking for the exact value of voxel / pixel which represent White
,Grey and CSF fluid matter in brain.

I am trying to draw contour, and to measure the count...or How to count the
pixel for particular region...?

Thanks in advance for your timely advise.

cheers
Saurabh Thakur,





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Re: [Freesurfer] Segmentation using Free Surfer.

2014-02-12 Thread Bruce Fischl

Hi Saurabh

have you run recon-all on your subjects? If so, you should be all set (see 
my previous email)


cheers
Bruce


On Wed, 12 Feb 2014, Saurabh Thakur 
wrote:



Hello Free surfer Expert,

I have started working on Free surfer. Now i m facing two issues such as :

1. I m trying to use contour ...

    but it is working as per guidance in website given.
   https://surfer.nmr.mgh.harvard.edu/fswiki/FreeviewGuide/FreeviewTools/Voxel
Edit

   Under heading of Contour Drawcan any tell me pre requisite to draw
contour.

   I have loaded T1 image and then made new volumeafter tat ctrl+alt+
left clicknot working...?

 Can any one help me with contour function, how to use in details.


2. I wanted to do segmentation of image into WM,GM and CSF.

    Please suggest what the best way/ Algorithm to so get MRI image
segmentation using Freesurfer.



Thanks in advance.


cheers
Saurabh Thakur,





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Re: [Freesurfer] Can -min_border_white and -min_gray_at_white_border be edited for single subject in a large group of subjects?

2014-02-12 Thread Bruce Fischl

Hi Erik

is there a reason not to do it for the whole group? I guess if the one 
subject you uploaded had significant motion (which caused the blurryness) 
then it might be the case that it needs separate parameters. In general 
though it's good to hold this kind of thing constant as it will definitely 
bias you to having greater thickness. Try it on some of the other subjects 
and see if the surfaces are at least as accurate as without, and if so do 
it uniformly


cheers
Bruce

On Wed, 12 Feb 2014, 
Erik Lindberg wrote:



Dear Freesufers,
I am trying to understand what happens if I go in and edit the numbers for
-min_border_white  -min_gray_at_white_border  in a single subjects in a
large group.

Generally we aim to set everything identical when running a group of
subjects in FS.  I went in and had a look at the recon-all log file and I
can see that the numbers for -min_border_white
 -min_gray_at_white_border  different for different subjects.

Thus - what will happened if I go and edit the -min_border_white
 -min_gray_at_white_border numbers for  a single subjects in a large bach
 will I still be able compare cortical thickness with subjects that I
did not edit?

Or is it necessary to keep the number identical for all subjects when
editing the min_border_white  -min_gray_at_white_border 

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Re: [Freesurfer] Can -min_border_white and -min_gray_at_white_border be edited for single subject in a large group of subjects?

2014-02-12 Thread Bruce Fischl

Hi Erik

yes, those numbers are always estimated from the data unless you specify 
otherwise. And please remember to cc the list so that others can answer/see 
the answers in case they are interested in the same type of issue.


cheers
Bruce

 On Wed, 12 Feb 2014, Erik Lindberg wrote:


OK Thanks 
- I suspected that. What made me a bit confused what that I went in and had
a look at the recon-all log file. And numbers from this file was different
for different subjects at the same batch.






two subjects
setting MIN_GRAY_AT_WHITE_BORDER to 67.9 (was 70)
setting MAX_BORDER_WHITE to 107.3 (was 105)
setting MIN_BORDER_WHITE to 79.0 (was 85)
setting MAX_CSF to 56.7 (was 40)
setting MAX_GRAY to 94.7 (was 95)
setting MAX_GRAY_AT_CSF_BORDER to 73.4 (was 75)
setting MIN_GRAY_AT_CSF_BORDER to 45.6 (was 40)


setting MIN_GRAY_AT_WHITE_BORDER to 71.5 (was 70)
setting MAX_BORDER_WHITE to 108.1 (was 105)
setting MIN_BORDER_WHITE to 82.0 (was 85)
setting MAX_CSF to 61.0 (was 40)
setting MAX_GRAY to 95.9 (was 95)
setting MAX_GRAY_AT_CSF_BORDER to 76.7 (was 75)
setting MIN_GRAY_AT_CSF_BORDER to 50.5 (was 40)


On Wed, Feb 12, 2014 at 2:31 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
wrote:
  Hi Erik

  is there a reason not to do it for the whole group? I guess if
  the one subject you uploaded had significant motion (which
  caused the blurryness) then it might be the case that it needs
  separate parameters. In general though it's good to hold this
  kind of thing constant as it will definitely bias you to having
  greater thickness. Try it on some of the other subjects and see
  if the surfaces are at least as accurate as without, and if so
  do it uniformly

  cheers
  Bruce

  On Wed, 12 Feb 2014, Erik Lindberg wrote:

Dear Freesufers,
I am trying to understand what happens if I go in
and edit the numbers for
-min_border_white  -min_gray_at_white_border  in a
single subjects in a
large group.

Generally we aim to set everything identical when
running a group of
subjects in FS.  I went in and had a look at the
recon-all log file and I
can see that the numbers for -min_border_white
 -min_gray_at_white_border  different for different
subjects.

Thus - what will happened if I go and edit the
-min_border_white
 -min_gray_at_white_border numbers for  a single
subjects in a large bach
 will I still be able compare cortical thickness
with subjects that I
did not edit?

