Re: [Freesurfer] longitudinal processing, template and flags

2014-01-31 Thread Daniel Ferreira
Thanks Martin for your reply,

I am agree with you on point 1. What would you say in the case that we are
interested in rates of decline from baseline to 12 months, but besides 6
months follow-up we also have 24 months?. Here I see more conceptual
problems. In an hypothetical context of severe atrophy from 12 to 24
months, adding the 24 mo follow-up perhaps difficult registration more than
improves it. What do you think?

Thanks a lot

Best

Daniel


Hi Daniel,

1. yes. But why not include 6 month in your study if you have those
scans??? You will get much more reliable slope estimates with 3 time points
compared to 2, so including that time point will not only help for the
image processing part, but also in your statistics (you gain power).

2. I am not familiar with the mprage flag and think it mainly affects the
normalization. If you are sure you need it, then also add it to the -base
and -long runs, just to be safe.

best, Martin

On 01/29/2014 09:08 AM, Daniel Ferreira wrote:

Dear experts,

I have two questions regarding the longitudinal stream:

- I am including Baseline and 12 months follow-up in my study. However, I
also have 6 months follow-up. I wonder if it is conceptually right to
include these 6 months scans in template creation with the idea of
increasing registration.

- I am applying the -mprage flag in the crossectional first step. Should I
use it in the -base and -longs steps too?

Thanks very much

Daniel Ferreira
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Re: [Freesurfer] Troubleshooting - uncertainty about adding control points

2014-01-31 Thread Janosch Linkersdörfer
Hi Bruce,

thanks for your answer!

Am 30.01.2014 um 14:40 schrieb Bruce Fischl fis...@nmr.mgh.harvard.edu:

 Hi Janosch
 
 it's impossible to tell from a single slice whether those points should be 
 added or not. The white matter in your image is *very* dark in these regions, 
 do you know why?

No, I don't know why, is that something to worry about? The screen shot is from 
a child participant, but it seems my images (includung the ones from adults) 
are darker than the ones provided in the tutorial overall. We used an optimized 
MDEFT sequence with the following settings

Slices  176
Voxel size  1x1x1mm
Orientation sagittal
FoV 256x224
Matrix  224x256
TR  7.92
FA  16
TE  2.48
TI  910
PAT modeGrappa 2
Fat suppr   fat sat
Coil8ch. Head
Bandwidth   195
Phase enc.dir   A-P

see Deichmann, R., Schwarzbauer, C.,  Turner, R. (2004). Optimisation of the 
3D MDEFT sequence for anatomical brain imaging: technical implications at 1.5 
and 3 T. NeuroImage, 21(2), 757–767.

 To decide whether to add them or not you should check a couple of slices in 
 each direction (or look in multiple orientations) to make sure that the white 
 matter is actually dark and it's not partial volume effects. The approach I 
 would take is iterative - add a couple then rerun up to the first inflation 
 and see if things have been improved significantly. This is fast, maybe 5-10 
 minutes, not sure.

Thanks, I will try this approach.

 You shouldn't need to add a ton. Even one control point in the middle of a 
 dark region can have a large effect.

I still wonder which is the desired outcome state. Is it important that the 
white matter border follows *exactly* the one I perceive on every slice or is 
it OK when on some sclices it does not.

Regarding the tutorial data: Can cp_after considered to be a completely 
corrected example subject or is only the one area corrected that the tutorial 
points to and the rest of the images would also have to be modified?! I see 
some areas in cp_before AND cp_after where I am not sure whether adding control 
points would be needed.

It would help me if you could point me to one or two completely corrected and 
perfectly processed images so I could determine what level of accuracy is 
desirable.

Sorry for all these questions, but I think modifying the images is a crucial 
point in the process that influences all further steps, and I just don't yet 
have a feeling for it...

Thanks,

Janosch

 
 cheers
 Bruce
 
 
 On Thu, 30 Jan 2014, Janosch Linkersdörfer wrote:
 
 Dear Freesurfers,
 
 I am just getting started using Freesurfer. I ran recon-all on my subjects 
 for the first time and now would like to troubleshoot the output.
 
 I watched the tutorial lectures and worked through the troubleshooting 
 tutorial. Nevertheless, I am still uncertain which things I will have to 
 correct (especially as editing too much and/or not to the same degree 
 between subjects might do more harm than good).
 
 Some errors are relatively obvious like the exclusion of white matter voxels 
 from the white matter surface (see *1* on the screen shot of my own data)
 
 
 
 I am far more uncertain about adding control points. For example, I do not 
 know whether I should add those at the location denoted with *2* in my own 
 data.
 
 If so, there would be a lot of other, similar locations where I would add 
 control points in my data. But this would also be true for the image used in 
 the Adding control points tutorial. In the second screen shot, which 
 displays this image, I have marked some locations where the white matter 
 surface does not follow the one I would draw if I had to do it manually.
 
