arriba_example | R Documentation |
detailed desc: TODO 25 rows are included, with details about 27 different features (see details below).
When read in via read.delim, the following information is available:
X.gene1: TODO - TODO: check if this is indeed the way it is supposed to be read in (if not, we would need to add a dependency to the data package as well)
gene2: TODO
strand1.gene.fusion.: TODO
strand2.gene.fusion.: TODO
breakpoint1: TODO
breakpoint2: TODO
site1: TODO
site2: TODO
type: TODO
direction1: TODO
direction2: TODO
split_reads1: TODO
split_reads2: TODO
discordant_mates: TODO
coverage1: TODO
coverage2: TODO
confidence: TODO
closest_genomic_breakpoint1: TODO
closest_genomic_breakpoint2: TODO
filters: TODO
fusion_transcript: TODO
reading_frame: TODO
peptide_sequence: TODO
read_identifiers: TODO
tumor_id: TODO
gene1..gene2: TODO
annots: TODO
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