### ###
### add data
### ###
input.path <- "../RCC/resources/input/"
output.path <- "/media/knt/sdb2//KN/RCC/resources/nfkb/bootstrap/" -> model.path
computation.path <- paste(output.path, "rcc_scc/", sep = "/")
confusion_matrix.path <- paste(computation.path, "confusion_matrix", sep = "/") ### full
output.analysis.path <- paste(output.path, "analysis", sep= "/")
rcc_clustering.path <- paste(computation.path, "clustering", sep = "/") ### full
data.list <- list()
data.list[["nfkb"]] <-
readRDS(
file =
paste(
input.path,
"nfkb_short_ts.rds", sep = "/")) %>%
dplyr::filter(Stim %in% c(
0,
0.01,
0.03,
0.1,
0.2,
0.5,
1,
2,
4,
8,
100
))
data.list[["nfkb"]] %>%
dplyr::mutate(Stim = dplyr::if_else(Stim == 8, 10, Stim)) %>%
dplyr::arrange(Stim) %>%
data.table::data.table() ->
data.list[["nfkb"]]
data <- data.list[["nfkb"]] %>%
reshape2::dcast(formula = "Stim+CellID2~Time", value.var = "intensity")
data %>% head()
data %>%
dplyr::rename(signal = Stim,
sample = CellID2) ->
data
data.nfkb <-
data %>%
data.table::data.table()
# data.nfkb %>%
# dplyr::filter(
# signal %in% c(
# 0,
# 0.01,
# 0.1,
# 1,
# 10,
# 100)) ->
# data.nfkb
#
# data.nfkb %>%
# dplyr::filter(signal != 8) %>%
# rbind(
# (data.nfkb %>%
# dplyr::filter(signal == 8) %>%
# dplyr::mutate(signal = 10))) ->
# data.nfkb
data.itrc.nfkb <- data.nfkb
data.itrc.nfkb.all <- data.nfkb
devtools::use_data(
data.itrc.nfkb.all,
overwrite = TRUE)
####
library(devtools)
data.fra.nfkb.all <- data.itrc.nfkb.all
data.fra.cytof <- FRA::data.fra.cytof %>% dplyr::filter(Stim != 50)
usethis::use_data(
data.fra.cytof,
overwrite = TRUE)
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