#' A function to normalize calcium-sensitivie dye data
#'
#' @param file Path to a csv file that contains the time-series data for multiple cells obtained in ImageJ
#' @keywords Calcium Imaging
#' @export
#' @examples
#' CalciumExperiment191 <- minmaxCalciumData('./Data/Wholeimage_Calcium_Experiment191.csv')
#'
#' Example of storing data:
#' wholeNormInt191 <- wholeCalciumExperiment191[[1]]
#' longWholeNormInt191 <-wholeCalciumExperiment191[[2]]
DeltafDivFoNormalizeData <- function(file) {
# Inputs csv file data into dataframe
rawCalcium <- read.csv(file)
# Removes final datapoint of the movie
rawCalcium <- dplyr::slice(rawCalcium, 1:(nrow(rawCalcium)-1))
# Initial cleanup of data - removes time column and rawIntDen column leaving only Area and IntDen
tempRawCalcium <- rawCalcium %>%
dplyr::select(-1) %>%
dplyr::select(-1*seq(2,ncol(rawCalcium),3))
# Divides even column by odd columns to normalize intensity by area of the ROI used
integratedDensity <- (tempRawCalcium[seq(0,ncol(tempRawCalcium),2)] )
# Normalizes intensities so it is on a scale of 0,1
normInt <- data.frame(lapply(integratedDensity, function(x) ((x - (mean(x[10:25]))) / mean(x[10:25])) ))
# Reintigrates time column
normInt <- cbind(rawCalcium[1], normInt)
# Creates a long, tidy dataframe
longNormInt <- normInt %>%
gather(key = Region, value = Intensity, starts_with('RawIntDen'))
# Rename the regions
longNormInt$Region <- gsub('RawIntDen','Cell ', longNormInt$Region)
# Returns a list of the dataframes, normInt is good for checking analysis and will be wide
# longNormInt is suitable for graphing and is 'Tidy'
return(list(normInt, longNormInt))
}
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