[Freesurfer] volume of CSF for hemispheres

2011-02-16 Thread Tetiana Dadakova
Dear list,

I would like to calculate CSF volume separately for left and right
hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
ventricles as a whole.
Is there any possibility to get volume values for right/left parts of
3rd, 4th and 5th ventricles?

Thank you,
Tanja.
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Re: [Freesurfer] volume of CSF for hemispheres

2011-02-16 Thread Bruce Fischl
Hi Tanja

we don't do this by default, but I guess you could use the Talairach x 
coordinate to try to differentiate.

cheers
Bruce
On Wed, 16 Feb 2011, Tetiana Dadakova wrote:

 Dear list,

 I would like to calculate CSF volume separately for left and right
 hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
 ventricles as a whole.
 Is there any possibility to get volume values for right/left parts of
 3rd, 4th and 5th ventricles?

 Thank you,
 Tanja.
 ___
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 Freesurfer@nmr.mgh.harvard.edu
 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer



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Re: [Freesurfer] volume of CSF for hemispheres

2011-02-16 Thread Tetiana Dadakova
Thank you, Bruce.

Could you recommend me any tutorial on this? Or probably can you just
mention some steps or commands, where I should insert coordinates?

Tanja.


On Wed, Feb 16, 2011 at 3:15 PM, Bruce Fischl
fis...@nmr.mgh.harvard.edu wrote:
 Hi Tanja

 we don't do this by default, but I guess you could use the Talairach x
 coordinate to try to differentiate.

 cheers
 Bruce
 On Wed, 16 Feb 2011, Tetiana Dadakova wrote:

 Dear list,

 I would like to calculate CSF volume separately for left and right
 hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
 ventricles as a whole.
 Is there any possibility to get volume values for right/left parts of
 3rd, 4th and 5th ventricles?

 Thank you,
 Tanja.
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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer





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 e-mail
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 HelpLine at
 http://www.partners.org/complianceline . If the e-mail was sent to you in
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Re: [Freesurfer] volume of CSF for hemispheres

2011-02-16 Thread Bruce Fischl
Hi Tanja,

I think Doug just put up a coordinate tutorial. For each voxel in the 
aseg label you are interested, compute it's tal coords and if the x is 
negative assign it to one pool and if it is positive assign it to the other

cheers
Bruce


On Wed, 16 Feb 2011, 
Tetiana Dadakova wrote:

 Thank you, Bruce.

 Could you recommend me any tutorial on this? Or probably can you just
 mention some steps or commands, where I should insert coordinates?

 Tanja.


 On Wed, Feb 16, 2011 at 3:15 PM, Bruce Fischl
 fis...@nmr.mgh.harvard.edu wrote:
 Hi Tanja

 we don't do this by default, but I guess you could use the Talairach x
 coordinate to try to differentiate.

 cheers
 Bruce
 On Wed, 16 Feb 2011, Tetiana Dadakova wrote:

 Dear list,

 I would like to calculate CSF volume separately for left and right
 hemispheres. In aseg.stats file I have volumes for 3rd, 4th and 5th
 ventricles as a whole.
 Is there any possibility to get volume values for right/left parts of
 3rd, 4th and 5th ventricles?

 Thank you,
 Tanja.
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 https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer





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 HelpLine at
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[Freesurfer] output of mris_anatomical_stats

2011-02-16 Thread Marco Loggia, PhD
Dear all,

 

In mris_anatomical_stats, the average cortical thickness value comes with
a measure of dispersion around the mean. Is this Standard Deviation? If so,
is there a way to plot the 95% confidence intervals instead?  

 

Thanks,

Marco

 


_ 

 

Marco L. Loggia, PhD 

Postdoctoral Fellow, Mass General Hospital  Brigham and Women's Hospital 

Harvard Medical School 

 

CNY Building 120, suite 101E 

Charlestown, Massachusetts 02129 

Phone: (617) 643-7267 

Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu 

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Re: [Freesurfer] (no subject)

2011-02-16 Thread Marco Loggia, PhD
Cara Angela,

 

La maggioranza degli utenti di questa mailing list (incluso il team di
freesurfer, che mi ha chiesto di risponderti) non parla italiano. Per
comunicazioni future ti suggerirei di scrivere in inglese, in modo da
assicurarti assistenza diretta dal team.

