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. 2015 Jan 27;5:8056. doi: 10.1038/srep08056

Table 1. Coverage necessary to reach a 99.9% probability of recovering three copies of the correct sequence for all alleles (based on the proportion of correct reads). Since not all alleles in a PCR amplify equally well, we calculated the coverage needed when two alleles amplify at the same rate (equal amplification), and when one allele yields twice as many products as the other (unequal amplification). Enzymes that did not amplify are marked n.a. and those which amplified but for which there was insufficient data to calculate coverage are labeled i.d. Abbreviations are those used in Figures 1 and 2 and the text.

Enzyme Abbreviation Test 1 Test 2 equal amplification Test 2 unequal amplification
Phusion® High Fidelity DNA Polymerase (Finnzymes) Phusion 7 42 87
KAPA HiFi™ (Kapa Biosystems) KapHF 7 i.d. i.d.
Pwo® DNA Polymerase (Roche) Pwo 7 n.a. n.a.
AmpliTaq Gold® (Applied Biosystems) Gold 9 48 88
i-MaxTM II DNA Polymerase (iNtRON Biotechnology) iMax 11 57 99
Taq DNA Polymerase (Roche) Roche Taq 11 120 185
Velocity DNA Polymerase (Bioline) Velocity 12 n.a. n.a.
HotStarTaq® DNA Polymerase (Qiagen) HotStar 14 97 152
FastStart® High Fidelity PCR System (Roche) FastStart 14 45 86
Biotaq® (Bioline) Biotaq 16 271 395
OneTaq™ DNA Polymerase (New England Biolabs) OneTaq i.d. n.a. n.a.
Vent® DNA Polymerase (New England Biolabs) Vent n.a. n.a. n.a.
Deep Vent® DNA Polymerase (New England Biolabs) DeepVent n.a. n.a. n.a.