readCNAProfile: Read CNA Profiles

View source: R/readCNAProfile.R

readCNAProfileR Documentation

Read CNA Profiles

Description

We used a CNAqc object, containing a set of mutations, CNA calls and tumor purity values. The CNAqc was used to deal with the allele-specific CNAs.

Usage

readCNAProfile(maf, seg, Patient_ID = NULL, purity = 1, ref = "hg19")

Arguments

maf

Maf or MafList object generated by readMaf() function

seg

seg or seglist.

Patient_ID

Patient_ID: select the specific patients. IF not indicate, the input is Maf and seg, or the input is MafList and segList.

purity

purity information for each samples.

ref

human reference genome version. Default 'hg19'. Optional: 'hg18' or 'hg38'.

Details

This code reads the CNA Profiles for each patient. The tumor names of maf and seg are required to match each other.

Value

cnaqc.list for cnaqc initiation.


qingjian1991/MPTevol documentation built on Jan. 30, 2023, 10:16 p.m.