Description Usage Arguments Value Examples
View source: R/shattered.regions.r
Caller for shattered genomic regions based on breakpoint densities
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 | shattered.regions(
cnv,
svc,
fc.pct = 0.2,
min.cnv.size = 0,
min.num.probes = 0,
low.cov = NULL,
clean.brk = NULL,
window.size = 10,
slide.size = 2,
num.cnv.breaks = 6,
num.cnv.sd = 5,
num.svc.breaks = 6,
num.svc.sd = 5,
num.common.breaks = 3,
num.common.sd = 3,
maxgap = 10000,
chrlist = NULL,
interleaved.cut = 0.5,
dist.iqm.cut = 1e+05,
verbose = TRUE
)
|
cnv |
(S4) an object of class svcnvio containing data type 'cnv' validated by validate.cnv |
svc |
(S4) an object of class svcnvio containing data type 'svc' validated by validate.svc |
fc.pct |
(numeric) inherited from cnv.breaks(); copy number change between 2 consecutive segments: i.e (default) cutoff = 0.2 represents a fold change of 0.8 or 1.2 |
min.cnv.size |
(numeric) inherited from cnv.breaks(); The minimun segment size (in base pairs) to include in the analysis |
min.num.probes |
(numeric) inherited from cnv.breaks(); The minimun number of probes per segment to include in the analysis |
low.cov |
(data.frame) inherited from cnv.breaks(), svc.breaks() and match.breaks; a data.frame (chr, start, end) indicating low coverage regions to exclude from the analysis |
clean.brk |
(numeric) inherited from cnv.breaks(); n of redundant breakpoints to filter out |
window.size |
(numeric) size in megabases of the genmome bin to compute break density |
slide.size |
(numeric) size in megabases of the sliding genmome window |
num.cnv.breaks |
(numeric) number of segmentation breakpoints per segments to be considered high-density break |
num.cnv.sd |
(numeric) number of standard deviations above the sample average for num.cnv.breaks |
num.svc.breaks |
(numeric) number of svc breakpoints per segments to be considered high-density break |
num.svc.sd |
(numeric) number of standard deviations above the sample average for num.svc.breaks |
num.common.breaks |
(numeric) number of common SV and segmentation breakpoints per segments to be considered high-density break |
num.common.sd |
(numeric) number of standard deviations above the sample average for num.common.breaks |
maxgap |
(numeric) inherited from match.breaks(); sets the maximum gap between co-localizing orthogonal breakpoints |
chrlist |
(character) vector containing chromosomes to include in the analysis; if NULL all chromosomes available in the input will be included |
interleaved.cut |
(numeric) 0-1 value indicating percentage of interleaved (non-contiguous) SV breakpoint pairs |
dist.iqm.cut |
(numeric) interquantile average of the distance between breakpoints within a shattered region |
an instance of the class 'chromo.regs' containing breakpoint mapping onto genes
1 2 3 4 5 | ## validate input data.frames
cnv <- validate.cnv(segdat_lung_ccle)
svc <- validate.svc(svdat_lung_ccle)
shattered.regions(cnv,svc)
|
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