Freesurfer team,
Hi. Our lab tried to unpack DICOM files using both freesurfer v4.5.0 and
v5.3.0.
The command line is:
unpacksdcmdir -src $DATA_DIR/$SUBJECT/DICOM/day1 -targ
$DATA_DIR/$SUBJECT/bold_decode -fsfast -seqcfg $LOG_DIR/$UNPACK
And I get the error message:
$Id: unpacksdcmdir,v 1.19.2
e];
}"
(file "/home/jbang/freesurfer//bin/unpacksdcmdir.tcl" line 1048)
This same error message appeared on both v4.5.0 and v5.3.0.
Do you have any clue to fix it?
Thank you for your help.
Best,
Ji Won Bang
___
Freesurfer mailing list
Fre
h run argument rather than using
numaris4-protocols.unpackcfg?
I'll be waiting for your reply.
Thank you.
Best,
Ji Won
2016-02-04 11:56 GMT-05:00 Douglas Greve :
> Hi Ji Won, can you try dcmunpack? Should take the same arguments
>
>
> On 2/4/16 10:28 AM, Ji Won Bang wrote:
>
/FsFastFunctionalConnectivityWalkthrough),
it says that 3 files are generated. which are paradigm file, f.nii, fmc.nii
Why don't I get paradigm file and fmc.nii?
Thank you!
Best,
Ji Won
2016-02-04 13:42 GMT-05:00 Ji Won Bang :
> Hi.
>
> When I tried dcmunpack:
> dcmunpack -src $DATA_D
Thank you!
Best,
Ji Won
> On Feb 4, 2016, at 7:01 PM, Douglas Greve wrote:
>
> that is not generated when unpacking. It is generated when you run
> preproc-sess
>
>
>> On 2/4/16 6:09 PM, Ji Won Bang wrote:
>> Hi, again.
>>
>> I tried dcmunpack:
Dear. Freesurfer team
I used dcmunpack to convert DCM to nii.
This command didn't generate seq.info (I couldn't find it).
I'd like to create one by myself
Do you know how I can check the scan parameters:
sequencename
nrows
ncols
nslcs
rowpixelsize
colpixelsize
slcpixelsize
ntrs
TR
I know t
If I use:
unpacksdcmdir -src dicomdir -targ targetdir -scanonly targetdir /scan.info
I can get sequencename, nrows, ncols, nslcs, ntrs, but how can I check the
exact value of slcpixelsize?
Thanks,
Ji Won
2016-02-05 14:54 GMT-05:00 Ji Won Bang :
> Dear. Freesurfer team
>
> I used dcm
Or my guess is that this seq.info is not necessary for the further
analysis.. so I can go ahead without it?
Best,
Ji Won
2016-02-05 15:06 GMT-05:00 Ji Won Bang :
> If I use:
> unpacksdcmdir -src dicomdir -targ targetdir -scanonly targetdir /scan.info
>
> I can get sequencename,
Dear. Freesurfer team.
Hi.
I'm using freesurfer 4.5 version.
While doing the motion correction, an error occurred.
the command I used:
mc-sess -s $SUBJECT -df sessdirfile -fsd bold_retino -targrun
$DATA_DIR/$SUBJECT/bold_decode/003
the error I have:
/home/jbang/Projects/replay/epi/replay01/bol
tino) were collected in one
scan per subject, so the head position should not be too different...
Do you have any suggestions for fixing this error?
Should I do 3dWarp -deoblique?
Thank you so much.
Best,
Ji Won
2016-02-08 16:30 GMT-05:00 Ji Won Bang :
> Dear. Freesurfer team.
>
>
2016-02-08 17:16 GMT-05:00 Ji Won Bang :
> Dear. Freesurfer team.
>
> I'd appreciate any advice from you.
>
> When doing the motion correction, I'd like to align all EPI
> data(bold_retino) to the first EPI of target run(bold_decode/003). However,
> the number of sl
unctional subdir (FSD, eg, bold), and create a new analysis for it, then
> combine them together after analysis. A bit of a hassle.
>
>
> On 2/8/16 5:58 PM, Ji Won Bang wrote:
>
> Dear. Freesurfer team.
>
> As another attempt, I run the motion correction without the argu
Dear. freesurfer experts.
Hi. I'm using freesurfer version 5.3.0.
I tried mc-sess onto runs that have different number of slices.
However, due to this different number of slices in different runs, mc-sess
gives an error.
