Re: [Freesurfer] longitudinal stream - template

2013-03-19 Thread Yolanda Vives
Hi Martin,

Thank you for your answer, but my idea was to compare the atrophy
rates when using scans at 6 months (0 - 6 months) and scans at 12
months (0 - 12 months). If my templates are built with more time
points, the results will be biased, right?

Regards,
Yolanda

2013/3/18 Martin Reuter :
> Hi Yolanda,
>
> actually it is advantageous if the template is build from more time points.
> You don't need to process the images again, just do your statistical
> analysis with the time points you are interested in.
>
> But: why restrict the statistics to a subset of the data? If you are
> interested in yearly change, you can compute that from all time points. If
> you are interested in seeing if the atrophy rate increases over time, use a
> piecewise linear model (node at 6 months) and see if the slopes increase,
> etc. Removing time points from the statistics is usually a bad idea as you
> loose power.
>
> Best, Martin
>
>
> On 03/18/2013 01:15 PM, Yolanda Vives wrote:
>>
>> Dear FreeSurfer experts,
>>
>> I have run a longitudinal study considering multiple time points (7
>> scans/subject on average) with FS 5.1. However, I am interested in the
>> percent changes between two time points only (between 0 and 6 months
>> and between 0 and 1 year). Should I run the longitudinal stream from
>> step 2 (template) two more times (1.- considering only 0 and 6 months
>> scans and 2.- considering only 0 and 12 months scans) or is it correct
>> even if my templates were built with all the time scans together?
>>
>> Thank you for your help,
>> Yolanda
>> ___
>> Freesurfer mailing list
>> Freesurfer@nmr.mgh.harvard.edu
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>>
>>
>
> --
> Dr. Martin Reuter
> 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
>
>
>
> 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
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Re: [Freesurfer] Very different results between 5.1.0 and 5.2.0

2013-03-19 Thread Yang, Daniel

Posting one of the brains.

https://yalesurvey.qualtrics.com/SE/?SID=SV_ddwW7I9yMQuCtPn


It seems to me that neither version is perfect; however, 5.2.0 is
capturing more "black spaces" in the region I'm looking at.

It's in the right hemisphere, TAL coordinate about ~ (44, -46, 20).

Given that the correlation between 5.1.0 and 5.2.0 is r = .33 in the
region I examined with my samples, it's not a systematic "predictable"
bias.

Any solution?

-- 
Yung-Jui "Daniel" Yang, PhD
Postdoctoral Researcher
Yale Child Study Center
New Haven, CT
(203) 737-5454






On 3/18/13 6:27 PM, "Matt Glasser"  wrote:

>Do the surfaces look correct in these regions?  You might post some
>screenshots of subjects who have a big difference between 5.1 and 5.2 with
>the 5.1 and 5.2 white and pial surfaces on volume slices that highlight
>the difference.  Without this kind of info, its hard to know which was
>more correct, 5.1 or 5.2.
>
>Peace,
>
>Matt.
>
>On 3/18/13 5:13 PM, "Ritobrato Datta"  wrote:
>
>>I concur. I have seen similar results in primary visual cortex from ~40
>>subjects. While fs 5.1 estimated mean thickness in the range of 1.5 to
>>1.9 in V1, fs 5.2 is giving me V1 thickness in the range of 2 to 2.3.
>>
>>Ritobrato Datta, Ph.D.
>>Post Doctoral Researcher
>>Department of Neurology
>>University of Pennsylvania School of Medicine
>>3rd Floor, Room 312
>>3710 Hamilton Walk (Goddard Laboratories)
>>Philadelphia, PA 19104-6241
>>email - rida...@mail.med.upenn.edu
>> 
>>
>>- Original Message -
>>From: Daniel Yang 
>>To: freesurfer@nmr.mgh.harvard.edu
>>Sent: Mon, 18 Mar 2013 17:44:44 -0400 (EDT)
>>Subject: [Freesurfer] Very different results between 5.1.0 and 5.2.0
>>
>>Dear FreeSurfer Experts,
>>
>>I ran FreeSurfer 5.1.0 and FreeSurfer 5.2.0 on identical set of 161
>>subjects, and I'm interested in rh_superior_temporal_sulcus_thickness in
>>particular.
>>
>>Previously, the mean thickness is 2.24 mm in 5.1.0; now it is 3.28 mm in
>>5.2.0. They are significantly different, t(160) = 56.71.
>>
>>The correlation between the two versions is r = .33
>>
>>Is this something possible?? I can't see what went wrong in my
>>procedures.
>>
>>Thanks!
>>Daniel
>>
>>--
>>Yung-Jui "Daniel" Yang, PhD
>>Postdoctoral Researcher
>>Yale Child Study Center
>>New Haven, CT
>>(203) 737-5454
>>
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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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Re: [Freesurfer] longitudinal analysis

2013-03-19 Thread Joy-Loi Chepkoech
Hello Martin,

Thank you for your swift reply.

