Hi Team,
I apologize, I am new to Freesurfer .
Currently we are processing PIB PET images.
When we compare the SPM data along with FREESURFER outputs. We
were able to see a large variation in the values.
Could you please guide us in processing PI
Hi all,
I sent a message previously and just wanted to check in one more time about
this question (apologies for the repeat message!).
I’m using Optseq2 to generate stimulus / jitter schedules and, depending on the
TR I use, in the output files I see onset times like 124.4001 (instead of
124.4
Hello Experts,
Can we do VBM in MNI template using the outputs from recon all? Which file
should I be using? And how do I smooth the volumes?
Thank you for the tips!
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Hi Idil
you have to figure out what the input volume has more than 1 frame (that
is, why is it 4d). It could be because you saved phase and mag, or because
there are multiple echoes, but until you understand what the additional
frames are we can't process it. YOu can start by bringing the orig.
Hello FreeSurfer experts,
I am trying to run recon-all on a nifti file converted from PAR/SEC using
dcm2niix, and this error came up pretty soon after the script started to run;
>> mri_convert.bin
>> /home/lab/Desktop/freesurfer/subjects/sub-06_run-01_T1w.nii.gz
>> /home/lab/Desktop/freesurfer
Hi Zach
I think if you cut and flatten the cortical part of the surfaces, convert
tha .annot files to separate label files, you can then use label2flat on
each label to generate a flattened patch that is just taht label. I haven't
used it in years (decades?), but I think it should work
cheer
Hello All,
I have been attempting to convert Label files generated using
mri_annotation2label into surface files for use in external programs. In
order to do this I first need to convert the label files into freesurfer
binary. I have attempted to use the mri_label2vol function to generate an
mgz f
It sounds like you have reported everything correctly. The clusterwise
p-value corresponds to a critical cluster size at the given cluster
forming threshold (4), sign (neg), and fwhm (fwhm.dat in the glmdir). So
the answer to the reviewer is "yes". If you want to report the critical
size, then
Dear freesurfers,
I have data collected here at the martinos using the Siemens ep2d_PASL
sequence. I run the command "rcbf-prep —s subject —rcbf asl.nii —o tesfolder"
or something like that. The resulting rcbf.nii looks good, but the values are
negative? Is this just a matter of tag and ref im
Hi,
One of my papers is under review showing significant differences in
cortical surface area between healthy controls and patients.
In this paper, regarding statistical results, for multiple comparison
correction, I ran Monte Carlo simulations using following command:
mri_glmfit-sim \
--cach
FYI
-- Forwarded message --
Date: Mon, 7 Aug 2017 12:54:29 +
From: Meritxell Bach Cuadra
To: Meritxell Bach Cuadra
Subject: Open position at Lausanne University Hospital: research and development
engineer
Dear colleague,
we are looking for a research and development e
Hello Freesurfer experts,
We have processed, hand-edited, and QA'ed over 130 subjects' scans with version
5.3.0 on a linux sci6 box, and extracted the atlas-based ROI values for
cortical thickness, volume, curvature, etc. The servers need upgrading but
there are still whole brain analyses to r
Hi everybody,
I have a .annot file and I would like to display a sphere above one
certain vertex.
(I know the coordinates of the vertex)
Someone knows a way to do that ?
Thank you very much,
Redwan
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Thank you Bruce, sure thing :)
Regards,
Sneha
From: freesurfer-boun...@nmr.mgh.harvard.edu
on behalf of Bruce Fischl
Sent: Monday, August 7, 2017 6:21:57 PM
To: Freesurfer support list
Subject: Re: [Freesurfer] Cortical thickness map for a pediatric case
th
Hi FreeSurfer Experts,
I am trying to run a dods cortical thickness analysis examining the interaction
of group on a continuous variable while controlling for other variables.
Specifically, I have 6 classes (gender by three groups [zero, one, two]). I am
interested in the group interaction wi
Dear FreeSurfer,
I have a longitudinal study (patients and controls) with two time points (i.e.,
baseline and six-weeks follow-up). I would like to use the LME model as it can
handle unequal timing and different number of time points across subjects due
to missing data.
I would like to test if t
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