New subject: Recon-all Soft Errors

30 Jul 2020

      External Email - Use Caution
Here is the recon-all.log file.
Thanks,
Elana
-----Original Message-----
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Sent: July 30, 2020 10:00 AM
To: freesurfer@nmr.mgh.harvard.edu
Subject: Freesurfer Digest, Vol 197, Issue 59
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When replying, please edit your Subject line so it is more specific than "Re: Contents of Freesurfer digest..."
Today's Topics:
1. FS 7.1.0 - Editing intensity values for WM (Nils B?er)
   2. Re: FS 7.1.0 - Editing intensity values for WM (Fischl, Bruce)
   3. Creating .annot file for a mri_decimate downsampeld       version
      of pial surface (Donelson Berger)
   4. GONE: -make to recon-all (Johnson, Hans J)
   5. Re: fsgd file - glmfit error
      (Lab of Autism and Developmental Neuroscience,    Lab of Autism and Developmental Neuroscience)
   6. Re: Recon-all Soft Errors (Zollei, Lilla,Ph.D.)
   7. bad interpreter: No such file or directory error
      (Hengameh Marzbani)
   8. Re: overlapping/ superimposing regions of one analysis over
      another (Douglas N. Greve)
   9. Re: Creating .annot file for a mri_decimate downsampeld
      version of pial surface (Douglas N. Greve)
  10. Re: Recon-all Soft Errors (Douglas N. Greve)
  11. Re: Coregistration to MNI (Douglas N. Greve)
  12. mri_aparc2aseg: how to remove redundant output labels? (Ellen Ji)
  13. Re: bad interpreter: No such file or directory error (fsbuild)
----------------------------------------------------------------------
Message: 1
Date: Wed, 29 Jul 2020 21:27:03 +0200
From: Nils B?er nils.tobias94@gmail.com
Subject: [Freesurfer] FS 7.1.0 - Editing intensity values for WM
To: freesurfer@nmr.mgh.harvard.edu
Message-ID:
        CALZW1G2=-OvWkL81sZxTBiMCKBwiOn6EwSfd2xP0NzEWQYBSTw@mail.gmail.com
Content-Type: text/plain; charset="utf-8"
External Email - Use Caution
Hello everyone,
I just have a short question, because I can't find anything helpful in the tutorials.
In my MRI scans freesurfer includes areas to the white matter, even though visual inspection concludes that the area should be grey matter. Is there a possibility to change the value at which freesurfer includes areas to the WM, which i can just change? For example freesurfer includes areas to the WM with intensity values below 85 and i want to change that.
I'd be thankful for any feedback/links to guides.
Best regards,
Nils
--
Nils B?er
Research Assistant with Bachelor Degree (WHB) *Psychology and Movement* University of Paderborn Department of Sports and Health Warburger Str. 100
33098 Paderborn
Room: Sp 1.401
Email: nils.tobias94@gmail.com / nboeer@mail.uni-paderborn.de nils.tobias94@gmail.com
Web: https://sug.uni-paderborn.de/en/sport/sportpsychologie/team/
         https://sug.uni-paderborn.de/department/it/
https://sug.uni-paderborn.de/en/sport/sportpsychologie/team/
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Message: 2
Date: Wed, 29 Jul 2020 20:32:34 +0000
From: "Fischl, Bruce" BFISCHL@mgh.harvard.edu
Subject: Re: [Freesurfer] FS 7.1.0 - Editing intensity values for WM
To: "freesurfer@nmr.mgh.harvard.edu" freesurfer@nmr.mgh.harvard.edu
Message-ID:
        BL0PR04MB660985EC505DEECB596362ADEF700@BL0PR04MB6609.namprd04.prod.outlook.com
Content-Type: text/plain; charset="utf-8"
Hi Nils
There are expert options for this. You can specify things like -min_white 90 to some of the programs like mri_segment and the surface placement stuff
Cheers
Bruce
From: freesurfer-bounces@nmr.mgh.harvard.edu freesurfer-bounces@nmr.mgh.harvard.edu On Behalf Of Nils B?er
Sent: Wednesday, July 29, 2020 3:27 PM
To: freesurfer@nmr.mgh.harvard.edu
Subject: [Freesurfer] FS 7.1.0 - Editing intensity values for WM
External Email - Use Caution
Hello everyone,
I just have a short question, because I can't find anything helpful in the tutorials.