Or is it necessary to keep the number identical for
all subjects when
editing the min_border_white
 -min_gray_at_white_border 




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[Freesurfer] distribute dots on the surface

2014-02-12 Thread peng
Dear Freesurfers,

   I have run recon-all and got a set of surfaces for the subjects. I wish
to distribute N dots about evenly on the surface to cover most gyri and
sulci , but I don't how to implement that. One way is to manually put them
in the GUI of freeview, but it is not so convenient if N is relative large
(say, 200). Can anyone give me a hint which function shall I use?


best
Peng
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Re: [Freesurfer] distribute dots on the surface

2014-02-12 Thread Douglas Greve


what do you mean by dots? Eg, a mask surface overlay with 1s in some 
vertices and 0s in others? Or a label?

doug



On 2/12/14 9:52 AM, peng wrote:

Dear Freesurfers,

   I have run recon-all and got a set of surfaces for the subjects. I 
wish to distribute N dots about evenly on the surface to cover most 
gyri and sulci , but I don't how to implement that. One way is to 
manually put them in the GUI of freeview, but it is not so convenient 
if N is relative large (say, 200). Can anyone give me a hint which 
function shall I use?



best
Peng


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[Freesurfer] freesurfer course

2014-02-12 Thread Jayachandra Raghava
Hello,

I am interested in attending a freesurfer course at  Martinos Center for
Biomedical Imaging in
Bostonhttp://maps.google.com/maps?q=%22114%20Sixteenth%20Street,%20Charlestown,%20MA%2002129%22


But, it says that the following  lectures are only during spring and fall.

1)Functional analysis (during the Spring course)
2)Diffusion processing (during the Fall course)

I would like to attend the course which covers the above topics. Can you
please give me the link for the details of the workshop which includes
diffusion and functional course.

Regards
Jay
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[Freesurfer] How to avoid tumour from being segmented out

2014-02-12 Thread Melanie Morrison
Hi there,

I am creating surfaces from my volume T1-weight scans so that I can run them in 
AFNI's SUMA program. 
Problem is that my tumour has been segmented out because its intensity and the 
intensity of its surround area is much lower that what is being segmented. 

How can I avoid this? Or edit this? I need my functional MRI data to be 
displayed around the tumour region which is now unfortunately cut out. 
(HELPP!!!) 


Thanks,
Melanie Morrison 
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Re: [Freesurfer] dt_recon error for Siemens mosaics image

2014-02-12 Thread Douglas N Greve
has it been anonymized?

On 02/11/2014 02:23 PM, Gennan Chen wrote:
 HI! All,

 I got an error when I ran dt_recon

 WARNING: file /Users/gnchen/tmp/3011_DTI/orig/MR01.dcm does not 
 contain a Siemens ASCII header

 has this file been anonymized?

 ERROR: cannot unpack mosiacs without ASCII header


 I can confirm it is Siemens mosaics format. Any idea how to by pass 
 this??


 -- 
 Gennan Chen


 
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Re: [Freesurfer] How to avoid tumour from being segmented out

2014-02-12 Thread Bruce Fischl
Hi Melanie

you should be able to fill it in in the wm.mgz volume in either tkmedit 
or freeview (using 255 if in freeview - tkmedit will do this by default)

cheers
Bruce
On 
Wed, 12 Feb 2014, Melanie Morrison wrote:

 Hi there,
 
 I am creating surfaces from my volume T1-weight scans so that I can run them
 in AFNI's SUMA program.
 Problem is that my tumour has been segmented out because its intensity and
 the intensity of its surround area is much lower that what is being
 segmented.
 
 How can I avoid this? Or edit this? I need my functional MRI data to be
 displayed around the tumour region which is now unfortunately cut out.
 (HELPP!!!)
 
 
 Thanks,
 Melanie Morrison
 

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[Freesurfer] Postdoc - ICM Paris - Morphometry using 7T MRI

2014-02-12 Thread Olivier Colliot

Dear colleagues,

Our team is looking for a postdoctoral fellow.
Please find below the informations about the position.

Many thanks
Olivier Colliot


_*Research topic: Computational anatomy of the hippocampus using very 
high resolution MRI at 7 Tesla: diffeomorphic registration and shape 
analysis
*_The hippocampus is an anatomical structure of the brain which plays 
critical roles in different brain disorders including Alzheimer's 
disease and epilepsy. The hippocampus has the particularity of 
presenting a highly complex tridimensional organization with a large 
number of substructures, fields and layers.


Current approaches for shape analysis of the hippocampus only consider 
its external boundary and do not model its complex internal 
architecture. Indeed, using conventional MRI at 1.5T or 3T, only the 
external boundaries of the hippocampus can be visualized and its 
internal subregions remain inaccessible. The advent of ultra-high field 
MRI (7T and higher) has opened new perspectives by providing increased 
signal-to-noise ratio, increased tissular contrast and increased spatial 
resolution, which allows visualizing in vivo tiny anatomical structures 
(~100-200 microns). New computational anatomy approaches are needed to 
handle these complex anatomical structures.


The aim of this postdoctoral project is to develop new approaches for 
diffeomorphic registration and shape analysis of the internal structures 
of the hippocampus using 7T MRI data with very high spatial resolution. 
The developments will be based on the framework of large diffeomorphic 
deformations and matching of currents. New developments based on 
varifolds and functional currents will be performed in order to handle 
the complex shapes of the internal structures. The work will be done in 
collaboration with our partners at ENS de Cachan (Alain Trouvé) and 
Université Paris-Descartes (Joan Glaunès).


The developed approaches will be applied to detect subtle alterations in 
patients with Alzheimer's disease and epilepsy in which 7T MRI has been 
acquired. These clinical applications will be done in collaboration with 
our partners at Neurospin, Pitié-Salpêtrière hospital, and University of 
Minnesota.



_*Profile of the candidate
*_The ideal candidate should have previous experience in the design of 
new methods for morphometry, shape analysis or registration of 
anatomical medical images. However, we will also consider outstanding 
scientific profiles in the fields of image processing/computer vision, 
without previous experience of the specific topics mentioned above.



_*About the ARAMIS team*_
ARAMIS is a joint research team between CNRS, INRIA, Inserm and UPMC 
within the Brain and Spine Institute (ICM). The ICM 
(http://icm-institute.org/menu/foundation/mission?lang=en) is a recently 
created neuroscience center based in the Pitié-Salpêtrière hospital in 
Paris, which is the largest adult hospital in Europe and has a long 
tradition of neuroscience and neurology. The ICM brings together 500 
researchers covering the whole field of neuroscience.


