fimport: Load any type of sequencing reads
In ORFik: Open Reading Frames in Genomics

Description Usage Arguments Details Value See Also Examples

Wraps around rtracklayer::import and tries to speed up loading with the use of data.table. Supports gzip, gz, bgz compression formats. Also safer chromosome naming with the argument chrStyle

1	fimport(path, chrStyle = NULL, param = NULL, strandMode = 0)

`path`	a character path to file (1 or 2 files), or data.table with 2 colums(forward&reverse) or a GRanges/Galignment/GAlignmentPairs object etc. If it is ranged object it will presume to be already loaded, so will return the object as it is, updating the seqlevelsStyle if given.
`chrStyle`	a GRanges object, TxDb, FaFile, or a `seqlevelsStyle` (Default: NULL) to get seqlevelsStyle from. Is chromosome 1 called chr1 or 1, is mitocondrial chromosome called MT or chrM etc. Will use 1st seqlevel-style if more are present. Like: c("NCBI", "UCSC") -> pick "NCBI"
`param`	`NULL` or a ScanBamParam object. Like for `scanBam`, this influences what fields and which records are imported. However, note that the fields specified thru this ScanBamParam object will be loaded in addition to any field required for generating the returned object (GAlignments, GAlignmentPairs, or GappedReads object), but only the fields requested by the user will actually be kept as metadata columns of the object. By default (i.e. `param=NULL` or `param=ScanBamParam()`), no additional field is loaded. The flag used is `scanBamFlag(isUnmappedQuery=FALSE)` for `readGAlignments`, `readGAlignmentsList`, and `readGappedReads`. (i.e. only records corresponding to mapped reads are loaded), and `scanBamFlag(isUnmappedQuery=FALSE, isPaired=TRUE, hasUnmappedMate=FALSE)` for `readGAlignmentPairs` (i.e. only records corresponding to paired-end reads with both ends mapped are loaded).
`strandMode`	numeric, default 0. Only used for paired end bam files. One of (0: strand = *, 1: first read of pair is +, 2: first read of pair is -). See ?strandMode. Note: Sets default to 0 instead of 1, as readGAlignmentPairs uses 1. This is to guarantee hits, but will also make mismatches of overlapping transcripts in opposite directions.

NOTE: For wig you can send in 2 files, so that it automaticly merges forward and reverse stranded objects. You can also just send 1 wig file, it will then have "*" as strand.

a GAlignments/GRanges object, depending on input.

Other utils: bedToGR(), convertToOneBasedRanges(), export.bed12(), export.wiggle(), findFa(), fread.bed(), optimizeReads(), readBam(), readWig()

bam_file <- system.file("extdata", "ribo-seq.bam", package = "ORFik")
fimport(bam_file)
# Certain chromosome naming
fimport(bam_file, "NCBI")
# Paired end bam strandMode 1:
fimport(bam_file, strandMode = 1)
# (will have no effect in this case, since it is not paired end)