Thank you very much.
I have placed file 3dvolreg.afni in Applications/freesurfer/bin/ but the error
persist.
Stefano
Messaggio originale
Da: std...@virgilio.it
Data: 7-gen-2015 11.14
A:
Ogg: [Freesurfer] Error first step FS-FAST
Hi list,
I'm running FS-FAST.
After this command
How can I check whether it is executable?
Thanks,
Setafno
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 7-gen-2015 22.51
A:
Ogg: Re: [Freesurfer] R: Error first step FS-FAST
And is it executable?
On 01/07/2015 04:35 PM, std...@virgilio.it wrote:
>
> Thank you very much.
>
>
-rwxr-xr-x 1 root wheel 60776 Jan 29 2013 #trac-all#
-rw-r--r--@ 1 Stefano staff 3985520 Jan 7 21:21 3dvolreg.afni
ls -l mris_register mris_register.cls: mris_register.c: No such file or
directory
-rwxr-xr-x 1 root wheel 7351544 May 14 2013 mris_register
Thanks,
Stefano
I have also installed AFNI as advise in
http://www.mail-archive.com/freesurfer%40nmr.mgh.harvard.edu/msg37796.html
but I did not resolved the problem.
Stefano
Messaggio originale
Da: std...@virgilio.it
Data: 8-gen-2015 0.25
A:
Ogg: [Freesurfer] R: Re: R: Re: R: Error first step
Porbably I have resolved by chmod +x 3dvolreg.afni
Messaggio originale
Da: std...@virgilio.it
Data: 8-gen-2015 12.45
A: ,
Ogg: [Freesurfer] R: R: Re: R: Re: R: Error first step FS-FAST
I have also installed AFNI as advise in
http://www.mail-archive.com/freesurfer%40nmr.mgh.h
Hi list,
I'm running FAST on resting state data.
After
fcseed-config -segid 9 -fcname L_Thalamus.dat -fsd rest -mean -cfg
mean.L_Thalamus.config
and
fcseed-sess -s Sess01 -cfg mean.L_Thalamus.config
gives this error:
Loading
/Applications/freesurfer/subjects/FUNCTIONAL_DATA/Sess01/rest/001/tmp.
Hi list,
the selxavg3-sess -s Sess01 -a fc.lpccseed.surf.lh in fcMRI analysis produces
this error.
rawfunc2surf-sess completed
Started at Sun Jan 11 00:50:53 CET 2015
Ended at Sun Jan 11 00:50:54 CET 2015
preproc-sess done
-
Hi list,I'd like to perform functional connectivity analysis between thalamus
and whole cortex. I have two groups (control and disease) and I' d like also to
assess between groups differences.I'm performing these steps. Please, could you
check if these are corrected and could you respond to some
Thank you very much. I have looked -mcreg in
http://freesurfer.net/fswiki/FsFastFunctionalConnectivityWalkthrough
Stefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 13-gen-2015 20.55
A:
Ogg: Re: [Freesurfer] functional connectivity analysis
Mostly looks ok to me, exce
Hi list
I'm running
preproc-sess -s Sess01 -fwhm 5 -surface fsaverage lhrh -mni305 -fsd rest
-per-run
fcseed-config -segid 10 -fcname L_Thalamus.dat -fsd rest -mean -cfg
mean.L_Thalamus.config
Create nuisance variables:fcseed-config -wm -fcname wm.dat -fsd bold -pca -cfg
wm.configfcseed-sess -s
Hi list,please, I have two questions:a) subcortical volume correction in
cross-sectional studies could be done by using total GM as covariate instead of
eTIV?b) relatively to group subcortical analysis in cross-sectional studies,
the anatomical images should be necessarily transformed in common
Hi list,please, I have two questions:a) subcortical volume correction in
cross-sectional studies could be done by using total GM as covariate instead of
eTIV?b) relatively to group subcortical analysis in cross-sectional studies,
the anatomical images should be necessarily transformed in commo
Hi,I'm using FS-FAST for seed based connectivity analysis.I'd like to visualize
the results for each subject in a plot as for qdec.Is it possible? If no, there
is an alternative interface to visualize the contribute of each subject in each
vertex/region?Thank you very much in advance.
Stefano
Hi list,
I'm performing the FS-FAST analysis.