ARAMIS is the methodological research team of the ICM. It is a 
multidisciplinary group (electrical engineering, computer science, 
neurology) with about 30 members. The team aims at designing new 
mathematical and computational approaches for the analysis of images and 
signals of the human brain. The key domains of expertise of the team 
are: i) automatic segmentation of brain structures; ii) shape analysis 
and longitudinal modeling; iii) machine learning; iv) analysis of brain 
connectivity. The team has developed advanced methods for the analysis 
of anatomical and functional neuroimaging data including the fully 
automatic approach SACHA to segment the hippocampus and the amygdala, 
pattern classification algorithms, the Deformetrica software for shape 
analysis, and graph-theory approaches to functional connectivity. The 
team also has strong expertise in the management of multi-center 
neuroimaging studies, including multi-site MRI harmonization, quality 
control and analysis of massive datasets. The team has close and 
enduring collaborations with different clinical teams of the ICM and the 
Pitié-Salpêtrière hospital to apply advanced image analysis approaches 
to neurological disorders, including Alzheimer's disease, epilepsy, 
fronto-temporal dementia, Parkinson's disease, Gilles de la Tourette 
syndrome.


_*Contact information*_
Olivier Colliot - olivier.coll...@upmc.fr - 
http://cogimage.dsi.cnrs.fr/perso/colliot/


_*More information:*_
https://www.inria.fr/en/institute/recruitment/offers/post-doctoral-research-fellowships/post-doctoral-research-fellowships/campaign-2014/(view)/details.html?id=PNGFK026203F3VBQB6G68LOE1ContractType=4546LG=ENResultsperpage=20nPostingID=8265nPostingTargetID=13985option=52sort=DESCnDepartmentID=19
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[Freesurfer] Running a template through recon-all

2014-02-12 Thread Danielle Sliva
Dear FreeSurfer experts,

I am trying to map volumetric ROIs obtained from VBM to surfaces in 5-6 
year old children. I saw in a couple previous posts that it is 
recommended to run the template brain through recon-all, map the ROIs to 
the template surface, and then propagate the ROIs to all subjects using 
either mri_surf2surf, or (after turning the ROIs into labels) using 
mri_label2label.

The problem I have is that we used a custom age-appropriate template 
that will not pass through recon-all. I have tried using -notalairach  
-notal-check.

Here is the output from the recon-all.log:

register_mri: find_optimal_transform
find_optimal_transform: nsamples 3481, passno 0, spacing 8
GCAhistoScaleImageIntensities: could not find wm peak
resetting wm mean[0]: 117 -- 126
resetting gm mean[0]: 74 -- 74
input volume #1 is the most T1-like
using real data threshold=24.0
skull bounding box = (128, 99, 138) -- (128, 154, 185)
using (128, 117, 162) as brain centroid...
mean wm in atlas = 126, using box (128,110,156) -- (127, 123,167) to 
find MRI wm
WARNING: gca.c::GCAhistoScaleImageIntensities: h_mri-nbins=255, 
mri_peak=-1
before smoothing, mri peak at 0
WARNING2: gca.c::GCAhistoScaleImageIntensities: h_mri-nbins=255, 
mri_peak=-1
after smoothing, mri peak at 0, scaling input intensities by inf
Linux rc-twice 3.2.21-mosix #1 SMP Mon Jul 2 08:55:48 EDT 2012 x86_64 
x86_64 x86_64 GNU/Linux
recon-all -s TOM_5yr_2 exited with ERRORS at Mon Feb 10 19:11:23 EST 2014

I am using version 5.3. Can you suggest any other options to get this 
template through recon-all?

Thanks in advance,
Danielle
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Re: [Freesurfer] dt_recon error for Siemens mosaics image

2014-02-12 Thread Gennan Chen
Possible. Can you give me DICOM tag/tags the program looks for??

Gen

-Original Message-
From: freesurfer-boun...@nmr.mgh.harvard.edu 
[mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Douglas N Greve
Sent: Wednesday, February 12, 2014 8:24 AM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] dt_recon error for Siemens mosaics image

has it been anonymized?

On 02/11/2014 02:23 PM, Gennan Chen wrote:
 HI! All,

 I got an error when I ran dt_recon

 WARNING: file /Users/gnchen/tmp/3011_DTI/orig/MR01.dcm does not
 contain a Siemens ASCII header

 has this file been anonymized?

 ERROR: cannot unpack mosiacs without ASCII header


 I can confirm it is Siemens mosaics format. Any idea how to by pass
 this??


 --
 Gennan Chen


 --
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[Freesurfer] Fwd: Problems dipslaying annotations in freeview

2014-02-12 Thread Laura Taylor
Hi Ruopeng and freesurfer folks,

I am still having trouble loading annotations in freeview, similar to what
I mentioned before.  When I load 'rh.aparc.a2009s.annot' in freeview, the
annotation loads onto the LEFT hemisphere and is tye-died in appearance.
In contrast, 'lh.aparc.a2009s.annot' loads correctly onto the left
hemisphere and looks normal.

I have had this problem with many of my subjects.  Can you help with this??

Thank you,

Laura

-- Forwarded message --

Date: Thu, Jan 2, 2014 at 9:53 AM
Subject: Fwd: [Freesurfer] Problems dipslaying annotations in freeview
To: rpw...@nmr.mgh.harvard.edu


Hi Ruopeng,

I am forwarding the messages I sent to the freesurfer mailing list and that
Doug suggested I ask you.

Basically when I try and load an annotation in freeview, the rh loads
properly (looks normal and is on the correct hemisphere), but the lh loads
onto the rh and is tye-died in appearance.

Can you help with this?

