Provided by: macs_2.2.7.1-5ubuntu1_amd64
NAME
macs2_pileup - Model-based Analysis for ChIP-Sequencing
DESCRIPTION
usage: macs2 pileup [-h] -i IFILE [IFILE ...] -o OUTPUTFILE [--outdir OUTDIR] [-f {AUTO,BAM,SAM,BED,ELAND,ELANDMULTI,ELANDEXPORT,BOWTIE,BAMPE,BEDPE}] [-B] [--extsize EXTSIZE] [--buffer-size BUFFER_SIZE] [--verbose VERBOSE] options: -h, --help show this help message and exit -i IFILE [IFILE ...], --ifile IFILE [IFILE ...] Alignment file. If multiple files are given as '-t A B C', then they will all be read and combined. Note that pair-end data is not supposed to work with this command. REQUIRED. -o OUTPUTFILE, --ofile OUTPUTFILE Output bedGraph file name. If not specified, will write to standard output. REQUIRED. --outdir OUTDIR If specified all output files will be written to that directory. Default: the current working directory -f {AUTO,BAM,SAM,BED,ELAND,ELANDMULTI,ELANDEXPORT,BOWTIE,BAMPE,BEDPE}, --format {AUTO,BAM,SAM,BED,ELAND,ELANDMULTI,ELANDEXPORT,BOWTIE,BAMPE,BEDPE} Format of tag file, "AUTO", "BED", "ELAND", "ELANDMULTI", "ELANDEXPORT", "SAM", "BAM", "BOWTIE", "BAMPE", or "BEDPE". The default AUTO option will let 'macs2 pileup' decide which format the file is. DEFAULT: "AUTO", MACS2 will pick a format from "AUTO", "BED", "ELAND", "ELANDMULTI", "ELANDEXPORT", "SAM", "BAM" and "BOWTIE". If the format is BAMPE or BEDPE, please specify it explicitly. Please note that when the format is BAMPE or BEDPE, the -B and --extsize options would be ignored. -B, --both-direction By default, any read will be extended towards downstream direction by extension size. So it's [0,size-1] (1-based index system) for plus strand read and [-size+1,0] for minus strand read where position 0 is 5' end of the aligned read. Default behavior can simulate MACS2 way of piling up ChIP sample reads where extension size is set as fragment size/d. If this option is set as on, aligned reads will be extended in both upstream and downstream directions by extension size. It means [-size,size] where 0 is the 5' end of a aligned read. It can partially simulate MACS2 way of piling up control reads. However MACS2 local bias is calculated by maximizing the expected pileup over a ChIP fragment size/d estimated from 10kb, 1kb, d and whole genome background. This option will be ignored when the format is set as BAMPE or BEDPE. DEFAULT: False --extsize EXTSIZE The extension size in bps. Each alignment read will become a EXTSIZE of fragment, then be piled up. Check description for -B for detail. It's twice the `shiftsize` in old MACSv1 language. This option will be ignored when the format is set as BAMPE or BEDPE. DEFAULT: 200 --buffer-size BUFFER_SIZE Buffer size for incrementally increasing internal array size to store reads alignment information. In most cases, you don't have to change this parameter. However, if there are large number of chromosomes/contigs/scaffolds in your alignment, it's recommended to specify a smaller buffer size in order to decrease memory usage (but it will take longer time to read alignment files). Minimum memory requested for reading an alignment file is about # of CHROMOSOME * BUFFER_SIZE * 8 Bytes. DEFAULT: 100000 --verbose VERBOSE Set verbose level. 0: only show critical message, 1: show additional warning message, 2: show process information, 3: show debug messages. If you want to know where are the duplicate reads, use 3. DEFAULT:2