Description Usage Arguments Details Value Examples
Uses a hidden Markov model to calculate the probabilities of the true underlying genotypes given the observed multipoint marker data, with possible allowance for genotyping errors.
1 2 3 | calc_genoprob(cross, step = 0, off_end = 0, stepwidth = c("fixed", "max"),
pseudomarker_map, error_prob = 0.0001, map_function = c("haldane",
"kosambi", "c-f", "morgan"), quiet = TRUE, n_cores = 1)
|
cross |
Object of class |
step |
Distance between pseudomarkers and markers; if
|
off_end |
Distance beyond terminal markers in which to insert pseudomarkers. |
stepwidth |
Indicates whether to use a fixed grid
( |
pseudomarker_map |
A map of pseudomarker locations; if provided the
|
error_prob |
Assumed genotyping error probability |
map_function |
Character string indicating the map function to use to convert genetic distances to recombination fractions. |
quiet |
If |
n_cores |
Number of CPU cores to use, for parallel calculations.
(If |
Let O[k] denote the observed marker genotype at position k, and g[k] denote the corresponding true underlying genotype.
We use the forward-backward equations to calculate a[k][v] = log Pr(O[1], …, O[k], g[k] = v) and b[k][v] = log Pr(O[k+1], …, O[n] | g[k] = v)
We then obtain Pr(g[k] | O[1], …, O[n] = exp(a[k][v] + b[k][v]) / s where s = sum_v exp(a[k][v] + b[k][v])
A list of three-dimensional arrays of probabilities, individuals x positions x genotypes
1 2 | grav2 <- read_cross2(system.file("extdata", "grav2.zip", package="qtl2"))
probs <- calc_genoprob(grav2, step=1, error_prob=0.002)
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