Skip to main content
. 2015 Apr 1;5:9570. doi: 10.1038/srep09570

Table 1. Statistics of libraries generated by TruSeq or LM-Seq.

Samples Multiplex per lane Total reads Percent of non-duplicated reads* Number of reads mapped to RefSeq Percent of reads mapping to RefSeq Number of genes withTPM > 1 Percent of mapped reads mapping on expected sense/antisense strand
TruSeq 12 12426491 62.4% 10929050 88% 13000 50.6%
TruSeq-Stranded mRNA Seq-1 6 28515378 33.5% 24787808 87% 12151 99.4%
TruSeq-Stranded mRNA Seq-1 94 2179618 72.3% 1910603 88% 12899 99.4%
LM-Seq-1 24 6417881 62.0% 5119315 80% 12484 97.2%
LM-Seq-2 24 8786110 53.6% 5985757 68% 12784 98.2%
LM-Seq-10 ng total RNA 24 5673905 21.1% 3770987 66% 12421 98.6%
LM-Seq-85°C 11 min 24 8391832 47.8% 5601727 68% 12752 98.2%
LM-Seq-94°C 6 min 24 8273910 27.0% 5545433 67% 12558 98.2%
LM-Seq-1 hr ligation 24 6116079 35.5% 4172809 68% 12624 98.0%
LM-Seq-3 hr ligation 24 6613601 42.7% 4381615 66% 12668 98.2%

*: As reported by FastQC version 0.11.2.