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This repository has been archived by the owner on Jul 29, 2023. It is now read-only.
I wanted to prepare training data that cover different modalities, so we can compare the impact of phase vs brightfield and deconvolved vs not deconvolved channels. However, I get an unexpected behavior of the z-alignment script. The script simply copies all single page tif file images into the new aligned folder, without aligning them (from the 97 z-ids per position all z-ids are saved in the aligned folder).
I plan to preparing following training data combinations:
Phase & non deconvolved fluorescence channels
Brightfield & deconvolved fluorescence channels
Brightfield & non deconvolved fluorescence channels
Phase & deconvolved fluorescence channels --> these are the modalities the current model is trained on, z-alignment works
The scripts are located here: /gpfs/CompMicro/projects/HEK/2022_03_15_orgs_nuc_mem_63x_04NA/all_pos_single_page/
align_z_focus_2022_03_15_refmem_min25_max60.py. -> this script works! Aligned images are saved at /gpfs/CompMicro/projects/HEK/2022_03_15_orgs_nuc_mem_63x_04NA/all_pos_single_page/all_pos_Phase1e-3_Denconv_Nuc8e-4_Mem8e-4_pad15_bg50_registered_refmem_min25_max60
Furthermore, the alignment script takes quite a while to run through. If anyone finds time it would be great to speed the script up with e.g. multiprocessing.
I ran the scripts on hulk in a microDL docker container with the command python <script name>
I would highly appreciate if anyone finds time to debug this issue! Please let me know if there are open questions / if I can help with anything.
Best,
Johanna
The text was updated successfully, but these errors were encountered:
Hi together,
I wanted to prepare training data that cover different modalities, so we can compare the impact of phase vs brightfield and deconvolved vs not deconvolved channels. However, I get an unexpected behavior of the z-alignment script. The script simply copies all single page tif file images into the new aligned folder, without aligning them (from the 97 z-ids per position all z-ids are saved in the aligned folder).
I plan to preparing following training data combinations:
The scripts are located here:
/gpfs/CompMicro/projects/HEK/2022_03_15_orgs_nuc_mem_63x_04NA/all_pos_single_page/
align_z_focus_2022_03_15_only_phase_refmem_min25_max60.py
align_z_focus_2022_03_15_only_deconv_refmem_min25_max60.py
align_z_focus_2022_03_15_raw_data_refmem_min25_max60.py
align_z_focus_2022_03_15_refmem_min25_max60.py
. -> this script works! Aligned images are saved at/gpfs/CompMicro/projects/HEK/2022_03_15_orgs_nuc_mem_63x_04NA/all_pos_single_page/all_pos_Phase1e-3_Denconv_Nuc8e-4_Mem8e-4_pad15_bg50_registered_refmem_min25_max60
Furthermore, the alignment script takes quite a while to run through. If anyone finds time it would be great to speed the script up with e.g. multiprocessing.
I ran the scripts on hulk in a microDL docker container with the command
python <script name>
I would highly appreciate if anyone finds time to debug this issue! Please let me know if there are open questions / if I can help with anything.
Best,
Johanna
The text was updated successfully, but these errors were encountered: