Entering edit mode
18 months ago
Pac314
▴
10
Should ambient RNA expression correction (e.g. with SoupX) occur before or after initial QC for low-quality cells (e.g. filtering using RNA counts, mitochondrial fraction etc. when performing single-cell RNAseq analysis?
Isn't ambient RNA filtered out by keeping only reads with cell barcodes that have a relatively high abundance?
Ambient RNA would have the same cell barcode as a valid cell-containing droplet since the RNA gets partitioned into the droplet with the cell.