Thanks,

Laura

-- Forwarded message --
From: Douglas N Greve gr...@nmr.mgh.harvard.edu
Date: Wed, Dec 18, 2013 at 2:14 PM
Subject: Re: [Freesurfer] Problems dipslaying annotations in freeview

Cc: freesurfer@nmr.mgh.harvard.edu



oh, if the lh annot is being loaded onto the rh surface, then that will
definitely create the tye-died appearance.* Maybe Ruopeng can weigh in on
the freeview issue.*

doug


On 12/18/2013 04:53 PM, Laura  wrote:

 Hi Douglas,

 I would go to the annotation drop down menu in freeview, select
 l/rh.aparc.a2009s.annot and then it would freeze.  I can't seem to
 reproduce that problem today, but for every subject that I load an
 annotation for now, the rh annotation loads properly,* but the lh
 annotation loads onto the right hemisphere and is tye-died in appearance.*

 Thanks,

 Laura


 On Tue, Dec 17, 2013 at 11:57 AM, Douglas N Greve 
 gr...@nmr.mgh.harvard.edu mailto:gr...@nmr.mgh.harvard.edu wrote:


 So when you say you cannot load it, what do you mean?
 doug




 On 12/17/2013 02:55 PM, Laura Taylor wrote:

 Hi Douglas,

 I checked the status of each subject once recon-all was
 completed (by looking in the terminal window before I closed
 it).  Each of my roughly 90 subects had the message
 /recon-all -s/ subjectID /finished without error/ at date and
 time.


 When I look at the recon-all.log file the same message is
 there at the end.  Is there somewhere else where i should look
 for an error message??

 Thank you,
 Laura


 On Tue, Dec 17, 2013 at 10:44 AM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu mailto:gr...@nmr.mgh.harvard.edu
  mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu wrote:


 For the subject that you were not able to load the annot,
 did you
 check the recon-all log file? Did recon-all complete properly?
 doug


 On 12/17/2013 01:35 PM, Laura  wrote:

 Hi again, Douglas and freesurfer experts.

 Unfortunately my problem cannot be explained by having
 made
 manual edits and then not finishing recon-all.  When I
 load
 subjects that I did not manually edit, I am either
 unable to
 load an annotation file (specifically
 r/lh.aparc.a2009s.annot)
 at all, or I can load it but have problems with the
 output.
  When I am able to load an image I get a the same tye-died
 appearing surface for one hemisphere (and it is
 projected onto
 the opposite hemisphere that the label is for) or I get a
 proper surface when I load the label for the other
 hemisphere
 (and it appears on the correct hemisphere).

 Can  you help at all with this?

 Thank you,

 Laura


 On Tue, Dec 10, 2013 at 11:45 AM, Laura Taylor
  wrote:

 Hi, yes thank you both.  That is exactly what the
 problem was.

 Laura


 On Tue, Dec 10, 2013 at 11:12 AM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu

 mailto:gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu wrote:

 Yep, looks like your annot is out of sync with the
 surfaces

 On 12/10/2013 01:51 PM, Chris Watson wrote:
  I've seen this happen after making manual
 edits and
 then not
 finishing
  a re-run 

[Freesurfer] Fwd: How to avoid tumour from being segmented out

2014-02-12 Thread Melanie Morrison


Thanks,
Melanie Morrison

Begin forwarded message:

 From: Bruce Fischl fis...@nmr.mgh.harvard.edu
 Date: 12 February, 2014 1:21:56 PM EST
 To: Melanie Morrison melanie.morri...@hotmail.com
 Subject: RE: [Freesurfer] How to avoid tumour from being segmented out
 
 Hi Melanie
 
 can you cc the list so that others can answer?
 
 thanks
 Bruce
 On Wed, 12 Feb 2014, Melanie Morrison wrote:
 
 Thanks. I can just do this manually? Can I over lay this on my anatomical
 map somehow so I can manually outline the correct boundaries.
  Date: Wed, 12 Feb 2014 11:51:14 -0500
  From: fis...@nmr.mgh.harvard.edu
  To: melanie.morri...@hotmail.com
  CC: freesurfer@nmr.mgh.harvard.edu; astev...@nmr.mgh.harvard.edu
  Subject: Re: [Freesurfer] How to avoid tumour from being segmented out
 
  Hi Melanie
 
  you should be able to fill it in in the wm.mgz volume in either tkmedit
  or freeview (using 255 if in freeview - tkmedit will do this by default)
 
  cheers
  Bruce
  On
  Wed, 12 Feb 2014, Melanie Morrison wrote:
 
   Hi there,
  
   I am creating surfaces from my volume T1-weight scans so that I can run
 them
   in AFNI's SUMA program.
   Problem is that my tumour has been segmented out because its intensity
 and
   the intensity of its surround area is much lower that what is being
   segmented.
  
   How can I avoid this? Or edit this? I need my functional MRI data to be
   displayed around the tumour region which is now unfortunately cut out.
   (HELPP!!!)
  
  
   Thanks,
   Melanie Morrison
  
  
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Re: [Freesurfer] local_gi problem

2014-02-12 Thread Marie Schaer

Hi Krista,

Try using the following command:

tksurfer BV2 lh inflated -overlay $SUBJECTS_DIR/BV2/surf/lh.pial_lgi -fthresh 1

The error you got is because the overlay needs the full path to the pial_lgi 
file. Then, not all regions are coloured because the default minimum threshold 
is 2, and you want to set it at 1 to see whether everything want fine (fthresh 
option).

If it's just for quality check it should not be a problem to transfer your 
subjects from one platform to another. 

Hope it helps,

Marie


On Feb 12, 2014, at 9:50 AM, krista kelly krista.kell...@gmail.com wrote:

 Hello,
 
 I am trying to do local gyrification with freesurfer and am having trouble. I 
 have the image processing toolbox and have set the path. I ran recon-all -s 
 BV21 -localGI and it exited without errors. Yet, when I try to view it in 
 tksurfer using tksurfer BV21 lh inflated -overlay lh.pial_lgi, I get this 
 error: cannot find rh.pial_lgi (even though it is in the surfs folder). I can 
 open the inflated brain in tksurfer and overlay lh.pial_lgi but there seems 
 to be a problem where not all of the brain is colored in (please see attached 
 pictures). 
 
