Hi all
I have a problem importing .liff format images coming from a Perkin Elmer spinning disk microscopy.
The stack to import consists of 3 channels on 54 Z stacks, but once i import it and open it with Insight i only find 162 Z Stacks, as the channels were intended like other Z stacks, without the possibility of splitting channels. Obviously the stack imported this way is not useful to us.
Thanks in advance to anyone that could help me