Dear Douglas,
Thank you for your reply. I run “mri_fdr –help” to get docs that include
some information for how to use this command. However, I still don’t know
how FDR was used to correct for multiple comparisons.
This question is an opinion given by one reviewer, and I really don’t know
how t
Hi Bruce,
If I *just run the mri_convert command that you provided, it did not
work. The result is the same, with randomly labeled voxels along the
boundaries of GM.
*Am I supposed to run mri_convert and then also run the mri_vol2vol command?
I don't understand what you mean by trilinear sampl
I probably shouldn’t say this too loud but, after many delays, I might be close
to having a working atlas of the thalamic nuclei that I would like to release
in FreeSurfer. Hopefully in a couple of months…
--
Juan Eugenio Iglesias
ERC Senior Research Fellow
Translational Imaging Group
University
Hi all,
Is there any way to obtain (automatically, n~1000 subjects), LGN volumes
from the Freesurfer set of tools?
Or somehow transform the ROI from an atlas into subject space, then extract
volume data?
Thanks,
Yash
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Hi there,
I wonder if the fsgd file and the command lines listed below are corrected.
My sample included 4 groups with different diagnosis (g1, g2, g3, g4).
I'm interested to map the vertices that show a relationship between the FC
(obtained by FS-FAST) and cortical thickeness, regressing out the
Hi,
I just wanted to ask again regarding my question below.
I've noticed that 2 of the centres contribute a smaller number of
subjects and don't in fact have any female controls. Should I remove
these as classes (ie. take out control_Female_centre1 and
control_Female_centre2) and then change t
You can also use mri_fdr Run it with --help to get docs
On 04/16/2018 10:23 AM, Livia Liu wrote:
>
> Dear FS experts,
>
> I'd like to know that how FDR was used to correct for multiple
> comparisons. I do FDR correction in two way in FreeSurfer.
>
> 1, Do the FDR correction in the qdec tool. An
Hi Doug,
I need your recommendations on two topics. I really appreciate your help.
1.) I have two runs of the same experiment, each for about 12 minutes.
These 2 runs are different only in the presentation order of the stimuli. I
also have one localizer session which first, I calculated my contra
Hello all,
I am performing DTI analysis and wanted to know if Freesurfer has a tool
for non-rigid registration.
I performed recon-all and dt_recon on my subject and then used the
register.dat file that was generated by dt_recon to convert the dt_recon
output files back into the space of my orig.ni
Dear FS experts,
I'd like to know that how FDR was used to correct for multiple comparisons.
I do FDR correction in two way in FreeSurfer.
1, Do the FDR correction in the qdec tool. And the page of “False Discovery
Rate” in the page “Multiple-Comparisons Correction in Qdec” was lost.
2, Use
Hi Martin,
thank you so much for the quick and helpful reply!
As I only edited the wm.mgz in the base, there was still some non-wm
included there in the long and also some minor edits to the brainmask.mgz
were necessary that I had probably overlooked in the cross.
To run this command
recon-all -
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Welcome to
Douglas,
I'm already extracting the data with mris_anatomical_stats -a
SUBJ225/label/lh.lobesStrict.annot -b SUBJ225 lh
But I would like to do it now for multiple subjects at once, as the data
extraction. Righ now I'm just copying it to a table, one by one.
Thank you!
On Fri, Apr 13, 2018 at 8:1
Thank you, Douglas,
do you have any suggestions on how to make you work?
Fernanda
On Fri, Apr 13, 2018 at 5:56 PM Douglas Greve
wrote:
> that should work, except the command line is not quite right
>
> On 4/13/18 4:22 PM, Fernanda Hansen P. de Moraes wrote:
>
> Good night,
>
> does anyone kn
Thanks to both of you.
On Mon, Apr 16, 2018 at 12:18 PM, Martin Reuter wrote:
> Hi Susanna,
>
> yes, as you feared, you should rerun the first time point so that all time
> points are run by the same version. Edits should be preserved (although
> maybe more or probably less edits would be necess
Hi Susanna,
yes, as you feared, you should rerun the first time point so that all time
points are run by the same version. Edits should be preserved (although maybe
more or probably less edits would be necessary).
And it is really a bad idea to compare across groups where the groups where
pr
Hi Anna,
yes, long can still be edited, but usually this is not necessary. What kind of
edits did you need to do in the long?
You would need to call with the long flag, and passing the cross and base name.
So just like the regular processing of the -long step, only replace -all with
-autorecon
Hi Katie,
yes, you should check the base (subject-template) if further editing is
necessary there, so that surfaces look good on the base.
Best, Martin
> On 4. Apr 2018, at 15:54, Mckay, Katie Geraldine
> wrote:
>
> Hi,
> I have a question regarding the longitudinal processing stream in Free
Hi Maria,
you can include all time points per subject in the longitudinal processing. For
the statistics I would add a time-varying co-variate with the head coil type.
Best, Martin
> On 13. Mar 2018, at 11:45, Maria Paternina Die wrote:
>
> Dear all,
>
> We want to run the longitudinal FS p
Hi Lisa,
1. It all depends on what kind of analysis you want to do. You can run
aparcstats2table without the long_stats_slopes. Then you will get an
entry for each time point. If you run long_stats_slopes it will compute
the within-subject difference first, put the result into each base
dire
Hi Lea,
sorry for the late reply, just in case this is still of interest:
1. It is possible to process all cross data with 5.3 and then base and
long with 6.0. As long as you do the same for all subjects it should be
fine, just don't mix across subjects. Also depending on the size if only
half
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