Dear FS team,
I am doing a cortical thickness study using QDEC. I used FDR and got the
following clusters:
Generating cluster stats using min threshold of 3.8...
Found 2 clusters
Contrast: 'lh-Diff-Class1-Class2-Intercept-thickness', 15fwhm, DOF: 69
ClusterNo Max VtxMax Size(mm2) TalX
Hi Doug,
Many
thanks for your prompt response and your help. I have one more question
please. I searched for mri_surfcluster command and I am not sure what
should be my input file.
Can you please clarify this for me? Should this be L-frontal.fsgd since I have
more subjects?
Thank you.
Antonel
From: Douglas N Greve
To: Antonella Kis ; "Freesurfer@nmr.mgh.harvard.edu"
Sent: Wednesday, July 18, 2012 12:03 PM
Subject: Re: [Freesurfer] FDR versus mri_glmfit-sim with --cache option
It should be the sig.mgh file in your contrast directory.
doug
ps. Please post to th
Hi Doug,
You mentioned that in my case when FDR found a voxel-wise threshold of 3.8
means p<1.5849e-04.
How exactly I you got this p-val?
How I can get myp-vals for clusters after FDR?
Many thanks.
Antonella
___
Freesurfer mailing list
Freesurf
: freesurfer@nmr.mgh.harvard.edu
Sent: Wednesday, July 18, 2012 1:24 PM
Subject: Re: [Freesurfer] p-val from FDR
3.8 = -log10(1.5849e-04)
On 07/18/2012 12:36 PM, Antonella Kis wrote:
> Hi Doug,
>
> You mentioned that in my case when FDR found a voxel-wise threshold
> of 3.8 means
Dear All,
I want to use cingulate bundle as ROIs more exactly mask for fiber tracking.
Can I use different aseg than the one from Freesurfer for examples can I use
segmentation from JHU-WhiteMatter-labels-1mm.nii.gz and their labels
JHU-WhiteMatter-labels-1mm.txt to get a mask of my cingula
Dear All,
I want to use cingulate bundle as ROIs more exactly mask for fiber tracking.
Can I use different aseg than the one from Freesurfer for examples can I use
segmentation from JHU-WhiteMatter-labels-1mm.nii.gz and their labels
JHU-WhiteMatter-labels-1mm.txt to get a mask of my cing
Dear All,
I want to use cingulate bundle as ROIs more exactly mask for fiber tracking.
Can someone explain please how I can use the JHU-WhiteMatter-labels-1mm.nii.gz
and their labels JHU-WhiteMatter-labels-1mm.txt to get a mask of my cingulate
bundle in my diffusion space for each indivi
. You need a
registration between the JHU atlas and the individual. The people who
developed the JHU atlas can probably tell you how to do this.
doug
On 07/27/2012 10:39 AM, Antonella Kis wrote:
>
>
>
> Dear All,
>
> I want to use cingulate bundle as ROIs more exactly mask for
Dear FS team,
I am trying to find what is the connection between white matter tracts
with reduced FA and a number of cortical regions/clusters with
significant reduction in cortical thickness from QDEC.
Is there a way to overlap my cortical regions with reduced thickness more
exactly the clus
Dear All,
Is possible to overlap my QDEC clusters onto MNI_152_T1 _1mm_brain template?
Thank you.
Antonella
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Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
The information in this
freesurfer@nmr.mgh.harvard.edu
Sent: Tuesday, August 21, 2012 4:55 PM
Subject: Re: [Freesurfer] Convert QDEC clusters on the MNI_152_T1 space
You can use mri_label2vol and $FREESURFER_HOME/average/mni152.register.dat
doug
On 08/21/2012 11:06 AM, Antonella Kis wrote:
> Dear All,
>
> Is possible to overl
/average/mni152.register.dat
doug
On 08/21/2012 11:06 AM, Antonella Kis wrote:
> Dear All,
>
> Is possible to overlap my QDEC clusters onto MNI_152_T1 _1mm_brain
> template?
>
> Thank you.
> Antonella
>
>
> ___
> Freesurfer maili
Re: [Freesurfer] Convert QDEC clusters on the MNI_152_T1 space
You can use mri_label2vol and $FREESURFER_HOME/average/mni152.register.dat
doug
On 08/21/2012 11:06 AM, Antonella Kis wrote:
> Dear All,
>
> Is possible to overlap my QDEC clusters onto MNI_152_T1 _1mm_brain
> template?
