## ----------------------------------------------------------------------------- # install.packages("tidyverse") ## ----------------------------------------------------------------------------- # library(tidyverse) ## ----------------------------------------------------------------------------- # setup <- function(){ # needed <- c( # # Imports: Required # "dplyr", "drc", "forcats", "ggplot2", "here", "janitor", # "kableExtra", "knitr", "magrittr", "openxlsx", "parsnip", # "purrr", "ranger", "readr", "readxl", "rmarkdown", "stats", # "stringr", "tidyr", "tidyselect", "utils", "workflows", # # Imports: Suggested # "glue", "htmltools", "httr", "jsonlite", "shiny.fluent", # "tidyverse", "zoo" # ) # for(package in needed){ # if(!sum(installed.packages() %in% package)){ # install.packages(package) # } # # require(package, character.only = TRUE) # } # } # # setup() ## ----------------------------------------------------------------------------- # my_raw_data <- "data/my_plate1.csv" # my_plate_layout <- "data/my_plate_layout.xlsx" ## ----------------------------------------------------------------------------- # getPlateLayout("your/folder/with/plate/layouts/") ## ----------------------------------------------------------------------------- # getPlateLayout("data/") ## ----------------------------------------------------------------------------- # getPlateLayout() ## ----------------------------------------------------------------------------- # getPlateLayout(folder_path = c("plate_layout_1.xlsx", "plate_layout_2.xlsx", "plate_layout_3.xlsx")) ## ----------------------------------------------------------------------------- library(SeroTrackR) library(tidyverse) bioplex_raw_plates <- c( system.file("extdata", "example_BioPlex_plate1.xlsx", package = "SeroTrackR"), system.file("extdata", "example_BioPlex_plate2.xlsx", package = "SeroTrackR") ) all_plate_layout <- system.file("extdata", "example_platelayout_1.xlsx", package = "SeroTrackR") ## ----------------------------------------------------------------------------- # bioplex_raw_plates <- c( # "data/example_BioPlex_plate1.xlsx", # "data/example_BioPlex_plate2.xlsx" # ) # all_plate_layout <- "data/example_platelayout_1.xlsx" ## ----------------------------------------------------------------------------- # magpix_raw_plate <- system.file("extdata", "example_MAGPIX_plate3.csv", package = "SeroTrackR") ## ----------------------------------------------------------------------------- # magpix_raw_plate <- "data/example_MAGPIX_plate3.csv" ## ----------------------------------------------------------------------------- # # Serological data # bioplex_sero_data <- readSeroData( # raw_data = bioplex_raw_plates, # platform = "bioplex" # ) # magpix_sero_data <- readSeroData( # raw_data = magpix_raw_plate, # platform = "magpix", # version = "4.2" # ) ## ----------------------------------------------------------------------------- # sero_data_merged <- NULL # # data_raw # sero_data_merged$data_raw <- bioplex_sero_data$data_raw %>% # bind_rows(magpix_sero_data$data_raw) # # # results # sero_data_merged$results <- bioplex_sero_data$results %>% # bind_rows(magpix_sero_data$results) # # # counts # sero_data_merged$counts <- bioplex_sero_data$counts %>% # bind_rows(magpix_sero_data$counts) # # # blanks # sero_data_merged$blanks <- bioplex_sero_data$blanks %>% # bind_rows(magpix_sero_data$blanks) # # # stds # sero_data_merged$stds <- bioplex_sero_data$stds %>% # bind_rows(magpix_sero_data$stds) # # # run # sero_data_merged$run <- bioplex_sero_data$run %>% # bind_rows(magpix_sero_data$run) ## ----------------------------------------------------------------------------- # plate_list_all <- readPlateLayout( # plate_layout = all_plate_layout, # sero_data = sero_data_merged # ) # # qc_results <- runQC( # sero_data = sero_data_merged, # plate_list = all_plate_layout # ) # # mfi_to_rau_output <- MFItoRAU( # sero_data = sero_data_merged, # plate_list = all_plate_layout, # qc_results = qc_results, # std_point = 10 # ) # # # etc..