Open vreuter opened 7 months ago
Requested by @josephneos1010
@josephneos1010 since these would be very large image files (effectively doubling the input size, regarding the "input" as post-zarr-conversion), can you say how you'd use these? It's very preferable to avoid this slow write process and huge data storage, and no part of the processing or analysis operates on entire drift-corrected images, so it would be ideal to address your question via another route.
For a FOV, I would like to align certain hybridization steps so that I could visualize different signals on top of each other. I guess it doesn't have to align all hybridizations in a FOV. What would be nice is for me to select images to align and there is someway to align them with a pipeline instead of manually aligning them one by one.
Thanks @josephneos1010
For a FOV, I would like to align certain hybridization steps...I guess it doesn't have to align all hybridizations in a FOV.
OK, so a subset could be specified...do you know anything about the structure of the timepoints you'd like to compare? (e.g., RNA t0 vs. DNA t0, RNA t1 vs. DNA t1, etc.)
so that I could visualize different signals on top of each other.
Once aligned, is only the FISH channel of interest? That would save us the space of the beads channel.
If there's any subsetting in xy
(i.e., certain regions) or in z
(certain slices), please also not here.
After discussion w/ @josephneos1010 it makes most sense to restrict FOVs but leave timepoints (hybridisation rounds) unrestricted, so write out full stacks in TZYX but only for one or a few FOVs.
A non-pipeline, standalone version of #151