 

Per preprocessare i tuoi dati devi seguire questi step:

 

1)  Utilizzando il comando 'setenv' devi specificare il path completo
della directory contenente i tuoi soggetti.

Per esempio, se la tua directory si trova in /DATI/SOGGETTI, devi usare il
comando: 

setenv SUBJECTS_DIR /DATI/SOGGETTI

 

2)  cd $SUBJECTS_DIR

3)  mkdir -p NOMESOGGETTO/mri/orig 

4)  mri_convert FILE_NAME.nii NOMESOGGETTO/mri/orig/001.mgz

5)  recon-all -s NOMESOGGETTO -autorecon-all

 

Questo dovrebbe funzionare. In bocca al lupo!

 

 

Marco

 

_ 

 

Marco L. Loggia, PhD 

Postdoctoral Fellow, Mass General Hospital  Brigham and Women's Hospital 

Harvard Medical School 

 

CNY Building 120, suite 101E 

Charlestown, Massachusetts 02129 

Phone: (617) 643-7267 

Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu 

 

 

 

 

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Re: [Freesurfer] output of mris_anatomical_stats

2011-02-16 Thread Bruce Fischl
Hi Marco

that is the spatial standard deviation, which probably isn't a very 
interesting #. Typically the more interesting variance is cross subject.

cheers
Bruce


On Wed, 16 Feb 2011, Marco 
Loggia, PhD wrote:

 Dear all,



 In mris_anatomical_stats, the average cortical thickness value comes with
 a measure of dispersion around the mean. Is this Standard Deviation? If so,
 is there a way to plot the 95% confidence intervals instead?



 Thanks,

 Marco




 _



 Marco L. Loggia, PhD

 Postdoctoral Fellow, Mass General Hospital  Brigham and Women's Hospital

 Harvard Medical School



 CNY Building 120, suite 101E

 Charlestown, Massachusetts 02129

 Phone: (617) 643-7267

 Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu


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Re: [Freesurfer] retinotopy manual?

2011-02-16 Thread Michelle Umali
Hi Doug,
Sorry for the dumb beginner question, but to view the results  
projected onto their own anatomy, do I have to do anything special to  
their high res structural scan(like do a recon-all) ?

Thanks.
Michelle


Quoting Douglas N Greve gr...@nmr.mgh.harvard.edu:

 I don't have a formal manual yet (working on it). Below are a list of
 steps that you need to run. The version 5 retinotopy stream is now
 integrated with the rest of FSFAST, which is documented here:
 http://nmr.mgh.harvard.edu/~greve/fsfast.intro.ppt

 doug

 1. Create retinotopy paradigm file in each run directory, eg,
  session/bold/001/rtopy.par
  session/bold/002/rtopy.par etc

   This text file identifies the data in the directory in terms of the
   stimulus type (polar or eccen) and the direction (pos or neg).  Its
   contents should look somethign like:

stimtype polar
direction pos

 2. Run preprocessing

   preproc-sess -surface self lhrh -fwhm 5

 3. Create analysis (30 sec period, 'rtopy.par' is the name of the
   paradigm file from above):

  mkanalysis-sess -a rtopy.self.lh -surface self lh -TR 2 \
-retinotopy 30 -paradigm rtopy.par
  mkanalysis-sess -a rtopy.self.rh -surface self rh -TR 2 \
-retinotopy 30 -paradigm rtopy.par

 4. Run analysis

  selxavg3-sess -a rtopy.self.lh -sf ...
  selxavg3-sess -a rtopy.self.rh -sf ...
  fieldsign-sess -a rtopy.self.lh -occip -sf ...
  fieldsign-sess -a rtopy.self.rh -occip -sf ...

