Re: [Freesurfer] how to interpret a change in area of 0.004 mm² per year?

2014-10-29 Thread Lars M. Rimol
Hi Bruce (and Jorge),

Yes, it's the wm surface.  I have also done the analyses with the pial
surface and the results are similar to wm surface.

To your second question: White matter volume increased over this time
period (lme analysis; controls: logP = 8.49, patients: logP =  6.34).

Since the cortical analyses were done using lme, which can handle missing
data, some of the subjects have only one time point. So I created a
difference map for
those subjects for whom we have data on both time points, to see if area on
the first time point is consistently larger than on the second time point.
Almost all subjects
showed larger values on tp1 than tp2 and the maps of average area change
(across subjects) confirm that.
In addition, I ran an lme analysis with the same subjects and found results
very similar to those for the entire sample.

Would you agree that this apparent reduction in cortical area seems
plausible? There is a reduction over time in raw data, and pial surface
area show the same trend as wm surface,
and the lme analysis with only subjects that have data on both time points
shows very similar results as the lme with all subjects.
On the other hand, I suppose we wouldn't expect increased wm volume
together with reduced area?

As for the effect size maps, I have worked on finding a way to represent
change in area over time that is intuitive for a reader not familiar with
FreeSurfer:
I figured one solution could be to log transform the dependent variable (wm
or pial area). This way the significance tests are done with log
transformed data and for purposes of illustration
I do exp(beta)*100-100 on the beta for time, which ensures that if there is
e.g. a 1% reduction, the figure shows -1, and 1 for a 1% increase. I find
this is a good way of demonstrating the
effects (attached figure:
lh_wmarea_logtransf_expBeta2_s30_inflated_lateral.tif ). What do you think?

I could of course also transform the dependent variable into percentages.
That is, baseline == 100 and tp2 expressed in percent of baseline. However,
I find this to be a less attractive solution because we basically lose the
baseline values, and this makes the model less useful for all other
purposes. For instance, we can't investigate group differences at the
various time points within the model. Perhaps more importantly, it's
unclear what assumptions we are making. The lme assumes a normal
distribution and it's unclear to me what the distribution of such ratios
are.


Thank you!

LMR

yours,

Lars M. Rimol, PhD
Norwegian University of Science and Technology (NTNU)
Trondheim,
Norway



 Bruce Fischl
 http://www.mail-archive.com/search?l=freesurfer@nmr.mgh.harvard.eduq=from:%22Bruce+Fischl%22
  Sat,
 06 Sep 2014 07:00:14 -0700
 http://www.mail-archive.com/search?l=freesurfer@nmr.mgh.harvard.eduq=date:20140906

 Hi Lars


 which surface are you using? If it's the white surface you might try looking
 at white matter volume to see if it is decreasing

 cheers
 Bruce

 On Sat, 6 Sep 2014, Lars M. Rimol wrote:


 Hi,

 I have performed a longitudinal analysis using the lme module in FreeSurfer,
 with this model:

 intercept(random effect) + centered age + group + group x centered age + sex

 I tested the effect of time with this contrast vector [ 0 1 0 0 0 ].
 Dependent variable is  area.

 Here, mapping the second beta means mapping the effect size for (change
 over) time. In the beta map, I find values from 0 to 0.004.  I would
 interpret that to mean that local area shrinks by at most 0.004 mm² per year
 in the reference group. But I'm not 100% sure about the biological (or
 geometrical) meaning of that.

 Can I interpret this literally as the mean yearly shrinkage of the three
 triangles surrounding a given vertex, the average of whose area comprises
 the area score of the vertex, being 4/1000 mm? Of course, these maps are
 smoothed with 30mm, so the real spatial resolution is nowhere near this


 Thank you!


 --
 yours,
 Lars M. Rimol, PhD
 St. Olavs Hospital
 Trondheim,
 Norway


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 yours,

 Lars M. Rimol, PhD
 Norwegian University of Science and Technology (NTNU)
 Trondheim,
 Norway

 On Mon, Oct 27, 2014 at 9:59 AM, Lars M. Rimol lari...@gmail.com wrote:

 Hi Bruce (and Jorge),

 Yes, it's the wm surface.  I have also done the analyses with the pial
 surface and the results are similar to wm surface (attached p-maps:
 

[Freesurfer] adding insula voxels

2014-10-29 Thread Adam Mezher
Hi Bruce and FS group,

Thanks again for the speedy replies and help with everything. Quick
question about editing voxels (specifically those in the lh/rh insula).
Should I simply add specific voxels to the aparc+aseg for this step? It was
a little unclear on the wiki.

Also, is there a specific command to re-run the stats/etc. after these
edits are performed?

Thanks a lot,
Adam
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[Freesurfer] Error when completing cortical thickness analysis

2014-10-29 Thread Claire Morley
I am conducting cortical thickness analyses between hundreds of individuals
for a study we are conducting. I was getting this error

Unrecognized sub-option flag 'annot_outline'.  and so I tried to do the
group analysis tutorial and input the command from the end of it (please
see command below) but still got the same error. Freeview would open but it
would not show any images. Could you help me to resolve this issue please?
Also, what does it mean when it spits out invalid drawable?

 freeview -f
$SUBJECTS_DIR/fsaverage/surf/lh.inflated:annot=aparc.annot:annot_outline=1:overlay=lh.gender_age.glmdir/lh-Avg-thickness-age-Cor/sig.mgh:overlay_threshold=4,5
-viewport 3d
Thank you so much for your help!
Claire
-- 

*We shall not cease from exploration. And the end of all our exploring will
be to arrive where we started and know the place for the first time- T.S.
Eliot*
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[Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Alexandre Routier
Dear all,

I would like to work with the pial surfaces of my database and more
particularly with a point-to-point correspondance between each subject. But
I didn't find how to do that, only for longitudinal analysis of a single
subject which I am not interested.

Thanks in advance for you help,
Alexandre
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Re: [Freesurfer] how to interpret a change in area of 0.004 mm² per year?

2014-10-29 Thread Bruce Fischl

Hi Lars

yes, it seems plausible, particularly since it is so universal.

cheers
Bruce

On Wed, 29 
Oct 2014, Lars M. Rimol wrote:



Hi Bruce (and Jorge),

Yes, it's the wm surface.  I have also done the analyses with the pial
surface and the results are similar to wm surface.

To your second question: White matter volume increased over this time period
(lme analysis; controls: logP = 8.49, patients: logP =  6.34).

Since the cortical analyses were done using lme, which can handle missing
data, some of the subjects have only one time point. So I created a
difference map for
those subjects for whom we have data on both time points, to see if area on
the first time point is consistently larger than on the second time point.
Almost all subjects
showed larger values on tp1 than tp2 and the maps of average area change
(across subjects) confirm that.
In addition, I ran an lme analysis with the same subjects and found results
very similar to those for the entire sample.

Would you agree that this apparent reduction in cortical area seems
plausible? There is a reduction over time in raw data, and pial surface area
show the same trend as wm surface,
and the lme analysis with only subjects that have data on both time points
shows very similar results as the lme with all subjects.
On the other hand, I suppose we wouldn't expect increased wm volume together
with reduced area?

As for the effect size maps, I have worked on finding a way to represent
change in area over time that is intuitive for a reader not familiar with
FreeSurfer:
I figured one solution could be to log transform the dependent variable (wm
or pial area). This way the significance tests are done with log transformed
data and for purposes of illustration
I do exp(beta)*100-100 on the beta for time, which ensures that if there is
e.g. a 1% reduction, the figure shows -1, and 1 for a 1% increase. I find
this is a good way of demonstrating the
effects (attached figure:
lh_wmarea_logtransf_expBeta2_s30_inflated_lateral.tif ). What do you think?

I could of course also transform the dependent variable into percentages.
That is, baseline == 100 and tp2 expressed in percent of baseline. However,
I find this to be a less attractive solution because we basically lose the
baseline values, and this makes the model less useful for all other
purposes. For instance, we can't investigate group differences at the
various time points within the model. Perhaps more importantly, it's unclear
what assumptions we are making. The lme assumes a normal distribution and
it's unclear to me what the distribution of such ratios are.


Thank you!

LMR

yours,
Lars M. Rimol, PhD
Norwegian University of Science and Technology (NTNU)
Trondheim,
Norway



  Bruce Fischl Sat, 06 Sep 2014 07:00:14 -0700

Hi Lars

  which surface are you using? If it's the white surface you might
  try looking at white matter volume to see if it is decreasing

cheers
Bruce

On Sat, 6 Sep 2014, Lars M. Rimol wrote:

Hi,

I have performed a longitudinal analysis using the lme module in FreeSurfer,
with this model: 

intercept(random effect) + centered age + group + group x centered age + sex

I tested the effect of time with this contrast vector [ 0 1 0 0 0 ].
Dependent variable is  area.

