View source: R/HoneyBADGER_comb.R
Calculate posterior probability of CNVs using normalized expression data and allele data
1 2 3 | calcCombCnvProb(gexp.norm, genes, mvFit, m = 0.15, r.maf, n.sc, l.maf, n.bulk,
snps, geneFactor, region = NULL, filter = FALSE, pe = 0.1, mono = 0.7,
verbose = FALSE)
|
gexp.norm |
Normalized gene expression matrix. |
genes |
GRanges annotation of gene names and coordinates |
mvFit |
Mean variance fit |
m |
Expression deviation due to copy number change (default: 0.15) |
r.maf |
Matrix of alt allele count in single cells. |
n.sc |
Matrix of site coverage count in single cells. |
l.maf |
Vector of alt allele count in pooled single cells or bulk. |
n.bulk |
Vector of site coverage count in pooled single cells or bulk. |
snps |
SNP annotations |
geneFactor |
Output of |
region |
Optional GenomicRanges region of interest such as expected CNV boundaries. (default: NULL) |
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) |
verbose |
Verbosity (default: FALSE) |
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