library(genotype)
n.sim = 10000
homogenotypes = rep('A')
Impacte de la profondeur de séquençage
p.hetero = 1/1000
error.rate = 1/100
merror = error_jc(rate = error.rate)
couvertures =1:50
success.homo = numeric(length = length(couvertures))
i = 0
for (c in couvertures) {
s = simulate_sites(rep('A',n.sim),
rep('A',n.sim),
coverage = c,
error = merror)
g = genotyping(s,sequencing.error = error.rate,phetero = p.hetero)
i = i+1
success.homo[i] = sum(g$ok)
}
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