sampP

tree


    default to be FALSE, TRUE if input sample is cell line (no normal cell
    contamination)

cell.line


To sample clonal frequency matrix $P$. Used in <code><a rd-options="" href="/link/canopy.sample?package=Canopy&version=1.0.0" data-mini-rdoc="Canopy::canopy.sample">canopy.sample</a></code>.


 package

A statistical framework and computational procedure for identifying the sub-populations within a tumor, determining the mutation profiles of each subpopulation, and inferring the tumor's phylogenetic history. The input are variant allele frequencies (VAFs) of somatic single nucleotide alterations (SNAs) along with allele-specific coverage ratios between the tumor and matched normal sample for somatic copy number alterations (CNAs). These quantities can be directly taken from the output of existing software. Canopy provides a general mathematical framework for pooling data across samples and sites to infer the underlying parameters. For SNAs that fall within CNA regions, Canopy infers their temporal ordering and resolves their phase.  When there are multiple evolutionary configurations consistent with the data, Canopy outputs all configurations along with their confidence assessment.

sampP: To sample clonal frequency

Description

Usage

Arguments

Value

Examples