 5. View results
  a. Significance maps:
  tksurfer-sess -a rtopy.self.lh -s sessid
  b. Display raw angle
  tksurfer-sess -a rtopy.self.lh -s sessid -map angle
  c. Display angle masked by by sig
  tksurfer-sess -a rtopy.self.lh -s sessid -map angle.masked
  d. Display field sign
  tksurfer-sess -a rtopy.self.lh -s sessid -fieldsign





 Michelle Umali wrote:
 Dear All,
 I was wondering if anyone knows of a step-by-step guide on how to do
 retinotopic analysis with freesurfer.

 Thanks.
 Michelle
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 Douglas N. Greve, Ph.D.
 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: www.nmr.mgh.harvard.edu/facility/filedrop/index.html



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Re: [Freesurfer] output of mris_anatomical_stats

2011-02-16 Thread Marco Loggia, PhD
Thanks Bruce for your prompt reply.

The surfaces I feed to mris_anatomical_stats are actually not thickness
data, but quantitative CBF maps, calculated using arterial spin labeling. 

I am trying to extract, for each subject, the average CBF value across the
whole cortical surface. Considering this, the dispersion should be the SD of
the CBF across all vertices, right?
 
Is it not possible to obtain 95% C.I. instead of the SD?

Marco

_ 
 
Marco L. Loggia, PhD 
Postdoctoral Fellow, Mass General Hospital  Brigham and Women's Hospital 
Harvard Medical School 
 
CNY Building 120, suite 101E 
Charlestown, Massachusetts 02129 
Phone: (617) 643-7267 
Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu 


-Original Message-
From: Bruce Fischl [mailto:fis...@nmr.mgh.harvard.edu] 
Sent: Wednesday, February 16, 2011 11:52 AM
To: Marco Loggia, PhD
Cc: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] output of mris_anatomical_stats

Hi Marco

that is the spatial standard deviation, which probably isn't a very
interesting #. Typically the more interesting variance is cross subject.

cheers
Bruce


On Wed, 16 Feb 2011, Marco
Loggia, PhD wrote:

 Dear all,



 In mris_anatomical_stats, the average cortical thickness value comes 
 with a measure of dispersion around the mean. Is this Standard 
 Deviation? If so, is there a way to plot the 95% confidence intervals
instead?



 Thanks,

 Marco




 _



 Marco L. Loggia, PhD

 Postdoctoral Fellow, Mass General Hospital  Brigham and Women's 
 Hospital

 Harvard Medical School



 CNY Building 120, suite 101E

 Charlestown, Massachusetts 02129

 Phone: (617) 643-7267

 Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu





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Re: [Freesurfer] FS 5.1

2011-02-16 Thread Michael Waskom
Hi,

For what it's worth, I have seen a very similar skull-strip failure on
at least one of my brains processed with Freesurfer 5.0 but not using
the -nuintensitycor-3T flag.  Happy to send data, if helpful.

Best.
Michael

On Wed, Feb 16, 2011 at 2:03 PM, Mehul Sampat mpsam...@gmail.com wrote:
 Hi Bruce,

 Okay. I will try it out 5.1 in the future and compare it to 4.5.

 I also have a question about comparisons between version 4.5 and 5.0

 In some cases, I saw that FS 4.5 does a slightly better job at skull
 stripping than FS 5.0.
 Esentially, FS 5.0 seems to make errors in the back of the brain and cuts
 out some tissue.
 (Please see attached images).

 The images are the same slice from the same subject processed with FS 4.5
 and 5.0 (This happens across 5-10 slices)
 In 5.0, I used the following command: recon-all -s subj--id -i
 nifti-file -all -nuintensitycor-3T
 (I have seen this issue in atleast 5 subjects in our data)

 Since 5.0 uses the graph cuts, could the error be due the combination of
 (graph cuts + -nuintensitycor-3T) ?
 Also, I guess I could run 5.0  and use only graph cuts or -nuintensitycor-3T
 to isolate the error ?

