You may have to give up the arcuate (slft) too, since part of the temporal lobes are chopped off. Although it didn't get to that tract so it's just a guess.

Yes, you should be fine by removing from pathlist (and the respective entries in ncpts) any tracts that are partly cut off in your images.

The registrations are fine, bbregister managed to align the DWI to the T1 even though only the former is truncated. And the registration to the atlas uses the T1, so that worked fine too.

Hope this helps,
a.y

On Fri, 27 Sep 2013, Garikoitz Lerma-Usabiaga wrote:

Many thanks Anastasia. So,  do you think it would work if I exclude this
tracts from the analysis and ask for the remaining ones? 
thanks again,
Gari


On Fri, Sep 27, 2013 at 4:35 PM, Anastasia Yendiki
<ayend...@nmr.mgh.harvard.edu> wrote:

      Hi Gari - Just looked at your subject. The bottom of the brain
      is truncated in the DWIs. The slices stop in the middle of the
      angular bundle, which is why the -prior step failed in that
      pathway. But I expect there'd be problems with other tracts that
      reach that inferior, even if they didn't fail completely -
      corticospinal, uncinate, inferior longitudinal fasciculus.

      a.y

      On Thu, 26 Sep 2013, Garikoitz Lerma-Usabiaga wrote:

            Hi Anastasia,
            I was  testing just with one subject and it finished
            the -prep part with
            error.
            Please find attached the trac-all.log file.
            As this is a test user you will see some other
            invocations of trac-all. The
            last build_stamp starts at row 54.500 aprox.
            (just in case: I started new from de DICOMS and the
            dcm2nii, and I am using
            the resulting .nii, .bvec and .bval, just in case I
            attached the dmrirc
            too).

            Thanks again for your help!
            Gari


            On Thu, Sep 26, 2013 at 8:01 AM, Anastasia Yendiki
            <ayend...@nmr.mgh.harvard.edu> wrote:

                  Hi Gari - Yes, that's your best option right
            now. Sorry for the
                  inconvenience. I'll make sure to add the
            option to have one
                  gradient file per subject in the next version.

                  a.y

                  On Thu, 26 Sep 2013, Garikoitz Lerma-Usabiaga
            wrote:

                        Hi! Thanks for the fast answer. If I do:
            diff
                        id1.bvec id2.bvec
                        I can see some clear differences. 

                        I was told that in FSL I should use the
            bvecs and
                        bvals created in dcm2nii
                        per subject, so I understand I should do
            the same
                        now?
                        Do you think an option would be to
            script the
                        creation of a dmrirc file per
                        each subject and then launch as many
            trac-alls as
                        subjects?

                        Thanks again,
                        Gari

                        On Thursday, September 26, 2013,
            Anastasia Yendiki
                        wrote:

                              Hi Gari - Sorry, right now the
            assumption is
                        that the gradient
                              vectors are the same for all
            subjects. How
                        different are they?

                              a.y

                              On Wed, 25 Sep 2013, Garikoitz
            Lerma-Usabiaga
                        wrote:

                                    Hi Anastasia,I am setting up
            the dmrirc
                        file to run
                                    Tracula. I am using
                                    Siemens Dicoms, so I did not
            specify any
                        setting for
                                    bval and bvec, but when
                                    trac-all -prep starts
            running it gives
                        the following
                                    error: mv: cannot stat
                                   
                       
            'paths.../SubjectID/dmri/dwi_orig_flip.mghdti.bvecs':
                                    No such file or
                                    directory

                                    Ok, so I understand that our
            problem is
                        that we
                                    don't have MGH Siemens
                                    Dicom. 

                                    So I used dcm2nii to convert
            it to .nii
                        files and
                                    each conversion gives me a
                                    SubjectID.bval and
            SubjectID.bvec. Every
                        .bval is
                                    the same file, but every
                                    .bvec file is a different
            one. 

                                    I can edit "set dcm_list = "
            to include
                        all the
                                    newly created .nii files,
                                    but

                                    My question is: 
                                    - How can I specify every
            .bvec value
                        for every
                                    subject? In the dmrirc file
                                    everything I see is a "set
            bvecfile = "
                        option.

                                    Thank you very much,
                                    Gari




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