| highlightFilters {QDNAseq} | R Documentation |
Highlights data points in a plotted profile to evaluate filtering
Description
Highlights data points in a plotted profile to evaluate filtering.
Usage
highlightFilters(object, col="red", residual=NA, blacklist=NA, mappability=NA, bases=NA,
type="union", ...)
Arguments
object |
A QDNAseqCopyNumbers object.
|
col |
The color used for highlighting.
|
residual |
Either a logical specifying whether to filter based on
loess residuals of the calibration set, or if a numeric, the cutoff
as number of standard deviations estimated with
madDiff to use for. Default is TRUE, which
corresponds to 4.0 standard deviations.
|
blacklist |
Either a logical specifying whether to filter based on
overlap with blacklisted regions, or if numeric, the maximum
percentage of overlap allowed. Default is TRUE, which corresponds to
no overlap allowed (i.e. value of 0).
|
mappability |
A numeric in [0,100] to specify filtering out
bins with mappabilities lower than the number specified. NA (default)
or FALSE will not filter based on mappability.
|
bases |
A numeric specifying the minimum percentage of characterized
bases (not Ns) in the reference genome sequence. NA (default) or
FALSE will not filter based on uncharacterized bases.
|
type |
When specifying multiple filters (residual,
blacklist, mappability, bases), whether to
highlight their union (default) or intersection.
|
... |
Further arguments to points.
|
Author(s)
Ilari Scheinin
Examples
data(LGG150)
readCounts <- LGG150
plot(readCounts)
highlightFilters(readCounts, residual=TRUE, blacklist=TRUE)
[Package
QDNAseq version 1.30.0
Index]