Some months ago, I have already preformed this analysis on some subjects
without problem.
Now, I have added some subjects. When I rerun the analysis i have these error:
for isxconcat-sess -sf sessidlist —analysis fc.lthalseed.surf.lh -contrast
L_Tha
Thank you very much. I have resolved Sess49 (--s) error but the "ERROR: Flag —s
unrecognized" is still remained.
Stefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 31-mar-2015 18.07
A:
Ogg: Re: [Freesurfer] isxconcat-sess problem
Not sure what is going wrong with the 1st
No, do you think that a folder is lacking (please see below)?Thanks
Stefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 3-apr-2015 7.34
A:
Ogg: Re: [Freesurfer] R: Re: isxconcat-sess problem
do you have another double dash (--s) in the command line?
Hi list,
I'm performing the FS-FAST for functional connectivity analysis on two groups.
I'm using tkmedit to visualize the results. Is possible to load a scatter plot
which describes the values of each subject for each selected voxel? e.g. I'd
like to verify the presence of outliers.Scatter plot
Hi,
I'm performing FS-FAST for functional connectivity analysis.I have performed
all step for cortical labels.Now, I'd like to perform the analysis for
subcortical structure.Which are the correct lines?
Using preproc-sess -s Sess01 -fwhm 5 -surface fsaverage lhrh -mni305 -fsd rest
-per-run for e
hi list,
where can I download the new version 6.0 of hippocampal subfields segmentation?
And in general the new FS version 6.0?
Thanks
Stefano
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Thanks. The new version will involve also changes in the measure of perirhinal
and parahippocampus?
Stefano
Messaggio originale
Da: fis...@nmr.mgh.harvard.edu
Data: 15-mag-2015 15.31
A: , "Freesurfer support
list"
Ogg: Re: [Freesurfer] Segmentation of hippocampal subfields version 6.0
Hi list,
I'm configuring mkanalysis-sess to configure an analysis for FC data by
FS-FAST.
No problem for cortical label:
mkanalysis-sess -analysis fc.lthalseed.surf.lh -surface fsaverage lh -fwhm 5
-notask -taskreg L_Thalamus.dat 1 -nuisreg vcsf.dat 5 -nuisreg wm.dat 5
-polyfit 5 -nskip 4 -mcex
Hi list,
I'm using version 5.3 and I have performed hippo-subfields analysis.
A- I'd like to visualize the mask of each subfield on the T1.
In subid/mri, I run the command line above:
freeview nu.mgz -p-labels posterior_left_* posterior_Left-Hippocampus.mgz
-p-labels posterior_right_* posterior_
Thanks Eugenio. Point A is resolved: some typos in line command.But, I do not
found the label of perirhinal in aparc+aseg.Is possible to visualize the
enthorhinal, perirhinal and parahippocampus on a surface?
Stefano
Messaggio originale
Da: e.igles...@bcbl.eu
Data: 20-mag-2015 23.05
A:
Thanks, I have resolved for tksurfer. However, in freeviewer I'm not able
visualize correctly the labels of perirhinal and entorhinal in aparc+aseg.
Stefano
Messaggio originale
Da: fis...@nmr.mgh.harvard.edu
Data: 21-mag-2015 21.48
A: , "Freesurfer support
list"
Ogg: Re: [Freesurfer] R:
Hi list,
I'm configuring mkanalysis-sess to configure an analysis for FC data by
FS-FAST. I do not understand how I can perform mni305 volume-based analysis.
How can I configure an analysis for mni305? Specifically, which is the paradigm
file in
-taskreg? How is the command for group level prepr
Hi list,
I'm configuring mkanalysis-sess to configure an analysis for FC data by
FS-FAST. I do not understand how I can perform mni305 volume-based analysis.
How can I configure an analysis for mni305? Specifically, which is the paradigm
file in
-taskreg? How is the command for group level prep
Hi list,
I 'm continuing to have problem to run mni305 volume-based analysis.I have read
the guide
(http://freesurfer.net/fswiki/FsFastFunctionalConnectivityWalkthrough?highlight=%28mkanalysis%5C-sess%29%7C%28connectivity%29).It
explains that separate mkanalysis-sess commands will need to be ru
I'm sorry Doug but I should run mkanalysis-sess -mni305 for both right and left
thalamus (which are taskreg).