Here, mapping the second beta means mapping the effect size for (change
over) time. In the beta map, I find values from 0 to 0.004.  I would
interpret that to mean that local area shrinks by at most 0.004 mm² per year
in the reference group. But I'm not 100% sure about the biological (or
geometrical) meaning of that.

Can I interpret this literally as the mean yearly shrinkage of the three
triangles surrounding a given vertex, the average of whose area comprises
the area score of the vertex, being 4/1000 mm? Of course, these maps are
smoothed with 30mm, so the real spatial resolution is nowhere near this


Thank you!


--
yours,
Lars M. Rimol, PhD
St. Olavs Hospital
Trondheim,
Norway

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yours,
Lars M. Rimol, PhD
Norwegian University of Science and Technology (NTNU)
Trondheim,
Norway

On Mon, Oct 27, 2014 at 9:59 AM, Lars M. Rimol lari...@gmail.com
wrote:
  Hi Bruce (and Jorge),

Yes, it's the wm surface.  I have also done the analyses with
the pial surface and the results are similar to wm surface
(attached p-maps:
lh_0-1000_wmarea_s30_log10p_inflated_lateral.tif vs.
lh_0-1000_wmarea_s30_log10p_inflated_lateral.tif).


Re: [Freesurfer] adding insula voxels

2014-10-29 Thread Bruce Fischl
Hi Adam

sorry, I've lost the context for this. Why are you adding voxels to the 
aparc+aseg in the insula?

cheers
Bruce
On Wed, 29 Oct 2014, Adam Mezher wrote:

 Hi Bruce and FS group,
 Thanks again for the speedy replies and help with everything. Quick question
 about editing voxels (specifically those in the lh/rh insula). Should I
 simply add specific voxels to the aparc+aseg for this step? It was a little
 unclear on the wiki.
 
 Also, is there a specific command to re-run the stats/etc. after these edits
 are performed?
 
 Thanks a lot,
 Adam
 

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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Bruce Fischl
Hi Alexandre

can you tell us what you want to do with the point-to-point 
correspondence? We don't usually map surfaces into a common space since 
we want to have  uniform resolution/sampling in the individual coords.

cheers
Bruce


On Wed, 29 Oct 2014, Alexandre Routier wrote:

 Dear all,
 
 I would like to work with the pial surfaces of my database and more
 particularly with a point-to-point correspondance between each subject. But
 I didn't find how to do that, only for longitudinal analysis of a single
 subject which I am not interested.
 
 Thanks in advance for you help,
 Alexandre
 

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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Alexandre Routier
Hello Bruce,

I would like to build an atlas of subcortical structures and pial surface
on my population of study. But given the anatomical complexity of the pial
surface (and the number of points), I would like to use point-to-point
correspondence so as to have a L^2 metric (I use another metric for
subcortical structures).
I don't know if I am clear enough but since I estimate the template and the
variability between the template and the subjects, I would like to detect
information such as atrophy thanks to the deformation parameters.

Is there any solution?

Alexandre


2014-10-29 13:49 GMT+01:00 Bruce Fischl fis...@nmr.mgh.harvard.edu:

 Hi Alexandre

 can you tell us what you want to do with the point-to-point
 correspondence? We don't usually map surfaces into a common space since
 we want to have  uniform resolution/sampling in the individual coords.

 cheers
 Bruce


 On Wed, 29 Oct 2014, Alexandre Routier wrote:

  Dear all,
 
  I would like to work with the pial surfaces of my database and more
  particularly with a point-to-point correspondance between each subject.
 But
  I didn't find how to do that, only for longitudinal analysis of a single
  subject which I am not interested.
 
  Thanks in advance for you help,
  Alexandre
 
 
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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Douglas N Greve

I'm not sure what you mean by working with the pial surfaces with 
respect to point-to-point correspondence. Can you give more info?
doug

On 10/29/2014 06:29 AM, Alexandre Routier wrote:
 Dear all,

 I would like to work with the pial surfaces of my database and more 
 particularly with a point-to-point correspondance between each 
 subject. But I didn't find how to do that, only for longitudinal 
 analysis of a single subject which I am not interested.

 Thanks in advance for you help,
 Alexandre


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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Alexandre Routier
What I wanted to say is that there is the exact number of points of the
pial surface for each subject and if I look to the i-th vertex of the pial
surface of a given subject, it should be located on the same area for
another subject.

Alexandre

2014-10-29 15:25 GMT+01:00 Douglas N Greve gr...@nmr.mgh.harvard.edu:


 I'm not sure what you mean by working with the pial surfaces with
 respect to point-to-point correspondence. Can you give more info?
 doug

 On 10/29/2014 06:29 AM, Alexandre Routier wrote:
  Dear all,
 
  I would like to work with the pial surfaces of my database and more
  particularly with a point-to-point correspondance between each
  subject. But I didn't find how to do that, only for longitudinal
  analysis of a single subject which I am not interested.
 
  Thanks in advance for you help,
  Alexandre
 
 
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 gr...@nmr.mgh.harvard.edu
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Re: [Freesurfer] 7T reconstruction

2014-10-29 Thread Douglas N Greve

Create a voxel shift map using epidewarp.fsl (only the shift map is 
needed, don't use this to dewarp the data). Save this in 
bold/b0dcmap.nii (or nii.gz). When you run preproc-sess and 
mkanalysis-sess add -b0dc (stands for B0 distortion correction).
doug



On 10/28/2014 01:14 PM, B V wrote:
 Hello,
 I am interested in using functional data collected from 7t using 
 freesurfer and fsfast. We would like to use EPI field maps to warp 
 this data to 3T anatomical space. Can anyone guide me as to how to do 
 this.
 Best,
 B


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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Douglas N Greve
This is not something we support.

On 10/29/2014 10:32 AM, Alexandre Routier wrote:
 What I wanted to say is that there is the exact number of points of 
 the pial surface for each subject and if I look to the i-th vertex of 
 the pial surface of a given subject, it should be located on the same 
 area for another subject.

 Alexandre

 2014-10-29 15:25 GMT+01:00 Douglas N Greve gr...@nmr.mgh.harvard.edu 
 mailto:gr...@nmr.mgh.harvard.edu:


 I'm not sure what you mean by working with the pial surfaces with
 respect to point-to-point correspondence. Can you give more info?
 doug

 On 10/29/2014 06:29 AM, Alexandre Routier wrote:
  Dear all,
 
  I would like to work with the pial surfaces of my database and more
  particularly with a point-to-point correspondance between each
  subject. But I didn't find how to do that, only for longitudinal
  analysis of a single subject which I am not interested.
 
  Thanks in advance for you help,
  Alexandre
 
 
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 --
 Douglas N. Greve, Ph.D.
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 Fax: 617-726-7422

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Re: [Freesurfer] how to interpret a change in area of 0.004 mm² per year?

2014-10-29 Thread Martin Reuter

Hi Lars,

two thoughts that came up reading this thread:
- each vertex has usually more than 3 triangles (your first mail), the 
number differs depending on where you are. With a uniform mesh you'd 
have nearly 60 degree angles so you'd have approx 6 triangles at a vertex.
- wm volume can increase when area shrinks. If especially the slucii 
move further outside the whole surface gets more spherical, decreasing 
area, but increasing volume.


Best, Martin


On 10/29/2014 08:44 AM, Bruce Fischl wrote:

Hi Lars

yes, it seems plausible, particularly since it is so universal.

cheers
Bruce

On Wed, 29 Oct 2014, Lars M. Rimol wrote:


Hi Bruce (and Jorge),

Yes, it's the wm surface.  I have also done the analyses with the pial
surface and the results are similar to wm surface.

To your second question: White matter volume increased over this time 
period

(lme analysis; controls: logP = 8.49, patients: logP =  6.34).

Since the cortical analyses were done using lme, which can handle 
missing

data, some of the subjects have only one time point. So I created a
difference map for
those subjects for whom we have data on both time points, to see if 
area on
the first time point is consistently larger than on the second time 
point.

Almost all subjects
showed larger values on tp1 than tp2 and the maps of average area change
(across subjects) confirm that.
In addition, I ran an lme analysis with the same subjects and found 
results

very similar to those for the entire sample.

Would you agree that this apparent reduction in cortical area seems
plausible? There is a reduction over time in raw data, and pial 
surface area

show the same trend as wm surface,
and the lme analysis with only subjects that have data on both time 
points

shows very similar results as the lme with all subjects.
On the other hand, I suppose we wouldn't expect increased wm volume 
together

with reduced area?

As for the effect size maps, I have worked on finding a way to represent
change in area over time that is intuitive for a reader not familiar 
with

FreeSurfer:
I figured one solution could be to log transform the dependent 
variable (wm
or pial area). This way the significance tests are done with log 
transformed

data and for purposes of illustration
I do exp(beta)*100-100 on the beta for time, which ensures that if 
there is
e.g. a 1% reduction, the figure shows -1, and 1 for a 1% increase. I 
find

this is a good way of demonstrating the
effects (attached figure:
lh_wmarea_logtransf_expBeta2_s30_inflated_lateral.tif ). What do you 
think?


