R/annotate_mut_effect.R
next_junctions.Rd
Get genomic coordinates of possible next donor and acceptor sides.
next_junctions(var_gr, transcripts, transcripts_gr)
a GenomicRanges object with variants (of length one).
It is assumed that it is named with a unique ID.
Usually this is <chr>_<pos>_<alt>
.
a GRangesList with transcripts defined as GRanges of exons
created by GenomicFeatures::exonsBy(txdb, by = c("tx"), use.names = TRUE)
.
a GRanges object with transcript ranges created by
GenomicFeatures::transcripts(txdb)
A data.frame with possible upstream and downstream exon coordinates for all overlapping transcripts. The data frame contains the following columns: mut_id, var_nr, tx_chr, tx_id, exon_idx, tx_strand, upstream_start, upstream_end, downstream_start, downstream_end, at_start, at_end.