Nothing
# Variable, global to REMP's namespace.
# This function is not exported to user space and does not need to be documented.
REMPOPTIONS <- settings::options_manager(
.default.AluFamily.grep = "^Alu|^FAM|^FLAM|^FRAM",
.default.L1Family.grep = "^L1|^HAL1",
.default.LTRFamily.grep = "ERV|LTR",
.default.chr = paste0("chr", c(seq_len(22), "X", "Y")),
.default.GM12878.450k.URL = "http://hgdownload.cse.ucsc.edu/goldenPath/hg19/encodeDCC/wgEncodeHaibMethyl450/wgEncodeHaibMethyl450Gm12878SitesRep1.bed.gz",
.default.RMSK.hg19.URL = "http://hgdownload.cse.ucsc.edu/goldenpath/hg19/database/rmsk.txt.gz",
.default.RMSK.hg38.URL = "http://hgdownload.cse.ucsc.edu/goldenpath/hg38/database/rmsk.txt.gz",
.default.refGene.hg19.URL = "https://hgdownload.soe.ucsc.edu/goldenPath/hg19/database/refGene.txt.gz",
.default.refGene.hg38.URL = "https://hgdownload.soe.ucsc.edu/goldenPath/hg38/database/refGene.txt.gz",
.default.AH.repeatmasker.hg19 = "AH5122",
.default.AH.refgene.hg19 = "AH5040",
.default.AH.hg38ToHg19.over.chain = "AH14108",
.default.AH.hg19ToHg38.over.chain = "AH14150",
.default.TSS.upstream = 2000,
.default.TSS.downstream = 0,
.default.max.flankWindow = 1200,
.default.27k.total.probes = 27578,
.default.450k.total.probes = 485577,
.default.epic.total.probes = 866895,
.default.450k.annotation = "ilmn12.hg19",
.default.epic.annotation = "ilm10b2.hg19",
.default.genomicRegionColNames = c(
"InNM", "InNR", "InTSS", "In5UTR",
"InCDS", "InExon", "In3UTR"
),
.default.predictors = c(
"RE.score", "RE.Length", "RE.CpG.density",
"RE.InTSS", "RE.In5UTR", "RE.InCDS",
"N.nbr", "distance.mean", "distance.std", "distance.min", "distance.min2",
"Methy.min", "Methy.min2", "Methy.mean.mov1", "Methy.mean.mov2",
"Methy.mean.mov3", "Methy.mean.mov4", "Methy.std"
),
.default.svmLinear.tune = list(C = 2^seq(-15, 3, 2)),
.default.svmRadial.tune = list(
C = 2^seq(-7, 7, 2),
sigma = 2^seq(-9, 1, 2)
),
.default.xgbTree.tune = list(
nrounds = 500,
eta = 0.01,
max_depth = 5,
gamma = seq(0, 1, 0.2),
colsample_bytree = 0.8,
min_child_weight = 4,
subsample = 0.8
)
)
#' @title Set or get options for REMP package
#'
#' @description Tools to manage global setting options for REMP package.
#'
#' @param ... Option names to retrieve option values or \code{[key]=[value]} pairs to set options.
#'
#' @section Supported options:
#' The following options are supported
#' \describe{
#' \item{\code{.default.AluFamily.grep}}{Regular expression for 'grep' to extract Alu subfamily to be included in the prediction.}
#' \item{\code{.default.L1Family.grep}}{Regular expression for 'grep' to extract L1 subfamily to be included in the prediction.}
#' \item{\code{.default.LTRFamily.grep}}{Regular expression for 'grep' to extract Long Terminal Repeat (LTR), including Endogenous
#' Retrovirus (ERV) subfamily to be included in the prediction (this includes Human Endogenous Retrovirus, HERV).}
#' \item{\code{.default.chr}}{List of human chromosome.}
#' \item{\code{.default.GM12878.450k.URL}}{URL to download GM12878 450k methylation profiling data.}
#' \item{\code{.default.RMSK.hg19.URL}}{URL to download RepeatMasker database in hg19 genome.}
#' \item{\code{.default.RMSK.hg38.URL}}{URL to download RepeatMasker database in hg38 genome.}
#' \item{\code{.default.refGene.hg19.URL}}{URL to download refSeq gene database in hg19 genome.}
#' \item{\code{.default.refGene.hg38.URL}}{URL to download refSeq gene database in hg38 genome.}
#' \item{\code{.default.AH.repeatmasker.hg19}}{\code{AnnotationHub} data ID linked to RepeatMasker
#' database (build hg19).}
#' \item{\code{.default.AH.refgene.hg19}}{\code{AnnotationHub} data ID linked to refSeq gene database
#' (build hg19)}
#' \item{\code{.default.AH.hg38ToHg19.over.chain}}{\code{AnnotationHub} hg38 to hg19 liftover chain data ID.}
#' \item{\code{.default.AH.hg19ToHg38.over.chain}}{\code{AnnotationHub} hg19 to hg38 liftover chain data ID.}
#' \item{\code{.default.TSS.upstream}}{Define the upstream range of transcription start site region.}
#' \item{\code{.default.TSS.downstream}}{Define the downstream range of transcription start site region.}
#' \item{\code{.default.max.flankWindow}}{Define the max size of the flanking window surrounding the
#' predicted RE-CpG.}
#' \item{\code{.default.27k.total.probes}}{Total number of probes designed in Illumina 27k array.}
#' \item{\code{.default.450k.total.probes}}{Total number of probes designed in Illumina 450k array.}
#' \item{\code{.default.epic.total.probes}}{Total number of probes designed in Illumina EPIC array.}
#' \item{\code{.default.450k.annotation}}{A character string associated with the Illumina 450k
#' array annotation dataset.}
#' \item{\code{.default.epic.annotation}}{A character string associated with the Illumina EPIC
#' array annotation dataset.}
#' \item{\code{.default.genomicRegionColNames}}{Define the names of the genomic regions for prediction.}
#' \item{\code{.default.predictors}}{Define the names of predictors for RE methylation prediction.}
#' \item{\code{.default.svmLinear.tune}}{Define the default \code{C} (Cost) parameter for Support
#' Vector Machine (SVM) using linear kernel.}
#' \item{\code{.default.svmRadial.tune}}{Define the default parameters (\code{C} and \code{sigma}) for SVM
#' using Radial basis function kernel.}
#' \item{\code{.default.xgbTree.tune}}{Define the default parameters (\code{nrounds}, \code{eta}, \code{max_depth},
#' \code{gamma}, \code{colsample_bytree}, \code{min_child_weight}, and \code{subsample}) for Extreme Gradient
#' Boosting.}
#' }
#'
#' @return \code{NULL}
#'
#' @examples
#' # Display all default settings
#' remp_options()
#'
#' # Display a specified setting
#' remp_options(".default.max.flankWindow")
#'
#' # Change default maximum flanking window size to 2000
#' remp_options(.default.max.flankWindow = 2000)
#'
#' # Reset all options
#' remp_reset()
#' @rdname options
#' @export
remp_options <- function(...) {
# protect against the use of reserved words.
settings::stop_if_reserved(...)
REMPOPTIONS(...)
}
#' @rdname options
#' @export
remp_reset <- function() {
settings::reset(REMPOPTIONS)
}
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