I could of course also transform the dependent variable into 
percentages.
That is, baseline == 100 and tp2 expressed in percent of baseline. 
However,
I find this to be a less attractive solution because we basically 
lose the

baseline values, and this makes the model less useful for all other
purposes. For instance, we can't investigate group differences at the
various time points within the model. Perhaps more importantly, it's 
unclear
what assumptions we are making. The lme assumes a normal distribution 
and

it's unclear to me what the distribution of such ratios are.


Thank you!

LMR

yours,
Lars M. Rimol, PhD
Norwegian University of Science and Technology (NTNU)
Trondheim,
Norway



  Bruce Fischl Sat, 06 Sep 2014 07:00:14 -0700

Hi Lars

  which surface are you using? If it's the white surface you might
  try looking at white matter volume to see if it is decreasing

cheers
Bruce

On Sat, 6 Sep 2014, Lars M. Rimol wrote:

Hi,

I have performed a longitudinal analysis using the lme module in 
FreeSurfer,

with this model:

intercept(random effect) + centered age + group + group x centered 
age + sex


I tested the effect of time with this contrast vector [ 0 1 0 0 0 ].
Dependent variable is  area.

Here, mapping the second beta means mapping the effect size for (change
over) time. In the beta map, I find values from 0 to 0.004.  I would
interpret that to mean that local area shrinks by at most 0.004 mm² 
per year

in the reference group. But I'm not 100% sure about the biological (or
geometrical) meaning of that.

Can I interpret this literally as the mean yearly shrinkage of the three
triangles surrounding a given vertex, the average of whose area 
comprises

the area score of the vertex, being 4/1000 mm? Of course, these maps are
smoothed with 30mm, so the real spatial resolution is nowhere near 
this



Thank you!


--
yours,
Lars M. Rimol, PhD
St. Olavs Hospital
Trondheim,
Norway

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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Alexandre Routier
Oh, okay. I thought this kind of data could be obtained since it exists for
longitudinal analysis.

Thanks for your answer anyway!

2014-10-29 15:35 GMT+01:00 Douglas N Greve gr...@nmr.mgh.harvard.edu:

 This is not something we support.

 On 10/29/2014 10:32 AM, Alexandre Routier wrote:
  What I wanted to say is that there is the exact number of points of
  the pial surface for each subject and if I look to the i-th vertex of
  the pial surface of a given subject, it should be located on the same
  area for another subject.
 
  Alexandre
 
  2014-10-29 15:25 GMT+01:00 Douglas N Greve gr...@nmr.mgh.harvard.edu
  mailto:gr...@nmr.mgh.harvard.edu:
 
 
  I'm not sure what you mean by working with the pial surfaces with
  respect to point-to-point correspondence. Can you give more info?
  doug
 
  On 10/29/2014 06:29 AM, Alexandre Routier wrote:
   Dear all,
  
   I would like to work with the pial surfaces of my database and more
   particularly with a point-to-point correspondance between each
   subject. But I didn't find how to do that, only for longitudinal
   analysis of a single subject which I am not interested.
  
   Thanks in advance for you help,
   Alexandre
  
  
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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Bruce Fischl
you can just compute the jacobian of the ?h.sphere.reg for deformation. I'm 
not sure I understand how you would use an L2 metric. There are tools in 
AFNI/SUMA for converting a freesurfer surface to a standard mesh that you 
could use


cheers
Bruce


On Wed, 29 Oct 2014, Alexandre Routier wrote:


Hello Bruce,

I would like to build an atlas of subcortical structures and pial surface on
my population of study. But given the anatomical complexity of the pial
surface (and the number of points), I would like to use point-to-point
correspondence so as to have a L^2 metric (I use another metric for
subcortical structures).
I don't know if I am clear enough but since I estimate the template and the
variability between the template and the subjects, I would like to detect
information such as atrophy thanks to the deformation parameters.

Is there any solution?

Alexandre


2014-10-29 13:49 GMT+01:00 Bruce Fischl fis...@nmr.mgh.harvard.edu:
  Hi Alexandre

  can you tell us what you want to do with the point-to-point
  correspondence? We don't usually map surfaces into a common
  space since
  we want to have  uniform resolution/sampling in the individual
  coords.

  cheers
  Bruce


  On Wed, 29 Oct 2014, Alexandre Routier wrote:

   Dear all,
  
   I would like to work with the pial surfaces of my database and
  more
   particularly with a point-to-point correspondance between each
  subject. But
   I didn't find how to do that, only for longitudinal analysis
  of a single
   subject which I am not interested.
  
   Thanks in advance for you help,
   Alexandre
  
  
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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Bruce Fischl
no, but I think SUMA does. Check it out. I'll cc Ziad so he can chime in.

cheers
Bruce
On 
Wed, 29 Oct 2014, Douglas N Greve wrote:

 This is not something we support.

 On 10/29/2014 10:32 AM, Alexandre Routier wrote:
 What I wanted to say is that there is the exact number of points of
 the pial surface for each subject and if I look to the i-th vertex of
 the pial surface of a given subject, it should be located on the same
 area for another subject.

 Alexandre

 2014-10-29 15:25 GMT+01:00 Douglas N Greve gr...@nmr.mgh.harvard.edu
 mailto:gr...@nmr.mgh.harvard.edu:


 I'm not sure what you mean by working with the pial surfaces with
 respect to point-to-point correspondence. Can you give more info?
 doug

 On 10/29/2014 06:29 AM, Alexandre Routier wrote:
 Dear all,

 I would like to work with the pial surfaces of my database and more
 particularly with a point-to-point correspondance between each
 subject. But I didn't find how to do that, only for longitudinal
 analysis of a single subject which I am not interested.

 Thanks in advance for you help,
 Alexandre


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Re: [Freesurfer] LGI fails for fsaverage

2014-10-29 Thread Pierre Mégevand
Our usual method for electrode localization remains in the patient's space:
co-register post-op MR and CT with pre-op MR brainmask (our reference
space) and snap electrodes to patient's outer pial surface.

My idea was: register the patient's (crappy) brainmask volume to the
Talairach fsaverage volume (not surface), which I can correct manually;
use the Talairach.xfm transform to bring the electrodes into that same
fsaverage volume, and then snap the electrodes to fsaverage's outer pial
surface. But that last step I can't perform. I'm aware that the
localization would be pretty inaccurate.

I'll look into what you suggest Marie. In case all else fails, the last
resort is to show the actual post-op MR and CT slices for electrodes of
interest, but that just does not look as appealing as pial surfaces!

--
Pierre Mégevand, MD, PhD
PLOS Neuro Community http://neuro.plos.org editor - Follow us on Twitter
http://twitter.com/PLOSNeuro
Postdoc @ Feinstein Institute for Medical Research (NY, USA)
Follow me on Twitter http://twitter.com/pierre_vanmedge - Read my blog
here http://neuroscimed.wordpress.com

On Wed, Oct 29, 2014 at 12:29 AM, Marie Schaer marie.sch...@unige.ch
wrote:


  So what I don't get in your pipeline is how you'll register the post-op
 brain to fsaverage if you don't have any cortical surface in the post-op?

  If I were you, if you want precise registration that includes the sulci,
 I'd go with the white surface from the pre-op gadolinium scan. And if you
 just want a rough registration of the skull shape, then you can probably
 find a way to create the outer surface directly on the gadolinium scan: if
 your brain mask is good, then mris_fill should work (maybe you need to
 binarize the data first (in any case a few lines of code in matlab should
 do the trick). If the brain mask is not good due to gadolinium, then either
 playing with mri_watershed (and maybe try mri_fill to separate the
 hemispheres / pons and cerebellum) and then mris_fill for the tessellation.
 Or if it doesn't work with mri_watershed, playing a bit with threshold with
 another skull-stripping program (e.g. MRIcro), then importing the volume
 back in FreeSurfer and use mris_fill to get a good tessellation. Both
 solutions will need you to play a bit, but I guess you cannot really afford
 to simply throw these data and take another subject!

  Good luck,

  Marie



  On Oct 28, 2014, at 2:57 PM, Pierre Mégevand pierre.megev...@gmail.com
 wrote:

  You're right, we can't use the post-op surface because of the
 deformation caused by surgery and the electrode artifacts.

  Getting a surface right from the brainmask would be OK, if we can't get
 anything better, but the nice thing about using the fsaverage surface is
 that you can plot and compare electrode locations from multiple patients.
 Just in case we have nothing better, though, how would you do it?

  Thanks again!

