callAlleleSpecificCNfromHSCN | R Documentation |
Call allele specific copy number in single cell datasets
callAlleleSpecificCNfromHSCN(
hscn,
eps = 1e-12,
maxCN = NULL,
selftransitionprob = 0.95,
progressbar = TRUE,
ncores = 1,
fillmissing = TRUE
)
hscn |
hscn object from callHaplotypeSpecificCN |
eps |
default 1e-12 |
maxCN |
maximum copy number to infer allele specific states, default=NULL which will use the maximum state from CNbins |
selftransitionprob |
probability to stay in the same state in the HMM, default = 0.999, set to 0.0 for an IID model |
progressbar |
Boolean to display progressbar or not, default = TRUE, will only show if ncores == 1 |
ncores |
Number of cores to use, default = 1 |
fillmissing |
For bins with missing counts fill in values based on neighbouring bins |
In the allele specific copy number inference A is always > B and state_AS_phased == state_AS
allele specific copy number object which includes dataframe similar to input with additional columns which include
* 'A' (Major allele copy number) * 'B' (Minor allele copy number) * 'state_AS_phased' (phased state of the form A|B ) * 'state_AS' (mirrored state of the form A|B) * 'LOH' (is bin LOH or not) * 'state_phase' (state describing which is the dominant allele and whether it is LOH or not) * 'state_BAF' (binned discretized BAF value calculated as B / (A + B))
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