Summarize detected transcript results
detectedTxInfo( detectedTxL, Gene = NULL, Tx = NULL, Groups = NULL, detectedOnly = NULL, ... )
| detectedTxL |
|
|---|---|
| Gene | optional |
| Tx | optional |
| Groups | optional |
| detectedOnly |
* `detectedOnly=NULL` then `Tx` is used as-is. * `detectedOnly=TRUE` and `Tx=NULL` then `Tx` uses all detected transcripts from `detectedTxL$detectedTx`. * `detectedOnly=TRUE` and `Tx` is supplied, it is restricted to detected transcripts from `detectedTxL$detectedTx`. * `detectedOnly=FALSE` and `Tx=NULL` then `Tx` uses all transcripts. * `detectedOnly=FALSE` and `Tx` is supplied, it is used as-is. |
| ... | additional arguments are ignored. |
list of data.frame objects, each containing one
summary table of data used to support whether each transcript
were called "detected."
This function provides a simple summary of the results of
defineDetectedTx(), typically for a given gene of interest.
By default, either Gene or Tx must be supplied, however
to return data for all genes, use either detectedOnly=TRUE
to return data only for detected transcripts, or
detectedOnly=FALSE to return all data including transcripts
that are not determined to be detected.
Other jam RNA-seq functions:
assignGRLexonNames(),
closestExonToJunctions(),
combineGRcoverage(),
defineDetectedTx(),
exoncov2polygon(),
flattenExonsBy(),
getGRcoverageFromBw(),
groups2contrasts(),
internal_junc_score(),
makeTx2geneFromGtf(),
make_ref2compressed(),
prepareSashimi(),
runDiffSplice(),
sortSamples(),
spliceGR2junctionDF()