Provided by: allelecount_4.3.0-2build2_amd64
NAME
alleleCounter - NGS copy number algorithms
SYNOPSIS
alleleCounter -l loci_file.txt -b sample.bam -o output.txt [-m int] [-r ref.fa.fai]
DESCRIPTION
Support code for NGS copy number algorithms. Takes a file of locations and a [cr|b]am file and generates a count of coverage of each allele [ACGT] at that location (given any filter settings).
OPTIONS
-l --loci-file [file] Path to loci file. -b --hts-file [file] Path to sample HTS file. -o --output-file [file] Path write output file. Optional -r --ref-file [file] Path to reference fasta index file. NB. If cram format is supplied via -b and the reference listed in the cram header can't be found alleleCounter may fail to work correctly. -m --min-base-qual [int] Minimum base quality [Default: 20]. -q --min-map-qual [int] Minimum mapping quality [Default: 35]. -c --contig [string] Limit calling to named contig. -d --dense-snps Improves performance where many positions are close together -x --is-10x Enables 10X processing mode. In this mode the HTS input file must be a cellranger produced BAM file. Allele counts are then given on a per-cellular barcode basis, with each count representing the consensus base for that UMI. by iterating through bam file rather than using a 'fetch' approach. -f --required-flag [int] Flag value of reads to retain in allele counting default: [3]. N.B. if the proper-pair flag is are selected, alleleCounter will assume paired-end and filter out any proper-pair flagged reads not in F/R orientation. -F --filtered-flag [int] Flag value of reads to exclude in allele counting default: [3852]. -v --version Display version number. -h --help Display this usage information.
AUTHOR
This manpage was written by Andreas Tille for the Debian distribution and can be used for any other usage of the program.