Calculate posterior probability of CNVs using allele data
r.sub |
Optional matrix of alt allele count in single cells. If not provided, internal r.sc matrix is used. |
n.sub |
Optional matrix of site coverage count in single cells. If not provided, internal n.sc matrix is used. |
l.sub |
Optional vector of alt allele count in pooled single cells or bulk. If not provided, internal l vector is used. |
n.bulk.sub |
Optional vector of site coverage count in pooled single cells or bulk. If not provided, internal n.bulk vector is used. |
region |
GenomicRanges region of interest such as expected CNV boundaries. |
filter |
Boolean for whether to filter out SNP sites with no coverage. (default: TRUE) |
pe |
Effective error rate to capture error from sequencing, etc. (default: 0.01) |
mono |
Rate of mono-allelic expression. (default: 0.7) |
n.iter |
Number of iterations in MCMC. (default: 1000) |
quiet |
Boolean of whether to suppress progress bar. (default: TRUE) |
verbose |
Verbosity(default: FALSE) |
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