View source: R/sc_atac_create_fragments.R
| sc_atac_create_fragments | R Documentation | 
Takes in a tagged and sorted BAM file and outputs the associated fragments in a .bed file
sc_atac_create_fragments(
  inbam,
  output_folder = "",
  min_mapq = 30,
  nproc = 1,
  cellbarcode = "CB",
  chromosomes = "^chr",
  readname_barcode = NULL,
  cells = NULL,
  max_distance = 5000,
  min_distance = 10,
  chunksize = 5e+05
)
| inbam | The tagged, sorted and duplicate-free input BAM file | 
| output_folder | The path of the output folder | 
| min_mapq | : int Minimum MAPQ to retain fragment | 
| nproc | : int, optional Number of processors to use. Default is 1. | 
| cellbarcode | : str Tag used for cell barcode. Default is CB (used by cellranger) | 
| chromosomes | : str, optional Regular expression used to match chromosome names to include in the output file. Default is "(?i)^chr" (starts with "chr", case-insensitive). If None, use all chromosomes in the BAM file. | 
| readname_barcode | : str, optional Regular expression used to match cell barocde stored in read name. If None (default), use read tags instead. Use "[^:]*" to match all characters before the first colon (":"). | 
| cells | : str File containing list of cell barcodes to retain. If None (default), use all cell barcodes found in the BAM file. | 
| max_distance | : int, optional Maximum distance between integration sites for the fragment to be retained. Allows filtering of implausible fragments that likely result from incorrect mapping positions. Default is 5000 bp. | 
| min_distance | : int, optional Minimum distance between integration sites for the fragment to be retained. Allows filtering implausible fragments that likely result from incorrect mapping positions. Default is 10 bp. | 
| chunksize | : int Number of BAM entries to read through before collapsing and writing fragments to disk. Higher chunksize will use more memory but will be faster. | 
returns NULL
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