 I'm wondering if someone can help me with this problem, it's happened on more 
 than one participant. When checking through the terminal, I found this at the 
 beginning of the processing: 
 
 INFO: FreeSurfer build stamps do not match
 Subject Stamp: freesurfer-Linux-centos4-stable-pub-v5.3.0
 Current Stamp: freesurfer-Darwin-lion-stable-pub-v5.3.0
 
 I initially did recon-all -all using a linux on a virtual machine, however 
 there wasn't enough working memory to do all of my analyses using linux, so I 
 transferred all of my data to a mac and did the quality checks, extracted roi 
 data (aparcstats2table) and ran glm analyses (qdec) from there. Do you think 
 that the problem lies in the fact that recon-all was originally ran in Linux? 
 I'd rather not do the local gyrification in Linux as I do not have matlab on 
 that machine. 
 
 Thanks!
 Krista
 Screen Shot 2014-02-12 at 12.49.23 PM.pngScreen Shot 2014-02-12 at 
 12.49.18 PM.png___
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Re: [Freesurfer] Fwd: How to avoid tumour from being segmented out

2014-02-12 Thread Bruce Fischl
Hi Melanie

doing it in tkmedit (or freeview) would be doing it manually. But if you 
do it this way it should allow you to correct the resulting surfaces and 
such

cheers
Bruce
On Wed, 12 Feb 2014, Melanie Morrison wrote:

 
 
 Thanks,Melanie Morrison
 
 Begin forwarded message:

   From: Bruce Fischl fis...@nmr.mgh.harvard.edu
   Date: 12 February, 2014 1:21:56 PM EST
   To: Melanie Morrison melanie.morri...@hotmail.com
   Subject: RE: [Freesurfer] How to avoid tumour from being
   segmented out

   Hi Melanie

   can you cc the list so that others can answer?

   thanks
   Bruce
   On Wed, 12 Feb 2014, Melanie Morrison wrote:

 Thanks. I can just do this manually? Can I over lay
 this on my anatomical

 map somehow so I can manually outline the correct
 boundaries.

  Date: Wed, 12 Feb 2014 11:51:14 -0500

  From: fis...@nmr.mgh.harvard.edu

  To: melanie.morri...@hotmail.com

  CC: freesurfer@nmr.mgh.harvard.edu;
 astev...@nmr.mgh.harvard.edu

  Subject: Re: [Freesurfer] How to avoid tumour from
 being segmented out

 

  Hi Melanie

 

  you should be able to fill it in in the wm.mgz
 volume in either tkmedit

  or freeview (using 255 if in freeview - tkmedit
 will do this by default)

 

  cheers

  Bruce

  On

  Wed, 12 Feb 2014, Melanie Morrison wrote:

 

   Hi there,

  

   I am creating surfaces from my volume T1-weight
 scans so that I can run

 them

   in AFNI's SUMA program.

   Problem is that my tumour has been segmented out
 because its intensity

 and

   the intensity of its surround area is much lower
 that what is being

   segmented.

  

   How can I avoid this? Or edit this? I need my
 functional MRI data to be

   displayed around the tumour region which is now
 unfortunately cut out.

   (HELPP!!!)

  

  

   Thanks,

   Melanie Morrison

  

  

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

 

 

  The information in this e-mail is intended only
 for the person to whom it

 is

  addressed. If you believe this e-mail was sent to
 you in error and the

 e-mail

  contains patient information, please contact the
 Partners Compliance

 HelpLine at

  http://www.partners.org/complianceline . If the
 e-mail was sent to you in

 error

  but does not contain patient information, please
 contact the sender and

 properly

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Re: [Freesurfer] dt_recon error for Siemens mosaics image

2014-02-12 Thread Douglas N Greve

It is looking for information in the Siemens ascii header. This is a 
bit of ascii text that gets stored in a private field in the dicom, but 
because it is ascii we can just parse the file. It uses this information 
to determine the size of the mosaic.

doug


On 02/12/2014 12:23 PM, Gennan Chen wrote:
 Possible. Can you give me DICOM tag/tags the program looks for??

 Gen

 -Original Message-
 From: freesurfer-boun...@nmr.mgh.harvard.edu 
 [mailto:freesurfer-boun...@nmr.mgh.harvard.edu] On Behalf Of Douglas N Greve
 Sent: Wednesday, February 12, 2014 8:24 AM
 To: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] dt_recon error for Siemens mosaics image

 has it been anonymized?

 On 02/11/2014 02:23 PM, Gennan Chen wrote:
 HI! All,

 I got an error when I ran dt_recon

 WARNING: file /Users/gnchen/tmp/3011_DTI/orig/MR01.dcm does not
 contain a Siemens ASCII header

 has this file been anonymized?

 ERROR: cannot unpack mosiacs without ASCII header


 I can confirm it is Siemens mosaics format. Any idea how to by pass
 this??


 --
 Gennan Chen


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Fax: 617-726-7422

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[Freesurfer] bbregister and fnirt

2014-02-12 Thread qtnguyen
Hi all,

We're conducting the registration using bbregister that gives us a
registration matrix (a .dat file) BUT the original structural file remains
intact, i.e. the registered output can be viewed but not stored. Can we
store the co-registered structural image as a .nii file? And if so, how?
We are using the Connectivity Toolbox that requires structural data to be
coregistered with functional data, and there is no way we can feed in the
.dat file.

Also, what are your thoughts on first using bbregister for linear
coregistration, and then use fnirt on the output to get nonlinear
coregistration? We ask this because we are working on a younger population
(ages 8-25) with autism spectrum disorder and the data is affected by
motion. Should we also be using --init-fsl instead of --init-spm if we
want to use fnirt?

