R/simSample.r
In OskarHansson/pcrsim: Simulation of the Forensic DNA Process
Defines functions
simSample
Documented in
simSample
################################################################################
# TODO LIST
# TODO: Introduce variation using sigma when calculating concentration for each allele?
################################################################################
# NOTES
# ...
################################################################################
# CHANGE LOG (10 last changes)
# 14.04.2016: Version 1.0.0 released.
# 13.08.2015: Fixed initiation of a vector (example from concentration did not work).
# 18.11.2014: Support simulation of mixtures and different haplotype state.
# 26.08.2014: More robust definition of .rows (can be different per sample).
# 24.02.2014: First version.
#' @title Forensic Sample Simulator
#'
#' @description Simulates the DNA content in forensic stain.
#'
#' @details Simulates the number of DNA molecules in a forensic stain either
#' from:
#' 1) An estimate of the number of cells in the stain.
#' 2) The DNA concentration.
#' 3) The slope and intercept values as obtained from log-linear regression
#' of DNA concentration by size in basepair.
#' The regression emulates degradation and should not be used together with
#' simulation of degradation using \code{\link{simDegradation}}.
#' Some parameters accept vectors so that simulated samples can have different
#' number of cells and be a mixture of haploid and diploid samples (see examples).
#' Note 1: Number of cells can be decimal values since it is an estimate.
#' Note 2: Number of cells will always be integer if haploid=TRUE because
#' binomial selection require integer values.
#' Note 3: To get the same total amount of DNA in samples with diploid and haploid cells.
#' the parameter for haploid cells must be: cells = 2 * number_of_diploid_cells
#' NB! Important that each marker has two rows (i.e. homozygotes is e.g. 16, 16).
#'
#' @param data data.frame with columns 'Marker', 'Allele', and 'Sim' defining
#' the DNA profiles and simulation id (counter).
#' Preferably output from \code{\link{simProfile}}.
#' @param cells integer for the estimated number of cells.
#' @param sd.cells numeric for the standard deviation of \code{cells}.
#' @param conc numeric for the estimated DNA concentration.
#' @param sd.conc numeric for the standard deviation of \code{conc}.
#' @param vol numeric for the estimated sample volume.
#' @param sd.vol numeric for the standard deviation of \code{vol}.
#' @param cell.dna numeric to indicate the DNA content of a diploid cell in
#' nanograms (ng).
#' @param haploid logical TRUE to indicate haploid cells.
#' @param intercept numeric from regression of log concentration by fragment
#' size (bp).
#' @param slope numeric from regression of log concentration by fragment
#' size (bp).
#' @param kit character string defining the DNA typing kit used to calculate
#' allele size (used to calculate allele sizes needed for the regression option
#' i.e. \code{slope} and \code{intercept}).
#' @param debug logical TRUE to indicate debug mode.
#'
#' @return data.frame with simulated result in columns 'Cells'.
#'
#' @importFrom plyr count
# @importFrom strvalidator addSize getKit
#' @importFrom utils head tail str
#' @importFrom stats rbinom rnorm
#'
#' @export
#'
#' @seealso \code{\link{simProfile}}
#'
#' @examples
#' # Create a data frame with a DNA profile.
#' markers = rep(c("D3S1358","TH01","FGA"), each=2)
#' alleles = c(15,18,6,10,25,25)
#' df <- data.frame(Marker=markers, Allele=alleles)
#' # Simulate profile.
#' prof <- simProfile(data=df, sim=3, name="Test")
#'
#' # Simulate diploid sample.
#' res <- simSample(data=prof, cells=100, sd.cells=20)
#' print(res)
#'
#' # Simulate haploid sample.
#' res <- simSample(data=prof, cells=100, sd.cells=20, haploid=TRUE)
#' print(res)
#'
#' # Simulate haploid sample from concentration.
#' res <- simSample(data=prof, conc=0.02, sd.conc=0.001, vol=100, haploid=TRUE)
#' print(res)
#'
#' # Simulate sample from slope and intercept.
