Fig. 3
From: Tandem-genotypes: robust detection of tandem repeat expansions from long DNA reads
a–j Distribution of predicted change in repeat copy number, for nanopore reads of human DNA with inserted repeats. Reads covering each of ten disease-associated repeat loci were selected, and the repeat region in each read was replaced by the repeat region of a plasmid nanopore read. y-axis: read count, x-axis: change in copy number relative to the reference human genome. Forward (red) and reverse strand reads (blue) are shown separately. Red arrows: projected repeat copy changes