BED12toGRangesList <- function(filepath) {
# message
print("Converting BED12 to GRangesList")
print("It may take a few minutes")
# read bed file
a = read.table(filepath,sep="\t",header=TRUE,stringsAsFactors =FALSE)
# mcols_info =a[,13:length(a[1,])]
a = a[,1:12]
# get transcripts
no_tx = length(a[,1])
tx_id = 1:no_tx;
tx_name = paste("line1",1:no_tx,sep="")
tx_chrom = a[,1]
tx_strand = a[,6]
tx_start = a[,2]+1
tx_end = a[,3]
transcripts= data.frame(tx_id,tx_name,tx_chrom,tx_strand,tx_start,tx_end)
head(transcripts)
# get genes
tx_name = tx_name
gene_id = as.character(a[,4])
gene_id[is.na(gene_id)]="NA"
gene=data.frame(tx_name,gene_id)
#
splicing <- lapply(1:no_tx, .spliceSingleTrans, a=a, tx_start=tx_start)
splicing <- .combineListOfSplicing(splicing)
# make txdb
peaks = suppressWarnings(
makeTxDb(transcripts=transcripts,
splicings=splicing,
genes=gene))
# generate GRangesList
tx <- exonsBy(peaks, "tx",use.names=TRUE)
mcols(tx) <- a
return(tx)
}
.combineListOfSplicing <- function(t){
a <- paste("t[[",1:length(t),"]]", sep="")
a <- paste(a,collapse =",")
a <- paste("rbind(",a,")",sep="")
c <- parse(text=a)
b <- suppressWarnings(eval(c))
return(b)
}
.spliceSingleTrans <- function(i,a,tx_start) {
tx = a[i,]
tx_id = i
exon_rank=1:as.integer(tx[10])
# get start
temp = as.integer(strsplit(as.character(tx[12]), ",")[[1]]) + tx_start[i]
exon_start=temp
# get end
temp = as.integer(strsplit(as.character(tx[11]), ",")[[1]])
temp2 = temp + exon_start - 1
exon_end=temp2
# get CDS
cds_start = exon_start
cds_end = exon_end
# get data frame
splicing_tx = data.frame(tx_id,exon_rank,exon_start,exon_end,cds_start,cds_end)
return(splicing_tx)
}
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