  --
 Pierre Mégevand, MD, PhD
 PLOS Neuro Community http://neuro.plos.org/ editor - Follow us on
 Twitter http://twitter.com/PLOSNeuro
 Postdoc @ Feinstein Institute for Medical Research (NY, USA)
 Follow me on Twitter http://twitter.com/pierre_vanmedge - Read my blog
 here http://neuroscimed.wordpress.com/

 On Tue, Oct 28, 2014 at 5:23 PM, Marie Schaer marie.sch...@unige.ch
 wrote:


  Hi Pierre,

  Tricky question. So you can't really use the post-op cortical surface
 for this participant, right? Otherwise I would simply use the outer
 smoothed pial for this subject directly, which would be much more similar
 to the pre-op than the outer surface from the fsaverage (?). Otherwise,
 with the gadolinium MRI, maybe you can still get an adequate white surface,
 but I'm not sure that it would help you. The other option is to use the
 brain mask volume (which may work even with gadolinium if you are lucky,
 otherwise you can play with the watershed parameters), and tesselate a
 surface directly on this volume. But you'll get the two hemispheres at once
 (and probably the cerebellum as well), which may not be what you want?

  Best,

  Marie


  On Oct 28, 2014, at 2:10 PM, Pierre Mégevand pierre.megev...@gmail.com
  wrote:

  Thanks Marie. Here is what I'm trying to do. In fact, all I need from
 LGI are the first few steps, until ?h.pial-outer-smoothed has been
 generated. I'm not actually interested in the local GI for fsaverage.

 Our intra-cranial electrode localization method relies on post-implant CT
 and MRI scans to localize the electrodes, and a pre-implant MR scan to
 which we co-register the post-op exams and to whose smoothed outer pial
 surface we then snap the electrodes to, in order to account for the brain
 shift caused by the implantation procedure (Dykstra et al., 2012).

 Now, for one of our patients, the pre-op MRI was acquired with a lot of
 gadolinium, and we can't get Freesurfer to compute the pial surface. So I
 thought I would co-register the post-op exams to the fsaverage brain, and
 then snap the electrodes to fsaverage's outer 

Re: [Freesurfer] LGI fails for fsaverage

2014-10-29 Thread Bruce Fischl
have you tried using bbregister to register post-op MRI with the pre-op 
surfaces?

On Wed, 29 Oct 2014, Pierre Mégevand wrote:


Our usual method for electrode localization remains in the patient's space:
co-register post-op MR and CT with pre-op MR brainmask (our reference space)
and snap electrodes to patient's outer pial surface.

My idea was: register the patient's (crappy) brainmask volume to the
Talairach fsaverage volume (not surface), which I can correct manually;
use the Talairach.xfm transform to bring the electrodes into that same
fsaverage volume, and then snap the electrodes to fsaverage's outer pial
surface. But that last step I can't perform. I'm aware that the localization
would be pretty inaccurate.
I'll look into what you suggest Marie. In case all else fails, the last
resort is to show the actual post-op MR and CT slices for electrodes of
interest, but that just does not look as appealing as pial surfaces!

--
Pierre Mégevand, MD, PhD
PLOS Neuro Community editor - Follow us on Twitter
Postdoc @ Feinstein Institute for Medical Research (NY, USA)
Follow me on Twitter - Read my blog here

On Wed, Oct 29, 2014 at 12:29 AM, Marie Schaer marie.sch...@unige.ch
wrote:

So what I don't get in your pipeline is how you'll register the
post-op brain to fsaverage if you don't have any cortical surface in
the post-op? 

If I were you, if you want precise registration that includes the
sulci, I'd go with the white surface from the pre-op gadolinium scan.
And if you just want a rough registration of the skull shape, then you
can probably find a way to create the outer surface directly on the
gadolinium scan: if your brain mask is good, then mris_fill should
work (maybe you need to binarize the data first (in any case a few
lines of code in matlab should do the trick). If the brain mask is not
good due to gadolinium, then either playing with mri_watershed (and
maybe try mri_fill to separate the hemispheres / pons and cerebellum)
and then mris_fill for the tessellation. Or if it doesn't work with
mri_watershed, playing a bit with threshold with another
skull-stripping program (e.g. MRIcro), then importing the volume back
in FreeSurfer and use mris_fill to get a good tessellation. Both
solutions will need you to play a bit, but I guess you cannot really
afford to simply throw these data and take another subject! 

Good luck,

Marie



On Oct 28, 2014, at 2:57 PM, Pierre Mégevand
pierre.megev...@gmail.com wrote:

  You're right, we can't use the post-op surface because of
  the deformation caused by surgery and the electrode
  artifacts.
Getting a surface right from the brainmask would be OK, if we
can't get anything better, but the nice thing about using the
fsaverage surface is that you can plot and compare electrode
locations from multiple patients. Just in case we have nothing
better, though, how would you do it?

Thanks again!

--
Pierre Mégevand, MD, PhD
PLOS Neuro Community editor - Follow us on Twitter
Postdoc @ Feinstein Institute for Medical Research (NY, USA)
Follow me on Twitter - Read my blog here

On Tue, Oct 28, 2014 at 5:23 PM, Marie Schaer
marie.sch...@unige.ch wrote:

Hi Pierre,

Tricky question. So you can't really use the post-op
cortical surface for this participant, right? Otherwise I
would simply use the outer smoothed pial for this subject
directly, which would be much more similar to the pre-op
than the outer surface from the fsaverage (?). Otherwise,
with the gadolinium MRI, maybe you can still get an
adequate white surface, but I'm not sure that it would
help you. The other option is to use the brain mask volume
(which may work even with gadolinium if you are lucky,
otherwise you can play with the watershed parameters), and
tesselate a surface directly on this volume. But you'll
get the two hemispheres at once (and probably the
cerebellum as well), which may not be what you want?

Best,

Marie


On Oct 28, 2014, at 2:10 PM, Pierre Mégevand
pierre.megev...@gmail.com
 wrote:

  Thanks Marie. Here is what I'm trying to do.
  In fact, all I need from LGI are the first few
  steps, until ?h.pial-outer-smoothed has been
  generated. I'm not actually interested in the
  local GI for fsaverage.

  Our intra-cranial electrode localization
  method relies on post-implant CT and MRI scans
  to localize the electrodes, and a pre-implant
  MR scan to which we co-register the post-op
  exams and to whose smoothed outer pial surface
  we then snap the electrodes to, in order to
  account for the brain shift caused by the
  implantation procedure (Dykstra et al., 2012).

  Now, for one of our patients, the pre-op MRI
  was acquired with a lot of gadolinium, and we
  can't get Freesurfer to compute the pial
  surface. So I thought I would co-register the
  post-op exams to the fsaverage brain, and then
  snap the electrodes to fsaverage's outer
  smoothed pial surface as an approximation. Any
  idea 

Re: [Freesurfer] LGI analysis of single subject

2014-10-29 Thread Maria Holland
Hi Marie -

Thanks for your response.  After sending my email I found the hemisphere
average values, but the values at each vertex and in each ROI will be very
helpful!

I tried the command you provided in tkmedit and it looks perfect - thanks!
But when I try what I think is the corresponding command in freeview:

freeview -v SUBJ/mri/brainmask.mgz   SUBJ/mri/T1.mgz -f
SUBJ/surf/lh.pial-outer-smoothed
the images don't align (see attached).  Am I doing something wrong?

~ Maria
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Re: [Freesurfer] Pial surface with point-to-point correspondance between subjects

2014-10-29 Thread Alexandre Routier
Okay, thanks for the answer, I'll have a look on this software.

Alexandre

2014-10-29 16:05 GMT+01:00 Bruce Fischl fis...@nmr.mgh.harvard.edu:

 no, but I think SUMA does. Check it out. I'll cc Ziad so he can chime in.

 cheers
 Bruce
 On
 Wed, 29 Oct 2014, Douglas N Greve wrote:

  This is not something we support.
 
  On 10/29/2014 10:32 AM, Alexandre Routier wrote:
  What I wanted to say is that there is the exact number of points of
  the pial surface for each subject and if I look to the i-th vertex of
  the pial surface of a given subject, it should be located on the same
  area for another subject.
 
  Alexandre
 
  2014-10-29 15:25 GMT+01:00 Douglas N Greve gr...@nmr.mgh.harvard.edu
  mailto:gr...@nmr.mgh.harvard.edu:
 
 
  I'm not sure what you mean by working with the pial surfaces with
  respect to point-to-point correspondence. Can you give more info?
  doug
 
  On 10/29/2014 06:29 AM, Alexandre Routier wrote:
  Dear all,
 
  I would like to work with the pial surfaces of my database and more
  particularly with a point-to-point correspondance between each
  subject. But I didn't find how to do that, only for longitudinal
  analysis of a single subject which I am not interested.
 
  Thanks in advance for you help,
  Alexandre
 
 
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Re: [Freesurfer] LGI fails for fsaverage

2014-10-29 Thread Pierre Mégevand
Unfortunately, our pre-implant MR was acquired with double-dose gadolinium
and we can't seem to extract the pial surface from it.


have you tried using bbregister to register post-op MRI with the pre-op
surfaces?
On Wed, 29 Oct 2014, Pierre M?gevand wrote:

 Our usual method for electrode localization remains in the patient's
space:
 co-register post-op MR and CT with pre-op MR brainmask (our reference
space)
 and snap electrodes to patient's outer pial surface.

