http://imagej.273.s1.nabble.com/SKM-Cross-sectional-area-measurement-tp5006330p5006344.html
> Yes they are all saved as tif files! The aim is to generate a CSA for each
> cell within the image, but ignoring those that come ito contact with the
> edges. So far I have been doing this by creating and ROI and then manually
> measuring a selections of cells, which is less than ideal! As you suggest,
> I
> have been doing this using the green channel alone, I just wanted to show a
> complete image as I'll also be analysing the density and activation of a
> number of other cell within the image.
>
> When I have tried to threshold the image, the problem that I get is that
> the
> fluoro isn't uniform throughout, so each cell often becomes grainy and is
> no
> longer recogonised as a single entity as defined by the cell membrane.
>
> I will have a number of images to analyse but so far they are just stored
> as
> each composite image (each filter) of the total overlay in a single file
> from a single field of view, all within a subject specific folder.
>
> Steve
>
>
>
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