 
 
 Is one supposed to correct all those imprecisions by adding control points?! 
 What are the criteria for adding vs. not adding control points?
 
 Thank you very much,
 
 Janosch
 
 
 
 
 
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 addressed. If you believe this e-mail was sent to you in error and the e-mail
 contains patient information, please contact the Partners Compliance HelpLine 
 at
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 error
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Re: [Freesurfer] longitudinal processing, template and flags

2014-01-31 Thread Martin Reuter
Hi Daniel,
I'd also include 24 month into both the processing and analysis. It is not 
really that we are trying to improve a registration here. We are trying to 
improve segmentation and surface placement of each time point.
I'd aways use all data, except there are good reasons to drop (eg strong motion 
artifacts).
Best Martin


Sent via my smartphone, please excuse brevity.

 Original message 
From: Daniel Ferreira dani...@ull.es 
Date:01/31/2014  3:41 AM  (GMT-05:00) 
To: freesurfer@nmr.mgh.harvard.edu,mreu...@nmr.mgh.harvard.edu 
Subject: Re: [Freesurfer] longitudinal processing, template and flags 

Thanks Martin for your reply,

I am agree with you on point 1. What would you say in the case that we are 
interested in rates of decline from baseline to 12 months, but besides 6 months 
follow-up we also have 24 months?. Here I see more conceptual problems. In an 
hypothetical context of severe atrophy from 12 to 24 months, adding the 24 mo 
follow-up perhaps difficult registration more than improves it. What do you 
think?

Thanks a lot

Best

Daniel


Hi Daniel,

1. yes. But why not include 6 month in your study if you have those scans??? 
You will get much more reliable slope estimates with 3 time points compared to 
2, so including that time point will not only help for the image processing 
part, but also in your statistics (you gain power).

2. I am not familiar with the mprage flag and think it mainly affects the 
normalization. If you are sure you need it, then also add it to the -base and 
-long runs, just to be safe.

best, Martin

On 01/29/2014 09:08 AM, Daniel Ferreira wrote:
Dear experts,

I have two questions regarding the longitudinal stream:

- I am including Baseline and 12 months follow-up in my study. However, I also 
have 6 months follow-up. I wonder if it is conceptually right to include these 
6 months scans in template creation with the idea of increasing registration.

- I am applying the -mprage flag in the crossectional first step. Should I use 
it in the -base and -longs steps too?

Thanks very much

Daniel Ferreira___
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Re: [Freesurfer] Longitudinal analysis within one group

2014-01-31 Thread amirhossein manzouri
Dear Doug and Martin,
Thanks a lot. I just have one group including 20 subjects. The scans have
been done in a range of 0.9 to 1.5 years difference (tp2-tp1). Is ooh if I
use the instructions from Paired Analysis :
https://surfer.nmr.mgh.harvard.edu/fswiki/PairedAnalysis ?
Regards,

Best regards,
Amirhossein Manzouri





On Thu, Jan 30, 2014 at 10:31 PM, Martin Reuter mreu...@nmr.mgh.harvard.edu
 wrote:

  Hi,

 with one group you want to check if atrophy is significantly different
 from zero? That is probably the case for any group (e.g. aging), so it
 won't tell you anything really. Also, if you don't find atrophy in a region
 it doesn't mean it's not there (only your group size is too small to detect
 it).
 So the only real use I can think of, would be a test-retest study, where
 the assumption is that there is no change?

 Sadly Qdec cannot do 'one sample group mean', otherwise you could do that
 in qdec. If only you had a second 'control' group, then it could be done.
 You can use long_mris_slopes to compute rate or percent change maps (one
 for each subjects) and then you can use qdec to analyze those rate maps
 across groups.
 If you don't have a control group, you could still use long_mris_slopes
 (it can also map and stack the rate maps on fsaverage) and then simply run
 the one sample group mean in mri_glmfit.

 some info is also here:

 https://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/LongitudinalTutorial_freeview
 and
 https://surfer.nmr.mgh.harvard.edu/fswiki/LongitudinalTwoStageModel


 Best, Martin


 On 01/30/2014 09:18 AM, amirhossein manzouri wrote:

  Hi,
 Would you please advise if it is possible to do longitudinal statistical
 analysis within a group with two time points in Qdec. And if it is not
 possible in Qdec how I suppose to do it?

  Best regards,
 Amirhossein Manzouri





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 Assistant in Neuroscience - Massachusetts General Hospital
 Instructor in Neurology   - Harvard Medical School
 MGH / HMS / MIT

 A.A.Martinos Center for Biomedical Imaging
 149 Thirteenth Street, Suite 2301
 Charlestown, MA 02129

 Phone: +1-617-724-5652
 Email:
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reu...@mit.edu
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 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
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Re: [Freesurfer] Troubleshooting - uncertainty about adding control points

2014-01-31 Thread Bruce Fischl

Hi Janosch

there should be some corrected subjects in the tutorial. The white matter 
surface shouldn follow the perceived boundary, although it may look wrong 
when it is when it is curving sharply out of plane. I don't have much 
experience with MDEFT, so I can't comment on the parameters


cheers
Bruce

On Fri, 31 Jan 
2014, Janosch Linkersdörfer wrote:



Hi Bruce,

thanks for your answer!