PM
Subject: Re: [Freesurfer] Convert QDEC clusters on the MNI_152_T1 space
You can use mri_label2vol and $FREESURFER_HOME/average/mni152.register.dat
doug
On 08/21/2012 11:06 AM, Antonella Kis wrote:
> Dear All,
>
> Is possible to overlap my QDEC clusters onto MNI_152_T1 _1mm_brain
&
e, it
would be fsaverage). Leave fillthresh at 0; the clusters cannot
overlap.
doug
On 8/27/12 4:17 PM, Antonella Kis wrote:
>
>
>
>
>
>
Hi,
>
> I want to overlay my QDEC clusters on the
connectivity maps in FSL on the MNI ( this is the
Hi,
I am trying to run the mri_label2vol but I am getting the following error. I am
not sure which annot file I should use for my QDEC clusters. I tried to use my
annot file from mri_glmfit-sim but it didn't work. I was running:
mri_label2vol --temp
MNI152_T1_1mm_brain.nii.gz --reg
$FREESURF
Hi,
I am trying to run the mri_label2vol but I am getting the following error. I am
not sure which annot file I should use for my QDEC clusters. I tried to use my
annot file from mri_glmfit-sim but it didn't work. I was running:
mri_label2vol --temp
MNI152_T1_1mm_brain.nii.gz --reg
$FREESU
Dear Experts,
What is the best way to get the average thickness for each subject in QDEC,
more exactly for the uncorrected clusters?
I know when running QDEC theer is a stats_tables file saved so I wonder if the
lh. aparc.thickness.stas.dat represents the mean cortical thickness.
Should this va
Dear FS team,
I would like to know if there is any options to get the
hippocampal subfield segmentation so I can get the volume for each segmentation
if I
was running only recon-all for all my subjects or I need to re-run recon-all
but with a
hippocampal subfield segmentation option this tim
Dear FS team,
I would like to know which subfield ( left_presubiculum, left_CA1,
left_CA2-3, left_fimbria, left_subiculum, left_CA4-DG,
left_hippocampal_fissure) contribute to the head, body and tail of left
hippocampus.
It also seems that the first column of nonPartialVolumeStat
Dear FS team,
After I ran the recon-all to get the total cortical thickness, the volume of
the left hypocampus ( = the number of voxels) equals to 2166 which I
thought should be the total hippocampal volume. But if we add all the
voxel numbers from the hippocampal subfield I will get a much large
x27;s studies?
Sorry for this silly question but for all my other subjects I had only one file
.nii.gz and I have no clue from where is coming.
Thank you very much.
Antonella
From: Bruce Fischl
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Dear Bruce,
I have two more questions for today, please:
1). Just to be sure that I understood correct: for my cortical thickness
studies and also for a group studies analysis I will use only the data from
the 3DAx_T1series which was converted to a .nii.gz file. Is this right?
2). If I want
labelling are correct?
Thank you very much.
Antonella
From: Bruce Fischl
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Friday, July 22, 2011 3:47 PM
Subject: Re: [Freesurfer] Pre-processing issues
Hi Antonella
do you know what t
Hi Bruce,
I forgot to ask why my data does not include an unknown region in my
aparc.stats file? My stats data starts with bankssts region and continue with
caudalanteriorcingulate, etc. Do I need to have the unknown region if I use the
new version of the FS 5.1.0?
Thank you.
Antonella
_
Hi,
I would like to check if my subcortical segmentation is correct so I was
running:
tkmedit SUBJECT1 brainmask.mgz \
-aux T1.mgz -surfs \
-segmentation aseg.mgz $FREESURFER_HOME/FreeSurferColorLUT.txt
1). Pial (red line), and white (yellow line) surfaces are shown and I wonde
Hi Bruce,
Thank again for your advice. I am not sure about the data collection but I will
find out soon. In the mean time I have two more questions:
1). The FS tutorial shows for the surface outlines (by loading the -surfs)
three line: the yellow indicating the white surface, the red for the pi
I can see the same point that I choose in one view
for example the coronal view in another view example horizontal view? How I can
select this point in one view and make it visible in another view?
Thanks,
Antonella
From: Bruce Fischl
To: Antonella Kis
Cc: &
nella
From: Bruce Fischl
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Thursday, July 28, 2011 11:15 AM
Subject: Re: "orig surface" button
Hi Antonella,
if it's not active then it probably failed loading the orig surface. Can
Dear Bruce,
1). What is the minimum value/the range for the intensity in order to be
considered acceptable? I know the value in wm should be very close to 110 but
what is the accepted value closed to this?
