Fig. 2: Comparison of the results of TAS-LRS with those of short-read WGS.
From: Genome profiling with targeted adaptive sampling long-read sequencing for pediatric leukemia
A Number of SNVs and small indels detected by TAS-LRS and/or short-read WGS. The variants detected by both TAS-LRS and short-read WGS are annotated as “Common.” B Number of SVs detected by TAS-LRS and/or short-read WGS. “Common (as SV)” represents variants commonly detected by TAS-LRS as SVs and short-read WGS as SVs, and “Common (as CNV)” represents variants commonly detected by TAS-LRS as CNVs and short-read WGS as SVs. C Allele frequency of variants detected by TAS-LRS (including those commonly detected by short-read WGS) and those detected only by short-read WGS. Asterisks represent statistically significant differences (* P ≤ 0.001). NS, not significant. D Blast fraction of variants detected by TAS-LRS (including those commonly detected by short-read WGS) and those detected only by short-read WGS. Mann–Whitney U test was applied for the statistical analyses.
