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. 2016 Jan 11;11(1):e0146638. doi: 10.1371/journal.pone.0146638

Table 8. PCR sampling efficiency for each genes in multiplex PCR.

Template # Reads # UID# % Template Sampled
FGFR3-E14 291850 64472 997 0.30%
FGFR3-E7 291850 6569826 104094 35.60%
FGFR3-E9 291850 57895 1589 0.50%
HRAS-E1 291850 133233 4856 1.70%
HRAS-E3 291850 111253 2476 0.80%
PIK3CA-E20 291850 13878 594 0.20%
PIK3CA-E9 291850 57895 2494 0.90%

0.1 ng input or 291850 copies of plasmid molecules was used as templates. High fidelity Q5 enzymes with spike-in Taq DNA polymerase was used for both Stage 1 and Stage 2 amplification.