Dear all,
I did some Fluorescence-based Cell Microscopequantifications of colocalization. The problem is that if I try to merge different channels into one picture (same cells, with different bio-markers), I don't get the right overlap. (I include a few pictures to show you an example)
Can someone help me how to solve it?
Thanks a lot for any kind of help you can bring
Best,
Ethan
Thanks so much for your help. You are very very kind! Your advice gave me a great help for my data processing.
I really appreciate it.
Best,
Ethan
Hi Ethan,You can use the Rigid Registration plugin (just type "Registration" in the Icy top search bar) to correct the channel drift, that should make it :)
Best,- Stephane
Le mercredi 31 octobre 2018 10:58:58 UTC+1, ethanwang0072018 a écrit :Dear all,
I did some Fluorescence-based Cell Microscopequantifications of colocalization. The problem is that if I try to merge different channels into one picture (same cells, with different bio-markers), I don't get the right overlap. (I include a few pictures to show you an example)
Can someone help me how to solve it?
Thanks a lot for any kind of help you can bring
Best,
Ethan
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