I expected that running mc-sess in freesurfer version 5.3.0 would handle
t
The command I used is:
mktemplate-sess -s $SUBJECT -df sessdirfile -fsd bold_retino
mc-sess -s $SUBJECT -df sessdirfile -fsd bold_retino -per-session
Thank you.
Best,
Ji Won
2016-03-03 12:22 GMT-05:00 Ji Won Bang :
> Dear. freesurfer experts.
>
> Hi. I'm using freesurfer
-see utilizes the template file created per
session(file under the functional subdirectory).
Is my understanding correct?
Thanks a lot!
Best,
Ji Won
2016-03-03 12:36 GMT-05:00 Douglas N Greve :
> you have to use -per-run not -per-session
>
>
> On 03/03/2016 12:27 PM, Ji Won Bang wrote:
&
Dear. Freesurfer experts.
Hi. How are you?
It might be very naive question.
When using version 4.5.0 I used the command:
mkbrainmask-sess -s $SUBJECT -funcstem fmc -df sessdirfile -fsd bold_retino
However under the version 5.3.0, mkbrainmask-sess does not have -funcstem.
May I use -maskstem in
In a simple word, my question is:
under version 5.3.0, how can I specify funcstem (stem of functional
volume)? I don't see any argument for that..
Thanks a lot.
Best,
Ji Won
2016-03-04 16:31 GMT-05:00 Ji Won Bang :
> Dear. Freesurfer experts.
>
> Hi. How are you?
>
> It
rm failed
Which part am I doing wrong?
Thank you so much.
Best,
Ji Won
2016-03-04 17:13 GMT-05:00 Douglas N Greve :
> The functional stream changed a lot from version 4 to version 5. The
> commands and workflow are very different now
>
> On 03/04/2016 04:31 PM, Ji Won Bang wrote:
Dear. Freesurfer experts.
Hi.
I'm using freesurfer version 5.3.0.
I tried:
mkanalysis-sess -analysis retino -TR 2 -paradigm para.para -event-related
-funcstem fmc -nconditions 4 -timewindow 34 -inorm -gammafit 2.25 1.25
-polyfit 2 -mcextreg -force -fsd bold_retino -per-run -native -refeventdur
ing ==> MRIread at 76
ERROR: cannot determine format of
/home/jbang/Projects/replay/epi/replay06/bold_retino/023/fmc (MRIread)
Error in ==> flac_customize at 87
mri = MRIread(fstem,1);
Error in ==> fast_selxavg3 at 65
flac0 = flac_customize(flac0);
>> -
Dear. Freesurfer experts.
Hi.
i appreciate your help in advance!
I'm using freesurfer version 5.3.0.
I tried selxavg3-sess and got the error dimension mismatch between mask and
2th run.
Actually, the number of slices of the 1st run and the rest are different.
Is it the reason why I get this err
ought preproc-sess -per-run creates mask for each run.. but probably
not...
Could you please advise me how to correct this dimension mismatch between
mask and 2th run?
Thank you very much!
Best,
Ji Won
2016-03-09 12:08 GMT-05:00 Ji Won Bang :
> Dear. Freesurfer experts.
>
> Hi.
>
&g
Dear. Freesurfer experts.
Hi. I'm trying retinotopy analysis using freesurfer version 5.3.0.
I'm having a problem when running selxavg3-sess...
Could you please help me with this issue?
I have 3 runs under bold_retino and all 3 scans have the same dimension..
The command line that I entered ar
Dear. All.
Hi. How are you?
It might be a very naive question, but your advice is greatly appreciated!
I'm trying to register 2 T1s obtained from 1 subject on different days and
then register the functional scans to their corresponding T1s (registering
the functional scans to the same day's T1).
tered to the
> same FS data?
>
> hth
> d
>
> On Thu, Mar 17, 2016 at 3:06 PM, Ji Won Bang wrote:
> > Dear. All.
> >
> > Hi. How are you?
> >
> > It might be a very naive question, but your advice is greatly
> appreciated!
> >
> > I'm t
Dear. Freesurfer experts.
Hi.
I'm having a problem with mris_flatten (version 5.3.0)
Could you please help me fix this problem?
My command line is:
mris_flatten -w 0 -distances 12 7
$SUBJECTS_DIR/$SUBJECT/surf/lh.oc.patch.3d
$SUBJECTS_DIR/$SUBJECT/surf/lh.oc.patch.flat
It returns the error:
u
Dear. Freesurfer experts.