Am 30.01.2014 um 14:40 schrieb Bruce Fischl fis...@nmr.mgh.harvard.edu:


Hi Janosch

it's impossible to tell from a single slice whether those points should be 
added or not. The white matter in your image is *very* dark in these regions, 
do you know why?


No, I don't know why, is that something to worry about? The screen shot is from 
a child participant, but it seems my images (includung the ones from adults) 
are darker than the ones provided in the tutorial overall. We used an optimized 
MDEFT sequence with the following settings

Slices  176
Voxel size  1x1x1mm
Orientation sagittal
FoV 256x224
Matrix  224x256
TR  7.92
FA  16
TE  2.48
TI  910
PAT modeGrappa 2
Fat suppr   fat sat
Coil8ch. Head
Bandwidth   195
Phase enc.dir   A-P

see Deichmann, R., Schwarzbauer, C.,  Turner, R. (2004). Optimisation of the 
3D MDEFT sequence for anatomical brain imaging: technical implications at 1.5 and 3 
T. NeuroImage, 21(2), 757–767.


To decide whether to add them or not you should check a couple of slices in 
each direction (or look in multiple orientations) to make sure that the white 
matter is actually dark and it's not partial volume effects. The approach I 
would take is iterative - add a couple then rerun up to the first inflation and 
see if things have been improved significantly. This is fast, maybe 5-10 
minutes, not sure.


Thanks, I will try this approach.


You shouldn't need to add a ton. Even one control point in the middle of a dark 
region can have a large effect.


I still wonder which is the desired outcome state. Is it important that the 
white matter border follows *exactly* the one I perceive on every slice or is 
it OK when on some sclices it does not.

Regarding the tutorial data: Can cp_after considered to be a completely 
corrected example subject or is only the one area corrected that the tutorial 
points to and the rest of the images would also have to be modified?! I see 
some areas in cp_before AND cp_after where I am not sure whether adding control 
points would be needed.

It would help me if you could point me to one or two completely corrected and 
perfectly processed images so I could determine what level of accuracy is 
desirable.

Sorry for all these questions, but I think modifying the images is a crucial 
point in the process that influences all further steps, and I just don't yet 
have a feeling for it...

Thanks,

Janosch



cheers
Bruce


On Thu, 30 Jan 2014, Janosch Linkersdörfer wrote:


Dear Freesurfers,

I am just getting started using Freesurfer. I ran recon-all on my subjects for 
the first time and now would like to troubleshoot the output.

I watched the tutorial lectures and worked through the troubleshooting 
tutorial. Nevertheless, I am still uncertain which things I will have to 
correct (especially as editing too much and/or not to the same degree between 
subjects might do more harm than good).

Some errors are relatively obvious like the exclusion of white matter voxels 
from the white matter surface (see *1* on the screen shot of my own data)



I am far more uncertain about adding control points. For example, I do not know 
whether I should add those at the location denoted with *2* in my own data.

If so, there would be a lot of other, similar locations where I would add control points 
in my data. But this would also be true for the image used in the Adding control 
points tutorial. In the second screen shot, which displays this image, I have 
marked some locations where the white matter surface does not follow the one I would draw 
if I had to do it manually.



Is one supposed to correct all those imprecisions by adding control points?! 
What are the criteria for adding vs. not adding control points?

Thank you very much,

Janosch






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Re: [Freesurfer] Longitudinal analysis within one group

2014-01-31 Thread Martin Reuter
Given the different time distances, the best would be mixed effects models. The 
2 stage model should also work as it incorporates time (but not different 
correlations according to time distance).

Again I don't see what you are analyzing with only one group. There will always 
be thinning, and you will find it in some regions more than in others 
(depending on how much power you have). 

Best Martin


Sent via my smartphone, please excuse brevity.

