View source: R/CNV_functions.R
CallCNV | R Documentation |
Calls CNV over genomic bins defined by binning
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 )
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 |
list of dataframes
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