##match gene count and methylation intensity
match_expr_methy <- function(gene_count_infor, gene_methy_infor,OUTPUT_DIR=NA){
##select DE gene data
gene_count <- gene_count_infor[[1]]
gene_count <- gene_count[which(rowSums(gene_count)>10),]
for (i in 1:nrow(gene_count)) {
for (j in 2:ncol(gene_count)) {
if(gene_count[i,j]==0){
gene_count[i,j] <- NA
}
}
}
select_genecount <- na.omit(gene_count)
size_factor <- gene_count_infor[[2]]
gene_name <- (as.character(rownames(select_genecount)))
select_genecount <- as.data.frame(cbind(gene_name,select_genecount))
rownames(select_genecount) <- NULL
intersect_gene <- intersect(select_genecount$gene_name, gene_methy_infor$gene_name)
match_data <- data.frame()
for (i in 1:length(intersect_gene)) {
methy_name <- intersect_gene[i]
match_gene <- as.data.frame(select_genecount[which(!is.na(match(select_genecount$gene_name, methy_name))),])
select_methy <- as.data.frame(gene_methy_infor[which(!is.na(match(gene_methy_infor$gene_name, methy_name))),])
match_methy_expr <- cbind(match_gene, select_methy[,-1])
match_data <- rbind(match_data, match_methy_expr)
}
if(is.na(OUTPUT_DIR)){
OUTPUT_DIR=getwd()
}
dir.create(paste0(OUTPUT_DIR,"/m6Aexpress_result"))
write.table(match_data, file = paste0(OUTPUT_DIR,"/m6Aexpress_result/","expr_methy.tab"), quote = FALSE, row.names = FALSE)
out_putfile <- paste0(OUTPUT_DIR,"/m6Aexpress_result/","expr_methy.tab")
m6A_express_input <- list(out_putfile,size_factor)
names(m6A_express_input) <- c("gene_express_methy_dir","size_factor")
return(m6A_express_input)
}
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