Description Usage Arguments Details Value Examples
View source: R/loadCopyNumberCallsPennCNV.R
Loads copy number calls from pennCNV.rawcnv file format
| 1 | 
| pennCNV.file | The name of the file with 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) | 
| 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) | 
| verbose | (logical) Whether to show information messages. (defaults to TRUE) | 
This function will load copy number calls from pennCNV.rawcnv file format. 
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 or a list of GRanges with a GRanges per sample.
| 1 2 3 4 5 | ## loadCopyNumberCallspennCNV from .rawcnv file format: 
## The file to run the example can be found in: http://penncnv.openbioinformatics.org/en/latest/user-guide/test/
pennCNV.file <- system.file("extdata", "pennCNV.rawcnv", package = "CopyNumberPlots", mustWork = TRUE)
cnv.call <- loadCopyNumberCallspennCNV(pennCNV.file = pennCNV.file)
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