In my MRI scans freesurfer includes areas to the white matter, even though visual inspection concludes that the area should be grey matter. Is there a possibility to change the value at which freesurfer includes areas to the WM, which i can just change? For example freesurfer includes areas to the WM with intensity values below 85 and i want to change that.
I'd be thankful for any feedback/links to guides.
Best regards,
Nils
--
Nils B?er
Research Assistant with Bachelor Degree (WHB) Psychology and Movement University of Paderborn Department of Sports and Health Warburger Str. 100
33098 Paderborn
Room: Sp 1.401
Email: nils.tobias94@gmail.com / nboeer@mail.uni-paderborn.demailto:nils.tobias94@gmail.com
Web: https://sug.uni-paderborn.de/en/sport/sportpsychologie/team/
         https://sug.uni-paderborn.de/department/it/https://sug.uni-paderborn.de/en/sport/sportpsychologie/team/
[https://ipmcdn.avast.com/images/icons/icon-envelope-tick-round-orange-animat...]https://www.avast.com/sig-email?utm_medium=email&utm_source=link&utm_campaign=sig-email&utm_content=webmail
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Message: 3
Date: Wed, 29 Jul 2020 15:51:03 -0500
From: Donelson Berger donelsongrahamberger@gmail.com
Subject: [Freesurfer] Creating .annot file for a mri_decimate
        downsampeld     version of pial surface
To: freesurfer@nmr.mgh.harvard.edu
Message-ID:
        CAAKWbtXL5vQOPXEoO6TUeRM_dHowghOYVX=ptXWPE8+GkAMENA@mail.gmail.com
Content-Type: text/plain; charset="utf-8"
External Email - Use Caution
Hello FreeSurfer Expert,
I've run into a problem that I just can't seem to solve. After downsampling teh ?.pial surfaces using mri_decimate to 20,000 surfaces and 10,002 points, I don't know how to create .annot files for the new surfaces I created. I want to be able to tell which ROI each vertex is in for my new surface based off a parcellation.
I've been trying to use mri_ca_label, mri_ca_train, and mris_sample_parc, but I can't seem to get anything to work.
Do you have any suggestions?
Thanks for your help,
Donelson Graham Berger
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Message: 4
Date: Wed, 29 Jul 2020 22:22:47 +0000
From: "Johnson, Hans J" hans-johnson@uiowa.edu
Subject: [Freesurfer] GONE: -make to recon-all
To: "freesurfer@nmr.mgh.harvard.edu" freesurfer@nmr.mgh.harvard.edu
Message-ID: 9DB20083-D647-47E0-9396-C24308B503B9@uiowa.edu
Content-Type: text/plain; charset="utf-8"
External Email - Use Caution
The release notes for 7.0.0 claim that the -make option is "Gone" from recon-all.  This option, however, is still available and does not seem to fail.
I am running several thousand data sets on a cluster through Freesurfer 7.1.0, and periodically the process fails for some subjects. In the past the "recon-all -make all" feature was a very convenient way to complete freesurfer runs that were terminated early for some unknown reason
Q1)  should "recon-all -make all" be avoided for FreeSurfer 7.1.0?
Q2) is there an alternate way to "continue form the point where results are missing" in the pipeline?
Thanks,
Hans
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Message: 5
Date: Wed, 29 Jul 2020 15:49:44 -0700
From: "Lab of Autism and Developmental Neuroscience,    Lab of Autism and
        Developmental Neuroscience" ladn@email.gwu.edu
Subject: Re: [Freesurfer] fsgd file - glmfit error
To: Freesurfer support list freesurfer@nmr.mgh.harvard.edu
Message-ID:
        CACE7MB+VaV5UyPsnRSfnyDA8XT0_dDhe1sxd2-rumCf3z0_PDA@mail.gmail.com
Content-Type: text/plain; charset="utf-8"
External Email - Use Caution
Thank you Douglas!
On Tue, Jul 28, 2020 at 9:34 AM Douglas N. Greve dgreve@mgh.harvard.edu
wrote:
...
Try putting 1 after GroupDescriptorFile, ie,
GroupDescriptorFile 1
On 7/28/2020 12:21 PM, Lab of Autism and Developmental Neuroscience, 
Lab of Autism and Developmental Neuroscience wrote:
    External Email - Use Caution

