View source: R/con_primer_efficiency.R
compute.efficiency | R Documentation |
Computes the efficiency of primer binding events for Taq polymerase.
compute.efficiency(
fw.primers,
fw.start,
fw.end,
covered,
taqEfficiency,
annealing.temp,
primer_conc,
sodium.eq.concentration,
mode.directionality = c("fw", "rev"),
seqs
)
fw.primers |
Primer sequence strings. |
fw.start |
Binding position (start). |
fw.end |
Binding position (end). |
covered |
List of covered template indices per primer. |
taqEfficiency |
Whether the efficiency shall be computed
using a mismatch-model developed for Taq polymerases. The default setting
is |
annealing.temp |
Annealing temperature for which to evaluate efficiency. |
primer_conc |
Primer concentration. |
sodium.eq.concentration |
The sodium-equivalent concentration of ions. |
mode.directionality |
Primer directionality. |
seqs |
Template sequence strings. |
This function uses DECIPHER's CalculateEfficiencyPCR.
The efficiencies of primer binding events.
Wright, Erik S., et al. "Exploiting extension bias in polymerase chain reaction to improve primer specificity in ensembles of nearly identical DNA templates." Environmental microbiology 16.5 (2014): 1354-1365.
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