Nothing
context("general usage")
test_that("general usage", {
data("dgrp2.3R.5k.data")
mks <- sample(dgrp2.3R.5k.data$markers, size = 100,
replace = FALSE, prob = NULL)
testthat::expect_silent(
simulated_pop <- simulate_admixture(
module = sequence_module(molecular_data = dgrp2.3R.5k.data,
morgan = 1,
markers = mks),
pop_size = 1000,
total_runtime = 11)
)
### The list option is working now with genomeadmixr_data type:
testthat::expect_output(
testthat::expect_message(
simulated_pop_2 <- simulate_admixture(
module = sequence_module(molecular_data =
list(dgrp2.3R.5k.data,
dgrp2.3R.5k.data),
markers = mks,
morgan = 1),
pop_size = 100,
total_runtime = 10,
verbose = TRUE),
"found multiple input populations"
)
)
testthat::expect_message(
testthat::expect_output(
simulated_pop_2 <- simulate_admixture(
module = sequence_module(molecular_data =
list(simulated_pop,
simulated_pop),
morgan = 1,
markers = mks),
pop_size = 100,
total_runtime = 10,
verbose = TRUE)
)
)
a1 <- calculate_marker_frequency(simulated_pop, location = mks[50])
a2 <- subset(simulated_pop$frequencies, time == 10 & location == mks[50])
for (x in unique(a1$ancestor)) {
a3 <- subset(a1, a1$ancestor == x)
if (x == 0) x = "-" # 0 is - in a2.
a4 <- subset(a2, a2$ancestor == x)
testthat::expect_equal(a3$frequency[1],
a4$frequency[1], tolerance = 0.05)
}
selection_matrix <- matrix(nrow = 1, ncol = 5)
selection_matrix[1, ] <- c(mks[50], 0.4, 0.7, 1.0, "t")
testthat::expect_silent(
iso_100 <- create_iso_female(
module = sequence_module(molecular_data = dgrp2.3R.5k.data,
morgan = 1),
inbreeding_pop_size = 100,
n = 20,
run_time = 20)
)
testthat::expect_silent(
iso_100 <- create_iso_female(
module = sequence_module(molecular_data = simulated_pop,
morgan = 1),
inbreeding_pop_size = 100,
n = 20,
run_time = 20)
)
testthat::expect_message(
selected_pop <- simulate_admixture(
module = sequence_module(molecular_data = simulated_pop,
morgan = 1,
markers = mks),
pop_size = 100,
total_runtime = 11,
select_matrix = selection_matrix)
)
testthat::expect_output(
testthat::expect_message(
two_pops <- simulate_admixture(
module = sequence_module(molecular_data = list(
simulated_pop, simulated_pop),
markers = mks,
morgan = 1),
verbose = TRUE,
migration = migration_settings(migration_rate = 0,
population_size = c(100, 100),
stop_at_critical_fst = TRUE,
critical_fst = 0.05,
generations_between_update = 100),
total_runtime = 10)
)
)
})
test_that("isofemale usage", {
data("dgrp2.3R.5k.data")
mks = sample(dgrp2.3R.5k.data$markers, size = 300, replace = FALSE, prob = NULL)
testthat::expect_silent(
simulated_pop <- simulate_admixture(
module = sequence_module(molecular_data = dgrp2.3R.5k.data,
morgan = 1,
markers = mks),
pop_size = 100,
total_runtime = 10)
)
testthat::expect_output(
isos <- create_iso_female(
module = sequence_module(molecular_data = simulated_pop),
n = 20,
inbreeding_pop_size = 100,
run_time = 50,
verbose = TRUE)
)
testthat::expect_output(
simulated_pop <- simulate_admixture(
module = sequence_module(molecular_data = isos[1],
morgan = 1,
markers = mks),
pop_size = 100,
total_runtime = 10,
verbose = TRUE)
)
})
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