library("serocalculator")
library(dplyr)
library(tibble)
# load in longitudinal parameters
curve_params <-
typhoid_curves_nostrat_100 |>
filter(antigen_iso %in% c("HlyE_IgA", "HlyE_IgG"))
# load in pop data
xs_data <-
sees_pop_data_pk_100
# Load noise params
noise_params <- tibble(
antigen_iso = c("HlyE_IgG", "HlyE_IgA"),
nu = c(0.5, 0.5), # Biologic noise (nu)
eps = c(0, 0), # M noise (eps)
y.low = c(1, 1), # low cutoff (llod)
y.high = c(5e6, 5e6)
) # high cutoff (y.high)
cur_antibody <- "HlyE_IgA"
cur_data <-
xs_data |>
dplyr::filter(
.data$antigen_iso == cur_antibody
) |>
dplyr::slice_head(n = 100)
cur_curve_params <-
curve_params |>
dplyr::filter(.data$antigen_iso == cur_antibody) |>
dplyr::slice_head(n = 100)
cur_noise_params <-
noise_params |>
dplyr::filter(.data$antigen_iso == cur_antibody)
if (!is.element("d", names(cur_curve_params))) {
cur_curve_params <-
cur_curve_params |>
dplyr::mutate(
alpha = .data$alpha * 365.25,
d = .data$r - 1
)
}
lambda <- 0.1
f_dev0(
lambda = lambda,
csdata = cur_data,
lnpars = cur_curve_params,
cond = cur_noise_params
)