Hi. How are you?
I have dataset where a single subject was scanned twice on different days.
I ran recon-all in logitudinal stream (cross, base, long).
The recon-all -base gave me the within-subject template and the recon-all
-long gave me the directory in the format of
o recon-all it will motion correct and
> > average and then all of your functionals will be registered to the
> > same FS data?
> >
> > hth
> > d
> >
> > On Thu, Mar 17, 2016 at 3:06 PM, Ji Won Bang
> wrote:
> >> Dear. All.
> >>
> >
> Hi Ji
>
> that does sound strange! Can you tar and gzip the subject and upload it to
> our website so I can see if I can replicate the problem?
>
> cheers
> Bruce
>
>
> On Thu, 17 Mar 2016, Ji Won Bang wrote:
>
> > Dear. Freesurfer experts.
> >
>
Dear. Freesurfer experts.
Hi. How are you?
I'm trying to flatten the visual cortex using the command mris_flatten
(freesurfer version 5.3.0).
The command line is:
mris_flatten -w 0 -distances 12 7
$SUBJECTS_DIR/$SUBJECT/surf/lh.oc.patch.3d
$SUBJECTS_DIR/$SUBJECT/surf/lh.oc.patch.flat
The error
> some of them won't, meaning that they need to be regenerated.
>
> cheers
> Bruce
>
>
>
>
> On Tue, 22 Mar 2016, Ji Won Bang wrote:
>
> > Dear. Freesurfer experts.
> >
> > Hi. How are you?
> >
> > I'm trying to flatten the visual
> you can try recon-all -make all for that subject and and see if it doesn
> anything. But run mris_euler_number on those surfaces and see if they
> match. They should all have the same number of faces/edges/vertices (for
> one hemisphere in the same subject)
>
> On Tue, 22 Ma
e
> lh.sphere.reg
>
>
>
> and same for the rh (but different from the lh ones)
>
>
> cheers
> Bruce
>
>
> On Tue, 22 Mar 2016, Ji Won Bang wrote:
>
> Dear. Bruce.
>>
>> Thanks for your help.
>>
>> When I tried:
>> mris_euler_number rh.in
cut the patch from those surfaces. The error is
> about a vertex # in the patch (147220), which is larger than the total
> number of vertices in those surfaces (144977), so it's out of bounds. How
> did you do the cutting?
>
>
> On Tue, 22 Mar 2016, Ji Won Bang wrote:
>
&g
tting
work was done in other surface that I did not intend...
If anyone knows why it's happening, let me know.
Thank you!
Best,
Ji Won
2016-03-22 13:18 GMT-04:00 Ji Won Bang :
> Oh, I see.
>
> I showed the contrast results on a surface using the command:
> tksurfer-sess -s $S
Dear. Freesurfer experts.
Hi. How are you?
I'd appreciate it a lot if you can help me with this problem.
I'm trying to check the ROI (.nii) after creating it by using mri_label2vol
command.
I used the command:
mri_label2vol --label $SUBJECTS_DIR/$SUBJECT/label/lh.v1vt.label --label
$SUBJECTS_D
Dear. Experts.
Please ignore the previous email.
It works.
Thank you.
Best,
Ji Won
2016-03-23 17:24 GMT-04:00 Ji Won Bang :
> Dear. Freesurfer experts.
>
> Hi. How are you?
>
> I'd appreciate it a lot if you can help me with this problem.
>
> I'm trying to chec
Dear. Freesurfer experts.
Hi. How are you?
I have a question about making ROI.
This might be a naive question, but any input would be greatly appreciated.
I preprocessed scans per run, thus I have register.dof6.dat file inside all
run epi directories.
Then, I made ROIs per single subject based
Brodmann areas under label
directory.
However, inside the lable directory, I see only
aparc.annot.a2009s.ctab
aparc.annot.ctab
lh.aparc.a2009s.annot
lh.aparc.annot
lh.cortex.label
rh.aparc.a2009s.annot
rh.aparc.annot
rh.cortex.label
Please leave me any comment!!
I appreciate it a lot!
Best
Dear Freesurfer experts,
I'd appreciate any of your comments a lot!
I'm trying to extract BOLD signals from subfields of hippocampus but
somehow I find resolution/size mismatch such that the assigned voxel number
of subfield hippocampus is greater than voxel numbers of whole brain BOLD
data.
I i
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