Figure 3.
Average over samples of cTPR (A,B) and common false-discovery rate (cFDR; C,D) versus alternate allele coverage for variants binned by total (e.g., pooled) alt-allele coverage (e.g., the point coverage = 400 would include variants from 400 to the next bin, which is 500), for each of the variant-calling approaches used, for both scRNA-seq (A,C) and scATAC-seq (B,D).
