plotTracks.PairedPSCNData | R Documentation |
Plots parental specific copy numbers along the genome for one or more chromosomes. It is possible to specify what type of tracks to plot. Each type of track is plotted in its own panel.
## S3 method for class 'PairedPSCNData'
plotTracks(x, tracks=c("tcn", "dh", "tcn,c1,c2", "tcn,c1", "tcn,c2", "c1,c2", "betaN",
"betaT", "betaTN")[1:3], pch=".", col=NULL, cex=1, grid=FALSE, xlim=NULL, Clim=c(0, 6),
Blim=c(0, 1), xScale=1e-06, ..., add=FALSE, subplots=!add && (length(tracks) > 1),
verbose=FALSE)
tracks |
A |
pch |
The type of the scatter points, if any. |
col |
The color of the scatter points, if any. |
cex |
The size of the scatter points, if any. |
grid |
If |
xlim |
(Optional) The genomic range to plot. |
Clim |
The range of copy numbers. |
Blim |
The range of allele B fractions (BAFs) and decrease of heterozygosity (DHs). |
xScale |
The scale factor used for genomic positions. |
... |
Not used. |
add |
If |
subplots |
If |
verbose |
See |
Returns nothing.
Henrik Bengtsson
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.