Good to hear. That was just a naming convention to keep track of how each version was generated.

To continue, all you need to do is rename the good brainmask (generated with the modified gcuts command) to brainmask.mgz.
-Louis

On Fri, 11 Apr 2014, Markus Gschwind wrote:

Thanks Louis!
Great. It seems I need -T 0.65. That looks fine.

Is it necessary 
- to name the modified brainmask.gcuts.T065.mgz? 
- and keep both brainmask.mgz and brainmask.gcuts.mgz in the mri folder?

And then continue with 
recon-all autorecon2 autorecon3 -s subjectid

Is that correct?

Thank you so much!
Markus


2014-04-11 17:23 GMT+02:00 Louis Nicholas Vinke <vi...@nmr.mgh.harvard.edu>:
      Hi Markus,
      You can try running mri_gcut with a slightly higher T value,
      default is 0.4.

      command would be something like (running from within subject's
      mri dir):
      mri_gcut -T 0.5 T1.mgz brainmask.gcuts.T-0.5.mgz

      Carefully inspect the output, overlaid as a heatmap on the T1
      and/or previous brainmask.mgz.  You might have to clone back in
      some brain voxels.

      -Louis

      On Fri, 11 Apr 2014, Markus Gschwind wrote:

            Dear Louis (and Bruce),
            So I have run 

            recon-all -skullstrip -clean-bm -gcut -subjid
            <subjid>
            on my subjects where remaining pieces of dura after
            a normal recon-all got
            included into pial surface. I am having a look at
            the result before
            continuing with autorecon2 etc.

            Results are not yet satisfactory as there is still
            several centimeters of
            dura included in the brainmask, mostly on the convex
            part of central regions

            Is there a possibility to make graph-cut slightly
            more agressive?

            Thank you for help!
            Markus


                  2014-04-07 22:40 GMT+02:00 Louis Nicholas
            Vinke
                  <vi...@nmr.mgh.harvard.edu>:
                        Hi Markus,
                        It will only skullstrip the T1 and
            generate a new
                        brainmask.mgz. So you'll need to run
            autorecon2 and
                        3 afterwards.
                        -Louis

                        On Mon, 7 Apr 2014, Markus Gschwind
            wrote:

                              Dear Louis!
                              Thank you for the link.

                              It says I should use 


                              recon-all -skullstrip -clean-bm
            -gcut
                              -subjid <subjid>
                              My question is if this command
            only
                              skullstrips and then stops and I
            would
                              have to resume with
                              autorecon2 etc. or if it continues
            until
                              the end and overwrites the whole
                              processing (I'd like to
                              know before I mess up with te
            subject
                              and have a further 16 hours
            processing
                              for nothing... ;-)

                              Thanks!
                              Markus


                              2014-04-07 20:01 GMT+02:00 Louis
                              Nicholas Vinke
                              <vi...@nmr.mgh.harvard.edu>:
                                    Hi Markus,
                                    Instructions for using gcut
            within
                              recon-all can be found on this
            wiki
                              page, near the
                                    bottom.

                                  
https://surfer.nmr.mgh.harvard.edu/fswiki/FsTutorial/SkullStripFix_freevie
            w


                                    -Louis

                                    On Mon, 7 Apr 2014, Bruce
            Fischl
                              wrote:

                                          Hi Markus

                                          that looks pretty
            blurry and
                              low contrast, although it's hard
            to tell
                                          without windowing it.
            Does
                              the intensity normalization remove
            the
                              contrast?
                                          If so, you can try
            making it
                              less aggressive with the -gentle
            flag or
                                          playing with
            individual
                              parameters (like -b).

                                          I can't remember the
            graph
                              cuts stuff. Hopefully Nick or Zeke
            or
                              someone
                                          will point you in the
            right
                              direction
                                          Bruce


                                          On Mon, 7 Apr 2014,
            Markus
                              Gschwind wrote:

                                                Dear Bruce,

                                                Thanks for your
                              detailed answer!

                                                      > it's
            tough to
                              tell for sure on just a single
            slice,
                                                particularly if
            it is
                              the intensity normalized one that
                                                      removes a
            lot of
                              the contrast if it is (as you
            suspect)
                                                doing the wrong
            thing.
                              What does the orig look like? We
            try
                                                      pretty
            hard to
                              avoid including deep, highly
            myelinated
                                                gray matter
            inside the
                              white matter surface, but of
            course if
                                                      the
            contrast is
                              low enough we can fail. If you
            scroll
                                                backwards and
            forward
                              a few slices does or look in a
            different
                                                     
            orientation does
                              it look different/better?
            Sometimes the
                                                surface is
            curving
                              sharply and this kind of thing
            will show
                                                      up on a
            single
                              slice, but actually isn't a
            significant
                                                inaccuracy.



