1/18/2013 12:09 PM, Laura M. Tully wrote:
> > Hello freesurfers,
> >
> > I'm trying to run mri_glmfit between groups analysis (patients vs.
> > controls) with gender, age, medication (continuous), and duration of
> > illness as covariates. Because the control group ha
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Laura M. Tully, PhD
Post-Doctoral Fellow in Psychiatry
UC Davis Imaging Research Center
4701 X Street,
Sacramento, CA 95817
Phone: (916) 734-7927
Fax: (916) 734-8750
Alumnus of Social Neuroscience & Psychopathology Lab, Harvard Universi
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Laura M. Tully, PhD
Post-Doctoral Fellow in Psychiatry
UC Davis Imaging Research Center
4701 X Street,
Sacramento, CA 95817
Phone: (916) 734-7927
Fax: (916) 734-8750
Alumnus of Social Neuroscience & Psychopathology Lab, Harvard Universi
I am interested in is
detecting group differences in thickness whilst controlling for confounds
such as age, medication, and duration of illness... if I recoded the HC
group wouldn't this change the analysis from between group to within?
>
> doug
>
> On 10/21/2013 11:01 PM, La
itioned or badly scaled, condno = 1e+08
--
--
Laura M. Tully, PhD
Post-Doctoral Fellow in Psychiatry
UC Davis Imaging Research Center
4701 X Street,
Sacramento, CA 95817
Phone: (916) 734-7927
Fax: (916) 734-8750
Alumnus of Social Neuroscience & Psychopathology Lab, Harvard
> Thank you so much.
> It worked well.
> Do you know how to make cuts on the merged label, for eg. if I need to
> seperate DLPFC from premotor cortex.
>
>
>----------
> *From:* Laura M. Tully
> *To:* Anupa AV
> *Cc:* "freesurfer@nmr.mg
nceline . 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.
>
>
--
--
Laura M. Tully, MA
Social Neuroscience & Psychopathology, Harvard University
Center for the Assessment
information is strictly
> prohibited and may be unlawful. If you have received this e-mail
> unintentionally, please immediately notify the sender via telephone at
> (773)
> 406-2464 or email.
>
>
> On Fri, Mar 22, 2013 at 11:38 AM, Laura M. Tully <
> tully.la...@goog
d run separate
GLMs within each group, as you suggested - I just want to make sure I am
understanding the weights correctly first...
LT
On Fri, Mar 22, 2013 at 8:23 AM, MCLAREN, Donald
wrote:
>
> On Thu, Mar 21, 2013 at 8:59 PM, Laura M. Tully <
> tully.la...@googlemail.com&g
information. Any unauthorized use, disclosure, copying or the taking of any
> action in reliance on the contents of this information is strictly
> prohibited and may be unlawful. If you have received this e-mail
> unintentionally, please immediately notify the sender via telephone at
> (773)
.5 .5 -.5 -.5
Does this look right?
Thanks!
Laura.
--
--
Laura M. Tully, MA
Social Neuroscience & Psychopathology, Harvard University
Center for the Assessment and Prevention of Prodromal States, UCLA Semel
Institute of Neuroscience
ltu...@mednet.ucla.edu
ltu...@fas.harvard.edu
310-267-0
to recompute rvarmat (don't load rvar or beta)
>
> [betamat rvarmat] = fast_glmfit(y,X);
>
> Make sure you have $FREESURFER_HOME/fsfast/**toolbox in your matlab path
>
> doug
>
>
>
> On 03/21/2013 05:04 PM, Laura M. Tully wrote:
>
>> Hi Doug,
>>
>
ontrasts that you specify. You can run the same commands
> on the cluster averaged data (xxx.y.ocn...). To do this, don't load in the
> beta file. Instead
>
> y = load('xxx.y.ocn...');
> beta = inv(X'*X)*X'*y;
> then proceed with the rest of the code
>
>
Thank you!
On Thu, Mar 21, 2013 at 10:56 AM, Douglas N Greve wrote:
> Yes, the average thickness over the cluster for each subject.
> doug
>
> On 03/21/2013 01:54 PM, Laura M. Tully wrote:
>
>> Thanks - one last clarification: just to confirm - the values of
>&g
ressed. 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 info
y.dat by the number of vertices in the cluster.