Thank you for your help,

Trang
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Re: [Freesurfer] Compute DTI metrics in NAWM in Tracula

2014-02-12 Thread Celine Louapre
Hi Anastasia
Thanks a lot for your very nice talk today. I would have another question
on top of the one below.
I have looked at the formula to calculate the total motion index, and for
the third motion parameter (percentage of slice with signal drop-out), all
subjects except 2 had a 0 value. So in the formula, I would not be able to
calculate the motion factor for this parameter because median, upper and
lower quartile are all 0, is that correct (it would make (x-0/0-0))?
Thanks for your help
Celine

 Hi Anastasia and freesurfer experts,
 I am trying to get DTI values along the tracts as in the pathstatbyvoxel
 file, but excluding inflammatory WM lesions. I have masks of the WM
 lesions that I could apply on the DTI maps, but then how could I compute
 the DTI metrics along the tract with the exclusion of the lesion? (I guess
 the last step of trac-all -path could be applied to DTI maps that were
 masked by the lesions?)
 I would like to keep the advantage of having the DTI weighted metrics in
 particular.
 Thanks a lot for your help!
 Celine

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

 Building 149, Room 2301
 13th Street
 Charlestown, MA  02129
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Re: [Freesurfer] Tracula version and download problem

2014-02-12 Thread Anastasia Yendiki


Hi Clive - So you are talking about the overall tract stats, averaged over 
the whole tract (and not the stats by position on the tract that trac-all 
-stat outputs). That phrase in the tutorial is not very clear - these 
could be used as a covariate in mri_glmfit, but the main input of 
mri_glmfit is on a surface or volume. These stats (e.g., average FA of the 
uncinate fasciculus) are only one value per subject.


Hope this helps,
a.y

On Tue, 11 Feb 2014, Clive Wong wrote:


Thanks Anastasia. I ask that because in the tracula stat page, it saids 
Measures can be extracted from these files to be
analyzed further, e.g., for tract-based group analysis. Specifically, the text 
files can be converted into a table using
the command tractstats2table and then used for doing GLM analyses with 
mri_glmfit or any other statistical software (SPSS,
Excel, Statview etc.). So I think I may reuse the GLM matrix.
Best,
Clive 


On Tue, Feb 11, 2014 at 8:29 AM, Anastasia Yendiki 
ayend...@nmr.mgh.harvard.edu wrote:

  Hi Clive - These are not stats in the volume or on the surface, so 
mri_glmfit doesn't apply. If you want to do
  group analyses along a tract on a table produced by trac-all -stat, you 
should import the table in any
  software that you use for statistics (matlab, SPSS, etc).

  Best,
  a.y

  On Mon, 10 Feb 2014, Clive Wong wrote:

Dear Anastasia,
Thanks very much. I have already downloaded the file. The wiki page 
was also down a few hours ago,
but it's ok now.

And I am interested in the tracula group stat. How could I use 
mri_glmfit on the text file? And
can I use the QDEC (or the
contrast generated by QDEC) to do the glm?

Thanks
Clive


On Mon, Feb 10, 2014 at 6:13 AM, Anastasia Yendiki 
ayend...@nmr.mgh.harvard.edu wrote:

      Hi Clive - Yes, you can use the recent tracula update on top 
your already processed data.
The new update only
      adds new functionality to trac-all, without changing any of 
the existing functionality in
5.3.

      Did you try downloading the update from here?
      http://surfer.nmr.mgh.harvard.edu/fswiki/Tracula#Updates

      a.y

      On Sun, 9 Feb 2014, Clive Wong wrote:

            Hi,
            I just want to confirm, is that I can use the new 
trac-all with the data
            processed in the original FS5.3 trac-all?

            And, I just want to download the new trac-all, but I 
have problem to connect
            to the ftp server. I can login to the server, but it 
does not response to
            any command. Please advise. 

            Best,
            Clive




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Re: [Freesurfer] Fwd: Tracula Error: bvecs and bvals don't have the same number of entries

2014-02-12 Thread Anastasia Yendiki


Ciao Francesco - Just to clarify, to be able to have your bvecs/bvals in 
rows, you should have, in addition to the latest version of freesurfer, 
the update that I linked to below:

http://surfer.nmr.mgh.harvard.edu/fswiki/Tracula/#Updates

a.y

On Tue, 11 Feb 2014, Francesco Baldacchini wrote:


Ciao Anastasia, I checked and I'm using the latest version of Freesurfer, 
version 5.3.0. It seems like that the command
trac-all path while working on the bvecs table and doing the corrections makes 
some errors and you can see it from the
bvecs file I found in the dmri directory which is only 4 rows long.


2014-02-06 1:18 GMT+01:00 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu:

  Hi Francesco - Which version of tracula are you running? To be able to 
use bvecs files that are in 3 rows
  instead of 3 columns, you need to make sure that you have the latest 
update to tracula, see here:
          http://surfer.nmr.mgh.harvard.edu/fswiki/Tracula/#Updates

  This option was not available in the previous releases of tracula.

  Hope this helps,
  a.y

  On Mon, 20 Jan 2014, Francesco Baldacchini wrote:

Hi, 
Sorry Anastasia, I'm seeing that my question was not so clear. The 
files I sent you in
the first mail are the bvecs and bvals saved by trac-all -prep in 
the dmri directory.
The original files are in attachment in this mail,

Francesco Baldacchini


2014/1/13 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu

      Hi Francesco - The bvecs file that you're attaching has only 
3 vectors,
      while the bvals file has 65 b-values. Are these your original 
files, or the
      ones saved by trac-all in the dmri/ directory?

      a.y

      On Mon, 13 Jan 2014, Francesco Baldacchini wrote:

            Hi everybody,
            I'm trying to run the trac all -prep command but after 
some
            times I get this
            error bvecs and bvals don't have the same number of 
entries.
            I've checked
            my bvals and bvecs, which are in attach, but they seems 
to be
            formatted in
            the right way. What can I do? Thanks,

            Francesco Baldacchini




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Re: [Freesurfer] Tracula version and download problem

2014-02-12 Thread Clive Wong
Dear Anastasia,

Thank you very much for the clarification.

Best,
Clive


On Thu, Feb 13, 2014 at 8:52 AM, Anastasia Yendiki 
ayend...@nmr.mgh.harvard.edu wrote:


 Hi Clive - So you are talking about the overall tract stats, averaged over
 the whole tract (and not the stats by position on the tract that trac-all
 -stat outputs). That phrase in the tutorial is not very clear - these could
 be used as a covariate in mri_glmfit, but the main input of mri_glmfit is
 on a surface or volume. These stats (e.g., average FA of the uncinate
 fasciculus) are only one value per subject.