Specifically, I'm performing
mkanalysis-sess -analysis fc.lthalseed.surf.lh -surface fsaverage lh -fwhm 5
-notask -taskreg L_Thalamus.dat 1 -nuisreg vcsf.dat 5 -nuisreg wm.dat 5
-polyfi
Hi list,
I'm performing FS-FAST for seed-based (thalamus). During mri_glmfit-sim
--glmdir my-glm.wls/ --grf 1.3 neg --cwpvalthresh .0166I have this error:Input
volume FOV xfm Matrix:
-2.000 0.000 0.000 76.000;
0.000 0.000 2.000 -93.000;
0.000 -2.000 0.000 76.000
Hi list, I working on the combination of MRS and FS-FAST analysis.I have
extracted the grey matter within voxel (I will call it "ROI_MASK") by using FSL
tools and now it is in the same space of orig.mgz (the roi mask is perfectly
overlapped on orig.nii.gz when I use fslview).
I'd like to import
Hi list, I working on the combination of MRS and FS-FAST analysis.I have
extracted the grey matter within voxel (I have called it "ROI_MASK") by using
FSL tools and it is in the same space of orig.mgz (the roi mask is perfectly
overlapped on orig.nii.gz when I use fslview).I'd like to import it
Hi list,I'd like to performed FS-FAST using a ROI as seed.Should I use
fcseed-config? Thus, what should I put instead of -segid?Thanks and regards.
Stefano ___
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Hi list,is it possible to put a constraint to FS-FAST analysis. More
specifically use as seed a subcortical region (e.g. thalamus) and a target
(e.g. frontal pole)?If yes which is the option in the command line?
Stefano ___
Freesurfer mailing list
Fre
Thank you very much.My mask is in .nii.gz. How can I transform it in .mgz?
Should I do it?
Stefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 30-giu-2015 0.36
A:
Ogg: Re: [Freesurfer] Import mask from FSL to FS for performing seed-based
FS-FAST functional connectivity
Hi
Hi list,
When I use tkmedit the overlap between orig and ROI_MASK.nii.gz seem to
correspond. However, when I added the ROI_MASK.nii.gz, the orig is vanished,
and is remained the ROI_MASK in correct position (and in white) and around all
black. My concern is the correct binarization of ROI_MASK w
Hi list,
I'm performing the functional connectivity analysis by FAST.Next, I'd like to
perform spectral dynamic causal model analysis (SPM, Friston et al. 2015; Crone
et al. 2015) on FS-FAST output.Have you any suggestion in this matter?Thanks,
Stefano __
Hi list,
in the previous mail you have suggested to run fcseed-config and specify -seg
ROI_MASK.mgz and -segid 1 (assuming my ROI_MASK is in
$SUBJECTS_DIR/subject/mri). I have two question please.A- my mask is on vmPFC,
thus it include the both hemispheres. Should I divide it in right and left?
Hi list,
I have a strange problem with TRACULA.The analysis run fine on all subjects but
on the last two, -prep command produces this error:
#@# Image corrections Mon Jul 20 09:09:54 CEST 2015mri_convert
$SUBJECT/data.nii.gz $SUBJECT/dmri/dwi_orig.nii.gzcp $SUBJECT/bvecs.txt
$SUBJECT/dmri/dwi_or
Hi list,mri_convert command line did not provide output file.This error was
produced during the first computations of trac-all -prep command line.
Stefano ___
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https://mail.nmr.mgh.harvard.edu/mailm
My concern is whether this command line is correctfcseed-config -segid 1 -seg
ROI_MASK. -fsd rest -mean -cfg mean.ROI_MASK.configfcseed-sess -s SessXXX -cfg
mean.ROI_MASK.configThank youStefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 20-lug-2015 19.17
A:
Ogg: Re: [Frees
Thanks
Here is attached.
