Dear all,
I am a new FreeSurfer user, and have a quick question before beginning to
process T1 data: on the beginners guide (entitled 'Cortical Reconstruction
with FreeSurfer'), it says that the input ought to be from MPRAGE or from
SPGR sequences. 1) Are these the only sequences that FreeSurfer
Hi Narly,
1) we've run a couple of mdeft and they seem fine.
2) It really depends on the CNR. The tools are much more robust these days,
and a single acquisition is usually fine. It also depends on what you want
to do with the data. If it's just for analysis of functional data then the
requir
Hi Bruce,
Thanks for your answers. It actually is for a thickness study. I hope
that one run will be adequate. Are there validity checks for the analysis
output?
thanks again,
Narly.
On Mon, 9 Jul 2007, Bruce Fischl wrote:
> Hi Narly,
>
> 1) we've run a couple of mdeft and they seem fine.
>
the easiest thing is just visual inspection. It depends on the coil and
the field strength. We routinely do a single 6.5 minute acquisition with
a 12 channel coil at 3T and it seems fine. You could do test/retest
studies of course, but that will tell you reliability, not sensitivity.
Bruce
On
Hi,
I am hoping to perform a retinotopic mapping fMRI study.
My paradigms consist of a reversing checkerboard annulus which increases and
decreases in size and a reversing checkerboard wedge which moves clockwise dor
180 degrees and then anticlockwise.
I am struggling to correctly perform the
Hello, Group
Could anybody please tell me how to get the mean thickness of whole cortex? I
got only the average thickness of each hemisphere with mris_anatomical_stats -a
subject/lable/lh.aparc.annot -b subject lh
Thank you in advance,
Xin Wang
___
you mean of both hemispheres together? We don't explicitly compute it,
but the mean of the two hemisphere means should be pretty close, since they
are similar in size
On Mon, 9
Jul 2007, Wang, Xin wrote:
Hello, Group
Could anybody please tell me how to get the mean thickness of whole cortex
Hi John,
you would use a sine and cos at the fundamental. Unfortunately, our
retinotopy analysis is rather finnicky about the data formats and
directory structure, so you might want to use the FreeSurfer functional
analysis tools. It's on my list to generalize it ...
doug
McLean John (NHS G
Greetings,
I am attempting to use FreeSurfer/Slicer to study data from a mass
sprectrometer. To be of use, the segmentation capability of
FreeSurfer/Slicer has to be based on quantitative data, not morphology. It
appears as if FreeSurfer uses a generic mapping of the brain's structure as
a st
Greetings,
The data at this lab initially comes in a RAW data format. When converted to
16-bit TIFF files, the quantitative data is retained.
I recognize that, in order for FreeSurfer to be of use, this data must be
converted to mgz files. However, does the process of converting this
informa
Hello,
I ran a group contrast in an ROI, correcting for multiple comparisons
using the cluster size threshold method. It seems to have worked,
however the one element that I don't understand as well is the basic
between group contrast using an fsgd file, so I'm wondering if my
commands real
The contrast is not specified in the fsgd. The fsgd just declares that
you have two classes. The contrast is specified in your .mat file. The
+1 -1 means that you will subtract ASD from Normals.
doug
Robert Levy wrote:
Hello,
I ran a group contrast in an ROI, correcting for multiple compari
Hi All:
After imposing labels to a T1.mgz files in tkmedit, is it possible to
write out dicom files with the label?
Thanks in advance!
Tao
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Hi Greg,
what structures exactly are you interested in? For the most part, we
only do brain and brain-related structures (eg, ventricles). I don't
know about Slicer, but FreeSurfer only handles T1-weighted MRI data.
doug
Greg Soltis wrote:
Greetings,
I am attempting to use FreeSurfer/
The conversion to mgz is lossless. Having said that, at some point along
the freesurfer stream, it does get converted to 8bit, but you can always
get back to the original data.
doug
Greg Soltis wrote:
Greetings,
The data at this lab initially comes in a RAW data format. When
converted to 1
Sorry, we do not have an option to write out dicoms.
doug
T. Song wrote:
Hi All:
After imposing labels to a T1.mgz files in tkmedit, is it possible to
write out dicom files with the label?
Thanks in advance!
Tao
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Hello, Group
I need to edit the pial surface. I learned to remove points with tkmedit from
the tutorial. But how to add gray matter in the pial surface?
Thank you in advance.
Xin
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hat point). At least for my data, acquired with
surface coils, sub-optimal intensity correction is really annoying.
ahoi & good luck
Sebastian
Thank you in advance.
Xin
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it depends why it's not getting out far enough. Usually you need to add
control points in the nearby white matter that are <110 on the
brainmask.mgz volume.
On Mon, 9 Jul
2007, Wang, Xin wrote:
Hello, Group
I need to edit the pial surface. I learned to remove points with tkmedit from
the
point). At least for my data, acquired with surface coils, sub-optimal
intensity correction is really annoying.
ahoi & good luck
Sebastian
Thank you in advance.
Xin
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