I am trying to segment a multiplexed cell imaging dataset. You usually get a 2D array of predicted cell/nucleus labels as the result. A figure to illustrate the input and output:
The next step is to quantify the intensities for each antibody/stain for each cell. Somehow I did not see that aspect discussed in any of the tutorials. Is there a proper way of doing that?
Update: There appears to be some confusion what the data represents. In the example image, you are trying to identify individual cells. Each blob is a cell. Every cell gets a different label. The predictions are colored by label. You want to determine how bright each cell is. Here is an example workflow.
