Provided by: allelecount_4.3.0-3_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. alleleCounter 4.1.0 May 2020 ALLELECOUNTER(1)