 Original message 
From: amirhossein manzouri a.h.manzo...@gmail.com 
Date:01/31/2014  7:27 AM  (GMT-05:00) 
To: Martin Reuter mreu...@nmr.mgh.harvard.edu 
Cc: Douglas Greve gr...@nmr.mgh.harvard.edu,free surfer 
freesurfer@nmr.mgh.harvard.edu 
Subject: Re: [Freesurfer] Longitudinal analysis within one group 

Dear Doug and Martin, 
Thanks a lot. I just have one group including 20 subjects. The scans have been 
done in a range of 0.9 to 1.5 years difference (tp2-tp1). Is ooh if I use the 
instructions from Paired Analysis 
:https://surfer.nmr.mgh.harvard.edu/fswiki/PairedAnalysis ?
Regards,  

Best regards,
Amirhossein Manzouri 

 



On Thu, Jan 30, 2014 at 10:31 PM, Martin Reuter mreu...@nmr.mgh.harvard.edu 
wrote:
Hi, 

with one group you want to check if atrophy is significantly different from 
zero? That is probably the case for any group (e.g. aging), so it won't tell 
you anything really. Also, if you don't find atrophy in a region it doesn't 
mean it's not there (only your group size is too small to detect it).
So the only real use I can think of, would be a test-retest study, where the 
assumption is that there is no change?

Sadly Qdec cannot do 'one sample group mean', otherwise you could do that in 
qdec. If only you had a second 'control' group, then it could be done. You can 
use long_mris_slopes to compute rate or percent change maps (one for each 
subjects) and then you can use qdec to analyze those rate maps across groups. 
If you don't have a control group, you could still use long_mris_slopes (it can 
also map and stack the rate maps on fsaverage) and then simply run the one 
sample group mean in mri_glmfit.

some info is also here:
https://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/LongitudinalTutorial_freeview
and
https://surfer.nmr.mgh.harvard.edu/fswiki/LongitudinalTwoStageModel


Best, Martin


On 01/30/2014 09:18 AM, amirhossein manzouri wrote:
Hi, 
Would you please advise if it is possible to do longitudinal statistical 
analysis within a group with two time points in Qdec. And if it is not possible 
in Qdec how I suppose to do it?
 
Best regards,
Amirhossein Manzouri 

 



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Assistant in Neuroscience - Massachusetts General Hospital
Instructor in Neurology   - Harvard Medical School
MGH / HMS / MIT

A.A.Martinos Center for Biomedical Imaging
149 Thirteenth Street, Suite 2301
Charlestown, MA 02129

Phone: +1-617-724-5652
Email: 
   mreu...@nmr.mgh.harvard.edu
   reu...@mit.edu
Web  : http://reuter.mit.edu 
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Re: [Freesurfer] brainmask VS wm correction

2014-01-31 Thread Bruce Fischl

Hi Elisa

it's tough to tell from just the wm.mgz image. Are the voxels excluded 
from the pial brain or are they dura? What does the orig surface show? If 
the orig doesn't follow the wm.mgz and you think it should, that means 
there is a topological defect that was inaccurately corrected and you 
need to fix that

cheers
Bruce
On Fri, 31 Jan 2014, elisa veronese wrote:


Dear all,
I am trying to manually correct the segmentation result in one subject. My
problem is that I am not sure if in the area highlighted with the green
circle (see attached file) the volume I should correct is the brainmask.mgz
or the wm.mgz.
The pial boundary looks uncorrect, so I'd correct the brainmask. But those
voxels seem to belong to the wm.mgz volume, as well...

Thank you.
Best,
Elisa

--
Elisa Veronese - PhD
Research Unit on Brain Imaging and Neuropsychology (RUBIN)
Inter-University Center for Behavioral Neurosciences (ICBN)
University of Udine and University of Verona, Italy
ICBN Website: http://icbn.uniud.it/tiki-index.php



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Re: [Freesurfer] bbregister and AFNI

2014-01-31 Thread Douglas N Greve

On 01/30/2014 06:34 PM, Ajay Kurani wrote:
 Hi all,
I used freesurfer to process my anatomical scans, followed by 
 BBregister to align my resting state scan to the anatomical and 
 finally afni to process the resting state fmri scans.  After recon-all 
 I used bbregister:
 *
 *
 *bbregister -s ${sub}_FS --mov ${sub}.RS.nii --reg 
 $sub_RS_register.dat --init-header --bold --frame $LAST --nearest 
 --template-out $sub.RS.template.nii*

 I used the following for manual adjustments (although none were needed!)
 *tkregister2 --mov $sub.RS.template.nii --reg $sub_RS_register.dat --surf*

 The plan is to apply the reg file to the entire resting state 
 timeseries ($sub.RS.nii).

 My question is the following:
 1) Does bbregister already move the last timepoint in $sub.RS.nii as 
 well as $sub.RS.template.nii or does it just store the rigid 
 transformation in the reg file (this is what I assume)?  This is the 
 reason I assume we supply reg into tkregister2 as I assume the 
 transform is not applied to the nifti file header itself.
Neither bbregister nor tkregister2 apply the transform

 2) Assuming the transformations are not applied to the file itself, 
 how would I go about doing this?  I used the following based on 
 previous posts:

 *mri_vol2vol --mov $sub.RS.nii --reg $sub_RS_register.dat --fstarg 
 --interp nearest --o $sub.RS.align.nii --precision short --no-resample
 *
 I used no-resample as I do not want to put the data into orig space.  
 The plan is to align all of my timepoints to the last time point (same 
 as $sub.RS.template.nii).

