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# Produces a cghRA.design object from a custom TSV file
# Author : Sylvain Mareschal <mareschal@ovsa.fr>
custom.design = function(
file,
name = NULL,
organism = as.character(NA),
assembly = as.character(NA),
chromosomes = NULL,
...
) {
# File parsing
dat <- utils::read.table(
file = file,
sep = "\t",
dec = ".",
header = TRUE,
comment.char = "",
quote = "\"",
na.strings = c("NA", ""),
stringsAsFactors = FALSE
)
# Mandatory columns
missing <- setdiff(c("chrom", "start", "end"), colnames(dat))
if(length(missing) > 0L) stop("Mandatory columns are missing : ", paste(missing, collapse=", "))
# Factorial strand
if("strand" %in% colnames(dat)) { dat$strand <- factor(dat$strand, levels=c("-","+"))
} else { dat$strand <- factor(NA, levels=c("-","+"))
}
# Use provided chromosome levels
if(is.null(chromosomes)) { dat$chrom <- factor(dat$chrom)
} else { dat$chrom <- factor(dat$chrom, levels=chromosomes)
}
# Merging ID
if(!"id" %in% colnames(dat)) {
dat$id <- 1:nrow(dat)
warning("No 'id' column provided, assuming that design and probe files will be ordered in the same way")
}
# Without name, use ID as name
if(!"name" %in% colnames(dat)) {
dat$name <- as.character(dat$id)
warning("No 'name' column provided (not recommended), using 'id' as probe name")
}
# Use file name as default
if(is.null(name)) {
name <- basename(file)
}
# New object
design <- cghRA.design(
dat,
.name = name,
.organism = organism,
.assembly = assembly
)
return(design)
}
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