Hello,
I am trying to count the number of white specles in the nucleus in a grayscale image. I’ve tweaked the speckle counting pipeline provided and it is picking up the nuclei and speckles well, however, it is counting oversaturated nuclei (completely white as opposed to gray with structures in it) as a large clump of speckles. Is there a way to filter out oversaturated cells such as this so that they are not picked up as specks? Thank you!