 Is --fstarg the best option (default orig.mgz vs --fstarg 
 rawavg.mgz)?
You have to use --fstarg in this case because that was the target when 
you ran bbregister
 Is the transform stored in the header of $sub.RS.align.nii and not 
 in the $sub.RS.template.nii file or $sub.RS.nii?
Yes, in the header.

I'm not sure what you are trying to do here. Usually, one runs 
bbregister using the middle time point as the mov template and one runs 
motion correction separately to the middle time point. One then applies 
the bbregister transform to the motion corrected time series to map it 
to the surface (mri_vol2surf) or another volume (mri_vol2vol).

 3) Using @SUMA_Make_Spec_FS did not correctly convert brain.mgz and 
 aseg.mgz correctly when overlaid with the original $sub.SPGR.FS.mgz as 
 well as $sub.RS.align.nii or $sub.RS.nii so I just used the following 
 instead /mri directory:

 *mri_convert -ot nii brain.mgz brain.nii
 *
 *mri_convert -ot nii aseg.mgz aseg.nii
 *
 *
 *
 *4) Following relates to viewing images created in AFNI correctly if 
 anyone knows:
 *
 When I tried to use AFNI to view the original anatomical scan 
 $sub.SPGR.FS.mgz and $sub.RS.align.nii it was not aligned (assume 
 anatomical is similar to rawavg.mgz).
 When I load brain.nii and $sub.RS.align.nii into afni they are not 
 overlapped perfectly as in tkregister2. Additionally I get an error 
 about deobliquing the $sub.RS.align.nii file.  Interestingly enough I 
 do not get this error with the $sub.RS.template.nii so I am not sure 
 if there is an error in applying the transform or if the template file 
 has no transform info stored while the aligned file does.  How would I 
 apply the reg file to all timepoints without getting the oblique error 
 or should I use the following command and is this correct:

 *3dWarp -deoblique -gridset $sub.RS.nii -prefix 
 $sub.RS.align.deobl.nii $sub.RS.align.nii*

 Would i deoblique using the gridset of the original $sub.RS.nii, the 
 aligned file $sub.RS.align.nii or just the template file (or does it 
 not matter since the voxel dimensions are the same even though centers 
 are different).



 Sorry for the long email but thanks in advance for any advice / 
 explanations.

 Sincerely,
 Ajay




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gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
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Re: [Freesurfer] mri_convert - Scaling of Values

2014-01-31 Thread Bruce Fischl

Hi Dan

I think specifying -ns 1 will do the trick

cheers
Bruce
On Fri, 31 Jan 2014, Daniel Carey 
wrote:



Dear All,
We have been using mri_convert to convert .nii format quantitative scans
(specifically R1 volumes) into .mgz (float) format, so they can be used as
input to mri_vol2surf. Inputting the .nii files to mri_vol2surf has produced
an error in values in the output paint file, whereas this issue appears not
to occur with the .mgz input.

In running mri_convert, we are encountering an issue with the scaling of
image values. Optimally, we would like to preserve the values within the
quantitative volume, such that mri_convert does not change these when we
output to .mgz. In some cases, we have noted non-linear differences in the
output .mgz values, compared to the input volume. We have been using the -ns
flag, and still see these issues.

Is there a way to set the output .mgz scale factor to preserve the existing
values exactly as per the quantitative input volume? 

Any advice would be greatly appreciated. Many thanks in advance.

Best wishes,
Dan

---

Daniel Carey
Marie Curie Ph.D. Fellow,
Centre for Brain and Cognitive Development,
32 Torrington Sq.,
London WC1E 7HX
UK

email: d.ca...@bbk.ac.uk
web: http://www.cbcd.bbk.ac.uk/people/students/daniel_carey

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[Freesurfer] mri_convert - Scaling of Values

2014-01-31 Thread Daniel Carey
Dear All,

We have been using mri_convert to convert .nii format quantitative scans 
(specifically R1 volumes) into .mgz (float) format, so they can be used as 
input to mri_vol2surf. Inputting the .nii files to mri_vol2surf has produced an 
error in values in the output paint file, whereas this issue appears not to 
occur with the .mgz input.

In running mri_convert, we are encountering an issue with the scaling of image 
values. Optimally, we would like to preserve the values within the quantitative 
volume, such that mri_convert does not change these when we output to .mgz. In 
some cases, we have noted non-linear differences in the output .mgz values, 
compared to the input volume. We have been using the -ns flag, and still see 
these issues.

Is there a way to set the output .mgz scale factor to preserve the existing 
values exactly as per the quantitative input volume? 

Any advice would be greatly appreciated. Many thanks in advance.

