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Hi Helmut,

Thank you so much for your great help! I will use your segmented GM for now
and continue trying to figure out why it fails at my side.

Thanks a lot!!
MA

On Sun, May 10, 2015 at 12:54 AM, H. Nebl <[log in to unmask]> wrote:

> Dear Marris,
>
> Well, I'm not really sure what this screenshot shows (the segmented grey
> matter image?), and how it was visualized. It looks like a binary image
> with zeros and ones, but maybe this is just due to some display settings,
> coding anything non-zero as white. See attachements for 1) the raw
> structure and the c1 grey matter image obtained with "Segment" in SPM12,
> visualized within SPM, and 2) the grey matter tissue probability map as
> provided with SPM and the wc1 normalized grey matter image as obtained with
> the same routine.
>
> The output seems to be reasonable. It is not perfect, e.g. some white
> matter is classified as GM (see raw&c1_WML). This is not surprising though,
> as the raw image clearly shows some intensity changes, pointing to
> periventricular white matter lesions (and/or artefacts). It's not a matter
> of algorithm (SPM12 Segment vs. SPM8 vs. VBM8), but would require a special
> preprocessing pipeline to avoid misclassifications (e.g. some additional
> tissue probabiliy maps coding regions where WML are likely to occur).
>
> What bothers me a little is the contrast of the raw image. When looking at
> e.g. the topmost slices or at some of the sulci there is hardly any
> contrast between grey matter and white matter. It would thus be impossible
> to properly segment the image manually. The segmentation algorithm results
> in a reasonable image, but this is also because it is forced to classify
> things as grey matter due to spatial constraints. Thus it would be
> interesting to see the true raw image. I have doubts the current one is
> really the true one. When displaying it with a different intensity mapping
> it becomes evident that voxels around the head are coded as zero = there is
> no noise, which is very surprising given the usual low-intensity noise.
> Based on the sharp edges some correction must have been performed on that
> image. And then the question arises, which type of correction was performed
> and how did the raw data look like before that step? It might just have
> been some bias correction, but it might also have been prospective motion
> corrections like PROMO.
>
> For illustrative purpose I've also attached an unaltered T1 image
> screenshot affected by motion (motion artefacts can be much worse).
> Posteriorly, at the enlarged sulci, it's (almost) impossible to identify
> the cortical sheet, it looks like CSF -> brain tissue, not CSF -> GM -> WM.
> Anteriorly, quite some smearing is evident. Maybe this was also the case in
> your file, after some motion correction the blurring might have been
> reduced, but the contrast might still be quite low. This is just guessing
> of course. It would be necessary to see some of the other images to get an
> impression whether this is due to the scanner/sequence settings or whether
> it's a problem in particular volumes. The contrast might have been low due
> to the settings, but it might also have been due to motion or an artefact
> introduced during the correction step.
>
> Best
>
> Helmut
>