 Thanks
 Mehul



 On Tue, Feb 15, 2011 at 12:05 PM, Bruce Fischl fis...@nmr.mgh.harvard.edu
 wrote:

 Hi Mehul,

 I think 5.1 will work better for large ventricles than 4.5, but I'll be
 interested to hear your experience.

 cheers
 Bruce
 On Tue, 15 Feb 2011, Mehul Sampat wrote:

 Hi Bruce,
 We have two studies being conducted (one cross-sectional and one
 longitudinal)
 Some of the subjects in have a lot of atrophy and have large ventircles.

 For the cross-sectional analysis stream are there many differences
 between
 4.5 and the forthcoming 5.1 ? Or would it be fine to use 4.5 for
 cross-sectional analysis ?

 (I understand that for the longitudinal study, I should wait for 5.1 and
 process all the timepoints with 5.1)


 Thanks
 Mehul



 On Thu, Jan 20, 2011 at 10:36 AM, Bruce Fischl
 fis...@nmr.mgh.harvard.eduwrote:

 Hi Derin

 we are tracking down some issues with it and hope to have it out within
 a
 month

 cheers
 Bruce
 On Thu, 20 Jan 2011, Derin Cobia wrote:

 All,

 Just curious about the current estimated timeline for version 5.1,
 trying

 to schedule some projects around it.  Thanks!

 -Derin



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Re: [Freesurfer] question regarding T1-data quality

2011-02-16 Thread Bruce Fischl
the surfaces look ok, although the data looks pretty low contrast. Was it 
a flash scan? what is the voxel resolution?

On Wed, 16 Feb 2011, Eveline Geiser 
wrote:

 Dear List,
 we recorded this anatomical data on a clinical scanner (Philips Achieva 3T) 
 with the following parameters: eight-channel sense head coil, TE 2.3 ms TR = 
 20ms, angle = 20degree.
 do you think it is usable?
 thanks for your reply


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Re: [Freesurfer] Between Task Analysis

2011-02-16 Thread Mandy Nagy
Thank you for your response!

We decided to run an isxconcat-sess on both analyses (day1 and day2),
and we used fscalc to do day1 - day2.  Now we're trying to run
mri_glmfit.  However, the FSGD files we used before either specified
day1 or day2 sessions.  How do we create an FSGD file now that each
data point is actually 'day1 - day2' for one subject and not one of
the pre-existing subject folders?

Thanks!
--Mandy Nagy

On Tue, Feb 15, 2011 at 5:12 PM, Douglas N Greve
gr...@nmr.mgh.harvard.edu wrote:
 In principle you can do it either way and get the same result. From a
 practical standpoint, it is probably easier to do the day2-day1 subtraction,
 then do the group analysis.

 doug

 Mandy Nagy wrote:

 Hi all,

 We are attempting to do an analysis for subjects that came in on two
 different days to perform two similar but different tasks (one
 learning condition, one control).  Each of the tasks is structured
 such that there are 30sec rest epochs alternating with 30sec active
 (typing) epochs for a total of 12.5 minutes (the task begins and ends
 with rest).  We are trying to compare the typing period for the
 control task to the typing period for the learning task.

 We currently have first-level analyses of each of the tasks (active
 condition vs. null rest condition).  Can we do within-subject
 comparisons and then do a group analysis on those?  Or did we need to
 concatenate the learning and control conditions in the first-level
 analysis?  If that is the case, how would you suggest that we do this?

 Paradigm file:

 0       0       30      1       Rest
 30      1       30      1       Typing
 60      0       30      1       Rest
 90      1       30      1       Typing
 120     0       30      1       Rest
 150     1       30      1       Typing
 180     0       30      1       Rest
 210     1       30      1       Typing
 240     0       30      1       Rest
 270     1       30      1       Typing
 300     0       30      1       Rest
 330     1       30      1       Typing
 360     0       30      1       Rest
 390     1       30      1       Typing
 420     0       30      1       Rest
 450     1       30      1       Typing
 480     0       30      1       Rest
 510     1       30      1       Typing
 540     0       30      1       Rest
 570     1       30      1       Typing
 600     0       30      1       Rest
 630     1       30      1       Typing
 660     0       30      1       Rest
 690     1       30      1       Typing
 720     0       30      1       Rest


 Thanks in advance!
 --Mandy Nagy
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 gr...@nmr.mgh.harvard.edu
 Phone Number: 617-724-2358 Fax: 617-726-7422

 Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
 FileDrop: www.nmr.mgh.harvard.edu/facility/filedrop/index.html



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Re: [Freesurfer] retinotopy manual?

