getMatricesSNVOnly: Generate the matrices C, W and M from a set of parameters...

Description Usage Arguments Value Examples

Description

This is a generic function to generate the matrices of the linear system (see the paper) from the allele counts and the copy number information under the SNVOnly mode.

Usage

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getMatricesSNVOnly(varcounts_snv, refcounts_snv, major_cn, minor_cn, context,
  sigma = NULL)

Arguments

varcounts_snv

A count of alleles supporting the variant sequence of the somatic mutation

refcounts_snv

A count of alleles supporting the reference sequence of the somatic mutation

major_cn

major Copy number at the locus of the mutation

minor_cn

minor copy number at the locus of the mutation

context

represents either the situation of a mutation which occurred after the CNV ("C1") or the context of a mutation which occurred before the CNV ("C2"). If not provided, the right context will be estimated from the input

sigma

Copy number of the parental chromosome harboring the mutation.

Value

the matrices W, C and M for the linear system of prevalence computation.

Examples

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Matrices = getMatricesSNVOnly(3,10,2,1,"C1")

print(Matrices)
#$context
#[1] "C1"
#
#$W
#SNV
#SNV 0.2307692
#
#$M
#Germ Alt Both
#SNV    0   0    1
#
#$C
#Germ Alt Both
#SNV    2   3    3

chedonat/OncoPhase documentation built on May 13, 2019, 3:39 p.m.