RoarDatasetMultipleAPA {roar} | R Documentation

## Creates a `RoarDatasetMultipleAPA` object

### Description

This function creates an `RoarDatasetMultipleAPA` object from two lists of of `GAlignments` and a `GRanges` containing a suitable annotation of alternative APA sites and gene exon structure. A MultipleAPA analysis computes several roar values and p-values for each gene: one for every possible combination of APA-canonical end of a gene (i.e. the end of its last exon). This is more efficient than performing several different “standard” roar analyses choosing the PRE and POST portions corresponding to different APAs because reads overlaps are computed only once.

### Usage

          RoarDatasetMultipleAPA(treatmentBamsGenomicAlignments, controlBamsGenomicAlignments, gtfGRanges)

### Arguments

`treatmentBamsGenomicAlignments` | A list of `GAlignments` representing alignment of samples for the treatment condition (by convention it is considered the “treated” condition: this simply means that the package will compute roar values (ratios of the m/M) using this condition as the numerator) to be considered.
`controlBamsGenomicAlignments` | A list of `GAlignments` representing alignment of samples for the control condition to be considered.
`gtfGRanges` | A `GRanges` containing a suitable annotation of alternative APA sites and gene exonic structure. Minimal requirements are: metadata columns called "gene", "apa" and "type." APA should be single bases falling over one of the given genes and need to have the metadata column "type" equal to "apa" and the "apa" column composed of unambiguous id and the corresponding gene id pasted together with an underscore. The "gene" metadata columns for these entries should not be initialized. All the studied gene exons need to be reported, in this case the metadata column "gene" should contain the gene id (the same one reported for each gene APAs) while "type" should be set to "gene" and "apa" to NA. All apa entries assigned to a gene should have coordinates that falls inside it and every gene that appears should contain at least one APA.

### Value

A `RoarDatasetMultipleAPA` object ready to be analyzed via the other methods.

### See Also

`RoarDatasetMultipleAPAFromFiles`

### Examples

          library(GenomicAlignments)
          gene <- c("A", "B", NA, NA)
          type <- c("gene","gene","apa", "apa")
          apa <- c(NA, NA, "apa1_A", "apa2_B")
          features <- GRanges(
             seqnames = Rle(c("chr1", "chr2", "chr1", "chr2")),
             strand = strand(rep("+", length(gene))),
             ranges = IRanges(
                start=c(1000, 2000, 1300, 2050),
                width=c(500, 900, 1, 1)),
             DataFrame(gene, apa, type)
          )
          rd1 <- GAlignments("a", seqnames = Rle("chr1"), pos = as.integer(1000), cigar = "300M", strand = strand("+"))
          rds <- RoarDatasetMultipleAPA(list(c(rd1,rd1)), list(c(rd1,rd1)), features)

[Package roar version 1.28.0 Index]