[Freesurfer] Questions aobut using monte carlo sim in Qdec

2014-03-29 Thread Ashley Shurick
Hi,

I have some questions about using monte carlo sim in qdec:

First of all, I just want to verify it's ok to use the simulation with a
whole-brain analysis and not just an ROI analysis.

Second, I'm a bit confused about how to calculate the p-threshold for my
max clusters. Looking here:
http://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/GroupAnalysisClusterSummary

tells me how to calculate the p-value of my clusters, but according to the
page, max = -log(base10) (pvalue). The example given is the 13th cluster
where max = -5.981, and the stated p value is p  .006. I can't figure out
how you came up with this p-value, can you please clarify your calculations?

Finally, in qdec when I change my threshold from say 1.3 (.05) to 2.0
(.01) I notice the CW Pvalue threshold doesn't change in the terminal
output, and remains at .05. Can you please explain this? What exactly am I
changing when I change the threshold in qdec?

Thank you in advance for your assistance,

Ashley


-- 
Ashley A. Shurick
Ph.D. Candidate
Department of Psychology
Stanford University
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Re: [Freesurfer] Combining scans with different scanning parameters

2014-03-13 Thread Ashley Shurick
Hi Bruce (and others),

We can balance the numbers to allow the same number in each configuration.
But just to clarify, are you saying we should do, for example, 10 patient
scan 1, 10 patient scan 2, 10 patient scan 3, and 10 HC scan 1, 10 HC scan
2, 10 HC scan 3, to perfectly balance everything out? Or do we just need to
have X patient and X HC in scan 1, Y patient and Y HC with scan 2, and Z
patient and Z HC with scanning parameter 3?

Thank you for your assistance.

Ashley


On Tue, Mar 11, 2014 at 5:22 PM, Bruce Fischl fis...@nmr.mgh.harvard.eduwrote:

 Hi Ashley

 that is probably trouble unless your groups are perfectly balanced across
 the datasets (that is, the same # in each group were scanned on each
 configuration).

 cheers
 Bruce



 On Tue, 11 Mar 2014, Ashley Shurick wrote:

  Hi,
 I'm interested in comparing CT differences between 2 different groups, and
 in order to increase my sample size I'm contemplating combining 3 datasets
 with different scanning parameters.

 Some scans were collected with a 3T1 with fmri head coil, while others
 were
 collected with a 3T2 magnet with 8 channel head coil. The scans also
 differ
 in FOV (25.6 vs 22cm) and resolution.

 Thank you in advance for your support.

 Ashley

 --
 Ashley A. ShurickPh.D. Candidate

 Department of Psychology
 Stanford University




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[Freesurfer] Combining scans with different scanning parameters

2014-03-11 Thread Ashley Shurick
Hi,

I'm interested in comparing CT differences between 2 different groups, and
in order to increase my sample size I'm contemplating combining 3 datasets
with different scanning parameters.

Some scans were collected with a 3T1 with fmri head coil, while others were
collected with a 3T2 magnet with 8 channel head coil. The scans also differ
in FOV (25.6 vs 22cm) and resolution.

Thank you in advance for your support.

Ashley

-- 
Ashley A. Shurick
Ph.D. Candidate
Department of Psychology
Stanford University
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[Freesurfer] Fwd: Qdec Questions

2013-10-30 Thread Ashley Shurick
Great - and this would be true for all models?

For example, in the attached graph, I'm looking at a region representing
increased cortical thickness for one group compared to the other (orange
blob, Q: Does the average thickness differ between HC and SAD? nuisance
factor: mean thickness). From this plot it appears that SAD  HC, but based
on your answer to the previous question I would think this region should
represent HC  SAD. Can you please explain this?

Thank you!


On Wed, Oct 30, 2013 at 7:33 AM, Douglas N Greve
gr...@nmr.mgh.harvard.eduwrote:


 In your case you have HC listed first, so red/yellow means HCSAD, blue
 means SADHC
 doug






 On 10/29/2013 11:03 PM, Ashley Shurick wrote:

 Hi Doug,

 Apologies, but I have a rather easy follow-up question that I can't
 figure out:

 How do you interpret the effect in each significant region? A previous
 post suggests using ctrl + left mouse click on a blob and examining the
 plot of the data. However, for the model I am looking at (Does the
 thickness-ERQ correlation differ between HC and SAD?) I still can't
 determine if cortical thinning represents HCSAD or SADHC. I'm attaching a
 representative plot here.

 Thank you,

 Ashley


 On Tue, Oct 29, 2013 at 10:25 AM, Ashley Shurick 
 ashley.shur...@gmail.com 
 mailto:ashley.shurick@gmail.**comashley.shur...@gmail.com
 wrote:

 Thank you!


