assignTSSByCage: Input a txdb and add a 5' leader for each transcript, that...

Description Usage Arguments Details Value See Also Examples

View source: R/cage_annotations.R

Description

For all cds in txdb, that does not have a 5' leader: Start at 1 base upstream of cds and use CAGE, to assign leader start. All these leaders will be 1 exon based, if you really want exon splicings, you can use exon prediction tools, or run sequencing experiments.

Usage

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assignTSSByCage(
  txdb,
  cage,
  extension = 1000,
  filterValue = 1,
  restrictUpstreamToTx = FALSE,
  removeUnused = FALSE,
  preCleanup = TRUE
)

Arguments

txdb

a TxDb file, a path to one of: (.gtf ,.gff, .gff2, .gff2, .db or .sqlite) or an ORFik experiment

cage

Either a filePath for the CageSeq file as .bed .bam or .wig, with possible compressions (".gzip", ".gz", ".bgz"), or already loaded CageSeq peak data as GRanges or GAlignment. NOTE: If it is a .bam file, it will add a score column by running: convertToOneBasedRanges(cage, method = "5prime", addScoreColumn = TRUE) The score column is then number of replicates of read, if score column is something else, like read length, set the score column to NULL first.

extension

The maximum number of basses upstream of the TSS to search for CageSeq peak.

filterValue

The minimum number of reads on cage position, for it to be counted as possible new tss. (represented in score column in CageSeq data) If you already filtered, set it to 0.

restrictUpstreamToTx

a logical (FALSE). If TRUE: restrict leaders to not extend closer than 5 bases from closest upstream leader, set this to TRUE.

removeUnused

logical (FALSE), if False: (standard is to set them to original annotation), If TRUE: remove leaders that did not have any cage support.

preCleanup

logical (TRUE), if TRUE, remove all reads in region (-5:-1, 1:5) of all original tss in leaders. This is to keep original TSS if it is only +/- 5 bases from the original.

Details

Given a TxDb object, reassign the start site per transcript using max peaks from CageSeq data. A max peak is defined as new TSS if it is within boundary of 5' leader range, specified by 'extension' in bp. A max peak must also be higher than minimum CageSeq peak cutoff specified in 'filterValue'. The new TSS will then be the positioned where the cage read (with highest read count in the interval).

Value

a TxDb obect of reassigned transcripts

See Also

Other CAGE: reassignTSSbyCage(), reassignTxDbByCage()

Examples

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txdbFile <- system.file("extdata", "hg19_knownGene_sample.sqlite",
 package = "GenomicFeatures")
cagePath <- system.file("extdata", "cage-seq-heart.bed.bgz",
 package = "ORFik")

## Not run: 
  assignTSSByCage(txdbFile, cagePath)
  Minimum 20 cage tags for new TSS
  assignTSSByCage(txdbFile, cagePath, filterValue = 20)

## End(Not run)

ORFik documentation built on March 27, 2021, 6 p.m.