When I change the filters of our fluorescent microscope, the sample moves slightly, no matter how carefully I do it.

As a result, images of different channels are not directly mergable. (See the attached picture, where the red and green channels, that are supposed to overlap, differ in at least 10 pixels horizontally)

I am looking for a program or plugin within a program (ImageJ ?) where I could fix this issue and align/move my images prior to merging. I would appreciate your ideas.

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