Last data update: 2014.03.03

R: ASEset from bam file
ASEsetFromBamR Documentation

ASEset from bam file

Description

count alleles and create an ASEset direct from bam file instead of reading into R first.

Usage

ASEsetFromBam(gr, ...)

## S4 method for signature 'GRanges'
ASEsetFromBam(gr, pathToDir, PE = TRUE,
  flagsMinusStrand = c(83, 163), flagsPlusStrand = c(99, 147),
  strandUnknown = FALSE, ...)

Arguments

gr

GenomicRanges of SNPs to create ASEset for

...

passed on to ASEsetFromBam function

pathToDir

Directory of bam files with index in same directory

PE

if paired end or not (default: TRUE)

flagsMinusStrand

flags that mark reads coming from minus strand

flagsPlusStrand

flags that mark reads coming from plus strand

strandUnknown

default: FALSE

Details

counts the alleles in a bam file based on GRanges positions.

Author(s)

Jesper R. Gadin

Examples


data(GRvariants)
gr <- GRvariants

##no execution at the moment
#pathToDir <- system.file('inst/extdata/ERP000101_subset', package='AllelicImbalance')
#a <- ASEsetFromBam(gr, pathToDir)
 

Results


R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
Copyright (C) 2016 The R Foundation for Statistical Computing
Platform: x86_64-pc-linux-gnu (64-bit)

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Type 'contributors()' for more information and
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Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> library(AllelicImbalance)
Loading required package: grid
Loading required package: GenomicRanges
Loading required package: BiocGenerics
Loading required package: parallel

Attaching package: 'BiocGenerics'

The following objects are masked from 'package:parallel':

    clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
    clusterExport, clusterMap, parApply, parCapply, parLapply,
    parLapplyLB, parRapply, parSapply, parSapplyLB

The following objects are masked from 'package:stats':

    IQR, mad, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, append,
    as.data.frame, cbind, colnames, do.call, duplicated, eval, evalq,
    get, grep, grepl, intersect, is.unsorted, lapply, lengths, mapply,
    match, mget, order, paste, pmax, pmax.int, pmin, pmin.int, rank,
    rbind, rownames, sapply, setdiff, sort, table, tapply, union,
    unique, unsplit

Loading required package: S4Vectors
Loading required package: stats4

Attaching package: 'S4Vectors'

The following objects are masked from 'package:base':

    colMeans, colSums, expand.grid, rowMeans, rowSums

Loading required package: IRanges
Loading required package: GenomeInfoDb
Loading required package: SummarizedExperiment
Loading required package: Biobase
Welcome to Bioconductor

    Vignettes contain introductory material; view with
    'browseVignettes()'. To cite Bioconductor, see
    'citation("Biobase")', and for packages 'citation("pkgname")'.

Loading required package: GenomicAlignments
Loading required package: Biostrings
Loading required package: XVector
Loading required package: Rsamtools
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/AllelicImbalance/ASEsetFromBam.Rd_%03d_medium.png", width=480, height=480)
> ### Name: ASEsetFromBam
> ### Title: ASEset from bam file
> ### Aliases: ASEsetFromBam ASEsetFromBam,GRanges-method
> ### Keywords: ASEset
> 
> ### ** Examples
> 
> 
> data(GRvariants)
> gr <- GRvariants
> 
> ##no execution at the moment
> #pathToDir <- system.file('inst/extdata/ERP000101_subset', package='AllelicImbalance')
> #a <- ASEsetFromBam(gr, pathToDir)
>  
> 
> 
> 
> 
> 
> dev.off()
null device 
          1 
>