Best wishes,
Dan

---

Daniel Carey
Marie Curie Ph.D. Fellow,
Centre for Brain and Cognitive Development,
32 Torrington Sq.,
London WC1E 7HX
UK

email: d.ca...@bbk.ac.uk
web: http://www.cbcd.bbk.ac.uk/people/students/daniel_carey___
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Re: [Freesurfer] mri_convert - Scaling of Values

2014-01-31 Thread Douglas N Greve
what is your mri_convert command line. Send the terminal output too.
doug


On 01/31/2014 12:14 PM, Daniel Carey wrote:
 Dear All,

 We have been using mri_convert to convert .nii format quantitative 
 scans (specifically R1 volumes) into .mgz (float) format, so they can 
 be used as input to mri_vol2surf. Inputting the .nii files to 
 mri_vol2surf has produced an error in values in the output paint file, 
 whereas this issue appears not to occur with the .mgz input.

 In running mri_convert, we are encountering an issue with the scaling 
 of image values. Optimally, we would like to preserve the values 
 within the quantitative volume, such that mri_convert does not change 
 these when we output to .mgz. In some cases, we have noted non-linear 
 differences in the output .mgz values, compared to the input volume. 
 We have been using the -ns flag, and still see these issues.

 Is there a way to set the output .mgz scale factor to preserve the 
 existing values exactly as per the quantitative input volume?

 Any advice would be greatly appreciated. Many thanks in advance.

 Best wishes,
 Dan

 ---

 Daniel Carey
 Marie Curie Ph.D. Fellow,
 Centre for Brain and Cognitive Development,
 32 Torrington Sq.,
 London WC1E 7HX
 UK

 email: d.ca...@bbk.ac.uk mailto:d.ca...@bbk.ac.uk
 web: http://www.cbcd.bbk.ac.uk/people/students/daniel_carey


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MGH-NMR Center
gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
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[Freesurfer] adding color scale to freeview

2014-01-31 Thread Fred Lado
Dear Freesurfer Experts,
Is there a way to create custom color scale - like “Heat”, “Jet”, etc - for use 
in Freeview?
Thanks,

Fred Lado
Montefiore Medical Center



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Re: [Freesurfer] LGI ERROR: make_roi_paths did not complete successfully!

2014-01-31 Thread Wanda Truong
Hi Marie,

Yes, I'm using matlab R3013a. In $FREESURFER_HOME/matlab folder I don't
have a file called SearchProjectionOnPial.m. Should I create it and paste
the updated function?

Thanks for your help!!

Wanda




On 30 January 2014 15:09, Marie Schaer marie.sch...@unige.ch wrote:


  Hi Wanda,

  I'm not sure to understand your problem. Do you get an error because of
 using matlab 2013? If yes, I'm not sure to understand whether you modified
 the SearchProjectionOnPial.m function properly.

  Can you download the updated function there:
 http://www.mail-archive.com/freesurfer@nmr.mgh.harvard.edu/msg30506.html
 and copy it in the $FREESURFER_HOME/matlab folder (replace the older one
 with this one).

  Let me know how it works,

  Marie

  On Jan 30, 2014, at 1:50 PM, Wanda Truong wanda.truong...@gmail.com
  wrote:

  Hello Marie,

  I am trying to conduct a local gyrification index analysis, however I am
 getting this error ERROR:  make_roi_paths did not complete successfully!

  Which is the same as the one posted earlier by someone else:
 https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-July/032203.html

  I added the patch:

  function
 [verticeslist]=SearchProjectionOnPial(mesh_total,mesh_outer,perim, step)

 % step is typically set between 5 and 10. Default is 7, increasing it will
 % limit redundancies in the resulting path file.

 verticeslist=[];
 si=max(size(perim));
 for t=1:step:si
 
 [nearestIndexMT,nearestValuesMT]=mesh_vertex_nearest(mesh_total.vertices,mesh_outer.vertices(perim(t),:));
 verticeslist= [verticeslist nearestIndexMT];
 end

 verticeslist=unique(verticeslist);


  to my $freesurfer_home/matlab directly as a .m file. However, I'm still
 getting the same error:

  Error in dsearchn (line 80)
 [d(i),t(i)] = min(sum((x-yi).^2,2));

  Error in mesh_vertex_nearest (line 29)
 nearestIndex = dsearchn(vertices,points);

  Error in reorganize_verticeslist (line 28)

 [nextindex,nextvalue]=mesh_vertex_nearest(mesh_total.vertices(remaininglist,:),mesh_total.vertices(verticeslist(start_vertex),:));

 Error in make_roi_paths (line 93)
 reorglist = reorganize_verticeslist (mesh_total, A, mesh_outer, perim,
 verticeslist, step);

 
 ERROR:  make_roi_paths did not complete successfully!
 Darwin Vinas-iMac.local 11.4.2 Darwin Kernel Version 11.4.2: Thu Aug 23
 16:25:48 PDT 2012; root:xnu-1699.32.7~1/RELEASE_X86_64 x86_64

  recon-all -s SFS026 exited with ERRORS at Thu Jan 30 14:26:16 MST 2014



  Thanks,
 Wanda


  --
  Wanda Truong, MSc
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 is
 addressed. If you believe this e-mail was sent to you in error and the
 e-mail
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 HelpLine at
 http://www.partners.org/complianceline . If the e-mail was sent to you in
 error
 but does not contain patient information, please contact the sender and
 properly
 dispose of the e-mail.





