for (i in 1:n) {
vec <- readdepth[[tids[i]]]
- if (is.null(vec)) exit_with_error(paste("Cannot find transcript", tids[i], sep = ""))
+ if (is.null(vec)) exit_with_error(paste("Unknown transcript detected,", tids[i], "is not included in RSEM's indices."))
if (is.na(vec[[2]])) wiggle <- rep(0, vec[[1]]) else wiggle <- as.numeric(unlist(strsplit(vec[[2]], split = " ")))
len <- length(wiggle)
if (!show_uniq) {
vec <- readdepth_uniq[[tids[i]]]
stopifnot(!is.null(vec))
if (is.na(vec[[2]])) wiggle_uniq <- rep(0, vec[[1]]) else wiggle_uniq <- as.numeric(unlist(strsplit(vec[[2]], split = " ")))
- stopifnot(len == length(wiggle_uniq), len == sum(wiggle >= wiggle_uniq))
+ stopifnot(len == length(wiggle_uniq))
+ if (len != sum(wiggle >= wiggle_uniq)) {
+ cat("Warning: transcript ", tids[i], " has position(s) that read covarege with multireads is smaller than read covarge without multireads.\n", " The 1-based position(s) is(are) : ", which(wiggle < wiggle_uniq), ".\n", " This may be due to floating point arithmetics.\n", sep = "")
+ }
+
heights <- rbind(wiggle_uniq, wiggle - wiggle_uniq)
barplot(heights, space = 0, border = NA, names.arg = 1:len, col = c("black", "red"))
}
}
} else {
for (gene_id in ids) {
- if (is.null(t2gmap[[gene_id]])) exit_with_error(paste("Cannot find gene", gene_id, sep = ""))
+ if (is.null(t2gmap[[gene_id]])) exit_with_error(paste("Unknown gene detected,", gene_id, "is not included in RSEM's in indices."))
generate_a_page(t2gmap[[gene_id]], gene_id)
}
}
cat("Plots are generated!\n)
dev.off.output <- dev.off()
-
-
-
-
-
-