2011-02-16 Thread Douglas N Greve
Yes, you need to run recon-all in order to run the FSFAST analysis.

doug

Michelle Umali wrote:
 Hi Doug,
 Sorry for the dumb beginner question, but to view the results 
 projected onto their own anatomy, do I have to do anything special to 
 their high res structural scan(like do a recon-all) ?

 Thanks.
 Michelle


 Quoting Douglas N Greve gr...@nmr.mgh.harvard.edu:

 I don't have a formal manual yet (working on it). Below are a list of
 steps that you need to run. The version 5 retinotopy stream is now
 integrated with the rest of FSFAST, which is documented here:
 http://nmr.mgh.harvard.edu/~greve/fsfast.intro.ppt

 doug

 1. Create retinotopy paradigm file in each run directory, eg,
  session/bold/001/rtopy.par
  session/bold/002/rtopy.par etc

   This text file identifies the data in the directory in terms of the
   stimulus type (polar or eccen) and the direction (pos or neg).  Its
   contents should look somethign like:

stimtype polar
direction pos

 2. Run preprocessing

   preproc-sess -surface self lhrh -fwhm 5

 3. Create analysis (30 sec period, 'rtopy.par' is the name of the
   paradigm file from above):

  mkanalysis-sess -a rtopy.self.lh -surface self lh -TR 2 \
-retinotopy 30 -paradigm rtopy.par
  mkanalysis-sess -a rtopy.self.rh -surface self rh -TR 2 \
-retinotopy 30 -paradigm rtopy.par

 4. Run analysis

  selxavg3-sess -a rtopy.self.lh -sf ...
  selxavg3-sess -a rtopy.self.rh -sf ...
  fieldsign-sess -a rtopy.self.lh -occip -sf ...
  fieldsign-sess -a rtopy.self.rh -occip -sf ...

 5. View results
  a. Significance maps:
  tksurfer-sess -a rtopy.self.lh -s sessid
  b. Display raw angle
  tksurfer-sess -a rtopy.self.lh -s sessid -map angle
  c. Display angle masked by by sig
  tksurfer-sess -a rtopy.self.lh -s sessid -map angle.masked
  d. Display field sign
  tksurfer-sess -a rtopy.self.lh -s sessid -fieldsign





 Michelle Umali wrote:
 Dear All,
 I was wondering if anyone knows of a step-by-step guide on how to do
 retinotopic analysis with freesurfer.

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

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Re: [Freesurfer] Between Task Analysis

2011-02-16 Thread Douglas N Greve
You mean you have used the day1 recon-all with the day1 functional (and 
same for day 2)? I would probably pick an anatomical from one day and 
use them with the functionals for both days. You can use either FSGD 
file assuming that the class membership and continuous variables are the 
same. If you're just doing an OSGM, then you don't even need a an FSGD 
file (but it does not hurt).

doug

Mandy Nagy wrote:
 Thank you for your response!

 We decided to run an isxconcat-sess on both analyses (day1 and day2),
 and we used fscalc to do day1 - day2.  Now we're trying to run
 mri_glmfit.  However, the FSGD files we used before either specified
 day1 or day2 sessions.  How do we create an FSGD file now that each
 data point is actually 'day1 - day2' for one subject and not one of
 the pre-existing subject folders?