 On Tue, Oct 29, 2013 at 10:19 AM, Douglas N Greve
 gr...@nmr.mgh.harvard.edu 
 mailto:gr...@nmr.mgh.harvard.**edugr...@nmr.mgh.harvard.edu
 wrote:


 On 10/29/2013 01:10 PM, Ashley Shurick wrote:
  Hi all,
 
  I'm running analyses in Qdec and want to verify a few things:
 
  1. When comparing two groups (HC vs patients) I am including
 mean
  cortical thickness as a covariate, using the following equation:
 
 
  bh.thickness = (lh.thickness*lh.surfarea +
 rh.thickness*rh.surfarea) /
  (lh.surfarea + rh.surfarea)
 
 
  Is this the best way to calculate global mean thickness?
 Yes
 
 
  2. I want to regress out any effects of age, therefore I need to
  demean the ages for my groups as a whole, and not perform this
  calculation on each group separately, correct?
 Yes, in which case the test of the difference between groups
 will be
 done at an age equal to the mean of the ages.
 
  3. I'm including questionnaires as a covariate of interest -
 do I need
  to demean these values as well?
 When you do a test on a continuous covariate, that test will be
 unaffected by demeaning of the covariate. Demeaning will
 affect the
 difference between groups if you use a separate covariate for each
 group. If you have a single covariate across groups, demeaning
 will have
 no effect.

 doug
 
 
  Thank you in advance for your help!
 
 
  Ashley
 
 
  --
  Ashley A. Shurick
  Ph.D. Candidate
  Department of Psychology
  Stanford University
 
 
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[Freesurfer] Qdec Questions

2013-10-29 Thread Ashley Shurick
Hi all,

I'm running analyses in Qdec and want to verify a few things:

1. When comparing two groups (HC vs patients) I am including mean cortical
thickness as a covariate, using the following equation:


bh.thickness = (lh.thickness*lh.surfarea + rh.thickness*rh.surfarea) /
(lh.surfarea + rh.surfarea)


Is this the best way to calculate global mean thickness?


2. I want to regress out any effects of age, therefore I need to demean the
ages for my groups as a whole, and not perform this calculation on each
group separately, correct?

3. I'm including questionnaires as a covariate of interest - do I need to
demean these values as well?


Thank you in advance for your help!


Ashley


-- 
Ashley A. Shurick
Ph.D. Candidate
Department of Psychology
Stanford University
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Re: [Freesurfer] libjpeg.so.62

2013-03-20 Thread Ashley Shurick
Hi all,

My RA's are having similar issues running Freeview on Ubuntu (I've read
others are having the same issue). They get the following error when trying
to call freeview:

freeview.bin: error while loading shared libraries: libXss.so.1: cannot
open shared object file: No such file or directory

We ran apt-get install libjpeg62 to install missing libraries, and when
that didn't fix the issue we tried Nick's fix below just in case it might
work. Unfortunately we are still getting the error. Any ideas about what's
going on?

Thank you in advance for your assistance!


On Tue, Feb 26, 2013 at 7:47 AM, Nick Schmansky
ni...@nmr.mgh.harvard.eduwrote:

 Chikku,

 I am guessing that you are using Ubuntu.  To fix this problem:

 cd /usr/lib
 sudo ln -s libjpeg.so.8 libjpeg.so.62


 in other words, link whatever libjpeg is already installed to the name
 libjpeg.so.62.

 Nick



  Hi
  I am getting an  error  while  using qdec. It  says  error while
  loading shared libraries ,libjpeg.so.62  cannot open shared object
  file No such file or directory
  I ran reconall  with out any problem.
  Any idea,
  tx
  chikku
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-- 
Ashley A. Shurick
Graduate Student, Psychology
Stanford University
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Re: [Freesurfer] Adding low-res T2 and PD images in the recon-all stream - any advantages?

2013-03-18 Thread Ashley Shurick
Hi all,

I have a similar question: My T2 scans are similar to Nicola's -
approximately .86 x .86 x 4.5mm. However, about 60/168 subjects don't have
T2 scans. Would you recommend including the T2's for the subjects who have
them, or excluding the T2 scans altogether?

Thank you in advance for your help!


On Wed, Feb 27, 2013 at 5:44 AM, Bruce Fischl fis...@nmr.mgh.harvard.eduwrote:

 Hi Nicola

 the T2 might in 5.2, but it is pretty thick slices so might hurt more
 than it helps. Not sure, but you can try it out

 cheers
 Bruce
 On Wed, 27 Feb 2013, Nicola
 Toschi wrote:

  Hello List,
 
  on out 3T scanner, in addition to MPRAGE images (1 mm^3), we usually
  acquire T2 and PD images - however they are at 1x1x5 mm resolution.
 
  Would you recommend passing these (T2+PD) to the recon-all stream anyway
  - would they add value/accuracy to the segmentation/parcellation (or
  would they possibly decrease accuracy)?
 
  Thanks in advance,
 
  Nicola
 
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-- 
Ashley A. Shurick
Graduate Student, Psychology
Stanford University
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