 My idea was: register the patient's (crappy) brainmask volume to the
 Talairach fsaverage volume (not surface), which I can correct manually;
 use the Talairach.xfm transform to bring the electrodes into that same
 fsaverage volume, and then snap the electrodes to fsaverage's outer pial
 surface. But that last step I can't perform. I'm aware that the
localization
 would be pretty inaccurate.
 I'll look into what you suggest Marie. In case all else fails, the last
 resort is to show the actual post-op MR and CT slices for electrodes of
 interest, but that just does not look as appealing as pial surfaces!

 --
 Pierre M?gevand, MD, PhD
 PLOS Neuro Community editor - Follow us on Twitter
 Postdoc @?Feinstein Institute for Medical Research (NY, USA)
 Follow me on Twitter - Read my blog here

 On Wed, Oct 29, 2014 at 12:29 AM, Marie Schaer marie.sch...@unige.ch
 wrote:

 So what I don't get in your pipeline is how you'll register the
 post-op brain to fsaverage if you don't have any cortical surface in
 the post-op??

 If I were you, if you want precise registration that includes the
 sulci, I'd go with the white surface from the pre-op gadolinium scan.
 And if you just want a rough registration of the skull shape, then you
 can probably find a way to create the outer surface directly on the
 gadolinium scan: if your brain mask is good, then mris_fill should
 work (maybe you need to binarize the data first (in any case a few
 lines of code in matlab should do the trick). If the brain mask is not
 good due to gadolinium, then either playing with mri_watershed (and
 maybe try mri_fill to separate the hemispheres / pons and cerebellum)
 and then mris_fill for the tessellation. Or if it doesn't work with
 mri_watershed,?playing a bit with threshold with another
 skull-stripping program (e.g. MRIcro), then importing the volume back
 in FreeSurfer and use mris_fill to get a good tessellation. Both
 solutions will need you to play a bit, but I guess you cannot really
 afford to simply throw these data and take another subject!?

 Good luck,

 Marie



 On Oct 28, 2014, at 2:57 PM, Pierre M?gevand
 pierre.megev...@gmail.com wrote:

   You're right, we can't use the post-op surface because of
   the deformation caused by surgery and the electrode
   artifacts.
 Getting a surface right from the brainmask would be OK, if we
 can't get anything better, but the nice thing about using the
 fsaverage surface is that you can plot and compare electrode
 locations from multiple patients. Just in case we have nothing
 better, though, how would you do it?

 Thanks again!

 --
 Pierre M?gevand, MD, PhD
 PLOS Neuro Community editor - Follow us on Twitter
 Postdoc @?Feinstein Institute for Medical Research (NY, USA)
 Follow me on Twitter - Read my blog here

 On Tue, Oct 28, 2014 at 5:23 PM, Marie Schaer
 marie.sch...@unige.ch wrote:

 Hi Pierre,

 Tricky question. So you can't really use the?post-op
 cortical surface for this participant, right? Otherwise I
 would simply use the outer smoothed pial for this subject
 directly, which would be much more similar to the pre-op
 than the outer surface from the fsaverage (?).?Otherwise,
 with the gadolinium MRI, maybe you can still get an
 adequate white surface, but I'm not sure that it would
 help you. The other option is to use the brain mask volume
 (which may work even with gadolinium if you are lucky,
 otherwise you can play with the watershed parameters), and
 tesselate a surface directly on this volume. But you'll
 get the two hemispheres at once (and probably the
 cerebellum as well), which may not be what you want?

 Best,

 Marie


 On Oct 28, 2014, at 2:10 PM, Pierre M?gevand
 pierre.megev...@gmail.com
 ?wrote:

   Thanks Marie. Here is what I'm trying to do.
   In fact, all I need from LGI are the first few
   steps, until ?h.pial-outer-smoothed has been
   generated. I'm not actually interested in the
   local GI for fsaverage.

   Our intra-cranial electrode localization
   method relies on post-implant CT and MRI scans
   to localize the electrodes, and a pre-implant
   MR scan to which we co-register the post-op
   exams and to whose smoothed outer pial surface
   we then snap the electrodes to, in order to
   account for the brain shift caused by the
   implantation procedure (Dykstra et al., 2012).

   Now, for one of our patients, the pre-op MRI
   was acquired with a lot of gadolinium, and we
   can't get Freesurfer to compute the 

Re: [Freesurfer] LGI analysis of single subject

2014-10-29 Thread Marie Schaer

Hi Maria,

I have to say that I rarely use freeview, I prefer tkmedit and tksurfer that I 
know better. So I didn't realize that the images were shifted, I guess it's 
some preference in how to read the surface. I just tried and have the same kind 
of shift when using freeview, so I don't think you are doing something wrong. 
Unless someone else know how to correct for the shift, I would advise you to 
use tkmedit...

Best,

Marie


On Oct 29, 2014, at 10:27 AM, Maria Holland 
mho...@stanford.edumailto:mho...@stanford.edu
 wrote:

Hi Marie -

Thanks for your response.  After sending my email I found the hemisphere 
average values, but the values at each vertex and in each ROI will be very 
helpful!

I tried the command you provided in tkmedit and it looks perfect - thanks!  But 
when I try what I think is the corresponding command in freeview:

freeview -v SUBJ/mri/brainmask.mgz   SUBJ/mri/T1.mgz -f   
SUBJ/surf/lh.pial-outer-smoothed

the images don't align (see attached).  Am I doing something wrong?

~ Maria
Screen Shot 2014-10-29 at 10.23.56 
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[Freesurfer] NIH funded postdoctoral position at Harvard Medical School/Brigham and Women's Hospital

2014-10-29 Thread Emily Goard Jacobs
Professor Jill Goldstein is recruiting a postdoctoral fellow with expertise
in affective or cognitive neuroscience to join her lab, the CNL-SD (
http://cnl-sd.bwh.harvard.edu)



*Job Description*



This position requires the individual to have expertise in functional
MRI.  Experience
with psychiatric disorders is preferable.  Knowledge of paradigm
development, data analytic software (e.g., SPM, FSL), and statistical
underpinnings of fMRI are required.



Responsibilities of this position include analyses of fMRI studies of the
stress response, mood and anxiety, and hormonal responses; fetal
programming of sex differences in mood and psychotic disorders; and
implementation and analyses involved in a new neurostimulation study of
mood and autonomic nervous system function.  Thus, the position includes
implementing methods for the analysis of fMRI data; developing
project-specific methods when necessary (i.e., ROI analysis); utilization
of advanced statistical methods to analyze fMRI, psychophysiological and
serology data; preparation of manuscripts for publication; preparation of
study findings and presentation at professional meetings; review and
summarization of relevant literature for manuscript background and grant
preparation; supervision of research assistant working on the study.



There are many opportunities for education and growth in multiple domains
in which we operate:  neuroendocrinology, further neuroimaging training,
neuroanatomy, neuro-immune interface.  We collaborate with world-class
scientists who are part of Brigham and Women’s Hospital, Massachusetts
General Hospital, and others outside of the Harvard system.



Applicant should have a PhD or ScD in clinical psychology, neuropsychology,
and/or neuroscience or have an MD with fMRI expertise.  We are committed to
diversity, and qualified women and minorities are strongly encouraged to
apply.



Please email a CV, cover letter of interest, 2-3 written references,
and a *brief
*writing sample to Ms. Abby Brockman*, (abrock...@partners.org
abrock...@partners.org), *Administrative Assistant to Jill Goldstein,
PhD, Professor of Psychiatry and Medicine, Harvard Medical School, Director
of Research, Connors Center for Women’s Health and Gender Biology, Brigham
and Women’s Hospital, Boston, MA 02120.
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[Freesurfer] FLASH protocol

2014-10-29 Thread Le Wang
Hi,

I want to do source localization on 128-channel EEG. For that, I need to
create 3-layer head models for our subjects. However, our current MRI
protocol only includes MPRAGE.

I've talked with the (f)MRI team on our project about adding a single FLASH
scan in their protocol. They are mainly concerned about the time
requirement.

So my questions are:

1) Is it possible to get a decent 3-layer head model just from MPRAGE using
FreeSurfer or other tools like SPM?

2) If we have to use FLASH, which protocol we should use?

I found one at
https://surfer.nmr.mgh.harvard.edu/fswiki/FreeSurferWiki?action=AttachFiledo=gettarget=FreeSurfer_Suggested_Morphometry_Protocols.pdf

I don't know if this is the most recent one -- is there a newer FLASH
protocol that can produce decent skull boundaries and takes less time to
run.

3) Is there a FLASH protocol already imported on Bay 1 (Skyra scanner) at
Martinos (where the MPRAGE was run)? If not, is it ok to run FLASH and
MPRAGE on different scanners for the same subject?

I know this is a lot of questions. I really appreciate any responses.

