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. 2018 Jul 20;8:10999. doi: 10.1038/s41598-018-29364-z

Table 1.

The specificity of binding to different template strands for three forward and four reverse primers. The performance of each primer was examined for the ten most abundant taxa in each PCR reaction (for which the template sequences were known).

Primer combination Primer tested Length variation Proportion with expected length (±SD) t-test (p value) Fig. Data set
P5_BF1_0 + P7_BR1_4 BF1 −1 to 2 bp for some taxa 80.42 (±18.94) 0.003 Fig. 1A (Elbrecht & Leese11)
BR1 No variation 99.44 (±0.04) NA Fig. S1A
P5_BF2_0 + P7_BR1_4 BF2 −1 to 2 bp for some taxa, +1 for all taxa 62.14 (±14.07) NA Fig. 1B (Elbrecht & Leese11)
BR1 No variation 99.45 (±0.04) NA Fig. S1B
P5_fwhF1_3 + P7_fwhR1_1 fwhR1 +1 for all taxa 96.24 (±1.22) NA Fig. S1C (Vamos et al.14)
P5_fwhR2_2 + P7_fwhF2_3 fwhR2 No variation 99.33 (±0.05) NA Fig. S1E (Vamos et al.14)
fwhF2 −1 to 2 bp for some taxa 82.23 (±22.05) 0.003 Fig. S1D (Vamos et al.14)
mlCOIintF + jgHCO2198, complete run 1 mlCOIintF −1 to 2 bp for some taxa 70.08 (±29.93) 0.003 Fig. S1F (Leray & Knowlton15)

The exact primer length distribution and number of sequences used for this analysis are also provided in Table S1. For primers where no length variation was observed or for primers where all taxa showed length variation, no t-test could be applied (NA) due to the lack of groups (slippage vs no slippage).