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. 2017 Jan 7;6(2):1–13. doi: 10.1093/gigascience/giw018

Table 2:

Metrics of the S288C assemblies after polishing. Assemblies were corrected using 300x of 2 × 250 bp Illumina reads as input to Pilon. The resulting corrected assembly was then aligned to the S288C reference genome using Quast.

Spades Canu Miniasm SMARTdenovo ABruijn
Reads dataset used Illumina PE 2 × 250 bp 2D pass Canu-corrected Longest 2D 2D
Coverage 300x 67x 108x 30x 120x
# reads > 10 kb 0 16 860 21 005 28 668 28 668
# contigs 376 37 28 26 23
Cumulative size 12 047 788 12 230 747 12 113 521 12 213 590 12 182 847
Genome fraction (%) 96.464 98.519 98.421 99.352 98.635
N50 149 184 610 494 736 456 783 336 816 355
N90 19 522 191 846 265 917 242 658 257 117
L50 27 8 7 7 6
L90 100 20 16 16 16
# mismatches 1126 1898 4455 4205 2138
# mismatches per 100 kb 9.47 15.85 37.23 34.27 17.88
# insertions 81 1657 3164 2384 1325
# deletions 439 1869 5208 5551 1838
# deletions in homopolymers 38 868 4248 4023 740
# indels per 100 kb 1.97 22.49 57.27 46.76 21.76
# genes 6087 + 177 partial 6241 + 32 partial 6215 + 37 partial 6266 + 33 partial 6243 + 45 partial
# genes without indels 6023 5921 5475 5881 6002