merged_arriba_tcga | R Documentation |
detailed desc 8983 * 28 columns
When read in via read.delim, the following information is available:
X.gene1
gene2
strand1.gene.fusion.
strand2.gene.fusion.
breakpoint1
breakpoint2
site1
site2
type
direction1
direction2
split_reads1
split_reads2
discordant_mates
coverage1
coverage2
confidence
closest_genomic_breakpoint1
closest_genomic_breakpoint2
filters
fusion_transcript
reading_frame
peptide_sequence
read_identifiers
Sample
gene1..gene2
annots
Caller
if any
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