Here is my fsgd file.
Thank you!
On Mon, Jul 27, 2020 at 8:44 PM Douglas N. Greve 
dgreve@mgh.harvard.edu
wrote:
...
Please send the fsgd file
On 7/27/2020 11:34 PM, Lab of Autism and Developmental Neuroscience, 
Lab of Autism and Developmental Neuroscience wrote:
    External Email - Use Caution

Dear Freesurfer experts,
Hope this email finds you well. I am having some trouble with the 
fsgd file for glmfit and I'm confused why. This is the error I'm 
getting when running glmfit:
iMac-Pro:BAP_complete ajobsaid$ mri_glmfit --y 
mrip.rh_volume_F7_BNB.00.mgh --fsgd fsgd_8.fsgd --C Cor_2.mtx --surf 
fsaverage rh --cortex --glmdir contrast2.rh_volume_BNB.glmdir
gdfRead(): reading fsgd_8.fsgd
ERROR: FSGDF version 0 unsupported (fsgd_8.fsgd) 
iMac-Pro:BAP_complete ajobsaid$
If needed, I can send you my fsgd file, but I have triple checked the 
design and format of the file (it is saved as .fsgd), and I'm still 
getting this error message.
Thank you,
Alex

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Message: 6
Date: Thu, 30 Jul 2020 09:34:12 +0000
From: "Zollei, Lilla,Ph.D." LZOLLEI@mgh.harvard.edu
Subject: Re: [Freesurfer] Recon-all Soft Errors
To: Freesurfer support list freesurfer@nmr.mgh.harvard.edu
Message-ID:
        DM6PR04MB44127C2DB157BB07AB669F41E3710@DM6PR04MB4412.namprd04.prod.outlook.com
Content-Type: text/plain; charset="windows-1252"
Hi Elena,
What is the age range of your subjects?
Best, Lilla
________________________________
From: freesurfer-bounces@nmr.mgh.harvard.edu freesurfer-bounces@nmr.mgh.harvard.edu on behalf of Elana Sarabin elana.sarabin1@ucalgary.ca
Sent: Wednesday, July 29, 2020 11:02 AM
To: Freesurfer support list freesurfer@nmr.mgh.harvard.edu
Subject: [Freesurfer] Recon-all Soft Errors
External Email - Use Caution
Hi Freesurfer experts,
I am a first time user of FreeSurfer and I haven?t been able to find any threads for how to fix some of my problems. I have a very large dataset and as I am editing on freeview I am noticing that ? or more of my participants have a large area missing in the brainmask.mgz file but the region is visible from the T1.file. In some participant scans the areas missing arent too big however other scans (the photo I attached) have a very large portion of the brain missing. I have tried quite a few things to fix this including re running recon-all, adding control points, and adjusting the wsthresh value, however, none have worked. Wondering if there is a way to fix this kind of error and if there is a way to prevent this from happening as I run recon-all on future participants. In addition, I have been duplicating my files before editing in order to always have the original files as a backup. With some participants when I duplicate the files their T1.mgz file ends up completely white (image attached). I have yet to see this in a none duplicated file however with some participants I can duplicate the files and have no issue. I have attached photos of both of my problems. Any suggestions for fixes would be greatly appreciated.
Thanks,
Elana
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Message: 7
Date: Thu, 30 Jul 2020 17:49:49 +0430
