Changes between Version 49 and Version 50 of SOPs/chip_seq_peaks
- Timestamp:
- 03/04/20 10:35:04 (5 years ago)
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TabularUnified SOPs/chip_seq_peaks
v49 v50 49 49 }}} 50 50 * -B create bedgraph output files 51 * -f Input format (typically BAM for single-end reads and BAMPE for paired-end reads). In BAMPE mode, MACS2 will only use properly-paired read alignments, see [[https://groups.google.com/forum/#!topic/macs-announcement/Vh916L3tOOE | MACS2 Forum ]] .51 * -f Input format (typically BAM for single-end reads and BAMPE for paired-end reads). In BAMPE mode, MACS2 will only use properly-paired read alignments, see [[https://groups.google.com/forum/#!topic/macs-announcement/Vh916L3tOOE | MACS2 Forum ]], also from the readme/manual, "when format BAMPE is specified, MACS will use the real fragments inferred from alignment results for reads pileup." If you have PE ChIP-Seq data, -f bampe option is recommended. 52 52 * --nomodel whether or not to build the shifting model. If True, MACS will not build model. By default it means shifting size = 100. 53 53 * --extsize When nomodel is true, MACS will use this value as fragment size to extend each read towards 3' end