#' res <- simSample(data=prof, vol=100, slope=-0.01, intercept=0.20, kit="SGMPlus")
#' print(res)
#'
#' # Simulate mixture of diploid and haploid sample types of two concentrations.
#' res <- simSample(data=prof, cells=c(1000,1000,250), haploid=c(FALSE,TRUE,FALSE))
#' print(res)
simSample <- function(data, cells=NULL, sd.cells=0,
conc=NULL, sd.conc=0, vol=NULL, sd.vol=0, cell.dna=0.006,
haploid=FALSE, kit=NULL, slope=NULL, intercept=NULL, debug=FALSE) {
# Debug info.
if(debug){
print(paste(">>>>>> IN:", match.call()[[1]]))
print("CALL:")
print(match.call())
print("###### PROVIDED ARGUMENTS")
print("STRUCTURE data:")
print(str(data))
print("HEAD data:")
print(head(data))
print("TAIL data:")
print(tail(data))
print("cells")
print(cells)
print("sd.cells")
print(sd.cells)
print("conc")
print(conc)
print("sd.conc")
print(sd.conc)
print("vol")
print(vol)
print("sd.vol")
print(sd.vol)
print("haploid")
print(haploid)
}
# CHECK PARAMETERS ##########################################################
if(!is.data.frame(data)){
stop(paste("'data' must be of type data.frame."))
}
if(!is.logical(haploid)){
stop(paste("'haploid' must be logical."))
}
if(!is.logical(debug)){
stop(paste("'debug' must be logical."))
}
if(!"Marker" %in% names(data)){
stop(paste("'data' must have a colum 'Marker'."))
}
if(!"Allele" %in% names(data)){
stop(paste("'data' must have a colum 'Allele'."))
}
if(!"Sim" %in% names(data)){
stop(paste("'data' must have a colum 'Sim'."))
}
if(!is.null(cells) & is.null(conc) & is.null(slope) & is.null(intercept)){
if(is.null(cells) || !is.numeric(cells) || cells < 0){
stop(paste("'cells' must be a positive numeric for the number of cells."))
}
if(is.null(sd.cells) || !is.numeric(sd.cells) || sd.cells < 0){
stop(paste("'sd.cells' must be a positive numeric for the standard",
"deviation of the number of cells."))
}
} else if(is.null(cells) & !is.null(conc) & is.null(slope) & is.null(intercept)){
if(is.null(conc) || !is.numeric(conc) || conc < 0){
stop(paste("'conc' must be a positive numeric for the concentration."))
}
if(is.null(sd.conc) || !is.numeric(sd.conc) || sd.conc < 0){
stop(paste("'sd.conc' must be a positive numeric for the standard",
"deviation of the concentration."))
}
if(is.null(vol) || !is.numeric(vol) || vol < 0){
stop(paste("'vol' must be a positive numeric for the sample volume."))
}
if(is.null(sd.vol) || !is.numeric(sd.vol) || sd.vol < 0){
stop(paste("'sd.vol' must be a positive numeric for the standard",
"deviation of the sample volume."))
}
} else if(is.null(cells) & is.null(conc) & !is.null(slope) & !is.null(intercept)){
if(is.null(slope) || !is.numeric(slope)){
stop(paste("'slope' must be a numeric."))
}
if(is.null(intercept) || !is.numeric(intercept)){
stop(paste("'intercept' must be a numeric"))
}
} else {
stop("Either 'cells', 'concentration', or 'slope' and 'intercept' must be specified!")
}
# PREPARE ###################################################################
message("SIMULATE SAMPLE")
# Get number of simulations.
.sim <- max(data$Sim)
# Get number of rows per simulation.
.rows <- plyr::count(data$Sim)$freq
# Initiate variables.
ncells <- rep(NA, times=nrow(data))
if(debug){
print(paste("Number of simulations:", .sim))
print(paste("Number of rows per simulation:", paste(.rows, collapse=",")))
}
# Haploid -------------------------------------------------------------------
if("Sample.Haploid" %in% names(data)){
data$Sample.Haploid <- NA
message("The 'Sample.Haploid' column was overwritten!")
