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Table 5 Number of insertions and deletions

From: Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems

  PhiX-95nt At-100nt
  Insertions Deletions Insertions Deletions
All 336 (100%) 3,453 (100%) 11,043 (100%) 15,087 (100%)
1 base of T, A, C or G 330 (98%) 3,381 (98%) 10,225 (93%) 12,936 (86%)
1 base of T or A 259 (77%) 2,100 (61%) 8,878 (80%) 10,940 (73%)
1 base of C or G 71 (21%) 1,281 (37%) 1,347 (12%) 1,996 (13%)
> 1 base 6 (2%) 72 (2%) 818 (7%) 2,151 (14%)