#'CalculateCoverage
#'@description
#'We calculate the coverage information per variant from the MAEGATK results.
# #'@import MatrixGenerics
#'@importFrom SummarizedExperiment rowRanges assays
#'@param SE SummarizedExperiment object.
#'@param chromosome_prefix List of matrices for the alternative reads.
#'@export
CalculateCoverage <- function(SE, chromosome_prefix = "chrM"){
ref_allele <- as.character(SummarizedExperiment::rowRanges(SE)$refAllele)
coverage <- SummarizedExperiment::assays(SE)[["coverage"]]
rownames(coverage) <- paste0(chromosome_prefix, "_", 1:nrow(coverage), "_", ref_allele, "_A")
coverage_A <- coverage[ref_allele != "A",]
rownames(coverage) <- paste0(chromosome_prefix, "_", 1:nrow(coverage), "_", ref_allele, "_C")
coverage_C <- coverage[ref_allele != "C",]
rownames(coverage) <- paste0(chromosome_prefix, "_", 1:nrow(coverage), "_", ref_allele, "_G")
coverage_G <- coverage[ref_allele != "G",]
rownames(coverage) <- paste0(chromosome_prefix, "_", 1:nrow(coverage), "_", ref_allele, "_T")
coverage_T <- coverage[ref_allele != "T",]
coverage <- rbind(coverage_A, coverage_C, coverage_G, coverage_T)
return(coverage)
}
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