Thanks!
Le
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Re: [Freesurfer] LGI fails for fsaverage

2014-10-29 Thread Douglas N Greve

That is not what Bruce is suggesting. Try to register the post-op to the 
pre-op using bbregister. You can then map the pre-op surfaces to the 
post-op brain

On 10/29/2014 01:58 PM, Pierre Mégevand wrote:
 Unfortunately, our pre-implant MR was acquired with double-dose 
 gadolinium and we can't seem to extract the pial surface from it.


 have you tried using bbregister to register post-op MRI with the pre-op
 surfaces?
 On Wed, 29 Oct 2014, Pierre M?gevand wrote:

  Our usual method for electrode localization remains in the patient's 
 space:
  co-register post-op MR and CT with pre-op MR brainmask (our reference 
 space)
  and snap electrodes to patient's outer pial surface.
 
  My idea was: register the patient's (crappy) brainmask volume to the
  Talairach fsaverage volume (not surface), which I can correct manually;
  use the Talairach.xfm transform to bring the electrodes into that same
  fsaverage volume, and then snap the electrodes to fsaverage's outer pial
  surface. But that last step I can't perform. I'm aware that the 
 localization
  would be pretty inaccurate.
  I'll look into what you suggest Marie. In case all else fails, the last
  resort is to show the actual post-op MR and CT slices for electrodes of
  interest, but that just does not look as appealing as pial surfaces!
 
  --
  Pierre M?gevand, MD, PhD
  PLOS Neuro Community editor - Follow us on Twitter
  Postdoc @?Feinstein Institute for Medical Research (NY, USA)
  Follow me on Twitter - Read my blog here
 
  On Wed, Oct 29, 2014 at 12:29 AM, Marie Schaer marie.sch...@unige.ch 
 mailto:marie.sch...@unige.ch
  wrote:
 
  So what I don't get in your pipeline is how you'll register the
  post-op brain to fsaverage if you don't have any cortical surface in
  the post-op??
 
  If I were you, if you want precise registration that includes the
  sulci, I'd go with the white surface from the pre-op gadolinium scan.
  And if you just want a rough registration of the skull shape, then you
  can probably find a way to create the outer surface directly on the
  gadolinium scan: if your brain mask is good, then mris_fill should
  work (maybe you need to binarize the data first (in any case a few
  lines of code in matlab should do the trick). If the brain mask is not
  good due to gadolinium, then either playing with mri_watershed (and
  maybe try mri_fill to separate the hemispheres / pons and cerebellum)
  and then mris_fill for the tessellation. Or if it doesn't work with
  mri_watershed,?playing a bit with threshold with another
  skull-stripping program (e.g. MRIcro), then importing the volume back
  in FreeSurfer and use mris_fill to get a good tessellation. Both
  solutions will need you to play a bit, but I guess you cannot really
  afford to simply throw these data and take another subject!?
 
  Good luck,
 
  Marie
 
 
 
  On Oct 28, 2014, at 2:57 PM, Pierre M?gevand
  pierre.megev...@gmail.com mailto:pierre.megev...@gmail.com wrote:
 
  You're right, we can't use the post-op surface because of
  the deformation caused by surgery and the electrode
  artifacts.
  Getting a surface right from the brainmask would be OK, if we
  can't get anything better, but the nice thing about using the
  fsaverage surface is that you can plot and compare electrode
  locations from multiple patients. Just in case we have nothing
  better, though, how would you do it?
 
  Thanks again!
 
  --
  Pierre M?gevand, MD, PhD
  PLOS Neuro Community editor - Follow us on Twitter
  Postdoc @?Feinstein Institute for Medical Research (NY, USA)
  Follow me on Twitter - Read my blog here
 
  On Tue, Oct 28, 2014 at 5:23 PM, Marie Schaer
  marie.sch...@unige.ch mailto:marie.sch...@unige.ch wrote:
 
  Hi Pierre,
 
  Tricky question. So you can't really use the?post-op
  cortical surface for this participant, right? Otherwise I
  would simply use the outer smoothed pial for this subject
  directly, which would be much more similar to the pre-op
  than the outer surface from the fsaverage (?).?Otherwise,
  with the gadolinium MRI, maybe you can still get an
  adequate white surface, but I'm not sure that it would
  help you. The other option is to use the brain mask volume
  (which may work even with gadolinium if you are lucky,
  otherwise you can play with the watershed parameters), and
  tesselate a surface directly on this volume. But you'll
  get the two hemispheres at once (and probably the
  cerebellum as well), which may not be what you want?
 
  Best,
 
  Marie
 
 
  On Oct 28, 2014, at 2:10 PM, Pierre M?gevand
  pierre.megev...@gmail.com mailto:pierre.megev...@gmail.com
  ?wrote:
 
  Thanks Marie. Here is what I'm trying to do.
  In fact, all I need from LGI are the first few
  steps, until ?h.pial-outer-smoothed has been
  generated. I'm not actually interested in the
  local GI for fsaverage.
 
  Our intra-cranial electrode localization
  method relies on post-implant CT and MRI scans
  to localize the 

Re: [Freesurfer] permission denied

2014-10-29 Thread Z K
I beleive it should have a lower case X, as in:

chmod -R a+x freesurfer/bin

-Zeke

On 10/28/2014 01:19 AM, Ali Radaideh wrote:
 Dear Douglas

 Thanks for your reply. unfortunatey I still get the same error. Here is
 the terminal output. Is there anything else I can do?

  freesurfer-Linux-centos6_x86_64-stable-pub-v5.3.0 
 Setting up environment for FreeSurfer/FS-FAST (and FSL)
 FREESURFER_HOME   /usr/local/freesurfer
 FSFAST_HOME   /usr/local/freesurfer/fsfast
 FSF_OUTPUT_FORMAT nii.gz
 SUBJECTS_DIR  /usr/local/freesurfer/subjects
 MNI_DIR   /usr/local/freesurfer/mni
 FSL_DIR   /usr/local/fsl
 imaging@imaging-ThinkCentre-23:~$ tcsh
 imaging-ThinkCentre-23:~ tkmedit
 /usr/local/freesurfer/bin/tkmedit: Permission denied.
 imaging-ThinkCentre-23:~


 On Mon, Oct 27, 2014 at 5:21 AM, Douglas Greve
 gr...@nmr.mgh.harvard.edu mailto:gr...@nmr.mgh.harvard.edu wrote:


 Try chmod -R a+X freesurfer/bin


 On 10/26/14 1:57 PM, Ali Radaideh wrote:
 Dear FreeSurfer users,

 I am using freesurfer on 16 PCs (Ubuntu 14.04 64 bit). One of the
 PCs has the latest version of freesurfer 5.3.0 while the others
 have the version 5.0.0. The PC that is installed with the latest
 version freesurfer 5.3.0 does not allow me to run any command and
 everytime I try a command such such as tkmedit i get the following
 error
 /usr/local/freesurfer/bin/tkmedit: permission denied.

 I have tried to change the permission settings
 sudo chown -R imaging:imaging freesurfer

 but did not work.

 Any ideas why is this happening although I have done the same
 thing to other PCs and they are working fine.

 ​Thanks in advance,
 Ali​

 --
 /Ali M. Al-Radaideh. PhD
 Assistant Professor
 Head of Department of Medical Imaging
 Vice Dean of the Faculty of Allied Health Sciences
 The Hashemite University,
 Zarqa, Jordan
 W.phone +962 5 390 ext.5422, 5355, 5364
 Email: ali.radai...@hu.edu.jo mailto:ali.radai...@hu.edu.jo
 /
 /webpage: http://staff.hu.edu.jo/Default.aspx?id=ABZUPDzYeqM=/



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 the e-mail
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 --
 /Ali M. Al-Radaideh. PhD
 Assistant Professor
 Head of Department of Medical Imaging
 Vice Dean of the Faculty of Allied Health Sciences
 The Hashemite University,
 Zarqa, Jordan
 W.phone +962 5 390 ext.5422, 5355, 5364
 Email: ali.radai...@hu.edu.jo mailto:ali.radai...@hu.edu.jo
 /
 /webpage: http://staff.hu.edu.jo/Default.aspx?id=ABZUPDzYeqM=/



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[Freesurfer] Venous system on 3D models

2014-10-29 Thread rwlod...@uic.edu
Hello my names Rich. I am working on a project that involves creating 3D
models of patient brains and placing ECoG (Electrocorticography) leads on
these models. I have intra-operative pictures of the leads placed on the
subjects and I'm using these pictures to attempt to accurately place the
leads. However, as you might guess, the 3D models are very different from
looking at a live brain and the true sulcal and gyral pattern is difficult
to determine from the pictures. I was wondering if it is possible to have
freesurfer create or mark, in some way, the veins on the models so that I
can use the venous system as points of reference when placing the leads.
If not, is there a better way to do so that you can think of? I am
relatively new to freesurfer so I don't fully understand its capability
yet. Thanks!!

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[Freesurfer] Local gyrification index

2014-10-29 Thread Sterling, Nicholas
Hello,

I am trying to obtain estimates for the local gyrification index (LGI) using 
Freesurfer. I have tried to compute LGI via two different commands... 
mris_compute_lgi --i lh.pial and  recon-all -lgi -s subjectName. Both of 
these return the same error after running for a while...

