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CNVKIT_REFERENCE(1) User Commands CNVKIT_REFERENCE(1)

NAME

cnvkit_reference - Compile a coverage reference from the given files (normal samples).

DESCRIPTION

usage: cnvkit reference [-h] [-f FASTA] [-o FILENAME] [-c]

[--min-cluster-size NUM]
[-x {m,y,male,Male,f,x,female,Female}] [-y] [-t TARGETS] [-a ANTITARGETS] [--no-gc] [--no-edge] [--no-rmask] [references ...]

positional arguments:

Normal-sample target or antitarget .cnn files, or the directory that contains them.

optional arguments:

show this help message and exit
Reference genome, FASTA format (e.g. UCSC hg19.fa)
Output file name.
Calculate and store summary stats for clustered subsets of the normal samples with similar coverage profiles.
Minimum cluster size to keep in reference profiles.
Specify the chromosomal sex of all given samples as male or female. (Default: guess each sample from coverage of X and Y chromosomes).
Create a male reference: shift female samples' chrX log-coverage by -1, so the reference chrX average is -1. Otherwise, shift male samples' chrX by +1, so the reference chrX average is 0.

To construct a generic, flat" copy number reference with neutral expected coverage:"

Target intervals (.bed or .list)
Antitarget intervals (.bed or .list)

To disable specific automatic bias corrections:

Skip GC correction.
Skip edge-effect correction.
Skip RepeatMasker correction.
October 2021 cnvkit reference 0.9.9