I failed to make myself clear, and will try describing my study again. 
First, an important point: the study is not longitudinal per se, but I 
am interested in applying the methods of longitudinal analysis. I only 
have one time point, all the scans have been collected within the same 
session.

I am studying a large group of subjects whom each underwent a scan 
session with 4 scans. Each of these scans were graded for quality on a 
scale from 1-4.
An example of what I then did was to process each subject twice, once 
with the scan of quality ”1”, and a second time averaging the scans of 
quality ”1” and ”2”, thus resulting in two groups between which each 
subject is compared to itself.

Now I am attempting to set up a longitudinal analysis with this data. I 
have processed through the longitudinal stream, and I guess my question 
starts at the point of post-processing: How, if feasible, can I transfer 
the idea of “across group comparison between time point and time point 
2” to “across group comparison between 1 scan and 2 scans” in setting up 
the QDEC table and continuing from there?

I hope this make sense, your help is greatly appreciated.

Best regards,

Joy-Loi





On 2013-03-18 19:13, Martin Reuter wrote:
> Hi Joy-Loi,
> 
> so you have 2 time points? the first with a single scan, the second
> with two within-session scans that you want to average? I don't
> understand exactly what you are trying to do.  To test differences in
> reliability you'd have to scan a bunch of subjects twice in a session
> and then twice in another session.
> Then you can look at reliability when using only one scan (e.g. the
> first) or when averaging both scans in both time points. 'varying
> quality' with respect to motion also scares me a little. There can be
> individual outliers that severely affect your mean response (unless
> you have lots of subjects).
> 
> Anyway for these things you would process your results through the
> longitudinal stream (this allows you also to be unbiased with respect
> to the time point). There are several design questions to consider
> (e.g. does it make sense to include all virtual time points into the
> same base, or run everything twice: one base for the averaged images ,
> another for the single images and then compare etc. ) Either way this
> is not a standard analysis and you'd be pretty much on your own with
> how to set it up.
> 
> Best, Martin
> 
> 
> On 03/18/2013 09:02 AM, Joy-Loi Chepkoech wrote:
>> Hello FreeSurfer experts,
>> 
>> I am currently trying to systematically investigate the differences 
>> in
>> cortical and subcortical estimates that occur when performing 
>> recon-all
>> on one scan, or when averaging across scans of varying quality with
>> regard to movement.
>> 
>> I have a list of subjects that each have been processed (recon-all)
>> twice (once with one scan and once with two scans), and would like to
>> run some FreeSurfer statistical analysis on them.
>> 
>> Is it feasible to set up a longitudinal analysis similar to the one
>> described here:
>> (http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/LongitudinalTutorial)?
>> If it is, could someone assist me in setting this analysis up?
>> (I have tried following the tutorial, where I on each subject set "0
>> years" for one scan, and "1 year" for two scans in the QDEC table, 
>> but
>> the results from the QDEC analysis don't seem to agree with previous
>> SPSS results that I have).
>> 
>> Thank you,
>> 
>> Joy-Loi
>> ___
>> Freesurfer mailing list
>> Freesurfer@nmr.mgh.harvard.edu
>> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>> 
>> 
> 
> --
> Dr. Martin Reuter
> 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
> 
> 
> 
> 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 
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Re: [Freesurfer] longitudinal analysis

2013-03-19 Thread Martin Reuter
Hi Joy-Loi,

yes, you can do that using the free surfer tools (e.g. check if 'atrophy', i.e. 
change across the two methods, is different from zero, meaning if there is a 
bias).

Any of the statistical methods described here:
http://surfer.nmr.mgh.harvard.edu/fswiki/LongitudinalStatistics 
can do that.

You will find that results differ, but you will not know if they differ because 
of the 
- different quality of the scans
- difference in processing (averaging 2 scans)
- or simply the noise one would always expect from the scanner (imaging / 
positioning etc).

It would be interesting to distinguish those sources of variability. But for 
that you'd need a second time point I think.


