fragCounter | R Documentation |
Runs entire fragCounter pipeline
fragCounter(
bam,
skeleton,
cov = NULL,
midpoint = TRUE,
window = 200,
gc.rds.dir,
map.rds.dir,
minmapq = 1,
reference = NULL,
paired = TRUE,
outdir = NULL,
exome = FALSE,
use.skel = FALSE,
chr.sub = TRUE
)
bam |
string path to .bam or .cram file |
skeleton |
string Input data.table with intervals for which there is coverage data |
cov |
string path to existing coverage rds or bedgraph |
midpoint |
boolean If TRUE only count midpoint if FALSE then count bin footprint of every fragment interval |
window |
integer window / bin size |
gc.rds.dir |
string for tiles of width W, will look here for a file named gcW.rds in this directory |
map.rds.dir |
string for tiles of width W will look here for a file named mapW.rds in this directory |
minmapq |
double Minimal map quality |
reference |
reference file (recommended for CRAM, [NULL] |
paired |
boolean wether or not paired |
outdir |
string Directory to dump output into |
exome |
boolean If TRUE, perform correction using exons as bins instead of fixed size |
use.skel |
boolean flag If false then default exome skeleton from gencode is used, if TRUE, user defined skeleton is usde |
chr.sub |
boolean if TRUE, remove 'chr' prefix on seqnames. default TRUE |
Marcin Imielinski
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