..
Saving label file 
//FS/subjects/test/surf/tmp-mris_compute_lgi-lh.pial/lh.pial.029901.label
Connecting and filling vertices in path at fillseed 69178
Finding 
path.
 done
Filling 69178
nlabel 9709
Saving label file 
//FS/subjects/test/surf/tmp-mris_compute_lgi-lh.pial/lh.pial.030001.label
Connecting and filling vertices in path at fillseed 68070
Finding 
path.Killed
ERROR: mri_path2label --confillxfn lh.pial 
//FS/subjects/test/surf/tmp-mris_compute_lgi-lh.pial/mri_path2label.input
 failed!

I've tried a couple of subjects and I get the error above. Would anyone please 
be able to offer suggestions regarding how to resolve this issue?

Many thanks for taking the time to read my inquiry.

Nick
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Re: [Freesurfer] 7T reconstruction

2014-10-29 Thread B V
Thanks! Best, B

On Wed, Oct 29, 2014 at 10:34 AM, Douglas N Greve gr...@nmr.mgh.harvard.edu
 wrote:


 Create a voxel shift map using epidewarp.fsl (only the shift map is
 needed, don't use this to dewarp the data). Save this in
 bold/b0dcmap.nii (or nii.gz). When you run preproc-sess and
 mkanalysis-sess add -b0dc (stands for B0 distortion correction).
 doug



 On 10/28/2014 01:14 PM, B V wrote:
  Hello,
  I am interested in using functional data collected from 7t using
  freesurfer and fsfast. We would like to use EPI field maps to warp
  this data to 3T anatomical space. Can anyone guide me as to how to do
  this.
  Best,
  B
 
 
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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
 Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/

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[Freesurfer] Unknown problem with fsgd file

2014-10-29 Thread Bronwyn Overs

Dear Freesurfer Mailing list,

I have been attempting to run mri_glmfit using a complicated fsgd file 
(1 categorical varible with 5 levels, 3 categorical variables with 2 
levels, age as covariate). When I run the command, I receive the 
following error:

gdfReadHeader: reading site-gender-group-riskhaplotype.fsgd
Input line 5, subjid = 100121, class 
siteMelbourne-anyRiskAnyRisk-genderFemale-groupControl not defined

FSGDF Format Error: file = site-gender-group-riskhaplotype.fsgd, tag=Input

I have double checked the fsgd file and confirmed that the class for 
participant 100121 was specific correctly at the beginning of the file 
(correct spelling and case was used). So  I cannot identify the source 
of the error. Can you advise me as to what may be going wrong?


My full fsgd file begins like this (I have 389 subjects but have 
provided only the first 20 for brevity):

GroupDescriptorFile 1
Title GLM_SiteGender
Class siteBrisbane-anyProtNoProt-genderMale-groupCase
Class siteBrisbane-anyProtNoProt-genderFemale-groupCase
Class siteBrisbane-anyProtNoProt-genderMale-groupControl
Class siteBrisbane-anyProtNoProt-genderFemale-groupControl
Class siteBrisbane-anyProtAnyProt-genderMale-groupCase
Class siteBrisbane-anyProtAnyProt-genderFemale-groupCase
Class siteBrisbane-anyProtAnyProt-genderMale-groupControl
Class siteBrisbane-anyProtAnyProt-genderFemale-groupControl
Class siteMelbourne-anyProtNoProt-genderMale-groupCase
Class siteMelbourne-anyProtNoProt-genderFemale-groupCase
Class siteMelbourne-anyProtNoProt-genderMale-groupControl
Class siteMelbourne-anyProtNoProt-genderFemale-groupControl
Class siteMelbourne-anyProtAnyProt-genderMale-groupCase
Class siteMelbourne-anyProtAnyProt-genderFemale-groupCase
Class siteMelbourne-anyProtAnyProt-genderMale-groupControl
Class siteMelbourne-anyProtAnyProt-genderFemale-groupControl
Class siteNewcastle-anyProtNoProt-genderMale-groupCase
Class siteNewcastle-anyProtNoProt-genderFemale-groupCase
Class siteNewcastle-anyProtNoProt-genderMale-groupControl
Class siteNewcastle-anyProtNoProt-genderFemale-groupControl
Class siteNewcastle-anyProtAnyProt-genderMale-groupCase
Class siteNewcastle-anyProtAnyProt-genderFemale-groupCase
Class siteNewcastle-anyProtAnyProt-genderMale-groupControl
Class siteNewcastle-anyProtAnyProt-genderFemale-groupControl
Class sitePerth-anyProtNoProt-genderMale-groupCase
Class sitePerth-anyProtNoProt-genderFemale-groupCase
Class sitePerth-anyProtNoProt-genderMale-groupControl
Class sitePerth-anyProtNoProt-genderFemale-groupControl
Class sitePerth-anyProtAnyProt-genderMale-groupCase
Class sitePerth-anyProtAnyProt-genderFemale-groupCase
Class sitePerth-anyProtAnyProt-genderMale-groupControl
Class sitePerth-anyProtAnyProt-genderFemale-groupControl
Class siteSydney-anyProtNoProt-genderMale-groupCase
Class siteSydney-anyProtNoProt-genderFemale-groupCase
Class siteSydney-anyProtNoProt-genderMale-groupControl
Class siteSydney-anyProtNoProt-genderFemale-groupControl
Class siteSydney-anyProtAnyProt-genderMale-groupCase
Class siteSydney-anyProtAnyProt-genderFemale-groupCase
Class siteSydney-anyProtAnyProt-genderMale-groupControl
Class siteSydney-anyProtAnyProt-genderFemale-groupControl
Variables age
Input 100105SA sitePerth-anyProtNoProt-genderMale-groupCase 23
Input 100112SA siteBrisbane-anyProtAnyProt-genderMale-groupCase 22
Input 100117SA siteBrisbane-anyProtNoProt-genderMale-groupCase 39
Input 100118 siteBrisbane-anyProtNoProt-genderFemale-groupCase 30
Input 100121 siteMelbourne-anyProtAnyProt-genderFemale-groupControl 21
Input 100122 siteMelbourne-anyProtAnyProt-genderMale-groupControl 53
Input 100151 siteMelbourne-anyProtNoProt-genderFemale-groupControl 58
Input 100185SA siteBrisbane-anyProtNoProt-genderFemale-groupControl 24
Input 100187 siteBrisbane-anyProtNoProt-genderMale-groupCase 24
Input 100189 siteBrisbane-anyProtNoProt-genderFemale-groupCase 21
Input 100190 siteSydney-anyProtNoProt-genderMale-groupControl 41
Input 100191 siteMelbourne-anyProtAnyProt-genderFemale-groupControl 19
Input 100193SA siteSydney-anyProtNoProt-genderMale-groupControl 26
Input 100196 siteBrisbane-anyProtNoProt-genderMale-groupControl 55
Input 100197SA siteBrisbane-anyProtNoProt-genderFemale-groupCase 30
Input 100200SA siteBrisbane-anyProtNoProt-genderMale-groupControl 39
Input 100204 siteSydney-anyProtAnyProt-genderFemale-groupControl 50
Input 100208 siteBrisbane-anyProtNoProt-genderMale-groupControl 25
Input 100209SA siteBrisbane-anyProtAnyProt-genderMale-groupCase 35
Input 100214 siteSydney-anyProtAnyProt-genderMale-groupCase 44

The mri_glmfit command I am using is as follows:
mri_glmfit --y site-gender-group-prothaplotype.thick.lh.10.mgh --fsgd 
site-gender-group-prothaplotype.fsgd dods --C gender.mtx --C group.mtx 
--C haplotype.mtx --C groupXgender.mtx --C haplotypeXgender.mtx --C 
groupXhaplotype.mtx --C genderXgroupXhaplotype.mtx --surf fsaverage lh 
--cortex --glmdir site-gender-group-prothaplotype.thick.lh.glmdir

--

Kind regards,

Bronwyn Overs
Research Assistant


Re: [Freesurfer] adding insula voxels

2014-10-29 Thread Adam Mezher
Hi Bruce,

Sorry for not clarifying. A number of subjects in our set have underestimated 
insula (usually anatomical right insula but sometimes both). I just uploaded an 
example to the ftp. 

I don’t think control points or wm edits can help with some of these so I 
wanted to see how we could go about editing them manually by adding the correct 
label to the empty voxels with the Edit Segmentation tool in tkmedit. 

Thank you,
Adam
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Re: [Freesurfer] Venous system on 3D models

2014-10-29 Thread Zachary Greenberg
Hi Rich,

Do you have a post-operative CT scan of your ECoG patient? If you have that
and a high-res T1, you can get very accurate reconstruction of electrode
positions on the brain surface by corregistering the two.

