Fig. 6
From: Comprehensive evaluation of structural variant genotyping methods based on long-read sequencing data
Impact of imprecise breakpoint on the F1 score of SV genotyping methods. a, b HG002 Tier 1 dataset. c, d HG002 Tier 2 dataset. e–i HG005 dataset. The x-axis is the offset (bp: base pair) between the original and shifted breakpoints, and the y-axis is the F1 score of each SV genotyping method in each breakpoint shift. Performance was evaluated on 30× PacBio CLR data and the alignment files were generated by minimap2. INS: insertion, DEL: deletion, DUP: duplication, INV: inversion, TRA: translocation