Fig. 2
From: Straglr: discovering and genotyping tandem repeat expansions using whole genome long-read sequences
Genotyping benchmark (simulated data): resolving power. A series of bi-allelic (a) and tri-allelic (b) samples composed of a “base” expansion (columns) at 17 disease loci (legend) combined with one (a) or two (b) larger alleles separated from the next smaller allele by a fixed separation size (rows). Red vertical lines indicate the targeted allele sizes for simulation in each sample. Colored circles represent the allele sizes (x-axis) reported by Straglr for each locus (y-axis)