CallCNV: Calls CNV over genomic bins defined by binning

View source: R/CNV_functions.R

CallCNVR Documentation

Calls CNV over genomic bins defined by binning

Description

Calls CNV over genomic bins defined by binning

Usage

CallCNV(
  directory,
  bins,
  chrom_size,
  basename = "Exp",
  group = NULL,
  tmp_dir = file.path(getwd(), "CNV"),
  min_n_reads = 2e+05,
  mim_mean_CN_accepted = 2,
  max_mean_CN_accepted = 8,
  ploidy = NULL,
  chr_prefix = "chr",
  chr_range = NULL,
  cores = 1
)

Arguments

directory,

Single cell Bamfiles directory

bins,

bins produced by binning

chrom_size,

a dataframe (chr=chrom name, size=chrom size)

basename,

sample name

group,

experimental group name

tmp_dir,

temporary folder.

min_n_reads,

Min n of reads to keep a cell in the analysis

mim_mean_CN_accepted,

Min mean CN accepted as result

max_mean_CN_accepted,

Max mean CN accepted as result

ploidy,

user estimated ploidy

chr_prefix,

Chromosome prefix, if there is no prefix use NULL

chr_range,

Chromosomes to consider in the analysis (example 1:5,8,15:18,X)

cores,

Number of cores to use

Value

list of dataframes


CL-CHEN-Lab/User_interface_for_Kronos_scRT documentation built on Aug. 1, 2022, 2:08 p.m.