#' launch_interpro
#'
#' JAMSalpha function
#' @export
launch_interpro <- function(opt = NULL){
#Set working directory to sampledir
setwd(opt$sampledir)
#Discard proteins with stop codons in them, as this blocks interpro
CDSswithstop<-names(which(sapply(names(opt$proteome), function (x) { length(grep("\\*", opt$proteome[[x]])) } ) > 0))
proteomeforipro <- filter_sequence_by_name(input_sequences = opt$proteome, sequencenames = CDSswithstop, keep = FALSE)
#Write a copy of contigs to be annotated to the system
flog.info("Writing proteome for Interproscan annotation.")
write.fasta(sequences = proteomeforipro, names = names(proteomeforipro), nbchar = 80, file.out = "proteome.faa")
if(length(opt$proteome) > 10000){
chksize = 1000
} else {
chksize = 500
}
#annotate with prokka
flog.info("Launching Interproscan analysis of proteome.")
interprocmd <- file.path(opt$bindir, "dointerproBW.sh")
interproargs <- c("-i", "proteome.faa", "-p", opt$prefix, "-c", chksize)
system2(interprocmd, args = interproargs, stdout = TRUE, stderr = TRUE)
opt$iprodir <- file.path(opt$sampledir, "interproscan")
file.remove("proteome.faa")
return(opt)
}
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