From: Hengameh Marzbani marzbani91@gmail.com
Subject: [Freesurfer] bad interpreter: No such file or directory error
To: Freesurfer support list freesurfer@nmr.mgh.harvard.edu
Message-ID:
        CAFn2Bowe=LPArymmLwu=K_3WgEZC0GnG9OkV5qAeBPdZuGV8zw@mail.gmail.com
Content-Type: text/plain; charset="utf-8"
External Email - Use Caution
Hello Freesurfer developers,
I have installed FreeSurfer v7 on 2 machines running Ubuntu and made sure that the setting are fine.
Also, freeview works by simply typing the freeview command.
However,I have tried to run recon-all. but, I have got the following error message on all PCs:
*bash: /usr/local/freesurfer/bin/recon-all: /bin/tcsh: bad interpreter: No such file or directory*
also The build-stamps.txt file contents:
*freesurfer-linux-centos7_x86_64-7.1.0-20200511-813297b*
Thank you in advance,
Best regards,
Hengameh
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Message: 8
Date: Thu, 30 Jul 2020 10:20:07 -0400
From: "Douglas N. Greve" dgreve@mgh.harvard.edu
Subject: Re: [Freesurfer] overlapping/ superimposing regions of one
        analysis over another
To: freesurfer@nmr.mgh.harvard.edu
Message-ID: c4e336e0-b3b8-89eb-e59b-1894fdf856b8@mgh.harvard.edu
Content-Type: text/plain; charset="utf-8"
To obtain the common regions, first binarize the clusterwise significance maps with something like mri_binarize --min 2.0 --i clustersigmap1.mgh --o bin.clustersigmap1.mgh Same for the other groups Then take the intersection fscalc clustersigmap1.mgh and clustersigmap2.mgh -o intersection.mgh
On 7/27/2020 2:17 PM, Sunil Khokhar wrote:
...
????????External Email - Use Caution
To operate the visualization and obtain the common regions of my 
between-group difference results and the correlation results in one 
image. In other?words, overlapping/ superimposing?my correlation 
results on the between-group results (to obtain the common regions 
from the two separate analysis).
Thanks
_______________
Sunil K Khokhar
PhD Scholar,
Department of Neuroimaging & Interventional Radiology, NIMHANS, 
Bengaluru, INDIA.
khokharsunil1@gmail.com mailto:khokharsunil1@gmail.com
+91-9413101839
On Mon, Jul 27, 2020 at 8:21 PM Douglas N. Greve 
<dgreve@mgh.harvard.edu mailto:dgreve@mgh.harvard.edu> wrote:
are you asking how to create positive and negative regions or are
you asking how to operate the visualization?

On 7/25/2020 9:40 AM, Sunil Khokhar wrote:

...
????????External Email - Use Caution

Dear Experts,

I have done a between group (2 groups) difference in whole brain
voxel based cortical thickness using QDEC, which showed
significant regional differences in certain clusters
bilaterally?in the brain. I also did a correlation between
cortical thickness and behavioral scores separately?in these two
groups. Now, I want to superimpose regions (clusters) which
showed positive and negative correlation on the?results/
regions?I obtained in my between group analysis. How can I do this?

Thanks in advance!
Sunil.
_______________
Sunil K Khokhar
PhD Scholar,
Department of Neuroimaging & Interventional Radiology,
NIMHANS, Bengaluru, INDIA.
khokharsunil1@gmail.com <mailto:khokharsunil1@gmail.com>
+91-9413101839