Best, Martin



On Mar 19, 2013, at 10:47 AM, Joy-Loi Chepkoech 
 wrote:

> Hello Martin,
> 
> Thank you for your swift reply.
> 
> I failed to make myself clear, and will try describing my study again. First, 
> an important point: the study is not longitudinal per se, but I am interested 
> in applying the methods of longitudinal analysis. I only have one time point, 
> all the scans have been collected within the same session.
> 
> I am studying a large group of subjects whom each underwent a scan session 
> with 4 scans. Each of these scans were graded for quality on a scale from 1-4.
> An example of what I then did was to process each subject twice, once with 
> the scan of quality ”1”, and a second time averaging the scans of quality ”1” 
> and ”2”, thus resulting in two groups between which each subject is compared 
> to itself.
> 
> Now I am attempting to set up a longitudinal analysis with this data. I have 
> processed through the longitudinal stream, and I guess my question starts at 
> the point of post-processing: How, if feasible, can I transfer the idea of 
> “across group comparison between time point and time point 2” to “across 
> group comparison between 1 scan and 2 scans” in setting up the QDEC table and 
> continuing from there?
> 
> I hope this make sense, your help is greatly appreciated.
> 
> Best regards,
> 
> Joy-Loi
> 
> 
> 
> 
> 
> On 2013-03-18 19:13, Martin Reuter wrote:
>> Hi Joy-Loi,
>> so you have 2 time points? the first with a single scan, the second
>> with two within-session scans that you want to average? I don't
>> understand exactly what you are trying to do.  To test differences in
>> reliability you'd have to scan a bunch of subjects twice in a session
>> and then twice in another session.
>> Then you can look at reliability when using only one scan (e.g. the
>> first) or when averaging both scans in both time points. 'varying
>> quality' with respect to motion also scares me a little. There can be
>> individual outliers that severely affect your mean response (unless
>> you have lots of subjects).
>> Anyway for these things you would process your results through the
>> longitudinal stream (this allows you also to be unbiased with respect
>> to the time point). There are several design questions to consider
>> (e.g. does it make sense to include all virtual time points into the
>> same base, or run everything twice: one base for the averaged images ,
>> another for the single images and then compare etc. ) Either way this
>> is not a standard analysis and you'd be pretty much on your own with
>> how to set it up.
>> Best, Martin
>> On 03/18/2013 09:02 AM, Joy-Loi Chepkoech wrote:
>>> Hello FreeSurfer experts,
>>> I am currently trying to systematically investigate the differences in
>>> cortical and subcortical estimates that occur when performing recon-all
>>> on one scan, or when averaging across scans of varying quality with
>>> regard to movement.
>>> I have a list of subjects that each have been processed (recon-all)
>>> twice (once with one scan and once with two scans), and would like to
>>> run some FreeSurfer statistical analysis on them.
>>> Is it feasible to set up a longitudinal analysis similar to the one
>>> described here:
>>> (http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/LongitudinalTutorial)?
>>> If it is, could someone assist me in setting this analysis up?
>>> (I have tried following the tutorial, where I on each subject set "0
>>> years" for one scan, and "1 year" for two scans in the QDEC table, but
>>> the results from the QDEC analysis don't seem to agree with previous
>>> SPSS results that I have).
>>> Thank you,
>>> Joy-Loi
>>> ___
>>> Freesurfer mailing list
>>> Freesurfer@nmr.mgh.harvard.edu
>>> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>> --
>> Dr. Martin Reuter
>> 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
>> The information in this e-mail is intended only for the person to 

Re: [Freesurfer] Correspondence of Talairach coordinates from one subject to other

2013-03-19 Thread Garikoitz Lerma-Usabiaga
Hi Doug,
I tried to do what you recommended but I am encountering an inconsistency.

(Note: I obtain the same results in R (with ginv() ) and Matlab (with
pinv() ) )


Could you please have a look at the code and the values please? I don't
know what else to do right now... (it is possible to copy paste everything
in Matlab)

 ***

TalXFM = [1.040797, 0.011370, -0.069615, -0.863770;0.031794, 0.939578,
0.254677 ,-32.126083; 0.048458, -0.236663 ,1.101207, -20.946930];

Norig = [-1.0 ,  -0.0  , -0.0 , 130.38606 ;-0.0 ,
0.0  ,  1.0, -109.95447 ;-0.0,   -1.0 ,   0.0 ,
150.14441 ; 0.0,0.0  ,  0.0  ,  1.0];

Torig = [-1.0 ,   0.0 ,   0.0 , 128.0; 0.0 ,   0.0
,  1.0, -128.0; 0.0 ,  -1.0  ,  0.0 , 128.0;
0.0 ,   0.0  ,  0.0 ,   1.0];



W = TalXFM * Norig * inv(Torig);

Volume_RAS = [1, -30, 1, 1];



MNI_Talairach = W * Volume_RAS'  % Coincides with Tkmedit

 % MNI_Talairach = (0.9133; -37.3562; 7.5331)

Volume_RAS = pinv(W)*MNI_Talairach % DOES NOT COINCIDE

  % Volume_RAS = (0.4324; -2.9014; 8.7350; 3.8992)  >> shouldn't be
 [1, -30, 1, 1]; ?



Is the transformation two-way? Should it be?


