closestExonToJunctions | R Documentation |
Find closest exon to splice junction ends
closestExonToJunctions(
spliceGRgene,
exonsGR,
flipNegativeStrand = TRUE,
sampleColname = "sample_id",
reportActualCoords = FALSE,
spliceBuffer = NULL,
verbose = FALSE,
...
)
spliceGRgene |
GRanges representing splice junctions |
exonsGR |
GRanges representing flattened exons per gene, as
is produced by |
flipNegativeStrand |
logical indicating whether to flip the orientation of features on the negative strand. |
sampleColname |
character value matching the colname that defines distinct sample identifier, for which junctions will be kept separate. |
reportActualCoords |
logical indicating whether to report genomic coordinates or transcriptome coordinates. (Work in progress.) |
spliceBuffer |
optional |
verbose |
logical indicating whether to print verbose output. |
... |
additional arguments are ignored. |
This function is used to annotate splice junction GRanges entries based upon the closest compatible stranded exon boundary.
This function should usually be called by spliceGR2junctionDF()
and not called directly.
Other jam RNA-seq functions:
assignGRLexonNames()
,
combineGRcoverage()
,
defineDetectedTx()
,
detectedTxInfo()
,
exoncov2polygon()
,
flattenExonsBy()
,
getGRcoverageFromBw()
,
groups2contrasts()
,
internal_junc_score()
,
makeTx2geneFromGtf()
,
make_ref2compressed()
,
prepareSashimi()
,
runDiffSplice()
,
sortSamples()
,
spliceGR2junctionDF()
Other jam GRanges functions:
addGRLgaps()
,
addGRgaps()
,
annotateGRLfromGRL()
,
annotateGRfromGR()
,
assignGRLexonNames()
,
combineGRcoverage()
,
exoncov2polygon()
,
findOverlapsGRL()
,
flattenExonsBy()
,
getFirstStrandedFromGRL()
,
getGRLgaps()
,
getGRcoverageFromBw()
,
getGRgaps()
,
grl2df()
,
jam_isDisjoint()
,
make_ref2compressed()
,
sortGRL()
,
spliceGR2junctionDF()
,
stackJunctions()
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