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Message: 9
Date: Thu, 30 Jul 2020 10:21:14 -0400
From: "Douglas N. Greve" dgreve@mgh.harvard.edu
Subject: Re: [Freesurfer] Creating .annot file for a mri_decimate
        downsampeld version of pial surface
To: freesurfer@nmr.mgh.harvard.edu
Message-ID: ec2eef74-6cd8-0c36-dbeb-983240090223@mgh.harvard.edu
Content-Type: text/plain; charset="utf-8"
Use
mris_apply_reg --sval-annot lh.your.annot --streg lh.pial lh.pial.decimated --o lh.your.decimated.annot
On 7/29/2020 4:51 PM, Donelson Berger wrote:
...
????????External Email - Use Caution
Hello FreeSurfer Expert,
I've run into a problem that I just can't seem to solve. After 
downsampling teh ?.pial surfaces using mri_decimate to 20,000 surfaces 
and 10,002 points, I don't know how to create .annot files for the new 
surfaces I created. I want to be able to tell which ROI each vertex is 
in for my new surface based off a parcellation.
I've been trying to use mri_ca_label, mri_ca_train, and 
mris_sample_parc, but I can't seem to get anything to work.
Do you have any suggestions?
Thanks for your help,
Donelson Graham Berger

Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
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Message: 10
Date: Thu, 30 Jul 2020 10:26:22 -0400
From: "Douglas N. Greve" dgreve@mgh.harvard.edu
Subject: Re: [Freesurfer] Recon-all Soft Errors
To: freesurfer@nmr.mgh.harvard.edu
Message-ID: 78c6cfdd-63ba-9ed1-1c26-fcbc76472ac8@mgh.harvard.edu
Content-Type: text/plain; charset="windows-1252"
for the first error, can you send the recon-all.log file?
For the second error, you need to adjust the intensity ranges. For some reason they are coming up as 0s.
On 7/29/2020 11:02 AM, Elana Sarabin wrote:
...
????????External Email - Use Caution
Hi Freesurfer experts,
I am a first time user of FreeSurfer and I haven?t been able to find 
any threads for how to fix some of my problems. I have a very large 
dataset and as I am editing on freeview I am noticing that ? or more 
of my participants have a large area missing in the brainmask.mgz file 
but the region is visible from the T1.file. In some participant scans 
the areas missing arent too big however other scans (the photo I
attached) have a very large portion of the brain missing. I have tried 
quite a few things to fix this including re running recon-all, adding 
control points, and adjusting the wsthresh value, however, none have 
worked. Wondering if there is a way to fix this kind of error and if 
there is a way to prevent this from happening as I run recon-all on 
future participants. In addition, I have been duplicating my files 
before editing in order to always have the original files as a backup.
With some participants when I duplicate the files their T1.mgz file 
ends up completely white (image attached). I have yet to see this in a 
none duplicated file however with some participants I can duplicate 
the files and have no issue. I have attached photos of both of my 
problems. Any suggestions for fixes would be greatly appreciated.
Thanks,
Elana

Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
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Message: 11
Date: Thu, 30 Jul 2020 11:31:47 -0400
From: "Douglas N. Greve" dgreve@mgh.harvard.edu
Subject: Re: [Freesurfer] Coregistration to MNI
To: "Camargo, Aldo" ACamargo@som.umaryland.edu, Freesurfer support
        list    freesurfer@nmr.mgh.harvard.edu
Message-ID: 9af8c73e-46a8-e9b6-4b84-ce507589efed@mgh.harvard.edu
Content-Type: text/plain; charset="windows-1252"
It looks like cvs failed. Can you send the log? Also, please remember to post to the list and not us personally.
On 7/30/2020 11:13 AM, Camargo, Aldo wrote:
...
????????External Email - Use Caution
Hi Douglas,
I was able to run the script to create the cvs folder and its files 
but still I can not run the script that does the coregistration of the 
Pet image to the MNI space.
I am getting the following error:
(base)
acamargo@acamargo-System-Product-Name:~/PET/MPRAGE/2006-09-27_14_15_46
.0/S19445/subj1/mri$
mri_vol2vol --gcam
/home/acamargo/PET/ADNI_Brain_PET__Raw/2006-11-01_11_56_37.0/I28835/me
anPET.nii.gz
register.dof6.lta
$SUBJECS_DIR/subj1/cvs/final_CVSmorph_tocvs_avg35_inMNI152.m3z
$FREESURFER_HOME/subject/cvs_avg35_inMNI152/mri.2mm/register.lta 0 1 
pet.cvs.2mm.sm00.ni.gz Loading mov 
/home/acamargo/PET/ADNI_Brain_PET__Raw/2006-11-01_11_56_37.0/I28835/me
anPET.nii.gz
Loading source LTA register.dof6.lta
Loading GCAM /subj1/cvs/final_CVSmorph_tocvs_avg35_inMNI152.m3z
ERROR: cannot find or read
/subj1/cvs/final_CVSmorph_tocvs_avg35_inMNI152.m3z