Many thanks again for your help,

Gari








On Wed, Mar 13, 2013 at 10:15 AM, Douglas Greve
wrote:

>  Hi Gary, you would use the MNI305 space as the common space. Eg, Case 2
> shows you how to go from RAS of a subject to MNI305 space. You would
> reverse that to go from MNI305 space to another subject's RAS space thus
> allowing a RAS-RAS transform. If you have a surface overlay for a subject,
> you can use mri_surf2surf to transfer it to another subject.
> doug
>
>
> On 3/12/13 11:54 PM, Garikoitz Lerma-Usabiaga wrote:
>
> Thanks Doug,
> I've seen the page, but I understand that everything is within the same
> subject. I want to find the equivalencies between subjects. I mean, the
> plane y = 30 in fsaverage, will correspond to a plane with a bigger Y for a
> larger head (could be defined anatomically, the most outer point of the
> hippocampus, for example.
>
>  When finding equivalencies for surface ROIs from one subject to another
> we used label2label for example. If I have an overlay in volume space, how
> should I "move" it to another subject?
>
>  Thanks again,
> Gari
>
>
>
>  On 12/03/2013, at 20:29, Douglas Greve  wrote:
>
>   Hi Gary, check out this wiki page and let me know if you still have
> questions
> http://surfer.nmr.mgh.harvard.edu/fswiki/CoordinateSystems
> doug
>
> On 3/12/13 8:04 PM, Garikoitz Lerma-Usabiaga wrote:
>
> Hi!
> how can I translate a coordinate in talairach space of one subject
> (Colin27), to every subject in a study? For example, I would like to know
> where is the coordinate Y = +30 Talairach of Colin27 in Subject_00,
> Subject_01, etc.
>
>  Should I use vol2vol to create a volume for every subject? Is there any
> direct method with register matrices or something like that?
>
>  Thank you very much,
> Gari
>
>
> ___
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>
>
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Re: [Freesurfer] longitudinal stream - template

2013-03-19 Thread Martin Reuter
Hi Yolanda,

if you want to simulate a study where one obtains 2 time points (6 months 
apart) or 2 time points (12 months apart) and then compare the results, you 
would need to run these two independently through free surfers longitudinal 
stream (one time including 0 and 6 month, the other time including 0 and 12 
months). 
If you are interested in measuring if for whatever reason there is a change in 
the slope at 6 months (e.g. a nonlinear trajectory) you can do the piecewise 
linear model that I described below on the full dataset.

Best, Martin

On Mar 19, 2013, at 4:26 AM, Yolanda Vives  wrote:

> Hi Martin,
> 
> Thank you for your answer, but my idea was to compare the atrophy
> rates when using scans at 6 months (0 - 6 months) and scans at 12
> months (0 - 12 months). If my templates are built with more time
> points, the results will be biased, right?
> 
> Regards,
> Yolanda
> 
> 2013/3/18 Martin Reuter :
>> Hi Yolanda,
>> 
>> actually it is advantageous if the template is build from more time points.
>> You don't need to process the images again, just do your statistical
>> analysis with the time points you are interested in.
>> 
>> But: why restrict the statistics to a subset of the data? If you are
>> interested in yearly change, you can compute that from all time points. If
>> you are interested in seeing if the atrophy rate increases over time, use a
>> piecewise linear model (node at 6 months) and see if the slopes increase,
>> etc. Removing time points from the statistics is usually a bad idea as you
>> loose power.
>> 
>> Best, Martin
>> 
>> 
>> On 03/18/2013 01:15 PM, Yolanda Vives wrote:
>>> 
>>> Dear FreeSurfer experts,
>>> 
>>> I have run a longitudinal study considering multiple time points (7
>>> scans/subject on average) with FS 5.1. However, I am interested in the
>>> percent changes between two time points only (between 0 and 6 months
>>> and between 0 and 1 year). Should I run the longitudinal stream from
>>> step 2 (template) two more times (1.- considering only 0 and 6 months
>>> scans and 2.- considering only 0 and 12 months scans) or is it correct
>>> even if my templates were built with all the time scans together?
>>> 
>>> Thank you for your help,
>>> Yolanda
>>> ___
>>> Freesurfer mailing list
>>> Freesurfer@nmr.mgh.harvard.edu
>>> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>>> 
>>> 
>> 
>> --
>> Dr. Martin Reuter
>> 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
>> 
>> 
>> 
>> 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.
>> 
> 
> 

-
Dr. Martin Reuter
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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[Freesurfer] multi-echo mprage

2013-03-19 Thread Inati, Souheil (NIH/NIMH) [E]
Hi All,

I have some multi-echo mprage images from a sequence and protocol set up to 
emulate Andre's 2008 paper.  What's are the "best-practices" for using data 
from this type of sequence in Freesurfer?

