View source: R/loadCopyNumberCalls.R
loadCopyNumberCalls | R Documentation |
Loads copy number calls from a tabular format
loadCopyNumberCalls(cnv.data, chr.col = NULL, start.col = NULL, end.col = NULL, cn.col = NULL, loh.col = NULL, segment.value.col = NULL, genome = NULL, zero.based = FALSE, verbose = TRUE)
cnv.data |
Either the name of the file with the data or a variable containing the data |
chr.col |
(number or character) The name or number of the column with chromosome information. If NULL, it is automatically identified. (defaults to NULL) |
start.col |
(number or character) The name or number of the column with start position information. If NULL, it is automatically identified. (defaults to NULL) |
end.col |
(number or character) The name or number of the column with end position information. If NULL, it is automatically identified. (defaults to NULL) |
cn.col |
(number or character) The name or number of the column with CN information. If NULL, it is automatically identified. (defaults to NULL) |
loh.col |
(number or character) The name or number of the column with LOH information. If NULL, it is automatically identified. (defaults to NULL) |
segment.value.col |
(number or character) The name or number of the column with segment value. If NULL, it is automatically identified. (defaults to NULL) |
genome |
(character) The name of the genome (defaults to NULL) |
zero.based |
(logical) Whether the data is zero-based and half open (i.e. ranges are defined by (start:end] so chr1:10-20 represents nine bases long features spanning from base 11 to 20). (defaults to FALSE) |
verbose |
(logical) Whether to show information messages. (defaults to TRUE) |
This function will load segments data from any "bed-like" data structure
in R or file. Internally it uses the toGRanges
function from regioneR
package and can work with any format accepted by it, including R objects
and local or remote files.
If no column names are specified, it will use simple heuristics to try to
identify the relevant data columns.
A GRanges with a range per copy number segment
df <- data.frame("id"= "rs1234","chromosome"="chr1", "Start"=0, "end.position"=100,
"copy.number.level"=3, "LOH"=0, "median.value.per.segment"=1.2,
"BAF"=0.2, "Log Ratio"=1.5, "strange.name"="strange.value")
cnv.call <- loadCopyNumberCalls(cnv.data = df)
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