INFO: SUBJECTS_DIR is /Applications/freesurfer/subjects/subject_provaINFO:
Diffusion root is /Applications/freesurfer/subjects/subject_provaActual
FREESURFER_HOME /Applications/freesurfertrac-preproc -c
$SUBJECTS/Control75/scripts/dmrirc.local -log
$SUBJECTS/Control75/s
Hi list,
preproc-sess -s Sess101 -fwhm 5 -surface fsaverage lhrh -mni305 -fsd rest
-per-runproduces fmc file but fmcstc and fmcstcsm are lacking.A- The slice
timing correction is performed with the command reported above? Or I should add
to command line -stc (furthemore, where I should put it? S
Ok.My acquisition slices interleaved.Should I add to the command line above the
flag -sliceorder so odd
preproc-sess -s Sess101 -fwhm 5 -surface fsaverage lhrh -mni305 -fsd rest
-per-run -sliceorder so
but this is the error:3dvolreg.afni -verbose -dfile 001/fmcpr.mcdat
-1Dmatrix_save 001/fmcpr.m
Hi list,
I'm performing slice time correction on preproc-sess -s Sess201 -fwhm 5
-surface fsaverage lhrh -mni305-1mm -fsd rest -per-run.I have acquired data
using a Philipps scanner (interleaved). Thefore, shuold I use "-sliceorder
siemens"?The command line:preproc-sess -s Sess201 -fwhm 5 -surfa
Hi list,
I'm performing slice time correction on preproc-sess -s Sess201 -fwhm 5
-surface fsaverage lhrh -mni305-1mm -fsd rest -per-run.I have acquired data
using a Philipps scanner (interleaved). Thefore, shuold I use "-sliceorder
siemens"?The command line:preproc-sess -s Sess201 -fwhm 5 -surf
Hi using Philips scanner (interleaved)Therefore, I'm running
preproc-sess -sf sessid -fwhm 5 -surface fsaverage lhrh -mni305-1mm -fsd rest
-per-run -sliceorder odd
However, as you can see below stc has been not produced.
file:///Applications/freesurfer/subjects/Sess101/rest/001/f.niifile:///Appli
Hi list,
is possible to obtained a conjunction map from vlrmerge command on FS-FAST
(resting state) results?
Stefano ___
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The informat
Hi list,I'm performing FS-FAST using as seed MRS voxel (MRS_MASK). MRS_MASK
shows a god overlap with orig and both of these are located in
$SUBJ/mri.Firstly, I have performed:fcseed-config -segid 1 -seg MRS_MASK.nii.gz
-fsd rest -mean -cfg mean.MRS_MASK.configNext,fcseed-sess -s Sess101 -cfg
me
Thanks. Another error is occurring:Writing to
/Applications/freesurfer/subjects/Sess102/rest/001/tmp.fcseed-sess.8002/avgwf.mgh
Segmentation fault
after fcseed-sess -s Sess102 -cfg mean.MRS_MASK.config
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 8-set-2015 19.02
A:
Ogg:
Hi list,I'm performing one group and one covariate on resting state FAST
analysis.Here, I'm reporting the error.ThanksBest regards,
Stefano
mri_glmfit --glmdir my-glm_age.wls --y y.mgh --nii.gz --fsgd file_age.fsgd --C
intercept_age.mtx —-C slope_age.mtx
gdfReadHeader: reading file_age.fsgd
INFO:
Hi list,
I'm performing FS-FAST on rsfMRI.The seed is MRS voxel.I have run:
1-mri_convert MRS_MASK.nii.gz $SUBJECTS_DIR/MRS_MASK.mgz
2-fcseed-config -segid 1 -seg MRS_MASK.mgz -fsd rest -mean -cfg
mean.MRS_MASK.config
3-fcseed-sess -sf sessid -cfg mean.MRS_MASK.config
4- mkanalysis-sess -ana
Hi listi,
the following error now occur:
--- matlab output
< M A T L A B (R) >
Copyright 1984-2014 The MathWorks, Inc.
R2014a (8.3.0.532) 64-bit (maci64)
February 11, 2014
Thanks,
the error occurred in the command line because I have used
fcseed-config -segid 1 -seg MRS_MASK.mgz -fsd rest -mean -cfg
mean.MRS_MASK.configfcseed-sess -sf sessid -cfg mean.MRS_MASK.config
and the correct form is MRS_MASK without mean.
fcseed-config -segid 1 -seg MRS_MASK.mgz -fsd rest -
Yes, selxavg3-sess runs fine.
Stefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 22-set-2015 20.50
A:
Ogg: Re: [Freesurfer] R: Re: R: Re: R: R: Re: Import mask from FSL to FS for
performing seed-based FS-FAST functional connectivity
So it is working now?