} else {
data$Sample.Haploid <- NA
message("'Sample.Haploid' column added.")
}
# Add haploid state to data.
if(length(haploid) == 1){
data$Sample.Haploid <- haploid
} else {
data$Sample.Haploid <- rep(haploid, times=.rows)
}
# SIMULATE ##################################################################
if(!is.null(cells) & is.null(conc)){
if(debug){
print("PARAMETERS TO SIMULATE THE NUMBER OF CELLS")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(cells)
print("sd:")
print(sd.cells)
}
# Draw the random number of cells for each simulation.
rcells <- rnorm(n=.sim, mean=cells, sd=sd.cells)
# Extend to all rows.
ncells <- rep(rcells, times=.rows)
} else if(!is.null(conc) & is.null(cells)){
# Concentration -----------------------------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE DNA CONCENTRATION")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(conc)
print("sd:")
print(sd.conc)
}
# Draw the random concentration for each simulation.
rconc <- rnorm(n=.sim, mean=conc, sd=sd.conc)
# Concentration cannot be negative.
rconc[rconc < 0] <- 0
if("Sample.Conc" %in% names(data)){
data$Sample.Conc <- NA
message("The 'Sample.Conc' column was overwritten!")
} else {
data$Sample.Conc <- NA
message("'Sample.Conc' column added.")
}
# Add concentration to data.
data$Sample.Conc <- rep(rconc, times=.rows)
# Volume ------------------------------------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE SAMPLE VOLUME")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(vol)
print("sd:")
print(sd.vol)
}
# Draw the random volumes for each simulation.
rvol <- rnorm(n=.sim, mean=vol, sd=sd.vol)
# Volume cannot be negative.
rvol[rvol < 0] <- 0
if("Sample.Vol" %in% names(data)){
data$Sample.Vol <- NA
message("The 'Sample.Vol' column was overwritten!")
} else {
data$Sample.Vol <- NA
message("'Sample.Vol' column added.")
}
# Extend to all rows.
voltmp <- rep(rvol, times=.rows)
# Add sample volume to data.
data$Sample.Vol <- voltmp
# Calculate number of cells -----------------------------------------------
hapState <- data$Sample.Haploid
# Convert to number of cells for haploid and diploid samples.
ncells[hapState] <- (data$Sample.Conc[hapState] * data$Sample.Vol[hapState]) / cell.dna * 2
ncells[!hapState] <- (data$Sample.Conc[!hapState] * data$Sample.Vol[!hapState]) / cell.dna
} else if(!is.null(slope) & !is.null(intercept)){
# Log-linear regression ---------------------------------------------------
# To simulate degraded samples.
if(debug){
print("PARAMETERS TO SIMULATE THE DNA CONCENTRATION FOR DEGRADED SAMPLES")
print("slope:")
print(slope)
print("intercept:")
print(intercept)
}
if(!"Size" %in% names(data)){
kitData <- getKit(kit=kit, what="Offset")
if(!all(is.na(kitData))){
data <- strvalidator::addSize(data=data, kit=kitData,
bins=FALSE, ignore.case=FALSE, debug=debug)
message("Added column 'Size'")
} else {
message("Could not calculate allele size!")
print(getKit())
stop(paste(kit, "is not a defined DNA typing kit (available kits are printed above)."))
}
}
# Calculate concentration for each allele.
# TODO: Introduce variation using sigma?
regconc <- 10^(slope * data$Size + intercept)
# Concentration cannot be negative.
regconc[regconc < 0] <- 0
if("Sample.Conc" %in% names(data)){
data$Sample.Conc <- NA
message("The 'Sample.Conc' column was overwritten!")