Related side questions: 
I have used the suggested morphometry protocols on the FS wiki (1mm iso 
resolution, same FOV, bandwidth matched, etc)
1) are people who are using this method using 4 echoes of alternating polarity, 
or 4 echoes of the same polarity?
2) for some subjects I have also acquired a 3D T2.  Any recommendations on 
using these data together?

Thanks,
Souheil



Souheil Inati, PhD
Staff Scientist
Functional MRI Facility
NIMH/NIH/DHHS
souheil.in...@nih.gov
301-402-9409




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Re: [Freesurfer] multi-echo mprage

2013-03-19 Thread Bruce Fischl
Hi Souheil

we usually compute the RMS across echoes and give that to recon-all as a 
normal mprage. It's a reasonable (although of course not optimal) weighting 
since the earlier echoes have more signal and more contrast.

For the T2s, there's a new post-hoc procedure for deformaing the surfaces 
to match them (-T2pial or something like that in recon-all)

cheers
Bruce


On Tue, 19 Mar 2013, Inati, 
Souheil (NIH/NIMH) [E] wrote:

> Hi All,
>
> I have some multi-echo mprage images from a sequence and protocol set up to 
> emulate Andre's 2008 paper.  What's are the "best-practices" for using data 
> from this type of sequence in Freesurfer?
>
> Related side questions:
> I have used the suggested morphometry protocols on the FS wiki (1mm iso 
> resolution, same FOV, bandwidth matched, etc)
> 1) are people who are using this method using 4 echoes of alternating 
> polarity, or 4 echoes of the same polarity?
> 2) for some subjects I have also acquired a 3D T2.  Any recommendations on 
> using these data together?
>
> Thanks,
> Souheil
>
> 
>
> Souheil Inati, PhD
> Staff Scientist
> Functional MRI Facility
> NIMH/NIH/DHHS
> souheil.in...@nih.gov
> 301-402-9409
>
>
>
>
> ___
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>
>
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Re: [Freesurfer] multi-echo mprage

2013-03-19 Thread Shantanu Ghosh
Hi Souheil

I would run the two sets of scans separately; I would expect a T2 bias in
the sample if they are run together with ones that have no T2. Perhaps see
how T2 images influence the output (maybe have a .fsgd file with T2/noT2
as two levels) to see if there are significnt differences- no?

Hth, shantanu


On Tue, March 19, 2013 1:22 pm, Bruce Fischl wrote:
> Hi Souheil
>
> we usually compute the RMS across echoes and give that to recon-all as a
> normal mprage. It's a reasonable (although of course not optimal)
> weighting
> since the earlier echoes have more signal and more contrast.
>
> For the T2s, there's a new post-hoc procedure for deformaing the surfaces
> to match them (-T2pial or something like that in recon-all)
>
> cheers
> Bruce
>
>
> On Tue, 19 Mar 2013, Inati,
> Souheil (NIH/NIMH) [E] wrote:
>
>> Hi All,
>>
>> I have some multi-echo mprage images from a sequence and protocol set up
>> to emulate Andre's 2008 paper.  What's are the "best-practices" for
>> using data from this type of sequence in Freesurfer?
>>
>> Related side questions:
>> I have used the suggested morphometry protocols on the FS wiki (1mm iso
>> resolution, same FOV, bandwidth matched, etc)
>> 1) are people who are using this method using 4 echoes of alternating
>> polarity, or 4 echoes of the same polarity?
>> 2) for some subjects I have also acquired a 3D T2.  Any recommendations
>> on using these data together?
>>
>> Thanks,
>> Souheil
>>
>> 
>>
>> Souheil Inati, PhD
>> Staff Scientist
>> Functional MRI Facility
>> NIMH/NIH/DHHS
>> souheil.in...@nih.gov
>> 301-402-9409
>>
>>
>>
>>
>> ___
>> Freesurfer mailing list
>> Freesurfer@nmr.mgh.harvard.edu
>> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>>
>>
>>
> ___
> Freesurfer mailing list
> Freesurfer@nmr.mgh.harvard.edu
> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>
>
>


-- 
Shantanu Ghosh, Ph.D.
Harvard Medical School & Massachusetts General Hospital
Martinos Center for Biomedical Imaging

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Re: [Freesurfer] make a volume template from the surface-based template for non-human primates

2013-03-19 Thread Bruce Fischl
can you send your mris_fill command line? And maybe the lh.white surface 
you are trying to fill?

Bruce
On Tue, 19 Mar 2013, Longchuan Li wrote:


Hi, Bruce

This is the lh.white that gives me the empty volume when I use mris_fill to
sample it to the volume space. Could you help diagnose what is causing it?
Thank you very much in advance!