>
> doug
>
> ps. What version of FS are you using? If not 5.2, do you have the patch to
> fix the area and volume analysis?
>
>
>
> On 03/21/2013 12:52 PM, Laura M. Tully wrote:
>
>> hi Doug,
>> A follow up question
the clusters.
> They are raw input, no detrending.
> doug
> On 03/20/2013 05:16 PM, Laura M. Tully wrote:
> > Hello experts,
> >
> > could someone clarify for me what the y values in the xxx.ocn.y.dat
> > files represent following glmfit-sim? are they the residualized y
.
--
--
Laura M. Tully, MA
Social Neuroscience & Psychopathology, Harvard University
Center for the Assessment and Prevention of Prodromal States, UCLA Semel
Institute of Neuroscience
ltu...@mednet.ucla.edu
ltu...@fas.harvard.edu
310-267-0170
--
My musings as a young clinical scientist:
.abs.sig.ocn.annot.annot
No such file or directory
Thanks!
LT
On Wed, Mar 20, 2013 at 9:54 AM, Douglas N Greve
wrote:
>
> On 03/20/2013 12:09 PM, Laura M. Tully wrote:
>
>> Sorry - meant to respond to list.
>>
>> Thanks for the response Doug - I have a few follow up question
overall model) but
>I could not find the .m scripts for the functions (MRIread
>or fast_glm_pcc?) - would these functions be appropriate and if so where
>might I find them?
>
> Thanks in advance for your help!
>
> Laura.
>
>
> On Wed, Mar 20, 2013 at 8:2
, Mar 18, 2013 at 5:05 PM, Laura M. Tully
wrote:
> Hi Freesurfer experts,
>
> I'm hoping you can help me understand how to interpret interactions in
> clusters identified in whole brain analysis using glmfit and glmfit-sim.
> Below I describe what I've done and what I
nking is that I do something similar in fMRI analysis in
spm where I can plot the contrasts in a significant cluster and then
extract both the average contrast estimates for each group and the contrast
estimates for each individual subject.
Thanks in advance!
Laura.
--
--
Laura M. Tully, M
times if the
> subjects changed between analyses. If it is the same subjects in the same
> order, then you only need to run it once.
> doug
>
>
>
> On 3/15/13 4:42 PM, Laura M. Tully wrote:
>
> Hi freesurfer experts,
>
> I'm planning to run a few different glms
ached, and it seems that there may be an option
(-cache--in?) that I can use on just one mris_preproc but I'm not sure if
this is correct, or what the -cache--in option does.
Thanks!
Laura.
--
--
Laura M. Tully, MA
Social Neuroscience & Psychopathology, Harvard University
Center for the
mit this is a rather weak justification and if the images
>> are good, perhaps the pial could be just as good, despite the fact that it
>> somewhat depends on the white for its construction.
>>
>>
>>
>>>
>>>1. Is there a way to run mri_anatomical_
ical_stats on multiple subjects at
>>once and write to a tablefile (similar to asegstats2table output)?
>>
>>
> I think you can use aparcstats2table, then add up all regions in a
> spreadsheet (or even with awk/gawk). Alternatively, you can use "grep" to
> pick the White
?
mri_anatomical_stats can produce both pial and white matter mean surface
area stats.
3. Is there a way to run mri_anatomical_stats on multiple subjects at
once and write to a tablefile (similar to asegstats2table output)?
Thanks!
Laura.
--
--
Laura M. Tully, MA
Social Neuroscience
@nmr.mgh.harvard.edu
Message-ID: <4fccd21d.4040...@nmr.mgh.harvard.edu>
Content-Type: text/plain; charset=ISO-8859-1; format=flowed
OK, I've replicated that this is happening, but Nick will have to take a
look.
doug
On 06/04/2012 11:05 AM, Laura M. Tully wrote:
>
>
>
> Hi Do
Hi Doug,
Attached is the qdec table file and associated levels files. It's strange
that qdec won't let me select more than one continuous variable. What's
even more strange is that I have been able to do that last month when I
originally looked at these data before doing manual edits and quality
c
Hi,
I am using freesurfer 5.1.0 and qdec 1.4. I'm interested in looking at
between group differences in thickness in relation to two other continuous
measures whilst controlling for ICV. However, qdec doesn't seem to let me
select more that one continuous variable even though I only have group
sel
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