On 09/22/2015 02
For some subject, analysis run fine.For others subjects (processes are the same
for all) I have this error
fcseed-sess -s Sess001 -cfg MRS_MASK.configmri_label2vol --seg
/Applications/freesurfer/subjects/subject_prova/Control01/mri/MRS_MASK.mgz
--reg /Applications/freesurfer/subjects/subj/Sess
Hi list,
I would like to import FS-FAST results in FSL, opening them by fslview.Could
you provide me some suggestion?
Thank you very much
Stefano___
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https://mail.nmr.mgh.harvard.edu/mailman/listinf
Hi list,
I would like to import FS-FAST results (conjunction maps) in FSL, opening them
by fslview.Could you provide me any suggestion?
Thank you very muchBest regards,
Stefano
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https://
Hi list,
I would like to import FS-FAST results (conjunction maps) in FSL, opening them
by fslview.Could you provide me any suggestion?
Thank you very muchBest regards,
Stefano
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Hi list,
after update with El Capitain, recon-all -all produce the error reported below.
Thanks
srclabel =
/Applications/freesurfer/subjects/subject_prova/subj/fsaverage/label/lh.BA1.label
srcsubject = fsaverage
trgsubject = SUBJECTS_DIR
trglabel = ./lh.BA1.label
regmethod = surface
srchemi = l
This is the command and the error line.
Thanks.
Stefano
recon-all -all -i $SUBJECTS_DIR/T1_STRUCT.nii.gz -subject SUBJECTS_DIR
#
INFO: fsaverage subject does not have perirhinal labels!
\n cd /Applications/freesurfer/subjects/subject_prova/Control89;
Hi list,I wonder whether is possible to:1) obtain cortical thickness from
cerebellum and its subregions2) use cerebellum (or its subregions) as seed for
FS-FAST analysis?
Thanks in advance
Kind regards
Stefano___
Freesurfer mailing list
Freesurfer@nmr.
Hi list,
I would like to obtain the functional connectivity maps of CA1, CA2/3... by
using FS-FAST (VERSION 5.3).
Which are the codes in FreeSurferColorLUT.txt, that I should use, please?
The ranges from 500 - 508 and from 550 - 558 are useful by using 5.3?
Thanks
Kind regards,
Stefano Delli Piz
Dear Eugenio,thank you very much.How can I obtain the beta version
6.0?Moreover, given that we are planning to analyze a big sample, I wonder when
will be approximately released the stable's 6.0?Thanks
Kind regards
Stefano
Messaggio originale
Da: "Iglesias Gonzalez, Eugenio"
Data: 3
Hi list,
I have 2 questions, please.
1-The bedpostX that I have run for TRACULA could be used for PROBTRACKX (FSL)?
2-I'd like to export cortical masks from FS to FSL.
An option is mri_binarize but this way failed in probtrackx (fsl).FSL list have
advised me that I should use label2surf command to
Thanks Anastasia. I have some problem when I use mri_binarize.FSL list and
guide advise me to use label2surf. There are a way to obtain specific labels in
.label instead of .nii.gz?
Stefano
Messaggio originale
Da: ayend...@nmr.mgh.harvard.edu
Data: 25-set-2013 17.49
A:
Cc:
Ogg: Re:
For FSL guide:
Normal
0
false
false
false
IT
JA
X-NONE
Hi list and Anastasia.
Thank you very much. mri_annotatiion2label works fine.
Becouse I should run this command:
label2surf -s -o -l
-s,--surf input surface-o,--outoutput surface
-l,--labels ascii list of label files
I should provide also surface file re
Anastasia thank you very much!
I have wrote to FSL mail list.
They have uploaded a new web page of FDT.
Anyway, these are the commands:
mris_convert lh.white lh.white.giiecho lh.BA44.label lh.BA45.label >
listOfAreas.txt
label2surf -s lh.white.gii -o lh.BA44.gii -l listOfAreas.txtStefano
---
Hi list,
there is a way to convert niifty or .par/.rec in DICOM?
Thank you very much,
Stefano ___
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The information in this e-mail is in
Hi list,
I have some questions, please.
I performed linear regression by qdec to find the regions where the cortical
thinning correlates with neuropsychological test (NPS), taking in account 3
nuisance factors.
A- I individuated some posterior regions and now I'd like to build a table with
part
Tank you very much.
