quiet <- suppressWarnings
test_GenomicRanges_distance <- function()
{
genes <- data.frame(
tx_id=1:3,
gene_id=c("gene1", "gene1", "gene2"))
transcripts <- data.frame(
tx_id=1:3,
tx_chrom="chr1",
tx_strand=c("+", "+", "-"),
tx_start=c(1, 2001, 3001),
tx_end=c(999, 2199, 3199))
splicings <- data.frame(
tx_id=c(1L, 2L, 2L, 2L, 3L, 3L),
cds_id=c(10L, 11L, 12L, 13L, 14L, 15L),
exon_rank=c(1, 1, 2, 3, 1, 2),
exon_start=c(1, 2001, 2101, 2131, 3001, 3131),
exon_end=c(999, 2085, 2144, 2199, 3085, 3199),
cds_start=c(1, 2022, 2101, 2131, 3001, 3131),
cds_end=c(999, 2085, 2144, 2193, 3085, 3199))
txdb <- quiet(makeTxDb(transcripts, splicings, genes))
gr <- GRanges("chr1", IRanges(1050, width=1))
strand(gr) <- "-"
d <- quiet(distance(gr, txdb, id="gene1", type="gene"))
checkTrue(is.na(d))
strand(gr) <- "+"
d_pos <- quiet(distance(gr, txdb, id="gene1", type="gene"))
strand(gr) <- "*"
d_star <- quiet(distance(gr, txdb, id="gene1", type="gene"))
checkIdentical(d_pos, d_star)
d_tx <- quiet(distance(gr, txdb, id="3", type="tx"))
d_cds <- quiet(distance(gr, txdb, id="14", type="cds"))
checkIdentical(d_tx, d_cds)
}
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