Fig. 4: Comparison analysis of variant detection between AGLR2 and ROCR2 in the overlapping region (replicate 1 as an example).
From: Augmenting precision medicine via targeted RNA-Seq detection of expressed mutations

a The number of variants detected in the overlapping region by AGLR2 and ROCR2 excluding known FP calls. b Comparison of the log2 variant depth (larger symbol sizes indicate lower variant position depths) and VAF for common variants shared between AGLR2 and ROCR2 in the overlapping region. c Distributions of total DP and VAF per variant category, comparing panel-unique and common variants to both. d Percentage of the four types of panel-unique variants explaining why the other panel missed them.