} else {
data$Sample.Conc <- NA
message("'Sample.Conc' column added.")
}
# Add concentration to data.
data$Sample.Conc <- regconc
# Volume ------------------------------------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE SAMPLE VOLUME")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(vol)
print("sd:")
print(sd.vol)
}
# Draw the random volumes for each simulation.
rvol <- rnorm(n=.sim, mean=vol, sd=sd.vol)
# Volume cannot be negative.
rvol[rvol < 0] <- 0
if("Sample.Vol" %in% names(data)){
data$Sample.Vol <- NA
message("The 'Sample.Vol' column was overwritten!")
} else {
data$Sample.Vol <- NA
message("'Sample.Vol' column added.")
}
# Extend to all rows.
voltmp <- rep(rvol, times=.rows)
# Add sample volume to data.
data$Sample.Vol <- voltmp
# Calculate number of cells -----------------------------------------------
# Get haploid state.
hapState <- data$Sample.Haploid
# Convert to number of cells for haploid and diploid samples.
ncells[hapState] <- (data$Sample.Conc[hapState] * data$Sample.Vol[hapState]) / cell.dna * 2
ncells[!hapState] <- (data$Sample.Conc[!hapState] * data$Sample.Vol[!hapState]) / cell.dna
# Convert to number of cells.
if(haploid){
ncells <- (data$Sample.Conc * data$Sample.Vol) / cell.dna * 2
} else {
ncells <- (data$Sample.Conc * data$Sample.Vol) / cell.dna
}
} else {
warning(paste("Combination cells=", cells,
", conc=", conc,
", and slope=", slope, "and intercept=", intercept,
"not supported!"))
}
# Polish result -------------------------------------------------------------
# Number of cells cannot be negative.
ncells[ncells < 0] <- 0
# Check if haploid cells.
if(any(haploid)){
# Get haploid state.
hapState <- data$Sample.Haploid
# Number of cells must be integer for binomial selection.
ncells[hapState] <- floor(ncells[hapState])
# Simulate number of haploid cells ----------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE NUMBER OF HAPLOID CELLS")
print("rbinom(n, size, prob)")
print("n:")
print(length(ncells))
print("size:")
print(head(ncells))
print("prob:")
print(0.5)
}
# Get the number of cells per marker.
# NB! Assumes two rows per marker (also for homozygotes).
ncellsTmp <- ncells[seq(1,length(ncells), by=2)]
# Randomly draw the number of cells containing allele 1.
allele1 <- rbinom(n=length(ncellsTmp),size=ncellsTmp,prob=0.5)
# Calculate the number of cells containing allele 2.
allele2 <- ncellsTmp - allele1
# Combine vectors alternated (take one from each vector) for haploid samples only.
ncells[hapState] <- c(rbind(allele1,allele2))[hapState]
if(debug){
print("Output:")
print(head(ncells))
}
}
# Add result ----------------------------------------------------------------
if("Sample.Cells" %in% names(data)){
data$Sample.Cells <- NA
message("The 'Sample.Cells' column was overwritten!")
} else {
data$Sample.Cells <- NA
message("'Sample.Cells' column added.")
}
# Add number of cells to data.
data$Sample.Cells <- ncells
# Update DNA column ---------------------------------------------------------
if("DNA" %in% names(data)){
data$DNA <- NULL # Remove first so that the column always appear to the right.
data$DNA <- NA
message("'DNA' column updated!")
} else {
data$DNA <- NA
message("'DNA' column added.")
}
# Add number of cells/molecules to data.
data$DNA <- ncells
# RETURN ####################################################################
# Debug info.
if(debug){
print("RETURN")
print("STRUCTURE:")
print(str(data))
print("HEAD:")
print(head(data))
print("TAIL:")
print(tail(data))
print(paste("<<<<<< EXIT:", match.call()[[1]]))
}
# Return result.
return(data)
}
OskarHansson/pcrsim documentation built on Jan. 22, 2022, 11:55 a.m.