A-Do you mean the partial correlation coeff (PCC) at each voxel averaged over
region? Finally a linear regression is done between cortical thickness of a
composite region and NPS. However the authors discuss every individual region
as related to disease. So a table with parti
Dear Douglas, thank you very much for you kind reply.In the paper I have 3
groups (2 diseases and 1 controls).I have performed cortical thickness analysis
among groups, individuating relevant difference in the posterior regions. Next,
for one group, I have used qdec to individuate statistically
originale
Da: charujing...@163.com
Data: 5-dic-2013 2.15
A: "stdp82", "freesurfer"
Ogg: Re: [Freesurfer] R: Re: R: Re: Linear regression
body{FONT-SIZE:12pt; FONT-FAMILY:宋体,serif;}
-->
Dear
Stefano,
I also want to make a corre
Hi list,
I'm performing -stat step but this command produces sementation fault after
loading affine registration .mat.
Thanks,
Stefan
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Hi list,
I have some question regarding hippo-subfield parcellation.If I understand the
final results are thickness of each ROI but assuming a voxel of
0.5x0.5x0.5.Therefore, a correction is request.
A-How is the best way to do it?B-Correction for mean thickness or ICV is
advised? C-Is possible
Hi list,
SLFP is SLF III?
Is there a way to obtain by TRACULA also SLF I and II, knowing the the cortical
targets of the tracts?
Thanks,
Stefano ___
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Normal
0
false
false
false
IT
JA
X-NONE
Hi list,
I have download the files of Yeo parcellation from
ftp://surfer.nmr.mgh.harvard.edu/pub/data/Yeo_JNeurophysiol11_MNI152.zip.
I have two questions, please.
A- Which is the directory where I should put these files?B-I have already run
by recon-all -all all my subjects. How can I added to t
Hi list,
in Wakana et al., 2007, the SLF was divided in parietal and temporal
components. As I understand it, the same subdivision has been made in Yendiki
et al, 2011. In details, SLFp should correspond to SLF III and SLFt to arcuate
fascicle.Tractography studies showed that the anatomy of the
Hi list,
I'm performing TRACULA on three groups for all 18 tracts and for FA, MD, RD, AD.
Which is the best way to perform statistic on TRACULA outcomes? I think that
MANCOVA is too hard and it delete interesting and consolidate (in literature)
results.
Thanks,
Stefano __
Ciao Eugenio,
thank you very much for your prompt and kind response.Yes, I'm looking average
over the entire support of the path distribution and their differences among 2
pathological and 1 control groups.I haven't a strong hypothesis.When I
performed MANOVA, Tukey or Bonferroni post hoc find d
Hi list,
we would like to perform cortical thickness analysis on fetal brain.
We have a single shot T2 image (good quality) and T1 image (poor quality). All
images are in 2D with overlapping and they are acquired by using 1.5 tesla.
We have some questions:
1. Do you know a post-processing way to
Hi list,
I'm noting these regions in FreeSurferColorLUT.txt. How can I obtained
structural information from them?
8001 Thalamus-Anterior 74 130 181 0
8002 Thalamus-Ventral-anterior 242 241 240 0
8003 Thalamus-Lateral-dorsal
Thank you very much!
A last question, please. Therefore, do you are working also on SLF I and SLF II
implementation in TRACULA? If yes, how much time might be required to do it?
(I'm writing a paper and I may wait these new tracts).
Stefano
Messaggio originale
Da: fis...@nmr.mgh.harv
My apology. Here, the responce
http://www.mail-archive.com/freesurfer%40nmr.mgh.harvard.edu/msg32645.html
Messaggio originale
Da: std...@virgilio.it
Data: 28-apr-2014 19.11
A:
Ogg: [Freesurfer] labels of thalami
Hi list,
I'd like to obtained .labels of thalami to use it in FSL.
H
Thank you very much!!
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 28-apr-2014 19.21
A:
Ogg: Re: [Freesurfer] labels of thalami
Use mri_cor2label
On 04/28/2014 01:11 PM, std...@virgilio.it wrote:
> Hi list,
>
> I'd like to obtained .labels of thalami to use it in FSL.
>
>
Hi list,
I'd like to obtained .labels of thalami to use it in FSL.
How can I do it?