Lognchuan



From: Bruce Fischl 
To: Longchuan Li 
Cc: FreeSurfer 
Sent: Sunday, March 17, 2013 11:47 AM
Subject: Re: [Freesurfer] make a volume template from the surface-based
template for non-human primates

Hi Longchuan

I'm not sure what space the volume average is constructed in - Doug would
know. Probably talairach, in which case it won't match the surfaces well.
Can you send along your mris_fill command line? It shouldn't produce an
empty volume. There's no reason to look at the inflated surfaces in the
volume though - they have no volumetric meaning.

cheers
Bruce


On Fri, 15 Mar 2013, Longchuan Li wrote:

> Hi, Bruce
>
> Sorry for the late reply as I was trying to figure it out by myself.
> I mean the average of the subjects in the volume space that were used for
> generating the surface template. Actually I kind of found a volume average
> in the mri folder named as T1.mgz that seems to correspond to the surface
> template for the non-human primates. Perhaps because my ?h.white and
?.pial
> surface files do not have the identical origins as that of the volume
> template, when I used the function "mri_surf2vol" to project the mgh
surface
> file to the volume average, I always got the outputs telling me there is 0
> hits. I tried to diagnose it by projecting the ?h.white and ?h.pial to the
> volume using "mri_fill" and I got an empty volume. I then tried to project
> ?h.inflated to the volume space using the "mri_fill" and this time, I got
a
> mask in the output volume space. Therefore, i suspect that there is a
> mismatch of the origins between the ?h.white and the volume template in
the
> mri folder.
>
> Could you please show me what are the best strategies to correctly project
> the mgh file to the volume template in the 'mri' folder?
>
> Many thanks
>
> Longchuan 
>
>___
_
> From: Bruce Fischl 
> To: Longchuan Li 
> Cc: FreeSurfer 
> Sent: Friday, March 15, 2013 4:56 PM
> Subject: Re: [Freesurfer] make a volume template from the surface-based
> template for non-human primates
>
> Hi Longchuan
>
> what kind of volume template do you mean?
> Bruce
> On Fri, 15 Mar 2013, Longchuan Li
> wrote:
>
> > Hi, FreeSurfer experts
> >
> > I have a question regarding making a volume template based on the
surface
> > template for non-human primates. I have made a surface template using a
> > group of monkeys and now, we want to see the result, which is a mgh
> surface
> > file, on the coronal slices of the template. So I am planning to
generate
> a
> > volume template corresponding to the surface template and then project
the
> > mgh file to the volume for viewing. Could someone tell me what is the
best
> > way to generate such a volume template?
> >
> > Many thanks in advance!
> >
> > Longchuan
> >
> >
> >
>
>
> 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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Re: [Freesurfer] Medial orbitofrontal QA question

2013-03-19 Thread Alice Burnett
Thanks very much, Doug and Bruce! 




  This e-mail and any attachments to it (the "Communication") are, unless 
otherwise stated, confidential, may contain copyright material and is for the 
use only of the intended recipient. If you receive the Communication in error, 
please notify the sender immediately by return e-mail, delete the Communication 
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Communication, computer virus, data corruption, interference or delay arising 
from or in respect of the Communication.
P  Please consider the environment before printing this email


From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
Sent: 19 March 2013 00:00
To: Alice Burnett
Cc: freesurfer@nmr.mgh.harvard.edu; rahul desikan
Subject: Re: [Freesurfer] Medial orbitofrontal QA question

Hi Alice,

you might also see what Rahul (ccd) thinks if you send an image.

cheers
Bruce
On Mon, 18
Mar 2013, Alice Burnett wrote:

> Hi FreeSurfer experts,
>
> I have been working with a dataset we have run through FreeSurfer 5.0 and am 
> interested in the medial orbitofrontal
> region (Desikan atlas). We have an unexpected surface area finding, so we 
> want to rule out any systematic error in the
> generation of the area measurements. We followed the wiki instructions for 
> processing and checked and edited all images
> as necessary, so the pial and white surface placement looks OK. I'm 
> wondering, would you have any particular
> recommendations for QA checking the mOFC or things we should be looking out 
> for?
>
> Thanks so much!
> Alice
>
>
>
>   This e-mail and any attachments to it (the "Communication") are, unless 
> otherwise stated, confidential, may contain
> copyright material and is for the use only of the intended recipient. If you 
> receive the Communication in error, please
> notify the sender immediately by return e-mail, delete the Communication and 
> the return e-mail, and do not read, copy,
> retransmit or otherwise deal with it. Any views expressed in the 
> Communication are those of the individual sender only,
> unless expressly stated to be those of Murdoch Childrens Research Institute 
> (MCRI) ABN 21 006 566 972 or any of its
> related entities. MCRI does not accept liability in connection with the 
> integrity of or errors in the Communication,
> computer virus, data corruption, interference or delay arising from or in 
> respect of the Communication.
> P  Please consider the environment before printing this email
>
> __
> This email has been scanned by the Symantec Email Security.cloud service.
> For more information please visit http://www.symanteccloud.com
> __
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Re: [Freesurfer] Medial orbitofrontal QA question

