PlotAllCNVs: PlotAllCNVs
In mbertalan/iPsychCNV: iPsychCNV

Description Usage Arguments Details Value Author(s) Source Examples

PlotAllCNVs: Plot all Copy Number Variations (CNVs) in one plot.

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PlotAllCNVs(df = CNV.Res, Name = "CNV.Res.Test.png", NCOL = 2,
  Roi = roi, width = 16, height = 30, hg = "hg19", chr = NA,
  start = NA, stop = NA, Order = TRUE)

`Df:`	Data frame with predicted CNVs for each sample, default = CNV.Res.
`Name:Unknown,`	default = Unknown.
`NCOL:`	Number of columns, default = 2.
`Roi:`	Regions of interest or hotspots, default = roi.
`Width:`	Unknown, defualt = 16.
`Height:`	Unknown, default = 30.
`Hg:`	Human genome version, default = hg19.
`Chr:`	Chromosome, default = NA.
`Start:`	The start position of each CNV, default = NA.
`Stop:`	The stop position of each CNV, default = NA.
`Order:`	Should the function order the CNVs ?, default = TRUE.