If is not exactly 110 (foe example if is 101) do I need to add control points
in order to
Hello everyone,
I was trying to create a table with my statistical results (the cortical
thickness and the number of vertices) and I was running:
aparcstats2table --hemi lh --subjects bert NPI001 --meas thickness -t
lh.aparcstas.THICKNESS.txt
When I tried to also get the number of vertices
Hi,
I was trying to create a table with my statistical results (the cortical
thickness and the number of vertices) and I was running:
aparcstats2table --hemi lh --subjects bert NPI001 --meas thickness -t
lh.aparcstas.THICKNESS.txt
When I tried to also get the number of vertices a table by
: Bruce Fischl
To: Antonella Kis
Sent: Friday, July 29, 2011 5:24 PM
Subject: Re: [Freesurfer] Error with aparcstats2table
doug and nick can help with that
On Fri, 29 Jul 2011, Antonella Kis wrote:
> Hi Bruce,
>
> Thanks again for helping. I mean in the aparc stats I have for each
>
Hi Bruce,
Many thanks for your answer and for your valuable help. I was just following
the the examples from the Free Surfer manual on the page 57 (please see the
attachment). I believe my image (the slice I sent you on yesterday) is similar
or closed looking with the one on the page 57.
Since
Hi,
When visualizing the wm.mgz in the coronal view we can see both hemispheres: lh
and rh. How do I know which hemisphere I am visualising in a sagittal view? Do
I have a transition from lh to the rh while passing through the slices?
Thank you,
Antonella
_
Dear Bruce,
I am ready to start my GLM group analysis. I am trying to construct the FSGDF
by constructing an my_age_fsgd.txt file. I was reading the tutorial and I am
not sure if I need to put together my patients and controls in my FSGDF since
my group study will be for patients versus contro
talairach.m3z. What is the difference between this two and
what should I choose or how I know which one I have to choose?
Thank you very much for your help.
Antonella
From: Bruce Fischl
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent:
Dear Freesurfers,
I am ready to run the make_average_subject and I need to specify
-xform for the talairach transform: talairach.lta , talairach.m3z or
talairach.xfm. What is the difference between
this and what should I use for the make_average_subject in order to prepare my
data for the GLM
talairach.m3z?
Many thanks.
Antonella
From: Bruce Fischl
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Thursday, August 11, 2011 12:52 PM
Subject: Re: [Freesurfer] (no subject)
Hi Antonella
talairach.lta and .xfm are linear trans
Dear freesurfers,
I am trying to see what are the group differences in cortical thickness of
patients with right and left FLE compared to controls using the GLM.
I created a txt file in gedit called my_age_fsgd.txt (please see the
attachment) containing my subjects (patients and controls) and
Dear Freesurfer experts,
I am doing a thickness-age correlation group difference study (patients versus
controls. I would like to know if:
1) my contrast vector defined as 0 0 0.5 0.5 is correct in order to test the
change in thickness with age
2)what is the best iteration number for the simul
e my treshold until I
find some activation?
Thank you very much for your valuable help.
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Tuesday, August 16, 2011 12:04 PM
Subject: Re: [Freesurfer] thickne
his mean a low activation? If yes, what I have to do?
Thank you very much!
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Wednesday, August 17, 2011 11:53 AM
Subject: Re: [Freesurfer] mri_glmfit-sim
iteration if I run this part? Do I need to add
this and do I need to mention the threshold in the above coding?
THANKS!
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Wednesday, August 17, 2011 1:10 PM
S
!
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Wednesday, August 17, 2011 2:55 PM
Subject: Re: [Freesurfer] mri_glmfit-sim
for the cache, the simulation has already been done (using 10,000). This
makes it m
lh.age.glmdir/lh-Avg-thickness-age-Cor/mc-z.neg4.sig.ocn.annot
How can I fix this error?
THANKS!
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Wednesday, August 17, 2011 2:55 PM
Subject: Re: [Freesurfer] mri_
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Wednesday, August 17, 2011 1:10 PM
Subject: Re: [Freesurfer] mri_glmfit-sim
Antonella Kis wrote:
> Hi Doug,
>
>
> Thanks again for your help. There are few more things no
Dear Doug,
I just checked my results for the average thickness from each subject
generated in the csdbase.y.ocn.dat file in different clusters (e.g. I have 5
clusters for p<0.05). For cluster #1 - posteriorcingulate, the average
thickness for subject 1 is different from the average thic
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Thursday, August 18, 2011 1:09 PM
Subject: Re: [Freesurfer] mri_glmfit-sim
No you don't. This is the reason I wrote mri_glmfit-sim -- so you don't
need to
Dear FS experts,
I finished
running the GLM and I wonder what is the best way to further analyse my data in
order to see if there is any relation between age (at seizure onset)
and cortical thickness for my patients versus control group.