2013-03-19 Thread Bruce Fischl
actually, I think you need to look up his email at UCSD as his MGH one 
bounced
Bruce
On Wed, 20 Mar 2013, Alice Burnett wrote:

> Thanks very much, Doug and Bruce!
>
>
>
>
>  This e-mail and any attachments to it (the "Communication") are, unless 
> otherwise stated, confidential, may contain copyright material and is for the 
> use only of the intended recipient. If you receive the Communication in 
> error, please notify the sender immediately by return e-mail, delete the 
> Communication and the return e-mail, and do not read, copy, retransmit or 
> otherwise deal with it. Any views expressed in the Communication are those of 
> the individual sender only, unless expressly stated to be those of Murdoch 
> Childrens Research Institute (MCRI) ABN 21 006 566 972 or any of its related 
> entities. MCRI does not accept liability in connection with the integrity of 
> or errors in the Communication, computer virus, data corruption, interference 
> or delay arising from or in respect of the Communication.
> P  Please consider the environment before printing this email
>
> 
> From: Bruce Fischl [fis...@nmr.mgh.harvard.edu]
> Sent: 19 March 2013 00:00
> To: Alice Burnett
> Cc: freesurfer@nmr.mgh.harvard.edu; rahul desikan
> Subject: Re: [Freesurfer] Medial orbitofrontal QA question
>
> Hi Alice,
>
> you might also see what Rahul (ccd) thinks if you send an image.
>
> cheers
> Bruce
> On Mon, 18
> Mar 2013, Alice Burnett wrote:
>
>> Hi FreeSurfer experts,
>>
>> I have been working with a dataset we have run through FreeSurfer 5.0 and am 
>> interested in the medial orbitofrontal
>> region (Desikan atlas). We have an unexpected surface area finding, so we 
>> want to rule out any systematic error in the
>> generation of the area measurements. We followed the wiki instructions for 
>> processing and checked and edited all images
>> as necessary, so the pial and white surface placement looks OK. I'm 
>> wondering, would you have any particular
>> recommendations for QA checking the mOFC or things we should be looking out 
>> for?
>>
>> Thanks so much!
>> Alice
>>
>>
>>
>>   This e-mail and any attachments to it (the "Communication") are, unless 
>> otherwise stated, confidential, may contain
>> copyright material and is for the use only of the intended recipient. If you 
>> receive the Communication in error, please
>> notify the sender immediately by return e-mail, delete the Communication and 
>> the return e-mail, and do not read, copy,
>> retransmit or otherwise deal with it. Any views expressed in the 
>> Communication are those of the individual sender only,
>> unless expressly stated to be those of Murdoch Childrens Research Institute 
>> (MCRI) ABN 21 006 566 972 or any of its
>> related entities. MCRI does not accept liability in connection with the 
>> integrity of or errors in the Communication,
>> computer virus, data corruption, interference or delay arising from or in 
>> respect of the Communication.
>> P  Please consider the environment before printing this email
>>
>> __
>> This email has been scanned by the Symantec Email Security.cloud service.
>> For more information please visit http://www.symanteccloud.com
>> __
>>
>>
>
>
> 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 
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>
> If you have any question, please contact MCRI IT Helpdesk for further 
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[Freesurfer] Brainsuite --> FreeSurfer

2013-03-19 Thread Valtina Pouegue
Hi, 
I've done a segmentation with Brainsuite ( and FreeSurfer) and I would like to 
get measurements with FreeSurfer. SO, I convert my rile ( readdfs --> 
write_surf ) from BRainsuite in Matlab to be usable with Freesurfer. Then, I 
tried to get measurements with the command .'mris_anatomical_stats' .  with the 
file created previously in Matlab (I called it  'rh.pial'). But I got this 
error like the system is not able to read wm.mgz.That's why I thought I could 
juste replace th 'rh.pial' of the segmentation with Freesurfey by the 'rh.pial' 
created with Matalb and then run mris_anatomical_Stats. IS this a good 
approximation. Could you recommand another way.