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Defines functions simSample
Documented in simSample
################################################################################
# TODO LIST
# TODO: Introduce variation using sigma when calculating concentration for each allele?
################################################################################
# NOTES
# ...
################################################################################
# CHANGE LOG (10 last changes)
# 14.04.2016: Version 1.0.0 released.
# 13.08.2015: Fixed initiation of a vector (example from concentration did not work).
# 18.11.2014: Support simulation of mixtures and different haplotype state.
# 26.08.2014: More robust definition of .rows (can be different per sample).
# 24.02.2014: First version.
#' @title Forensic Sample Simulator
#'
#' @description Simulates the DNA content in forensic stain.
#'
#' @details Simulates the number of DNA molecules in a forensic stain either
#' from:
#' 1) An estimate of the number of cells in the stain.
#' 2) The DNA concentration.
#' 3) The slope and intercept values as obtained from log-linear regression
#' of DNA concentration by size in basepair.
#' The regression emulates degradation and should not be used together with
#' simulation of degradation using \code{\link{simDegradation}}.
#' Some parameters accept vectors so that simulated samples can have different
#' number of cells and be a mixture of haploid and diploid samples (see examples).
#' Note 1: Number of cells can be decimal values since it is an estimate.
#' Note 2: Number of cells will always be integer if haploid=TRUE because
#' binomial selection require integer values.
#' Note 3: To get the same total amount of DNA in samples with diploid and haploid cells.
#' the parameter for haploid cells must be: cells = 2 * number_of_diploid_cells
#' NB! Important that each marker has two rows (i.e. homozygotes is e.g. 16, 16).
#'
#' @param data data.frame with columns 'Marker', 'Allele', and 'Sim' defining
#' the DNA profiles and simulation id (counter).
#' Preferably output from \code{\link{simProfile}}.
#' @param cells integer for the estimated number of cells.
#' @param sd.cells numeric for the standard deviation of \code{cells}.
#' @param conc numeric for the estimated DNA concentration.
#' @param sd.conc numeric for the standard deviation of \code{conc}.
#' @param vol numeric for the estimated sample volume.
#' @param sd.vol numeric for the standard deviation of \code{vol}.
#' @param cell.dna numeric to indicate the DNA content of a diploid cell in
#' nanograms (ng).
#' @param haploid logical TRUE to indicate haploid cells.
#' @param intercept numeric from regression of log concentration by fragment
#' size (bp).
#' @param slope numeric from regression of log concentration by fragment
#' size (bp).
#' @param kit character string defining the DNA typing kit used to calculate
#' allele size (used to calculate allele sizes needed for the regression option
#' i.e. \code{slope} and \code{intercept}).
#' @param debug logical TRUE to indicate debug mode.
#'
#' @return data.frame with simulated result in columns 'Cells'.
#'
#' @importFrom plyr count
# @importFrom strvalidator addSize getKit
#' @importFrom utils head tail str
#' @importFrom stats rbinom rnorm
#'
#' @export
#'
#' @seealso \code{\link{simProfile}}
#'
#' @examples
#' # Create a data frame with a DNA profile.
#' markers = rep(c("D3S1358","TH01","FGA"), each=2)
#' alleles = c(15,18,6,10,25,25)
#' df <- data.frame(Marker=markers, Allele=alleles)
#' # Simulate profile.
#' prof <- simProfile(data=df, sim=3, name="Test")
#'
#' # Simulate diploid sample.
#' res <- simSample(data=prof, cells=100, sd.cells=20)
#' print(res)
#'
#' # Simulate haploid sample.
#' res <- simSample(data=prof, cells=100, sd.cells=20, haploid=TRUE)
#' print(res)
#'
#' # Simulate haploid sample from concentration.
#' res <- simSample(data=prof, conc=0.02, sd.conc=0.001, vol=100, haploid=TRUE)
#' print(res)
#'
#' # Simulate sample from slope and intercept.
