Richard Gillilan:
|While you guys are looking at tiff code, I have a question. Ever
|encounter a multi-tiff? This seems to be the standard in confocal
|microscopy and I'm starting to see them more often. ReadImage will treat
|one like an ordinary tiff, displaying only the first frame in the
|stack. What I really need is a module that will detect the appropriate
|tags and output a series or other group that can then be stacked for
|volumetric work.
We've worked with stacked confocal TIFFs here. Pointing ReadImage at
one of these (such as one from a Leica scanner), yields a series of image
fields.
ReadImage(delayed=0) => Stack => Scale z => Inquire("apply transform")
and the volume is ready to go.
Randall
--
Randall Hopper (mailto:[EMAIL PROTECTED])
EPA Scientific Visualization Center
US EPA MD/24 ERC-1A; RTP, NC 27711
