Nothing
t_dat <- read_hdx(system.file(package = "HaDeX2", "HaDeX/data/KD_180110_CD160_HVEM.csv"))
############
## PARAMS ##
############
t_protein <- "db_CD160"
t_states <- c("CD160", "CD160_HVEM")
t_state_1 <- "CD160"
t_state_2 <- "CD160_HVEM"
t_time_0 <- 0.001
t_time_100 <- 1440
t_time_t <- 5
t_deut_part <- 0.9
t_p_adjustment_method <- "none"
t_confidence_level <- 0.98
t_start <- min(t_dat[["Start"]])
t_end <- max(t_dat[["End"]])
t_peptide <- "INITSSASQEGTRLN"
t_peptide_start <- 1
t_peptide_end <- 15
state_uptake_dat <- create_state_uptake_dataset(t_dat,
protein = t_protein,
state = t_state_1,
time_0 = t_time_0,
time_100 = t_time_100,
deut_part = t_deut_part)
diff_uptake_dat <- create_diff_uptake_dataset(t_dat,
protein = t_protein,
state_1 = t_state_1,
state_2 = t_state_2,
time_0 = t_time_0,
time_100 = t_time_100,
deut_part = t_deut_part)
diff_p_uptake_dat <- create_p_diff_uptake_dataset(t_dat,
protein = t_protein,
state_1 = t_state_1,
state_2 = t_state_2,
p_adjustment_method = t_p_adjustment_method,
confidence_level = t_confidence_level,
time_0 = t_time_0,
time_100 = t_time_100,
deut_part = t_deut_part)
p_dat <- calculate_p_value(t_dat,
protein = t_protein,
state_1 = t_state_1,
state_2 = t_state_2,
p_adjustment_method = t_p_adjustment_method,
confidence_level = t_confidence_level)
uptake_dat <- create_uptake_dataset(t_dat,
protein = t_protein,
states = t_states,
time_0 = t_time_0,
time_100 = t_time_100)
auc_dat <- calculate_auc(uptake_dat,
protein = t_protein,
state = t_state_1,
preserve_values = F)
bx_dat <- calculate_back_exchange(t_dat,
protein = t_protein,
states = t_states,
time_100 = t_time_100)
p_diff_uptake_conf_dat <- create_p_diff_uptake_dataset_with_confidence(diff_p_uptake_dat)
agg_test_dat <- calculate_aggregated_test_results(p_diff_uptake_conf_dat,
method = "significance")
overlap_dist_dat <- create_overlap_distribution_dataset(dat = t_dat,
protein = t_protein,
state = t_state_1,
protein_sequence = reconstruct_sequence(t_dat))
pep_kinetics_dat <- calculate_peptide_kinetics(t_dat,
protein = t_protein,
sequence = t_peptide,
states = t_states,
start = t_peptide_start,
end = t_peptide_end,
time_0 = t_time_0,
time_100 = t_time_100,
deut_part = t_deut_part)
rep_mass_dat <- calculate_exp_masses_per_replicate(t_dat)
rep_dat <- create_replicate_dataset(t_dat)
Any scripts or data that you put into this service are public.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.