Hi Clay,
> Do y'all have any ideas as to how I can accurately close such
> cells and fill them, which out interrupting anything else?
Without seeing your original data, I can only suggest checking out:
http://imagej.net/Segmentationand in particular
http://imagej.net/Trainable_Weka_SegmentationRegards,
Curtis
On Fri, Jan 16, 2015 at 12:24 PM, Clay Morton <
[hidden email]> wrote:
> Hey guys,?
>
>
> I am currently working on a python pipeline to identify?sickle cells in
> photos of blood samples. Im trying to use Fiji for the preprocessing steps.
> My idea is to first convert the images to binary and then to fill any holes
> left in the cells. I then use watershedding to correctly separate cells
> that are in clusters. As you can see from the attached image Fiji does a
> pretty good job. The only issues?arise when healthy blood cells take on a
> "C"-shape due to curvature of their membrane. This prevents such cells from
> being filled in and then leads to incorrect watershedding. Do y'all have
> any ideas as to how I can accurately close such cells and fill them, which
> out?interrupting?anything else?
>
>
> Thanks,
> Clay
>
>
>
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