Hi,
I am wondering if there is a way to apply the default surface based
registration that is done during recon-all to surfaces other than the sphere
so that the nodes are all lined up? I am wanting to have registered white
matter surfaces that I can map data from the volume to the surface to a
And for the comparison to be appropriate, you further have to make sure
that you are using the exact same main and interaction terms in SPSS as
are being used in QDEC. The mere presence of interaction terms in a model
can have big effects on the significance (or lack thereof) of the main
effects.
Hi:
I was processing a longitudinal processing using a command line like:
recon-all -base -tp -tp ... -all
but it couldn't finished because the power cut produced by a 8.8 magnitude
earthquake here in Chile... How can I continue the processing without starting
again from the beginning ?...
Try creating a file with the list of files that should be converted,
then run mri_convert with
--sdcmlist file-with-list
If that does not work, you can always just copy the files to a new
directory.
doug
Satrajit Ghosh wrote:
> hi,
>
> mri_convert TrioTim/123456-10-1.dcm test.nii.gz
>
> wil
hi,
mri_convert TrioTim/123456-10-1.dcm test.nii.gz
will scan all files in the dicom directory to get at series 10. in the above
scenario, i know that the files corresponding to the run are
123456-10-*.dcm. is there a way to leverage this information, so that it
does not scan the entire directory
Optseq2 does not have the ability to change the identity of the stimuli
during the run.
doug
Gaber, Tilman wrote:
> Thank you for your quick response. Initially I had the same idea.
> Unfortunately, this easy solution does not work. All trials are successor of
> the previous and predecessor o
It's hard to tell from the coronal, but it looks ok. The problem is more
visible in the sagittal.
doug
Jeff Sadino wrote:
> Hello Doug,
>
> I loaded up the tkregister2 program and I think I see some poor
> transformations. I've never really used it before though. Am I just
> looking at wheth
If you use mri_surfcluster, it will output an annotation of the
clusters. You can then use mris_anatomical_stats to compute the mean
value inside those clusters.
doug
Cindy Eckart wrote:
> Dear FreeSurfers,
>
> is there an easy way to extract the mean cortical thickness of clusters
> according
Depends on some of the details. Is spss demeaning the age? If so, are
you passing qdec demeaned ages? It can also be that it shows up better
in the ROI analysis (ROI analyses are often more powerful than map-based).
doug
Dankner, Nathan (NIH/NIMH) [F] wrote:
> Hi all,
>
> I've covaried age in a
The last column in the matrix is all 0s. This means that there are no
members of that group (PTSDPTSD-diagnostikKG).
doug
=?iso-8859-1?q?=22br=f...@nmr.mgh.harvard.edu wrote:
> Hi to All,
>
> I have come across a problem using qdec, specified below. What I am trying to
> do is to look for an int
Hi all,
I've covaried age in a group difference analyses on cortical thickness data
both in qdec for vertex-based and in spss for the gyral-based data. For the
vertex-based data, covarying age has almost no effect, and if anything
intensifies the group differences. However, when run in qdec,
Hi, there,
I have a question about FS longitudinal stream,
I have data from two time points which have been processed by FreeSurfer
cross-sectional stream.
I also built the base template using recon-all -base command, everything looks
fine.
When I ran the longitudinal stream, one of them stop
Hi:
I was processing a longitudinal processing (previous the 8.8 earthquake)
using a command line like:
recon-all -base -tp -tp ... -all
but it couldn't finished because the power cut... How can I continue the
processing without starting again from the beginning ?...
Sincerely,
Gonzalo
Dear FreeSurfers,
is there an easy way to extract the mean cortical thickness of clusters
according to a predefined t-value threshold? I performed a cortical thickness
analysis between 3 groups and found some clusters where the groups differed
significantly. Now, I would like to extract the mea
Hi to All,
I have come across a problem using qdec, specified below. What I am trying to
do is to look for an interaction between two discrete variables (diagnostik and
PTSD). It is my understanding that this appears to be a common problem.
However, is there a way around it, such as conceptuali
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