#' res <- simSample(data=prof, vol=100, slope=-0.01, intercept=0.20, kit="SGMPlus")
#' print(res)
#'
#' # Simulate mixture of diploid and haploid sample types of two concentrations.
#' res <- simSample(data=prof, cells=c(1000,1000,250), haploid=c(FALSE,TRUE,FALSE))
#' print(res)
simSample <- function(data, cells=NULL, sd.cells=0,
conc=NULL, sd.conc=0, vol=NULL, sd.vol=0, cell.dna=0.006,
haploid=FALSE, kit=NULL, slope=NULL, intercept=NULL, debug=FALSE) {
# Debug info.
if(debug){
print(paste(">>>>>> IN:", match.call()[[1]]))
print("CALL:")
print(match.call())
print("###### PROVIDED ARGUMENTS")
print("STRUCTURE data:")
print(str(data))
print("HEAD data:")
print(head(data))
print("TAIL data:")
print(tail(data))
print("cells")
print(cells)
print("sd.cells")
print(sd.cells)
print("conc")
print(conc)
print("sd.conc")
print(sd.conc)
print("vol")
print(vol)
print("sd.vol")
print(sd.vol)
print("haploid")
print(haploid)
}
# CHECK PARAMETERS ##########################################################
if(!is.data.frame(data)){
stop(paste("'data' must be of type data.frame."))
}
if(!is.logical(haploid)){
stop(paste("'haploid' must be logical."))
}
if(!is.logical(debug)){
stop(paste("'debug' must be logical."))
}
if(!"Marker" %in% names(data)){
stop(paste("'data' must have a colum 'Marker'."))
}
if(!"Allele" %in% names(data)){
stop(paste("'data' must have a colum 'Allele'."))
}
if(!"Sim" %in% names(data)){
stop(paste("'data' must have a colum 'Sim'."))
}
if(!is.null(cells) & is.null(conc) & is.null(slope) & is.null(intercept)){
if(is.null(cells) || !is.numeric(cells) || cells < 0){
stop(paste("'cells' must be a positive numeric for the number of cells."))
}
if(is.null(sd.cells) || !is.numeric(sd.cells) || sd.cells < 0){
stop(paste("'sd.cells' must be a positive numeric for the standard",
"deviation of the number of cells."))
}
} else if(is.null(cells) & !is.null(conc) & is.null(slope) & is.null(intercept)){
if(is.null(conc) || !is.numeric(conc) || conc < 0){
stop(paste("'conc' must be a positive numeric for the concentration."))
}
if(is.null(sd.conc) || !is.numeric(sd.conc) || sd.conc < 0){
stop(paste("'sd.conc' must be a positive numeric for the standard",
"deviation of the concentration."))
}
if(is.null(vol) || !is.numeric(vol) || vol < 0){
stop(paste("'vol' must be a positive numeric for the sample volume."))
}
if(is.null(sd.vol) || !is.numeric(sd.vol) || sd.vol < 0){
stop(paste("'sd.vol' must be a positive numeric for the standard",
"deviation of the sample volume."))
}
} else if(is.null(cells) & is.null(conc) & !is.null(slope) & !is.null(intercept)){
if(is.null(slope) || !is.numeric(slope)){
stop(paste("'slope' must be a numeric."))
}
if(is.null(intercept) || !is.numeric(intercept)){
stop(paste("'intercept' must be a numeric"))
}
} else {
stop("Either 'cells', 'concentration', or 'slope' and 'intercept' must be specified!")
}
# PREPARE ###################################################################
message("SIMULATE SAMPLE")
# Get number of simulations.
.sim <- max(data$Sim)
# Get number of rows per simulation.
.rows <- plyr::count(data$Sim)$freq
# Initiate variables.
ncells <- rep(NA, times=nrow(data))
if(debug){
print(paste("Number of simulations:", .sim))
print(paste("Number of rows per simulation:", paste(.rows, collapse=",")))
}
# Haploid -------------------------------------------------------------------
if("Sample.Haploid" %in% names(data)){
data$Sample.Haploid <- NA
message("The 'Sample.Haploid' column was overwritten!")
