Fig. 2
From: Long-read-based human genomic structural variation detection with cuteSV
Benchmark results of the SV callers on various simulated datasets. F1 scores of a deletion, b insertion, c duplication, d inversion, e translocation at breakpoint level, and f translocation at breakend level, for the simulated datasets in various coverages and w/o genotyping. In the figure, “N×” and “N×-GT” indicate the statistics without and with genotyping, respectively