Fig. 3From: PyBSASeq: a simple and effective algorithm for bulked segregant analysis with whole-genome sequencing dataGenomic distribution of ∆(SNP index) at different sequencing coverage levels. The red curves indicate 99% confidence intervals obtained via simulation. a The original sequence reads. b 40% of the original sequence reads. c 30% of the original sequence reads. d 20% of the original sequence readsBack to article page