--
*From:* Douglas N. Greve dgreve@mgh.harvard.edu
*Sent:* Wednesday, July 29, 2020 10:39 AM
*To:* Camargo, Aldo ACamargo@som.umaryland.edu; Freesurfer support 
list freesurfer@nmr.mgh.harvard.edu
*Subject:* Re: [Freesurfer] Coregistration to MNI Here is the command 
mri_cvs_register --mov $subject --mni --openmp N
This command can take a very long time to run. The --openmp N 
indicates the number of processors to use if you have a multiprocessor 
system. Even with N=3, it can take 18 hours.
On 7/29/2020 12:35 AM, Camargo, Aldo wrote:
...
????????External Email - Use Caution
Hi Douglas,
I don't have the folder cvs and I don't have the files bellow:
cvs/final_CVSmorph_tocvs_avg35_inMNI152.m3z
$FREESURFER_HOME/subjects/cvs_avg35_inMNI152/mri.2mm/register.lta
How can I get these files,
Aldo

*From:* Camargo, Aldo ACamargo@som.umaryland.edu 
mailto:ACamargo@som.umaryland.edu
*Sent:* Monday, July 27, 2020 11:46 PM
*To:* Douglas N. Greve dgreve@mgh.harvard.edu 
mailto:dgreve@mgh.harvard.edu
*Subject:* Re: [Freesurfer] Coregistration to MNI Thanks a lot 
Douglas for your great input,
Aldo

*From:* freesurfer-bounces@nmr.mgh.harvard.edu
mailto:freesurfer-bounces@nmr.mgh.harvard.edu
freesurfer-bounces@nmr.mgh.harvard.edu
mailto:freesurfer-bounces@nmr.mgh.harvard.edu on behalf of Douglas 
N. Greve dgreve@mgh.harvard.edu mailto:dgreve@mgh.harvard.edu
*Sent:* Monday, July 27, 2020 10:46 AM
*To:* freesurfer@nmr.mgh.harvard.edu
mailto:freesurfer@nmr.mgh.harvard.edu
freesurfer@nmr.mgh.harvard.edu 
mailto:freesurfer@nmr.mgh.harvard.edu
*Subject:* Re: [Freesurfer] Coregistration to MNI This command will 
allow you to have a registration file and sample into MNI152 2mm 
space
mri_vol2vol --gcam pet.nii.gz register.dof6.lta 
$SUBJECTS_DIR/$subject/cvs/final_CVSmorph_tocvs_avg35_inMNI152.m3z
$FREESURFER_HOME/subjects/cvs_avg35_inMNI152/mri.2mm/register.lta 0 1 
pet.cvs.2mm.sm00.nii.gz
you can get the registration file with mri_coreg --mov pet.nii.gz --s 
$subject --reg register.dof6.lta
On 7/26/2020 9:19 AM, Zollei, Lilla,Ph.D. wrote:
...
Hi Aldo,
If you have a recon-ned structural MRI corresponding to your PET 
scan then the answer is yes.
Lilla

