BayesNMF.MutationalSignatures: Perform Bayesian NMF mutational signature analysis

Description Usage Arguments See Also

Description

Perform Bayesian NMF mutational signature analysis. Source code borrowed from Broad Institute CGA.

Usage

1
BayesNMF.MutationalSignatures(x, tumor.type="tumor.type", hyper=FALSE, fafile=NULL, out.dir="OUTPUT_lego96", prior="L1KL")

Arguments

x

A data frame with at least 6 named columns, i.e. 'chr', 'start', 'end', 'ref', 'alt' and 'sampleid'. The seqlevels of mutation data and reference must be identical, or ERROR will occur during mutation context extraction.

tumor.type

A character string specify tumor type analyzed.

hyper

Default = FALSE ; TRUE - to reduce the effect of hyper-mutant samples in the signature discovery.

fafile

BWA-indexed reference sequence. If this is NULL (default), the Homo sapiens hg19 in package BSgenome.Hsapiens.UCSC.hg19 is used. In this case, BSgenome.Hsapiens.UCSC.hg19 must be installed in advanced.

out.dir

The output directory.

prior

Default = L1KL (expoential priors); L2KL (half-normal priors).

See Also

Mutational signature analysis framework in package SomaticSignatures


lixiangchun/lxctk documentation built on May 21, 2019, 6:44 a.m.