                                                Yes, when
            scrolling
                              throug the slides it really
            appears
                                                consistent
            across
                              several slides (actually the
            attached
                                                screenshots
                                                showed Freeview
            in
                              coronal, sagittal and axial
            perspective
                              of
                                                the same
            region). Here
                              is the orig attached together with
            the
                                                wm,
                                                pial and white.
                                                So how should I
            treat
                              it?

                                                      > As for
            the
                              dura, that certainly looks like a
                              problem for
                                                thickness
            estimates.
                              Have you tried using the graph
            cuts
                                                      skull
            stripping?
                              That is more aggressive than
                                                mri_watershed.
            You can
                              also play with the watershed
            parameters
                                                to try
                                                      to get
            more dura
                              removed. Finally, if you have a
            T2-space
                                                FLAIR scan we
            can use
                              that to properly reposition the
                                                      surfaces
            (or
                              less ideally, a T2-space scan
            without a
                              FLAIR
                                                inversion).



                                                No,
            unfortunately
                              there are no other images at
                              disposition.

                                                How would one go
            with
                              the graph cuts ?
                                                I found
            "mri_gcut
                              [-110| -mult <filename> |-T
            <value>]
                                                in_filename
                              out_filename",

                                                but how is it
            run
                              within recon-all in order to
            repair (FS
                                                version 5.3)?

                                                Thank you so
            much!
                                                Markus


                                                2014-04-07 14:47
                              GMT+02:00 Bruce Fischl
                                               
                              <fis...@nmr.mgh.harvard.edu>:
                                                      Hi Markus

                                                      it's tough
            to
                              tell for sure on just a single
            slice,
                                                particularly if
            it is
                              the intensity normalized one that
                              removes
                                                      a lot of
            the
                              contrast if it is (as you suspect)
            doing
                              the
                                                wrong thing.
            What does
                              the orig look like? We try pretty
                                                      hard to
            avoid
                              including deep, highly myelinated
            gray
                                                matter inside
            the
                              white matter surface, but of
            course if
                              the
                                                      contrast
            is low
                              enough we can fail. If you scroll
                                                backwards and
            forward
                              a few slices does or look in a
            different
                                                     
            orientation does
                              it look different/better?
            Sometimes the
                                                surface is
            curving
                              sharply and this kind of thing
            will show
                                                      up on a
            single
                              slice, but actually isn't a
            significant
                                                inaccuracy.


                                                      As for the
            dura,
                              that certainly looks like a
            problem for
                                                thickness
            estimates.
                              Have you tried using the graph
            cuts
                                                      skull
            stripping?
                              That is more aggressive than
                                                mri_watershed.
            You can
                              also play with the watershed
            parameters
                                                to try
                                                      to get
            more dura
                              removed. Finally, if you have a
            T2-space
                                                FLAIR scan we
            can use
                              that to properly reposition the
                                                      surfaces
            (or
                              less ideally, a T2-space scan
            without a
                              FLAIR
                                                inversion).

                                                      cheers
                                                      Bruce


                                                      On Mon, 7
            Apr
                              2014, Markus Gschwind wrote:

                                                            Dear
            all,
                                                            I
            would
                              like to show some very frequent
            and
                              typical
                                                cases of
            segmentation
                                                           
            problems
                              in my bunch of data of normal
            subjects
                                                (after
            recon-all), of
                              which
                                                            I
            couldn't
                              find a description in the
                                                           
                                              
wiki(http://surfer.nmr.mgh.harvard.edu/fswiki/FreeviewGuide/FreeviewWorkin
            g
                              With
                                                           
                              Data/FreeviewEditingaRecon).

                                                            I am
                              therefore not sure if these types
            of
                              error are
                                                serious and will
                              affect
                                                           
            later
                              results like thickness, curvature,
            GWR,
                              etc.

                                                            Here
            are
                              the examples (c.f. attached
            screenshots
                                                from Freeview)

                                                            1)
            In the
                              primary sensory-motor cortex it
                              frequently
                                                happens that the
                                                           
            "?h.white"
                              line lies several mm within the wm
                              border
                                                (c.f. yellow
            arrow), I
                                                            did
            not
                              observe this behavior in other
            places.
                                                           
            >>Would I
                              need to edit that?

                                                            2)
                              Sometimes the "?h.pial" line
            includes
                              also dura
                                                or parts of the
            skull
                                                           
            (green
                              arrow).
                                                            >>Is
            it
                              necessary to edit that as well?

                                                            3)
            Another
                              question concerns the yellow parts
            of
                              the
                                                wm which
            sometimes are
                                                            much
                              larger than the ventricles and
            also
                              include
                                                both caudate
            nuclei
                              (not
                                                           
            shown). 
                                                            >>Is
            this
                              a problem? 

                                                           
            Thanks in
                              advance!!

                                                           
            Markus







                             
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