 Hope this helps,
 a.y

 On Tue, 11 Feb 2014, Clive Wong wrote:

  Thanks Anastasia. I ask that because in the tracula stat page, it saids
 Measures can be extracted from these files to be
 analyzed further, e.g., for tract-based group analysis. Specifically, the
 text files can be converted into a table using
 the command tractstats2table and then used for doing GLM analyses with
 mri_glmfit or any other statistical software (SPSS,
 Excel, Statview etc.). So I think I may reuse the GLM matrix.
 Best,
 Clive


 On Tue, Feb 11, 2014 at 8:29 AM, Anastasia Yendiki 
 ayend...@nmr.mgh.harvard.edu wrote:

   Hi Clive - These are not stats in the volume or on the surface, so
 mri_glmfit doesn't apply. If you want to do
   group analyses along a tract on a table produced by trac-all -stat,
 you should import the table in any
   software that you use for statistics (matlab, SPSS, etc).

   Best,
   a.y

   On Mon, 10 Feb 2014, Clive Wong wrote:

 Dear Anastasia,
 Thanks very much. I have already downloaded the file. The
 wiki page was also down a few hours ago,
 but it's ok now.

 And I am interested in the tracula group stat. How could I
 use mri_glmfit on the text file? And
 can I use the QDEC (or the
 contrast generated by QDEC) to do the glm?

 Thanks
 Clive


 On Mon, Feb 10, 2014 at 6:13 AM, Anastasia Yendiki 
 ayend...@nmr.mgh.harvard.edu wrote:

   Hi Clive - Yes, you can use the recent tracula update
 on top your already processed data.
 The new update only
   adds new functionality to trac-all, without changing
 any of the existing functionality in
 5.3.

   Did you try downloading the update from here?
   http://surfer.nmr.mgh.harvard.
 edu/fswiki/Tracula#Updates

   a.y

   On Sun, 9 Feb 2014, Clive Wong wrote:

 Hi,
 I just want to confirm, is that I can use the new
 trac-all with the data
 processed in the original FS5.3 trac-all?

 And, I just want to download the new trac-all,
 but I have problem to connect
 to the ftp server. I can login to the server, but
 it does not response to
 any command. Please advise.

 Best,
 Clive




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Re: [Freesurfer] Fwd: Tracula Error: bvecs and bvals don't have the same number of entries

2014-02-12 Thread Anastasia Yendiki


Hi Francesco  - The decimal separator should be dot, not comma. Can you 
send me the bvecs/bvals that you get after you change from row to column 
format? (Both the ones that you feed into trac-all and the ones that get 
created under dmri/.)


Thanks,
a.y

On Tue, 11 Feb 2014, Francesco Baldacchini wrote:


Hi again Anastasia,

I tried also to convert my three row bvecs file in a three column one but I still 
got the same bvecs and bvals don't have
the same number of entries error. I then tried also to change the dot to comma 
as the decimal separator but still nothing

Francesco Baldacchini


2014-02-11 15:06 GMT+01:00 Francesco Baldacchini frankb...@gmail.com:
  Ciao Anastasia, I checked and I'm using the latest version of Freesurfer, 
version 5.3.0. It seems like that
  the command trac-all path while working on the bvecs table and doing the 
corrections makes some errors and you
  can see it from the bvecs file I found in the dmri directory which is 
only 4 rows long.


2014-02-06 1:18 GMT+01:00 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu:

  Hi Francesco - Which version of tracula are you running? To be able to 
use bvecs files that are in 3
  rows instead of 3 columns, you need to make sure that you have the latest 
update to tracula, see here:
          http://surfer.nmr.mgh.harvard.edu/fswiki/Tracula/#Updates

  This option was not available in the previous releases of tracula.

  Hope this helps,
  a.y

  On Mon, 20 Jan 2014, Francesco Baldacchini wrote:

Hi, 
Sorry Anastasia, I'm seeing that my question was not so clear. The 
files I sent you in
the first mail are the bvecs and bvals saved by trac-all -prep in 
the dmri directory.
The original files are in attachment in this mail,

Francesco Baldacchini


2014/1/13 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu

      Hi Francesco - The bvecs file that you're attaching has only 
3 vectors,
      while the bvals file has 65 b-values. Are these your original 
files, or the
      ones saved by trac-all in the dmri/ directory?

      a.y

      On Mon, 13 Jan 2014, Francesco Baldacchini wrote:

            Hi everybody,
            I'm trying to run the trac all -prep command but after 
some
            times I get this
            error bvecs and bvals don't have the same number of 
entries.
            I've checked
            my bvals and bvecs, which are in attach, but they seems 
to be
            formatted in
            the right way. What can I do? Thanks,

            Francesco Baldacchini




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Re: [Freesurfer] Variability in bedpostx output

2014-02-12 Thread Anastasia Yendiki

Hi Jeff - Questions about bedpostx output files are best addressed to the 
FSL list, as it's an FSL program that is not developped by us. The 
appropriate info to provide them is the FSL (rather than freesurfer) 
version numbers.

a.y

On Tue, 11 Feb 2014, jwa...@nmr.mgh.harvard.edu wrote:

 Hello all,

   I have run bedpostx on a series of DTI scans over ~1 year, the earlier
 ones in stable 5.1 and later ones in 5.3. I'm seeing quite a lot of
 variability in intensity from the earlier to later versions - re-running
 bedpostx in 5.3 on an older scan and comparing with 5.1 yields up to 10%
 variation in intensity at any given voxel between versions. I've
 been comparing the mean_f1 images by subtracting the (new - old) using
 fslmaths.  The differences are not isolaed to surfaces, but can also be
 deep in the white matter or parenchyma. Has anyone else seen this?

