For example reduced representation experiments (230 genes; 2-4 wells) (~150,000 cells) we are able to normalize single cells in a single file using standard approaches. Two important notes:
this approach will not adjust for technical artifacts induced by site and well
this approach will not scale particularly easily to the millions of cells in whole genome experiments
We need to find a solution to normalize single cells within each site. This will also likely help us a bunch in our gene- and guide-level aggregated perturbation profiles.
For example reduced representation experiments (230 genes; 2-4 wells) (~150,000 cells) we are able to normalize single cells in a single file using standard approaches. Two important notes:
We need to find a solution to normalize single cells within each site. This will also likely help us a bunch in our gene- and guide-level aggregated perturbation profiles.