Fig. 5: HiRise scaffolding for 11 genomes.
From: Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes
a, NGx plots for each of the 11 genomes, before (dashed) and after (solid) scaffolding with HiC sequencing reads, GRCh38 minus alternate sequences is shown for comparison. b, Dot plot showing alignments between the scaffolded HG00733 Shasta assembly and GRCh38 chromosome scaffolds. Blue indicates forward aligning segments, green indicates reverse, with both indicating unique alignments.