} else {
data$Sample.Haploid <- NA
message("'Sample.Haploid' column added.")
}
# Add haploid state to data.
if(length(haploid) == 1){
data$Sample.Haploid <- haploid
} else {
data$Sample.Haploid <- rep(haploid, times=.rows)
}
# SIMULATE ##################################################################
if(!is.null(cells) & is.null(conc)){
if(debug){
print("PARAMETERS TO SIMULATE THE NUMBER OF CELLS")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(cells)
print("sd:")
print(sd.cells)
}
# Draw the random number of cells for each simulation.
rcells <- rnorm(n=.sim, mean=cells, sd=sd.cells)
# Extend to all rows.
ncells <- rep(rcells, times=.rows)
} else if(!is.null(conc) & is.null(cells)){
# Concentration -----------------------------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE DNA CONCENTRATION")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(conc)
print("sd:")
print(sd.conc)
}
# Draw the random concentration for each simulation.
rconc <- rnorm(n=.sim, mean=conc, sd=sd.conc)
# Concentration cannot be negative.
rconc[rconc < 0] <- 0
if("Sample.Conc" %in% names(data)){
data$Sample.Conc <- NA
message("The 'Sample.Conc' column was overwritten!")
} else {
data$Sample.Conc <- NA
message("'Sample.Conc' column added.")
}
# Add concentration to data.
data$Sample.Conc <- rep(rconc, times=.rows)
# Volume ------------------------------------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE SAMPLE VOLUME")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(vol)
print("sd:")
print(sd.vol)
}
# Draw the random volumes for each simulation.
rvol <- rnorm(n=.sim, mean=vol, sd=sd.vol)
# Volume cannot be negative.
rvol[rvol < 0] <- 0
if("Sample.Vol" %in% names(data)){
data$Sample.Vol <- NA
message("The 'Sample.Vol' column was overwritten!")
} else {
data$Sample.Vol <- NA
message("'Sample.Vol' column added.")
}
# Extend to all rows.
voltmp <- rep(rvol, times=.rows)
# Add sample volume to data.
data$Sample.Vol <- voltmp
# Calculate number of cells -----------------------------------------------
hapState <- data$Sample.Haploid
# Convert to number of cells for haploid and diploid samples.
ncells[hapState] <- (data$Sample.Conc[hapState] * data$Sample.Vol[hapState]) / cell.dna * 2
ncells[!hapState] <- (data$Sample.Conc[!hapState] * data$Sample.Vol[!hapState]) / cell.dna
} else if(!is.null(slope) & !is.null(intercept)){
# Log-linear regression ---------------------------------------------------
# To simulate degraded samples.
if(debug){
print("PARAMETERS TO SIMULATE THE DNA CONCENTRATION FOR DEGRADED SAMPLES")
print("slope:")
print(slope)
print("intercept:")
print(intercept)
}
if(!"Size" %in% names(data)){
kitData <- getKit(kit=kit, what="Offset")
if(!all(is.na(kitData))){
data <- strvalidator::addSize(data=data, kit=kitData,
bins=FALSE, ignore.case=FALSE, debug=debug)
message("Added column 'Size'")
} else {
message("Could not calculate allele size!")
print(getKit())
stop(paste(kit, "is not a defined DNA typing kit (available kits are printed above)."))
}
}
# Calculate concentration for each allele.
# TODO: Introduce variation using sigma?
regconc <- 10^(slope * data$Size + intercept)
# Concentration cannot be negative.
regconc[regconc < 0] <- 0
if("Sample.Conc" %in% names(data)){
data$Sample.Conc <- NA
message("The 'Sample.Conc' column was overwritten!")
} else {
data$Sample.Conc <- NA
message("'Sample.Conc' column added.")
