Fig. 1: Nanopore sequencing data.
From: Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes
a, Throughput in gigabases from each of three flow cells for 11 samples, with total throughput at top. Each point is a flow cell. b, Read N50 values for each flow cell. Each point is a flow cell. c, Alignment identities against GRCh38. Medians in a–c shown by dashed lines, dotted line in c is the mode. Each line is a single sample comprising three flow cells. d, Genome coverage as a function of read length. Dashed lines indicate coverage at 10 and 100 kb. HG00733 is accentuated in dark blue as an example. Each line is a single sample comprising three flow cells. e, Alignment identity for standard and RLE reads. Data for HG00733 chromosome 1 flow cell 1 are shown (4.6 Gb raw sequence). Dashed lines denote quartiles.