-- 
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[Freesurfer] Recon-all error

2014-01-31 Thread Emad Ahmadi
Hello,

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

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


Thank you very much,
Emad


Emad Ahmadi, MD

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

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



recon-all.log
Description: Binary data


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

2014-01-31 Thread Douglas N Greve
Emad, please run

mri_converrt 
/Users/louispuybasset/Desktop/Zebouni_Fadi/T1/IM-0002-0001.dcm junk.mgh

and send us the terminal output


On 01/31/2014 03:28 PM, Emad Ahmadi wrote:
 Hello,

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

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


 Thank you very much,
 Emad


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

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



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-- 
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MGH-NMR Center
gr...@nmr.mgh.harvard.edu
Phone Number: 617-724-2358
Fax: 617-726-7422

Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
FileDrop: https://gate.nmr.mgh.harvard.edu/filedrop2
www.nmr.mgh.harvard.edu/facility/filedrop/index.html
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Re: [Freesurfer] ERROR: dimension mismatch between y and X.

2014-01-31 Thread Douglas N Greve

that looks like the right size. I am stumped. What version of FS are you 
using? Do you have access to other versions?


On 01/31/2014 02:50 PM, Wanda Truong wrote:
 This is what I get:
 [Vinas-iMac:Wanda_SFS/qdec/Untitled] vinagoghari% ls -l y.mgh
 -rw-r--r--  1 vinagoghari  staff  1055844047 30 Jan 14:54 y.mgh


 On 31 January 2014 12:41, Douglas N Greve gr...@nmr.mgh.harvard.edu 
 mailto:gr...@nmr.mgh.harvard.edu wrote:

 OK, it is y.mgh that is definitely wrong. Can you send me the
 result of
 ls -l y.mgh



 On 01/31/2014 02:37 PM, Wanda Truong wrote:

 Hi Doug,

 Here's what I get for mri_info lh.area.fwhm10.fsaverage.mgh:

 [Vinas-iMac:~/Documents/Wanda/Wanda_SFS] vinagoghari% mri_info
 lh.area.fwhm10.fsaverage.mgh
 Volume information for lh.area.fwhm10.fsaverage.mgh
   type: MGH
 dimensions: 163842 x 1 x 1 x 46
voxel sizes: 1., 1., 1.
   type: FLOAT (3)
fov: 163842.000
dof: 0
 xstart: -81921.0, xend: 81921.0
 ystart: -0.5, yend: 0.5
 zstart: -0.5, zend: 0.5
 TR: 0.00 msec, TE: 0.00 msec, TI: 0.00 msec, flip
 angle: 0.00 degrees
nframes: 46
PhEncDir: UNKNOWN
 ras xform present
 xform info: x_r =  -1., y_r =   0., z_r = 0.,
 c_r = 0.
   : x_a =   0., y_a =   0., z_a = 1.,
 c_a = 0.
   : x_s =   0., y_s =  -1., z_s = 0.,
 c_s = 0.

 talairach xfm :
 Orientation   : LIA
 Primary Slice Direction: coronal

 voxel to ras transform:
-1.   0.   0. 81921.
 0.   0.   1.-0.5000
 0.  -1.   0. 0.5000
 0.   0.   0. 1.

 voxel-to-ras determinant -1

 ras to voxel transform:
-1.   0.   0. 81921.
-0.  -0.  -1. 0.5000
-0.   1.  -0. 0.5000
 0.   0.   0. 1.

 [Vinas-iMac:~/Documents/Wanda/Wanda_SFS] vinagoghari% mri_info
 /Users/vinagoghari/Documents/Wanda/Wanda_SFS/qdec/Untitled/y.mgh
 Volume information for
 /Users/vinagoghari/Documents/Wanda/Wanda_SFS/qdec/Untitled/y.mgh
   type: MGH
 dimensions: 163842 x 1 x 1 x 1584
voxel sizes: 1., 1., 1.
   type: FLOAT (3)
fov: 163842.000
dof: 0
 xstart: -81921.0, xend: 81921.0
 ystart: -0.5, yend: 0.5
 zstart: -0.5, zend: 0.5
 TR: 0.00 msec, TE: 0.00 msec, TI: 0.00 msec, flip
 angle: 0.00 degrees
nframes: 1584
PhEncDir: UNKNOWN
 ras xform present
 xform info: x_r =  -1., y_r =   0., z_r = 0.,
 c_r = 0.
   : x_a =   0., y_a =   0., z_a = 1.,
 c_a = 0.
   : x_s =   0., y_s =  -1., z_s = 0.,
 c_s = 0.

 talairach xfm :
 Orientation   : LIA
 Primary Slice Direction: coronal

 voxel to ras transform:
-1.   0.   0. 81921.
 0.   0.   1.-0.5000
 0.  -1.   0. 0.5000
 0.   0.   0. 1.

 voxel-to-ras determinant -1

 ras to voxel transform:
-1.   0.   0. 81921.
-0.  -0.  -1. 0.5000
-0.   1.  -0. 0.5000
 0.   0.   0. 1.

