callCNV: call copy number variation using QDNAseq utilities
In hw538/cfDNAPro: cfDNAPro extracts and Visualises biological features from whole genome sequencing data of cell-free DNA
callCNV R Documentation
call copy number variation using QDNAseq utilities
Description
call copy number variation using QDNAseq utilities
Usage
callCNV(bamfile, bin_size = 1000, genome_label = "hg19")
Arguments
bamfile
string. path to a single bam file.
bin_size
numerical. available options are
genome_label
Value
QDNAseqCopyNumbers object
hw538/cfDNAPro documentation built on Nov. 28, 2024, 12:13 p.m.
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| callCNV | R Documentation |
call copy number variation using QDNAseq utilities
Description
call copy number variation using QDNAseq utilities
Usage
callCNV(bamfile, bin_size = 1000, genome_label = "hg19")
Arguments
bamfile |
string. path to a single bam file. |
bin_size |
numerical. available options are |
genome_label |
Value
QDNAseqCopyNumbers object
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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