}
# Add concentration to data.
data$Sample.Conc <- regconc
# Volume ------------------------------------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE SAMPLE VOLUME")
print("rnorm(n, mean, sd)")
print("n:")
print(.sim)
print("mean:")
print(vol)
print("sd:")
print(sd.vol)
}
# Draw the random volumes for each simulation.
rvol <- rnorm(n=.sim, mean=vol, sd=sd.vol)
# Volume cannot be negative.
rvol[rvol < 0] <- 0
if("Sample.Vol" %in% names(data)){
data$Sample.Vol <- NA
message("The 'Sample.Vol' column was overwritten!")
} else {
data$Sample.Vol <- NA
message("'Sample.Vol' column added.")
}
# Extend to all rows.
voltmp <- rep(rvol, times=.rows)
# Add sample volume to data.
data$Sample.Vol <- voltmp
# Calculate number of cells -----------------------------------------------
# Get haploid state.
hapState <- data$Sample.Haploid
# Convert to number of cells for haploid and diploid samples.
ncells[hapState] <- (data$Sample.Conc[hapState] * data$Sample.Vol[hapState]) / cell.dna * 2
ncells[!hapState] <- (data$Sample.Conc[!hapState] * data$Sample.Vol[!hapState]) / cell.dna
# Convert to number of cells.
if(haploid){
ncells <- (data$Sample.Conc * data$Sample.Vol) / cell.dna * 2
} else {
ncells <- (data$Sample.Conc * data$Sample.Vol) / cell.dna
}
} else {
warning(paste("Combination cells=", cells,
", conc=", conc,
", and slope=", slope, "and intercept=", intercept,
"not supported!"))
}
# Polish result -------------------------------------------------------------
# Number of cells cannot be negative.
ncells[ncells < 0] <- 0
# Check if haploid cells.
if(any(haploid)){
# Get haploid state.
hapState <- data$Sample.Haploid
# Number of cells must be integer for binomial selection.
ncells[hapState] <- floor(ncells[hapState])
# Simulate number of haploid cells ----------------------------------------
if(debug){
print("PARAMETERS TO SIMULATE THE NUMBER OF HAPLOID CELLS")
print("rbinom(n, size, prob)")
print("n:")
print(length(ncells))
print("size:")
print(head(ncells))
print("prob:")
print(0.5)
}
# Get the number of cells per marker.
# NB! Assumes two rows per marker (also for homozygotes).
ncellsTmp <- ncells[seq(1,length(ncells), by=2)]
# Randomly draw the number of cells containing allele 1.
allele1 <- rbinom(n=length(ncellsTmp),size=ncellsTmp,prob=0.5)
# Calculate the number of cells containing allele 2.
allele2 <- ncellsTmp - allele1
# Combine vectors alternated (take one from each vector) for haploid samples only.
ncells[hapState] <- c(rbind(allele1,allele2))[hapState]
if(debug){
print("Output:")
print(head(ncells))
}
}
# Add result ----------------------------------------------------------------
if("Sample.Cells" %in% names(data)){
data$Sample.Cells <- NA
message("The 'Sample.Cells' column was overwritten!")
} else {
data$Sample.Cells <- NA
message("'Sample.Cells' column added.")
}
# Add number of cells to data.
data$Sample.Cells <- ncells
# Update DNA column ---------------------------------------------------------
if("DNA" %in% names(data)){
data$DNA <- NULL # Remove first so that the column always appear to the right.
data$DNA <- NA
message("'DNA' column updated!")
} else {
data$DNA <- NA
message("'DNA' column added.")
}
# Add number of cells/molecules to data.
data$DNA <- ncells
# RETURN ####################################################################
# Debug info.
if(debug){
print("RETURN")
print("STRUCTURE:")
print(str(data))
print("HEAD:")
print(head(data))
print("TAIL:")
print(tail(data))
print(paste("<<<<<< EXIT:", match.call()[[1]]))
}
# Return result.
return(data)
}
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