1). Why when I overlay the sig.mgh in tksurfer lh infla
Dear FS experts,
I finished
running the GLM and I wonder what is the best way to further analyse my data in
order to see if there is any relation between age (at seizure onset)
and cortical thickness for my patients versus control group.
1). Why when I overlay the sig.mgh in tksurfer lh inf
So to run for multiple corrections in fact I will need to run:
mri_glmfit-sim \
--glmdir rh.age.glmdir \
--cache 2 neg \
--cwpvalthresh .025
--overwrite
Please advise me.
Thank you for your time and help.
Antonella
From: Douglas N Greve
To: Antonella K
right?
Please advise.
Thank you.
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Tuesday, August 23, 2011 4:33 PM
Subject: Re: [Freesurfer] correction for multiple comparisons
Yes, that is correct, you sh
Dear All:
I wonder if for a new FSGD file (e.g. age.fsgd) the resample of each subjects
data to fsaverage (into a common space), as well as concatenating all the
subjects' into a single file, will change my old fsaverage.
Thank you.
Antonella
___
F
.
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Tuesday, August 23, 2011 4:33 PM
Subject: Re: [Freesurfer] correction for multiple comparisons
Yes, that is correct, you should use .025 if you are correcting
Hi Doug,
Many thanks for your valuable answer. Can you please briefly explain some other
issues:
1). what exactly means Correction for Multiple Comparisons and how this is done
when using --sim method with --cache.
2). do I need to do an estimation FDRthresholding in tksurfer for GLM meth
elp.
Antonella
From: Douglas N Greve
To: Bruce Fischl
Cc: Antonella Kis ; "freesurfer@nmr.mgh.harvard.edu"
Sent: Thursday, August 25, 2011 12:23 PM
Subject: Re: [Freesurfer] Fw: fsaverage
That "2" is a voxel-wise threshold used to form the
Dear All,
I would like to do DTI analysis on my subjects data. I finished the
pre-processing using recon-all and also I used GLm for the group study.
Can you please let me know how I can do DTI analysis using FSL in Freesurfer?
What steps I need to follow?
Many thanks,
Antonella
__
Dear FS experts,
I'm interested in doing DTI analysis, using FS.
Do I need to have functional data (feat) and then do I need to register the
anatomical data on the functional one?
My MRI data contains the following folders: 3DAx_T1, Ax_Flair, Ax_T2PD, DTI_15,
DTI_30. I am not sure for a DTI /FS
Dear All:
I am running the dt_recon:# setenv FREESURFER_HOME
/usr/local/freesurfer
# setenv SUBJECTS_DIR $FREESURFER_HOME
# cd /usr/local/freesurfer/NPI001
# dt_recon --i
/usr/local/freesurfer/NPI001/dti/1.3.46.670589.11.17385.5.0.7524.2009112812454960001.dcm
--s /usr/local/freesur
Dear Bruce:
I am running the dt_recon:# setenv FREESURFER_HOME
/usr/local/freesurfer
# setenv SUBJECTS_DIR $FREESURFER_HOME
# cd /usr/local/freesurfer/NPI001
# dt_recon --i
/usr/local/freesurfer/NPI001/dti/1.3.46.670589.11.17385.5.0.7524.2009112812454960001.dcm
--s /usr/local/fr
Dear FS experts,
While doing a NIFTI conversion for my dicom files I tried near mri_convert the
MRIcron conversion. I saw that during this conversion the MRIcron is doing a
correction and image orientation such that one of my final NIFTI file is having
a smaller size that the NIFTI file coming
Dear Doug,
Can you please give me some details about how the corrections by multiple
comparisons are done?
Which step in the following code is doing the corrections?
Are the corrections for multiple comparisons done by cache or by cwpvalthresh
or the corrections are done by some parts that are
Hi,
Based on Group Analysis tutorial by loading the cluster annotation in tksurfer
you can visualize all clusters, regardless of significance. Then changing
the label mode to "Outline" by hitting the outline button and loading the
cluster p-value overlay I can see all the significant cluste
Dear Doug,
I know as you told me in past that the average value for the cortical thickness
in significant clusters is given in the cache.th20.neg.y.ocn.dat file under
lh-Avg-thickness-age-Cor file.
