aThe total volume of PCR reaction was 25 µl and the PCR conditions were as follows: 50°C for 2 min, 95°C for 10 min, followed by 40 cycles of 95°C, 15 s for denaturation and 60°C, 1 min for annealing

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Additional file 3: Table S6. of Single molecule counting and assessment of random molecular tagging errors with transposable giga-scale error-correcting barcodes

单分子测序

基因表达定量

Comparison of MAQC qPCR and EXB-based quantification methods. (TXT 90 kb)

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qPCR primer sequences.

qPCR引物序列

基因表达定量

qPCR primer sequences.

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ORF_counts

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