 Thank you!
 Wanda


 On 30 January 2014 15:30, 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:


 I don't know, it is a bit bizarre. Can you run mri_info on
 both
 lh.area.fwhm10.fsaverage.mgh and Untitled/y.mgh and send
 me the
 results?


 On 01/30/2014 05:01 PM, Wanda Truong wrote:
  Hi Doug,
 
  Same thing happens with the other half. I'm wondering
 what file is
  used for Y - is it lh.area.fwhm10.fsaverage.mgh? and why
 does it
 have
  an input number that is different from X, which should
 be the number
  of subjects?
 

Re: [Freesurfer] LGI ERROR: make_roi_paths did not complete successfully!

2014-01-31 Thread Marie Schaer

Hi Wanda,

You should have this function in $FREESURFER_HOME/matlab, the same way you 
should have compute_lgi.m and many other matlab functions there. Are you sure 
that you are looking at the correct location and / or that you didn't delete it?

Marie


On Jan 31, 2014, at 11:32 AM, Wanda Truong 
wanda.truong...@gmail.commailto:wanda.truong...@gmail.com
 wrote:

Hi Marie,

Yes, I'm using matlab R3013a. In $FREESURFER_HOME/matlab folder I don't have a 
file called SearchProjectionOnPial.m. Should I create it and paste the updated 
function?

Thanks for your help!!

Wanda




On 30 January 2014 15:09, Marie Schaer 
marie.sch...@unige.chmailto:marie.sch...@unige.ch wrote:

Hi Wanda,

I'm not sure to understand your problem. Do you get an error because of using 
matlab 2013? If yes, I'm not sure to understand whether you modified the 
SearchProjectionOnPial.m function properly.

Can you download the updated function there: 
http://www.mail-archive.com/freesurfer@nmr.mgh.harvard.edu/msg30506.html
and copy it in the $FREESURFER_HOME/matlab folder (replace the older one with 
this one).

Let me know how it works,

Marie

On Jan 30, 2014, at 1:50 PM, Wanda Truong 
wanda.truong...@gmail.commailto:wanda.truong...@gmail.com
 wrote:

Hello Marie,

I am trying to conduct a local gyrification index analysis, however I am 
getting this error ERROR:  make_roi_paths did not complete successfully!

Which is the same as the one posted earlier by someone else: 
https://mail.nmr.mgh.harvard.edu/pipermail//freesurfer/2013-July/032203.html

I added the patch:

function [verticeslist]=SearchProjectionOnPial(mesh_total,mesh_outer,perim, 
step)

% step is typically set between 5 and 10. Default is 7, increasing it will
% limit redundancies in the resulting path file.

verticeslist=[];
si=max(size(perim));
for t=1:step:si

[nearestIndexMT,nearestValuesMT]=mesh_vertex_nearest(mesh_total.vertices,mesh_outer.vertices(perim(t),:));
verticeslist= [verticeslist nearestIndexMT];
end

verticeslist=unique(verticeslist);


to my $freesurfer_home/matlab directly as a .m file. However, I'm still getting 
the same error:

Error in dsearchn (line 80)
[d(i),t(i)] = min(sum((x-yi).^2,2));

Error in mesh_vertex_nearest (line 29)
nearestIndex = dsearchn(vertices,points);

Error in reorganize_verticeslist (line 28)

[nextindex,nextvalue]=mesh_vertex_nearest(mesh_total.vertices(remaininglist,:),mesh_total.vertices(verticeslist(start_vertex),:));

Error in make_roi_paths (line 93)
reorglist = reorganize_verticeslist (mesh_total, A, mesh_outer, perim,
verticeslist, step);


ERROR:  make_roi_paths did not complete successfully!
Darwin Vinas-iMac.local 11.4.2 Darwin Kernel Version 11.4.2: Thu Aug 23 
16:25:48 PDT 2012; root:xnu-1699.32.7~1/RELEASE_X86_64 x86_64

recon-all -s SFS026 exited with ERRORS at Thu Jan 30 14:26:16 MST 2014



Thanks,
Wanda


--
Wanda Truong, MSc
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dispose of the e-mail.




--
Wanda Truong, MSc

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