Thanks,
Stefano ___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
The information in this e-mai
My apologies, but how can I visualize and check the labels obtained by
mri_cor2label?
Thanks,
Stefano
Messaggio originale
Da: std...@virgilio.it
Data: 28-apr-2014 19.23
A:
Ogg: [Freesurfer] R: Re: labels of thalami
Thank you very much!!
Messaggio originale
Da: gr..
Hi list,
I'd like obtain FS thalami mask (nii.gz) to import in FSL and use it as seed
mask in probtrackx.
Thanks,
Stefano___
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
The in
My apologies, how can I visualize mri_binarize output? I tried in fslview but
orientation is wrong. Different orientation is a file's feature or swapdim is
request?
Thanks,
Stefano
Messaggio originale
Da: fis...@nmr.mgh.harvard.edu
Data: 29-apr-2014 16.01
A: , "Freesurfer support
lis
My apologies, how can I visualize mri_binarize output. I tried in fslview but
orientation is wrong. Different orientation is a file's feature or swapdim is
request?
Thanks,
Stefano
Messaggio originale
Da: fis...@nmr.mgh.harvard.edu
Data: 29-apr-2014 16.01
A: , "Freesurfer support
li
Hi Bruce,
in tkmedit the orientation is ok. Is wrong in fslview. Now, I'm running
probtrackx. I'll update you on results.
Thanks,
Stefano
Messaggio originale
Da: gr...@nmr.mgh.harvard.edu
Data: 29-apr-2014 17.52
A:
Ogg: Re: [Freesurfer] R: Re: thalami mask (nii.gz) to import in FSL
I'm trying to do it. But I have an error. It shoud be due to difference in
size? In freeviewer the files are shown in fslview no.
fslinfo T1_STRUCT.nii.gz (T1 used for recon-all)data_type FLOAT32dim1
212dim2 320dim3 320dim4 1datatype
16pixdim1
Thank you very much Michael.
Now I'm running probtrackx, I will update you.
Stefano
Messaggio originale
Da: mha...@wustl.edu
Data: 29-apr-2014 22.25
A: "std...@virgilio.it",
"freesurfer@nmr.mgh.harvard.edu", "Harms,
Michael"
Ogg: Re: [Freesurfer] R: Re: R: Re: R: Re: R: R
Hi list,
I'd like to perform FAST preprocessing for functional connectivity (seed-based
analysis).Data have been already preprocessed by AFNI.Therefore, no smoothing,
motion and slice timing corrections are requested.
When I run:preproc-sess -sf sessid -nomc -fwhm 0 -surface fsaverage lhrh
-mni
Hi list,
I'd like to perform FAST preprocessing for functional connectivity (seed-based
analysis).Data have been already preprocessed by AFNI.Therefore, no smoothing,
motion and slice timing corrections are requested.
When I run:preproc-sess -sf sessid -nomc -fwhm 0 -surface fsaverage lhrh
-mni
I'd like to open with FSLview the sig.nii.gz which is produced by
selxavg3-sess.
If I use mri_surf2vol, which is the template to added in --template?
It should be in Tailairach space? Where can I find the template that I
should added?
Thanks,
Stefano
subj/rest/fc.seed.surf.lh/L_seed/sig.nii.gz
Yes I would like to open with fslview (FSL) the sig.nii.gz of each
subject which is computed by seed-based analysis by FS-FAST.
I have mask the sig.nii.gz by fslmaths -div
I have run:
mri_vol2surf --src sig_mask.nii.gz --src_type nii.gz --srcreg
subj/rest/001/register.dof6.dat --hemi rh --o prova
Thank you very much,
How can I export a conjunction maps from surf to volume?
I need to make it to perform the DCM analysis by SPM.
Stefano
>Messaggio originale
>Da: fis...@nmr.mgh.harvard.edu
>Data: 27-ott-2015 13.21
>A: , "Freesurfer support list"
>Ogg: Re: [Freesurfer] R: Re: R: imp
Hi list,
I'm using FS-FAST. For a subject I have the error reported below after
fcseed-sess -s subj -cfg vcsf.config.The segmentation of the structural image
is fine.
$Id: mri_glmfit.c,v 1.196.2.8 2012/11/01 18:51:41 greve Exp $
cwd /Applications/freesurfer/subjects/fMRI
cmdline mri_glmfit --y
/
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