ssvFetchBam {seqsetvis} | R Documentation

## Iterates a character vector (ideally named) and calls `ssvFetchBam.single` on each. Appends grouping variable to each resulting data.table and uses rbindlist to efficiently combine results

### Description

`ssvFetchBam` iteratively calls `fetchWindowedBam.single`. See `ssvFetchBam.single` for more info.

### Usage

    ssvFetchBam(file_paths, qgr, unique_names = NULL, win_size = 50,
      win_method = c("sample", "summary")[1],
      summary_FUN = stats::weighted.mean, fragLens = "auto",
      target_strand = c("*", "+", "-", "both")[1], flip_strand = FALSE,
      anchor = c("left", "left_unstranded", "center",
      "center_unstranded")[3], names_variable = "sample",
      return_data.table = FALSE, max_dupes = Inf,
      splice_strategy = c("none", "ignore", "add", "only",
      "splice_count")[1], n_cores = getOption("mc.cores", 1), ...)

### Arguments

`file_paths` | character vector of file_paths to load from. Alternatively, file_paths can be a data.frame or data.table whose first column is a character vector of paths and additial columns will be used as metadata.
`qgr` | Set of GRanges to query. For valid results the width of each interval should be identical and evenly divisible by `win_size`.
`unique_names` | names to use in final data.table to designate source bigwig. Default is 'sample'
`win_size` | The window size that evenly divides widths in `qgr`.
`win_method` | character. one of c("sample", "summary"). Determines if `viewGRangesWinSample_dt` or `viewGRangesWinSummary_dt` is used to represent each region in qgr.
`summary_FUN` | function. only relevant if win_method is "summary". passed to `viewGRangesWinSummary_dt`.
`fragLens` | numeric. The fragment length to use to extend reads. The default value "auto" causes an automatic calculation from 100 regions in qgr. NA causes no extension of reads to fragment size.
`target_strand` | character. One of c("*", "+", "-"). Controls filtering of reads by strand. Default of "*" combines both strands.
`flip_strand` | boolean. if TRUE strands are flipped.
`anchor` | character, one of c("center", "center_unstranded", "left", "left_unstranded")
`names_variable` | The column name where unique_names are stored.
`return_data.table` | logical. If TRUE the internal data.table is returned instead of GRanges. Default is FALSE.
`max_dupes` | numeric >= 1. duplicate reads by strandd start position over this number are removed, Default is Inf.
`splice_strategy` | character, one of c("none", "ignore", "add", "only", "splice_count"). Default is "none" and spliced alignment are asssumed not present. fragLen must be NA for any other value to be valid. "ignore" will not count spliced regions. add" counts spliced regions along with others, "only" will only count spliced regions and ignore others.
`n_cores` | integer number of cores to use.
`...` | passed to Rsamtools::ScanBamParam() Uses mc.cores option if not supplied.

### Details

if `qgr` contains the range chr1:1-100 and `win_size` is 10, values from positions chr1 5,15,25...85, and 95 will be retrieved from `bw_file`

### Value

A tidy formatted GRanges (or data.table if specified) containing fetched values.

### Examples

    if(Sys.info()['sysname'] != "Windows"){
    library(GenomicRanges)
    bam_f = system.file("extdata/test.bam",
        package = "seqsetvis", mustWork = TRUE)
    bam_files = c("a" = bam_f, "b" = bam_f)
    qgr = CTCF_in_10a_overlaps_gr[1:5]
    bw_gr = ssvFetchBam(bam_files, qgr, win_size = 10)
    bw_gr2 = ssvFetchBam(as.list(bam_files), qgr, win_size = 10)

    bw_dt = ssvFetchBam(bam_files, qgr, win_size = 10,
        return_data.table = TRUE)
    }

[Package seqsetvis version 1.4.1 Index]