Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation

(Downloading may take up to 30 seconds. If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.

Figure 6.
Figure 6.

A highly continuous S. cerevisae assembly from noisy 1D and 2D MinION reads. (A) A histogram of read error rates (1D and 2D) versus the reference. Alignment identity was computed only for reads with an alignment >90% of their length. The majority of reads were <75% identity with an overall average of 70%. (B) Assembled Canu contigs were aligned to the reference, and all alignments >1 kbp in length and >90% identity were then plotted using the ColoredChromosomes package (Böhringer et al. 2002). Alternating shades indicate adjacent alignments, so each transition from gray to black represents a contig boundary or alignment breakpoint. White regions indicate regions missing from the assembly. Most chromosomes are in less than three contigs, indicating structural agreement with the reference.

This Article

  1. Genome Res. 27: 722-736

Preprint Server