| ImportPacBioGFF | R Documentation | 
Import PacBio GFF file, extract one modification, rename this modification and convert it as a GRanges object with new colnames similar to PacBio CSV file containing data from all bases sequenced.
ImportPacBioGFF( cPacBioGFFPath, cNameModToExtract, cModNameInOutput, cContigToBeAnalyzed = NULL, lKeepSequence = TRUE )
| cPacBioGFFPath | Path to a PacBio GFF file containing modification detection data. | 
| cNameModToExtract | Name of modification to be extracted. | 
| cModNameInOutput | Name for the extracted modification in the output. | 
| cContigToBeAnalyzed | Names of contigs for which the data will be kept. If NULL, data from all contigs available will be imported. Defaults to NULL. | 
| lKeepSequence | If TRUE, the sequence of the base will be retained in one column. Otherwise, it will be discarded to reduce object size. Defaults to TRUE. | 
# Loading genome data
myGenome <- Biostrings::readDNAStringSet(system.file(
  package = "DNAModAnnot", "extdata",
  "ptetraurelia_mac_51_sca171819.fa"
))
names(myGenome)
# Loading PacBio data
myGrangesPacBioGFF <-
  ImportPacBioGFF(
    cPacBioGFFPath = system.file(
      package = "DNAModAnnot", "extdata",
      "ptetraurelia.modifications.sca171819.gff"
    ),
    cNameModToExtract = "m6A",
    cModNameInOutput = "6mA",
    cContigToBeAnalyzed = names(myGenome)
  )
myGrangesPacBioGFF
# Loading PacBio data for 2 scaffolds only
myGrangesPacBioGFF <-
  ImportPacBioGFF(
    cPacBioGFFPath = system.file(
      package = "DNAModAnnot", "extdata",
      "ptetraurelia.modifications.sca171819.gff"
    ),
    cNameModToExtract = "m6A",
    cModNameInOutput = "6mA",
    cContigToBeAnalyzed = c("scaffold51_18", "scaffold51_19")
  )
myGrangesPacBioGFF
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