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Data from merged batches 5, 6, and 7 looking good so far
Batch correction not necessary
There might be some minor well effects
We discussed randomizing platemaps to the extent possible
Morphology signature is interesting, and worth having a biologist dig a bit deeper into
Still some concern over confluence issues
While it doesn't seem to impact profiles, it is impacting explanatory morphology features that are typically only important in high confluence settings
There might be something additionally interesting about the way the clones were selected
We talked about how they were all selected from the same cluster of resistant clones
Can you check me on this @mekelley? It is likely I didn't truly appreciate this point and I think it is important. (if possible, please add this to a new issue similar to Cloning Details #45 )
We know which cluster each sample belongs to which will help with:
Sequence specific clusters to determine molecular resistance mechanism
Use cluster info in future covariate models to observe which features are important for cluster of origin
The Rockefeller team is actively onboarding new clones and a new proteasome inhibitor
They will present at next check-in
We also briefly discussed presentations at next CSHL
It will be analysis heavy and @AnneCarpenter will represent (I don't remember if we've discussed this elsewhere before!)
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