1).Is there another way to get the cortical thickness for the significant
clusters, other than
Dear All,
When I designed the matrix consisted of two discrete groups, (patients vs.
controls),
I choose age as a covariate so during my analysis I was lookingif there is a
difference in the cortical thickness within patients
versus controls while accounting for age.
Should I change my FSGD i
Dear All,
When I designed the matrix consisted of two discrete groups, (patients vs.
controls),
I choose age as a covariate so during my analysis I was lookingif there is a
difference in the cortical thickness within patients
versus controls while accounting for age.
Should I change my
Dear All,
What should be my contrast vector if I want to do a direct comparison between
groups (patients vs. controls) after eliminating gender and age? Should this be
[1 -1]?
Should I change my FSGD in
order to be able to compare between patients and controls accounting
for age (I want t
Hi Doug,
One more question please: if I want to do a cortical thickness study between
two groups (patients and controls) and I want to eliminate the age and gender
what should be my Discrete and Continuous factors in QDEC?
Thank you.
AK
___
Freesurf
possible to get more clusters after running FDR in
comparison with the no. of clusters when I set up the thresh 2?
Thank you very much and have a great weekend!
Antonella
From: Douglas N Greve
To: Antonella Kis ; freesurfer
Sent: Thursday, September 22, 2011 3:53
Hi,
After running QDEC, I would like to output in a table the thickness values
within each clusters. I know this is a dependent variable and I can see the
values on the plot but is there a way that I can get this values in a table?
Thanks,
Antonella
From:
Hi,
After running QDEC, I would like to output in a table the average value for
the cortical thickness within each clusters. I know this is a dependent
variable and I can see the values on the plot but is there a way that I can get
this values in a table ?
Thanks,
Antonella___
clusters?
Many thanks,
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Monday, September 26, 2011 10:23 AM
Subject: Re: [Freesurfer] QDEC stats table output
Will this work (this is from running mri_
of the clusters?
Many thanks,
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Monday, September 26, 2011 10:23 AM
Subject: Re: [Freesurfer] QDEC stats table output
Will this work (this is from running
k you very much for your help.
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Monday, September 26, 2011 11:19 AM
Subject: Re: [Freesurfer] QDEC stats table output
You can run mri_glmfit-sim on the QDEC o
k you very much for your help.
Antonella
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Monday, September 26, 2011 11:19 AM
Subject: Re: [Freesurfer] QDEC stats table output
You can run mri_glmfit-sim on
Good morning Doug,
I will really appreciate if you can give me an advise on how I can get the mean
average of the cortical thickness value for the FDR clusters so before Monte
Carlo Simulation.
Many thanks,
Antonella___
Freesurfer mailing list
Freesu
Good morning Doug,
I tried running the -sim on my QDEC output (as you recommended me last days)
but for some data the FDR gives me error (cannot calculate clusters statistics)
so mri_glmfit-sim is not working either since the corrections by multiple
comparisons is not working. What should I do
Good afternoon,
I tried running the -sim on my QDEC output (as recommended last days) but for
some data the FDR gives me error (cannot calculate clusters statistics) so
mri_glmfit-sim is not working either since the corrections by multiple
comparisons is not working. What should I do in t
Dear Doug,
Sorry, I am coming up with the same problem. I am running the mri_glmfit_sim on
the QDEC results to get the text file with the cortical thickness average and
cluster summary but unfortunately I see for one side the --sim is not give me
any clusters even if I can see 5 in QDEC after c
Hi,
Sorry, I am coming up with the same problem. I am running the mri_glmfit_sim on
the QDEC results to get the text file with the cortical thickness average and
cluster summary but unfortunately I see for one side the --sim is not give me
any clusters even if I can see 5 in QDEC after ch
Dear Doug,
Seems that this will never end...It is so painful already.
I was running the --sim as you told me and it worked out for my Sample data
formed by controls and patients with Abnormal side Left.
Now, I am doing the same thing but I am getting an error for both lh and rh.
Here is what I
Hi Doug,
Seems that this will never end...
I was running the --sim as you told me and it worked out for my Sample data
formed by controls and patients with Abnormal side Left.
Now, I am doing the same thing but I am getting an error for both lh and rh.