  Thanks,
   Jeff
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Re: [Freesurfer] Compute DTI metrics in NAWM in Tracula

2014-02-12 Thread Anastasia Yendiki

Hi Celine - That's an interesting question. There's nothing implemented in 
there right now that would allow you to skip part of the tract in the 
along-the-tract stats. One (not very elegant) way to try to do something 
like this is:

1. Set the lesion voxels in the dmri/dtifit_FA.nii.gz volume to zero. 
(You'll want to save the original volume under some other name for backup 
first.) If you want the same for the diffusivities, repeat for the also 
for the MD, L1, L2, L3 volumes.

2. Run the dmri_pathstats command line that you'll find in trac-all.log 
for that subject.

This will regenerate all the pathstats.* files, but now the parts of the 
tract that go through the lesions will have zero values (or very low, if 
they're mixed in with some neighboring voxels).

Let us know if this worked! If not I may be able to implement something.

a.y

On Tue, 11 Feb 2014, Celine Louapre wrote:

 Hi Anastasia and freesurfer experts,
 I am trying to get DTI values along the tracts as in the pathstatbyvoxel
 file, but excluding inflammatory WM lesions. I have masks of the WM
 lesions that I could apply on the DTI maps, but then how could I compute
 the DTI metrics along the tract with the exclusion of the lesion? (I guess
 the last step of trac-all -path could be applied to DTI maps that were
 masked by the lesions?)
 I would like to keep the advantage of having the DTI weighted metrics in
 particular.
 Thanks a lot for your help!
 Celine


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Re: [Freesurfer] Compute DTI metrics in NAWM in Tracula

2014-02-12 Thread Anastasia Yendiki

Celine - You're very welcome!

If this particular motion measure is identical for pretty much all your 
subjects, there is no point in including it. So you can just use the other 
3 motion measures.

a.y

On Wed, 12 Feb 2014, Celine Louapre wrote:

 Hi Anastasia
 Thanks a lot for your very nice talk today. I would have another question
 on top of the one below.
 I have looked at the formula to calculate the total motion index, and for
 the third motion parameter (percentage of slice with signal drop-out), all
 subjects except 2 had a 0 value. So in the formula, I would not be able to
 calculate the motion factor for this parameter because median, upper and
 lower quartile are all 0, is that correct (it would make (x-0/0-0))?
 Thanks for your help
 Celine

 Hi Anastasia and freesurfer experts,
 I am trying to get DTI values along the tracts as in the pathstatbyvoxel
 file, but excluding inflammatory WM lesions. I have masks of the WM
 lesions that I could apply on the DTI maps, but then how could I compute
 the DTI metrics along the tract with the exclusion of the lesion? (I guess
 the last step of trac-all -path could be applied to DTI maps that were
 masked by the lesions?)
 I would like to keep the advantage of having the DTI weighted metrics in
 particular.
 Thanks a lot for your help!
 Celine

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

 Building 149, Room 2301
 13th Street
 Charlestown, MA  02129
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Re: [Freesurfer] Variability in bedpostx output

2014-02-12 Thread Anastasia Yendiki

Wow, that's interesting. In both cases it's called with the default 
settings, without specifying any special options on the command line. You 
could verify this by running the respective versions of bedpostx 
independently of tracula and looking at the outputs. Unless of course 
something has changed with the inputs to bedpostx (so in the 
pre-processing steps), in which case the differences wouldn't have to do 
with bedpostx itself.

On Wed, 12 Feb 2014, jwa...@nmr.mgh.harvard.edu wrote:

 Thank you Anastasia.
 Unfortunately, I posted the question to the FSL list first and after
 a few go-rounds with clarification and more info, they felt like it
 was potentially a problem of the calls to the bedposts command from
 within Freesurfer. Their final assessment was that there should be no
 differences in output between different versions of bedpostx, so
 there must be some difference in how stable 5.1 and 5.3 call the
 command.  Can you provide any more details about how 5.1 and 5.3
 differ in this way?

   Thank you,
   Jeff


 Hi Jeff - Questions about bedpostx output files are best addressed to the
 FSL list, as it's an FSL program that is not developped by us. The
 appropriate info to provide them is the FSL (rather than freesurfer)
 version numbers.

 a.y

 On Tue, 11 Feb 2014, jwa...@nmr.mgh.harvard.edu wrote:

 Hello all,

   I have run bedpostx on a series of DTI scans over ~1 year, the earlier
 ones in stable 5.1 and later ones in 5.3. I'm seeing quite a lot of
 variability in intensity from the earlier to later versions - re-running
 bedpostx in 5.3 on an older scan and comparing with 5.1 yields up to 10%
 variation in intensity at any given voxel between versions. I've
 been comparing the mean_f1 images by subtracting the (new - old) using
 fslmaths.  The differences are not isolaed to surfaces, but can also be
 deep in the white matter or parenchyma. Has anyone else seen this?

  Thanks,
   Jeff
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[Freesurfer] recon-all CTABreadASCII error

2014-02-12 Thread charujing123
Dear FS experts,
It represents this message in the command window after ran recon-all 
-autorecon-pial -s CON_EIU01 -no-isrunning:
Reading annotation reading colortable from annotation file...
colortable with 36 entries read originally 
/autofs/space/terrier_001/users/nicks/freesurfer/average/colortable_desikan_killiany.txt)
CTABwriteFileASCII(/tmp/mri_segstats.tmp.CON_EIU04.lh.64.ctab): could not open 
for writing

Seg base 1000 Permission denied
CTABreadASCII(/tmp/mri_segstats.tmp.CON_EIU04.lh.64.ctab): could not open file
No such file or directory
ERROR: reading /tmp/mri_segstats.tmp.CON_EIU04.lh.64.ctab
Linux centos2 2.6.18-308.20.1.el5xen #1 SMP Tue Nov 13 11:03:56 EST 2012 x86_64 
x86_64 x86_64 GNU/Linux

recon-all -s CON_EIU04 exited with ERRORS at Thu Feb 13 14:01:12 CST 2014

Thanks.
All the best.
Rujing Zha

2014-02-13



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