-zack

On Wed, Oct 29, 2014 at 3:32 PM, rwlod...@uic.edu rwlod...@uic.edu wrote:

 Hello my names Rich. I am working on a project that involves creating 3D
 models of patient brains and placing ECoG (Electrocorticography) leads on
 these models. I have intra-operative pictures of the leads placed on the
 subjects and I'm using these pictures to attempt to accurately place the
 leads. However, as you might guess, the 3D models are very different from
 looking at a live brain and the true sulcal and gyral pattern is difficult
 to determine from the pictures. I was wondering if it is possible to have
 freesurfer create or mark, in some way, the veins on the models so that I
 can use the venous system as points of reference when placing the leads.
 If not, is there a better way to do so that you can think of? I am
 relatively new to freesurfer so I don't fully understand its capability
 yet. Thanks!!

 ___
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 Freesurfer@nmr.mgh.harvard.edu
 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
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 but does not contain patient information, please contact the sender and
 properly
 dispose of the e-mail.




-- 
*Zachary Greenberg*
*Assistant Imaging Specialist*
*Department of Neurological Surgery*
*University of California, San Francisco*
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Re: [Freesurfer] Venous system on 3D models

2014-10-29 Thread rwlod...@uic.edu
I have some post-op CT's for some of my patients but not all, do you have
a link or could you explain how to coregister so I can do it for the ones
I have? Thank you!

On Wed, October 29, 2014 9:18 pm, Zachary Greenberg wrote:
 Hi Rich,

 Do you have a post-operative CT scan of your ECoG patient? If you have
 that
 and a high-res T1, you can get very accurate reconstruction of electrode
 positions on the brain surface by corregistering the two.

 -zack

 On Wed, Oct 29, 2014 at 3:32 PM, rwlod...@uic.edu rwlod...@uic.edu
 wrote:

 Hello my names Rich. I am working on a project that involves creating 3D
 models of patient brains and placing ECoG (Electrocorticography) leads
 on
 these models. I have intra-operative pictures of the leads placed on the
 subjects and I'm using these pictures to attempt to accurately place the
 leads. However, as you might guess, the 3D models are very different
 from
 looking at a live brain and the true sulcal and gyral pattern is
 difficult
 to determine from the pictures. I was wondering if it is possible to
 have
 freesurfer create or mark, in some way, the veins on the models so that
 I
 can use the venous system as points of reference when placing the leads.
 If not, is there a better way to do so that you can think of? I am
 relatively new to freesurfer so I don't fully understand its capability
 yet. Thanks!!

 ___
 Freesurfer mailing list
 Freesurfer@nmr.mgh.harvard.edu
 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
 dispose of the e-mail.




 --
 *Zachary Greenberg*
 *Assistant Imaging Specialist*
 *Department of Neurological Surgery*
 *University of California, San Francisco*
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 HelpLine at
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Re: [Freesurfer] Venous system on 3D models

2014-10-29 Thread Zachary Greenberg
Rich,

You need SPM preferably (http://www.fil.ion.ucl.ac.uk/spm/) for matlab, and
freesurfer.

First run recon-all on the patients T1 (after acpc aligning in Spm). Then
take the resultant orig.mgz file (convert to .nii using mri_convert
orig.mgz orig.nii), and corregister the post-op CT to it using SPM's
normalized mutual info. routine. To do this: 1.) open matlab, 2.)type spm
at the prompt, 3.) chose fMRI from the gui pop up, 4.) pick corregister
(est. and write) from the top left of the spm gui. Then chose the Orig.nii
as the reference image, and the patients pos-op CT as the target.

Open the corregisterd CT (rCT.nii), the Orig.nii, and pial surface in
freeview. Click on each electrode in the CT, and copy the xyz coords from
the bottom left into a text file or matlab matrix (it will list the surface
RAS coords in bottem left of freeview, which is what you want to display on
the freesurfer pial surface).

Let me know when you get that far and I'll send you a link to some code
that will help you visualize the pial surface with overlaid electrodes.

-zack

On Wed, Oct 29, 2014 at 7:28 PM, rwlod...@uic.edu rwlod...@uic.edu wrote:

 I have some post-op CT's for some of my patients but not all, do you have
 a link or could you explain how to coregister so I can do it for the ones
 I have? Thank you!

 On Wed, October 29, 2014 9:18 pm, Zachary Greenberg wrote:
  Hi Rich,
 
  Do you have a post-operative CT scan of your ECoG patient? If you have
  that
  and a high-res T1, you can get very accurate reconstruction of electrode
  positions on the brain surface by corregistering the two.
 
  -zack
 
  On Wed, Oct 29, 2014 at 3:32 PM, rwlod...@uic.edu rwlod...@uic.edu
  wrote:
 
  Hello my names Rich. I am working on a project that involves creating 3D
  models of patient brains and placing ECoG (Electrocorticography) leads
  on
  these models. I have intra-operative pictures of the leads placed on the
  subjects and I'm using these pictures to attempt to accurately place the
  leads. However, as you might guess, the 3D models are very different
  from
  looking at a live brain and the true sulcal and gyral pattern is
  difficult
  to determine from the pictures. I was wondering if it is possible to
  have
  freesurfer create or mark, in some way, the veins on the models so that
  I
  can use the venous system as points of reference when placing the leads.
  If not, is there a better way to do so that you can think of? I am
  relatively new to freesurfer so I don't fully understand its capability
  yet. Thanks!!
 
  ___
  Freesurfer mailing list
  Freesurfer@nmr.mgh.harvard.edu
  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
  dispose of the e-mail.
 
 
 
 
  --
  *Zachary Greenberg*
  *Assistant Imaging Specialist*
  *Department of Neurological Surgery*
  *University of California, San Francisco*
  ___
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  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
  dispose of the e-mail.
 


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

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contains patient information, please contact the Partners Compliance HelpLine at
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Re: [Freesurfer] Venous system on 3D models

2014-10-29 Thread rwlod...@uic.edu
Thank you so much! This will take me some time, but i'll get back to you
when I get that far.

On Wed, October 29, 2014 9:47 pm, Zachary Greenberg wrote:
 Rich,

 You need SPM preferably (http://www.fil.ion.ucl.ac.uk/spm/) for matlab,
 and
 freesurfer.

 First run recon-all on the patients T1 (after acpc aligning in Spm). Then
 take the resultant orig.mgz file (convert to .nii using mri_convert
 orig.mgz orig.nii), and corregister the post-op CT to it using SPM's
 normalized mutual info. routine. To do this: 1.) open matlab, 2.)type spm
 at the prompt, 3.) chose fMRI from the gui pop up, 4.) pick corregister
 (est. and write) from the top left of the spm gui. Then chose the Orig.nii
 as the reference image, and the patients pos-op CT as the target.

 Open the corregisterd CT (rCT.nii), the Orig.nii, and pial surface in
 freeview. Click on each electrode in the CT, and copy the xyz coords from
 the bottom left into a text file or matlab matrix (it will list the
 surface
 RAS coords in bottem left of freeview, which is what you want to display
 on
 the freesurfer pial surface).

 Let me know when you get that far and I'll send you a link to some code
 that will help you visualize the pial surface with overlaid electrodes.

 -zack

 On Wed, Oct 29, 2014 at 7:28 PM, rwlod...@uic.edu rwlod...@uic.edu
 wrote:

 I have some post-op CT's for some of my patients but not all, do you
 have
 a link or could you explain how to coregister so I can do it for the
 ones
 I have? Thank you!

 On Wed, October 29, 2014 9:18 pm, Zachary Greenberg wrote:
  Hi Rich,
 
  Do you have a post-operative CT scan of your ECoG patient? If you have
  that
  and a high-res T1, you can get very accurate reconstruction of
 electrode
  positions on the brain surface by corregistering the two.
 
  -zack
 
  On Wed, Oct 29, 2014 at 3:32 PM, rwlod...@uic.edu rwlod...@uic.edu
  wrote:
 
  Hello my names Rich. I am working on a project that involves creating
 3D
  models of patient brains and placing ECoG (Electrocorticography)
 leads
  on
  these models. I have intra-operative pictures of the leads placed on
 the
  subjects and I'm using these pictures to attempt to accurately place
 the
  leads. However, as you might guess, the 3D models are very different
  from
  looking at a live brain and the true sulcal and gyral pattern is
  difficult
  to determine from the pictures. I was wondering if it is possible to
  have
  freesurfer create or mark, in some way, the veins on the models so
 that
  I
  can use the venous system as points of reference when placing the
 leads.
  If not, is there a better way to do so that you can think of? I am
  relatively new to freesurfer so I don't fully understand its
 capability
  yet. Thanks!!
 
  ___
  Freesurfer mailing list
  Freesurfer@nmr.mgh.harvard.edu
  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
  dispose of the e-mail.
 
 
 
 
  --
  *Zachary Greenberg*
  *Assistant Imaging Specialist*
  *Department of Neurological Surgery*
  *University of California, San Francisco*
  ___
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  Freesurfer@nmr.mgh.harvard.edu
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  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
  dispose of the e-mail.
 


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

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