##' Reads in plate setup worksheets
##'
##' @description Parses column names for tabular fluorescence data (where rows indicate separate sampling times)
##' @export
##'
read_plate_setup <- function(d) {
# New plan:
# 1. Get passed the raw data frame from .csv
# 2. Split the column names by columns
# 3. Add a column to hte data frame for each variable from the column names.
# Populate each column with data from the column names (using format "value units,")
#nms <- col
}
# read_plate_setup <- function(fn=NA, ncol=13,
# #key=c("std.or.sample", "conc", "fluorophore", "medium")) {
# key=NULL) {
#
#
#
# # Open dialog box if no file is specified
# if (is.na(fn)) {
# fn <- file.choose()
# }
#
# # Read plate setup worksheet
# d <- read.csv(fn)
# first_col <- names(d)[1]
#
# # Melt df & create column of plate IDs
# dm <- melt(d, id.vars=first_col, value.name="sample.name")
# dm$well <- toupper(paste(dm$variable, dm[, first_col], sep=""))
# #dm_skinny <- subset(dm, select="well", "value")
# dm_skinny <- dm[ , c("well", "sample.name")]
#
# # Parse sample names
# # I guess I need to write sample_name_parser as vectorized
# d_parsed <- sample_name_parser(dm_skinny)
#
# ###
# # Assign names to columns. I'd like to do this automatically, but I'm not yet sure how
# # For now, I'll assign them capital letters by default
# ###
# browser()
# new.col.names <- c(key, LETTERS[1: (ncol(d_parsed)-length(key) - 2)])
# names(d_parsed)[3:ncol(d_parsed)] <- new.col.names
#
# # Parse the concentration vector in the legend, if there is a conc column
# if("conc" %in% names(d_parsed)) {
# d_parsed$conc <- parse_numeric(d_parsed$conc)
# }
#
# d_parsed
#
# }
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