Open shntnu opened 4 months ago
I am starting to work on this using the new recipe version. Regarding the recipes to use, besides the compound recipe, should I use CRISPR or ORF? Do you have any preference? Suganya and I discussed using her documentation for the recipes, then I can provide feedback if necessary
Please go with ORF
I noticed that some of the plates have metadata corresponding to the control.txt platemap. This file only includes the well names and an empty column for the condition.
I’m wondering if I should consider this as DMSO, a negative control, or something else. Could you please clarify? thank you!
I've attached a screenshot of the platemap for reference:
I noticed that some of the plates have metadata corresponding to the control.txt platemap. This file only includes the well names and an empty column for the condition.
I’m wondering if I should consider this as DMSO, a negative control, or something else. Could you please clarify? thank you!
I've attached a screenshot of the platemap for reference:
@jump-cellpainting/broad-claussnitzer can you help address the question above?
Additional info that might help: Here are the platemaps for a single batch; each batch has these control plates (they are different from the Target2 plates)
Update: I was able to run the ORF jump recipe with some changes that I will document soon, after discuss about it with Suganya and John. I run it considering that empty columns as a 'control' until I get the correct information from @jump-cellpainting/broad-claussnitzer.
We need to reprocess the profiles in this repo, starting from the augmented profiles.