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Re: [Freesurfer] Brainsuite --> FreeSurfer

2013-03-19 Thread Valtina Pouegue
I could  see the  created surface in MAtlab ( 'read_surf,) but I could't open 
the file in Freesurfer with tksurfer 

VP
From: pval...@hotmail.com
To: freesurfer@nmr.mgh.harvard.edu
Subject: Brainsuite --> FreeSurfer
Date: Tue, 19 Mar 2013 22:34:39 -0400




Hi, 
I've done a segmentation with Brainsuite ( and FreeSurfer) and I would like to 
get measurements with FreeSurfer. SO, I convert my rile ( readdfs --> 
write_surf ) from BRainsuite in Matlab to be usable with Freesurfer. Then, I 
tried to get measurements with the command .'mris_anatomical_stats' .  with the 
file created previously in Matlab (I called it  'rh.pial'). But I got this 
error like the system is not able to read wm.mgz.That's why I thought I could 
juste replace th 'rh.pial' of the segmentation with Freesurfey by the 'rh.pial' 
created with Matalb and then run mris_anatomical_Stats. IS this a good 
approximation. Could you recommand another way.

VP  
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Re: [Freesurfer] make a volume template from the surface-based template for non-human primates

2013-03-19 Thread Longchuan Li
Hi, Bruce

The command line I used is: 

mris_fill -r 1 -c rh.white rh.white.nii.gz

I attached the rh.white in my previous mail. Could you see it in the attachment?

Thank you!

Longchuan



 From: Bruce Fischl 
To: Longchuan Li  
Cc: FreeSurfer  
Sent: Tuesday, March 19, 2013 8:10 PM
Subject: Re: [Freesurfer] make a volume template from the surface-based 
template for non-human primates
 
can you send your mris_fill command line? And maybe the lh.white surface 
you are trying to fill?
Bruce
On Tue, 19 Mar 2013, Longchuan Li wrote:

> Hi, Bruce
> 
> This is the lh.white that gives me the empty volume when I use mris_fill to
> sample it to the volume space. Could you help diagnose what is causing it?
> Thank you very much in advance!
> 
> Lognchuan
> 
> 
> 
> From: Bruce Fischl 
> To: Longchuan Li 
> Cc: FreeSurfer 
> Sent: Sunday, March 17, 2013 11:47 AM
> Subject: Re: [Freesurfer] make a volume template from the surface-based
> template for non-human primates
> 
> Hi Longchuan
> 
> I'm not sure what space the volume average is constructed in - Doug would
> know. Probably talairach, in which case it won't match the surfaces well.
> Can you send along your mris_fill command line? It shouldn't produce an
> empty volume. There's no reason to look at the inflated surfaces in the
> volume though - they have no volumetric meaning.
> 
> cheers
> Bruce
> 
> 
> On Fri, 15 Mar 2013, Longchuan Li wrote:
> 
> > Hi, Bruce
> >
> > Sorry for the late reply as I was trying to figure it out by myself.
> > I mean the average of the subjects in the volume space that were used for
> > generating the surface template. Actually I kind of found a volume average
> > in the mri folder named as T1.mgz that seems to correspond to the surface
> > template for the non-human primates. Perhaps because my ?h.white and
> ?.pial
> > surface files do not have the identical origins as that of the volume
> > template, when I used the function "mri_surf2vol" to project the mgh
> surface
> > file to the volume average, I always got the outputs telling me there is 0
> > hits. I tried to diagnose it by projecting the ?h.white and ?h.pial to the
> > volume using "mri_fill" and I got an empty volume. I then tried to project
> > ?h.inflated to the volume space using the "mri_fill" and this time, I got
> a
> > mask in the output volume space. Therefore, i suspect that there is a
> > mismatch of the origins between the ?h.white and the volume template in
> the
> > mri folder.
> >
> > Could you please show me what are the best strategies to correctly project
> > the mgh file to the volume template in the 'mri' folder?
> >
> > Many thanks
> >
> > Longchuan 
> >
> >___
> _
> > From: Bruce Fischl 
> > To: Longchuan Li 
> > Cc: FreeSurfer 
> > Sent: Friday, March 15, 2013 4:56 PM
> > Subject: Re: [Freesurfer] make a volume template from the surface-based
> > template for non-human primates
> >
> > Hi Longchuan
> >
> > what kind of volume template do you mean?
> > Bruce
> > On Fri, 15 Mar 2013, Longchuan Li
> > wrote:
> >
> > > Hi, FreeSurfer experts
> > >
> > > I have a question regarding making a volume template based on the
> surface
> > > template for non-human primates. I have made a surface template using a
> > > group of monkeys and now, we want to see the result, which is a mgh
> > surface
> > > file, on the coronal slices of the template. So I am planning to
> generate
> > a
> > > volume template corresponding to the surface template and then project
> the
> > > mgh file to the volume for viewing. Could someone tell me what is the
> best
> > > way to generate such a volume template?
> > >
> > > Many thanks in advance!
> > >
> > > Longchuan
> > >
> > >
> > >
> >
> >
> > 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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> contains patient information, please contact the Partners Compliance
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>