cnvkit-coverage(1)
Calculate coverage in the given regions from BAM read depths.
Description
CNVKIT_COVERAGE
NAME
cnvkit_coverage - Calculate coverage in the given regions from BAM read depths.
DESCRIPTION
usage: cnvkit
coverage [-h] [-f FILENAME] [-c] [-q MIN_MAPQ] [-o FILENAME]
[-p [PROCESSES]]
bam_file interval
positional arguments:
bam_file
Mapped sequence reads (.bam)
interval
Intervals (.bed or .list)
options:
-h, --help
show this help message and exit
-f FILENAME, --fasta FILENAME
Reference genome, FASTA format (e.g. UCSC hg19.fa)
-c, --count
Get read depths by counting read midpoints within each bin. (An alternative algorithm).
-q MIN_MAPQ, --min-mapq MIN_MAPQ
Minimum mapping quality score (phred scale 0-60) to count a read for coverage depth. [Default: 0]
-o FILENAME, --output FILENAME
Output file name.
-p [PROCESSES], --processes [PROCESSES]
Number of subprocesses to calculate coverage in parallel. Without an argument, use the maximum number of available CPUs. [Default: use 1 process]