Here is what I was running:
mri_glmfit
Hi Doug,
I believe I got the error for the Abnormal Side R because the fwhm for the
clusters with thresh 2 in QDEC is fwhm = 31.843147 as you can see below: and
when I run mri_glmfit-sim it gives me the error:
and when I run mri_glmfit-sim it gives me the error that cannot find fwhm 32:
ERROR
Hi,
When I ran the QDEC on patients with abnormal side right, the fwhm for the
clusters at thresh 2 is fwhm = 31.843147.
Then, I ran mri_glmfit-sim on the QDEC output and it gives me the following
error (cannot find fwhm 32):
ERROR: cannot find
/usr/local/freesurfer/average/mult-comp-cor/fs
advise.
Thank you.
AK
From: Douglas N Greve
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu" ;
"fis...@nmr.mgh.harvard.edu"
Sent: Friday, September 30, 2011 10:52 AM
Subject: Re: Error due to fwhm
That exceeds the valued for which the tab
the default in FS while running the mri_gmlfit (mri_surfcluster?
What if my data was smoothed at 10 while running the mris_preproc --cache-in
thickness.fwhm20.fsaverage \
Please advise.
Thank you.
AK
From: Douglas N Greve
To: Antonella Kis
Cc: "frees
- Forwarded Message -
From: Antonella Kis
To: Douglas N Greve
Sent: Friday, September 30, 2011 12:31 PM
Subject: Re: [Freesurfer] Default for fwhm while running mri_glmfit
I see.I am not sure what exactly you mean by an outlier in my data,but if there
will be an outlier, why the
Hello Surfers,
I would appreciate if you can help me with the following question: what should
be the range values on the QDEC and/or GLM color scale if the cwp values for
the cached clusters at thresh 2 and cwpvalthresh .99 are between 0.4465 and
0.9710?
Many thanks.
AK__
Hello Surfers,
I would appreciate if you can help me with the following question: what should
be the range values on the QDEC and/or GLM color scale if the cwp values for
the cached clusters at thresh 2 and cwpvalthresh .99 are between 0.4465 and
0.9710?
Many thanks.
AK__
Dear FreeSurfers,
I would like to know if there is a way to re-sample a NIFTI image (obtained
after MRIcron conversion, from a dcm image) in Freesurfer with a scale factor
of 2.
I saw about mri_convert but this doesn't give me any option for the scale
factor (for e.g. I want to drop each second
Dear FreeSurfers,
This is a question I posted yesterday and I got not answer yet. I am trying to
re-sample a NIFTI image (obtained after MRIcron conversion, from a dcm image)
in Freesurfer with a scale factor of 2.
I know about mri_convert with the option -rt but this doesn't give me any
opti
Hi,
I would appreciate if you can help me with the following question: what should
be the range values on the QDEC and/or GLM color scale if the cwp values for
the cached clusters at thresh 2 and cwpvalthresh .99 are between 0.4465 and
0.9710? Also, I wonder if there is a way in QDEC to
Hi Bruce,
I will be very grateful if you can give me an advise regarding registration. In
TBSS there is recommended if the
subjects are young children (the adult-derived
FMRIB58_FA target is inappropriate), to
identify the "most representative" one, and use this as the target
image. This target
Dear Freesurfers,
I have a set of MRI data collected in an Axial_T1 and some in Sag3D_T1. I
wonder if after dcm to nii conversion when I get a 3D or 4D volume (if further
use for FSL) it really matter how my data was acquired (Axial or Sag) since the
NIFTI file is in fact a volume. Should I do
Dear Freesurfers,
I have a set of MRI data collected in an Axial_T1 and some in Sag3D_T1. I
wonder if after dcm to nii conversion when I get a 3D or 4D volume (if further
use for FSL) it really matter how my data was acquired (Axial or Sag) since the
NIFTI file is in fact a volume. Should I d
Hi,
I am trying to do a DTI Group Analysis study using a MNI152 standard space for
registration.
1). I wonder in case I want to use MNI 152 and not CVS space using TRACULA if I
have to follow all the steps
starting Setting Up a Configuration File to run Tracula and then to
continue
results from FSl with th eone from Freesurfer: TRACULA or dt_recon method.
Please advise.
Many thanks,
Antonella
From: Anastasia Yendiki
To: Antonella Kis
Cc: "freesurfer@nmr.mgh.harvard.edu"
Sent: Friday, November 11, 2011 4:45 PM
Subject: Re: [Frees
Dear all:
Based on the DTI Basic Tutorial I understood that MRI data can be resampled &
registered in CVS space (by running mri_cvs_register), but alternatively can
be normalized in any other (for example, MNI or Talairach). Can you please let
me know how this can be done in MNI152 space? Sho
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