View source: R/annotate_mut_effect.R
next_junctions | R Documentation |
Get genomic coordinates of possible next donor and acceptor sides.
next_junctions(var_gr, transcripts, transcripts_gr)
var_gr |
a GenomicRanges object with variants (of length one).
It is assumed that it is named with a unique ID.
Usually this is |
transcripts |
a GRangesList with transcripts defined as GRanges of exons
created by |
transcripts_gr |
a GRanges object with transcript ranges created by
|
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.
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.