*From:* freesurfer-bounces@nmr.mgh.harvard.edu
mailto:freesurfer-bounces@nmr.mgh.harvard.edu
freesurfer-bounces@nmr.mgh.harvard.edu
mailto:freesurfer-bounces@nmr.mgh.harvard.edu on behalf of 
Camargo, Aldo ACamargo@som.umaryland.edu 
mailto:ACamargo@som.umaryland.edu
*Sent:* Saturday, July 25, 2020 12:19 AM
*To:* Freesurfer support list freesurfer@nmr.mgh.harvard.edu 
mailto:freesurfer@nmr.mgh.harvard.edu
*Subject:* [Freesurfer] Coregistration to MNI
????????External Email - Use Caution
Hi Freesurfer experts,
I want to coregister a PET image to the MNI space, can I use 
mri_cvs_register ?
Thanks a lot,
Aldo Camargo

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Message: 12
Date: Thu, 30 Jul 2020 17:39:06 +0200
From: Ellen Ji ellen.ji@bli.uzh.ch
Subject: [Freesurfer] mri_aparc2aseg: how to remove redundant output
        labels?
To: freesurfer@nmr.mgh.harvard.edu
Message-ID: 24cc8874-81ee-1e68-85ad-b8fe662c4fc3@bli.uzh.ch
Content-Type: text/plain; charset="utf-8"; format="flowed"
External Email - Use Caution
Dear experts,
I am running mri_aparc2aseg using two annotations as input (one for each hemisphere), each with 159 labels, and wish to end up with a single output segmentation of 318 labels. However, when I run the below, this is not the case:
mri_aparc2aseg \
 ??????????????? --s subject1 \
 ??????????????? --annot 500_sym.aparc \  ??????????????? --wmparc-dmax 2 \  ??????????????? --labelwm \  ??????????????? --hypo-as-wm? \  ??????????????? --o subject1/mri/parcellation.nii.gz
In fact, the output has 680 labels rather than 318 labels. A few questions.
- How can I see what exactly the 680 label names are (how to extract from the .nii.gz output file)? Currently, I have just quantified it to be 680 by doing this in matlab: gunzip('parcellation.nii.gz')  ???? a = MRIread('parcellation.nii');  ???? u = unique(a.vol(:));  ???? length(u) % total number of labels
- I believe the extra labels are from the Freesurfer LUT. How can I make sure they are not added when running mri_aparc2aseg? (such that only my annotation labels are included in the output)
Thank you very much,
Ellen
*****
Ellen Ji, PhD
Postdoctoral Research Fellow
Psychiatric University Hospital
University of Z?rich
ellen.ji@bli.uzh.ch
homanlab.github.io/ellen/
------------------------------
Message: 13
Date: Thu, 30 Jul 2020 17:48:25 +0200
From: fsbuild fsbuild@contbay.com
Subject: Re: [Freesurfer] bad interpreter: No such file or directory
        error
To: freesurfer@nmr.mgh.harvard.edu
Cc: marzbani91@gmail.com
Message-ID: 1596124105.5f22ebc98f04a@trashmail.com
Content-Type: text/plain; charset="utf-8"
External Email - Use Caution
Hello Hengameh,
You probably need to install tcsh (and or csh).
I would try,
$&nbsp;sudo&nbsp;apt-get install csh tcsh
- R..
On Jul 30, 2020, at 09:19, Hengameh Marzbani &lt;marzbani91@gmail.com&gt; wrote:&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;External Email - Use Caution&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Hello Freesurfer developers,I have installed FreeSurfer v7 on 2 machines running Ubuntu and made sure that the setting are fine. Also, freeview works by simply typing the freeview command.However,I have tried to run recon-all. but, I have got the following error message on all PCs:bash: /usr/local/freesurfer/bin/recon-all: /bin/tcsh: bad interpreter: No such file or directoryalso&nbsp;The build-stamps.txt file contents:freesurfer-linux-centos7_x86_64-7.1.0-20200511-813297bThank you in advance, Best regards, Hengameh_______________________________________________Freesurfer mailing listFreesurfer@nmr.mgh.harvard.eduhttps://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
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