Additional file 1: Table S1.
Barcodes and read coverage are presented. The barcode sequence, the number of total associated reads, the average number of reads per unique sequence in the 4 bp, 6 bp, 8 bp, and 10 bp windows, and the DNA polymerase used are provided for each of the pooled amplification experiments. During pooling, more of the SL and amplified background were included in the pool (as evidenced by the read distribution) to ensure that both of these libraries had an ample number of reads for downstream analysis.
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Pan et al. BMC Biotechnology 2014 14:10 doi:10.1186/1472-6750-14-10