#' Set Settings.
#'
#' @param zent_obj ZentTools object.
#' @param analysis_type Type of experiment.
#' Either 'RNA-seq', 'ChIP-seq', or 'ChEC-seq'.
#' @param paired Paired-end status of the reads.
#' Either TRUE or FALSE.
#' @param ncores The number of cores/threads to use.
#' @param genome_dir The directory of the genome index.
#' @param genome_annotation The directory and file name of the
#' the genome index GTF file.
#' @param genome_assembly The directory and file name of the
#' the gnome assembly FASTA file.
#' @param alignment_dir The directory containing the aligned reads.
#' @param peak_dir The directory containing the called peaks.
#'
#' @export
set_settings <- function(
zent_obj,
analysis_type = NA,
paired = NA,
ncores = NA,
genome_dir = NA,
genome_annotation = NA,
genome_assembly = NA,
alignment_dir = NA,
peak_dir = NA
) {
settings <- copy(zent_obj@settings)
if (!is.na(analysis_type)) {
settings[parameter == "analysis_type", value := analysis_type]
}
if (!is.na(paired)) {
settings[parameter == "paired", value := paired]
}
if (!is.na(ncores)) {
settings[parameter == "ncores", value := ncores]
}
if (!is.na(genome_dir)) {
settings[parameter == "genome_dir", value := genome_dir]
}
if (!is.na(genome_annotation)) {
settings[parameter == "genome_annotation", value := genome_annotation]
}
if (!is.na(genome_assembly)) {
settings[parameter == "genome_assembly", value := genome_assembly]
}
if (!is.na(alignment_dir)) {
settings[parameter == "alignment_dir", value := alignment_dir]
}
if (!is.na(peak_dir)) {
settings[parameter == "peak_dir", value := peak_dir]
}
zent_obj@settings <- settings
return(zent_obj)
}
#' Pull Settings
#'
#' @param zent_obj ZentTools object.
#' @param setting Setting to pull.
#'
#' @export
pull_setting <- function(
zent_obj,
setting
) {
setting_value <- zent_obj@settings[parameter == setting, value]
return(setting_value)
}
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