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Table 4 Indels and substitution errors in B-tail trimmed reads

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

Data set Uniquely aligned bases Substitution errors (rate) Indels (rate)
Bv-95nt 4,900,840 7,615 (0.16%) 84 (1.7 E-5)
PhiX-95nt 778,014,176 830,351 (0.11%) 3,789 (4.9 E-6)
At-100nt 1,111,314,053 1,792,190 (0.16%) 26,130 (2.4 E-5)
PhiX-100nt 170,078,494 203,729 (0.12%) 546 (3.2 E-6)
PhiX-GAIIx 1,760,062,929 4,936,167 (0.28%) 7,077 (4.0 E-6)