 Thanks!
 --Mandy Nagy

 On Tue, Feb 15, 2011 at 5:12 PM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu wrote:
   
 In principle you can do it either way and get the same result. From a
 practical standpoint, it is probably easier to do the day2-day1 subtraction,
 then do the group analysis.

 doug

 Mandy Nagy wrote:
 
 Hi all,

 We are attempting to do an analysis for subjects that came in on two
 different days to perform two similar but different tasks (one
 learning condition, one control).  Each of the tasks is structured
 such that there are 30sec rest epochs alternating with 30sec active
 (typing) epochs for a total of 12.5 minutes (the task begins and ends
 with rest).  We are trying to compare the typing period for the
 control task to the typing period for the learning task.

 We currently have first-level analyses of each of the tasks (active
 condition vs. null rest condition).  Can we do within-subject
 comparisons and then do a group analysis on those?  Or did we need to
 concatenate the learning and control conditions in the first-level
 analysis?  If that is the case, how would you suggest that we do this?

 Paradigm file:

 0   0   30  1   Rest
 30  1   30  1   Typing
 60  0   30  1   Rest
 90  1   30  1   Typing
 120 0   30  1   Rest
 150 1   30  1   Typing
 180 0   30  1   Rest
 210 1   30  1   Typing
 240 0   30  1   Rest
 270 1   30  1   Typing
 300 0   30  1   Rest
 330 1   30  1   Typing
 360 0   30  1   Rest
 390 1   30  1   Typing
 420 0   30  1   Rest
 450 1   30  1   Typing
 480 0   30  1   Rest
 510 1   30  1   Typing
 540 0   30  1   Rest
 570 1   30  1   Typing
 600 0   30  1   Rest
 630 1   30  1   Typing
 660 0   30  1   Rest
 690 1   30  1   Typing
 720 0   30  1   Rest


 Thanks in advance!
 --Mandy Nagy
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 MGH-NMR Center
 gr...@nmr.mgh.harvard.edu
 Phone Number: 617-724-2358 Fax: 617-726-7422

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 addressed. If you believe this e-mail was sent to you in error and the
 e-mail
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 error
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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
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Re: [Freesurfer] output of mris_anatomical_stats

2011-02-16 Thread Douglas N Greve
Hi Marco, no, there's not a way to get 95% conf intervals out of it. sorry,
doug

Marco Loggia, PhD wrote:
 Thanks Bruce for your prompt reply.

 The surfaces I feed to mris_anatomical_stats are actually not thickness
 data, but quantitative CBF maps, calculated using arterial spin labeling. 

 I am trying to extract, for each subject, the average CBF value across the
 whole cortical surface. Considering this, the dispersion should be the SD of
 the CBF across all vertices, right?
  
 Is it not possible to obtain 95% C.I. instead of the SD?

 Marco

 _ 
  
 Marco L. Loggia, PhD 
 Postdoctoral Fellow, Mass General Hospital  Brigham and Women's Hospital 
 Harvard Medical School 
  
 CNY Building 120, suite 101E 
 Charlestown, Massachusetts 02129 
 Phone: (617) 643-7267 
 Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu 


 -Original Message-
 From: Bruce Fischl [mailto:fis...@nmr.mgh.harvard.edu] 
 Sent: Wednesday, February 16, 2011 11:52 AM
 To: Marco Loggia, PhD
 Cc: freesurfer@nmr.mgh.harvard.edu
 Subject: Re: [Freesurfer] output of mris_anatomical_stats

 Hi Marco

 that is the spatial standard deviation, which probably isn't a very
 interesting #. Typically the more interesting variance is cross subject.

 cheers
 Bruce


 On Wed, 16 Feb 2011, Marco
 Loggia, PhD wrote:

   
 Dear all,



 In mris_anatomical_stats, the average cortical thickness value comes 
 with a measure of dispersion around the mean. Is this Standard 
 Deviation? If so, is there a way to plot the 95% confidence intervals
 
 instead?
   

 Thanks,

 Marco




 _



 Marco L. Loggia, PhD

 Postdoctoral Fellow, Mass General Hospital  Brigham and Women's 
 Hospital

 Harvard Medical School



 CNY Building 120, suite 101E

 Charlestown, Massachusetts 02129

 Phone: (617) 643-7267

 Fax: (617) 643-7340 ma...@nmr.mgh.harvard.edu


 



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

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