Quantify colocalized foci/speckels in nucleus stained with Dapi

cellprofiler

#1

Hello all
I am looking to identify how many of my green foci overlap with red foci in nuclei stained with DAPI. How should the pipeline be written for Cell profiler to do this automatically.

Thank you
Sharmistha


#2

Hi,

Have you searched the forum, or checked out our examples page?