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superFreq (version 1.2.3)

getStories: Combines variants and CNAs to clonal evolution

Description

Combines variants and CNAs to clonal evolution

Usage

getStories(variants, cnvs, timeSeries, normals, genome,
  cloneDistanceCut = -qnorm(0.01), Rdirectory, plotDirectory, cpus = 1,
  forceRedo = F, manualStoryMerge = F, correctReferenceBias = T,
  rareGermline = T, maxStories = 3000)

Arguments

variants

variants: The variants.

cnvs

cnvs: The copy number calls.

timeSeries

names list of vectors: samples to be analysed together, named by individual.

normals

named boolean vector: which sameples (names of vector) are normal.

genome

character: the genome.

Rdirectory

character: The save directory.

plotDirectory

character: the directory to plot to.

cpus

integer: maximum number of parallel processes. Default 1.

forceRedo

boolen: if redoing calculations even if saved data is available. Default FALSE.

Details

This function calls VEP on the output from outputSomaticVariants. For this, VEP needs to be callable by system('vep').