Get a Data Frame of Base Frequency Data from a SequenceSummary Object

Description

An object that inherits from class SequenceSummary contains base frequency data by position gathered by readSeqFile. getBase is an accessor function that reshapes the base frequency data by position into a data frame.

This accessor function is useful if you want to map variables to custom ggplot2 aesthetics. Base proportions can be accessed with getBaseProp.

Usage

  getBase(x, drop=TRUE)

Arguments

Value

getBase returns a data.frame with columns:

Methods

signature(x = "SequenceSummary")

getBase is an accessor function that works on any object read in with readSeqFile; that is, objects that inherit from SequenceSummary.

Author(s)

Vince Buffalo <vsbuffalo@ucdavis.edu>

See Also

getGC, getSeqlen, getBaseProp, getQual, getMCQual, basePlot

Examples

  ## Load a FASTQ file, with sequence hashing.
  s.fastq <- readSeqFile(system.file('extdata', 'test.fastq',
    package='qrqc'))

  # A custom base plot
  ggplot(getBase(s.fastq)) + geom_line(aes(x=position, y=frequency,
    color=base)) + facet_grid(. ~ base) + scale_color_dna()

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)

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

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(qrqc)
Loading required package: reshape
Loading required package: ggplot2
Loading required package: Biostrings
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:reshape':

    expand, rename

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

    colMeans, colSums, expand.grid, rowMeans, rowSums

Loading required package: IRanges
Loading required package: XVector
Loading required package: biovizBase
Loading required package: brew
Loading required package: xtable
Loading required package: Rsamtools
Loading required package: GenomeInfoDb
Loading required package: GenomicRanges
Loading required package: testthat

Attaching package: 'testthat'

The following object is masked from 'package:S4Vectors':

    compare

> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/qrqc/getBase-methods.Rd_%03d_medium.png", width=480, height=480)
> ### Name: getBase-methods
> ### Title: Get a Data Frame of Base Frequency Data from a 'SequenceSummary'
> ###   Object
> ### Aliases: getBase getBase-methods getBase,SequenceSummary-method
> ### Keywords: methods accessor
> 
> ### ** Examples
> 
>   ## Load a FASTQ file, with sequence hashing.
>   s.fastq <- readSeqFile(system.file('extdata', 'test.fastq',
+     package='qrqc'))
> 
>   # A custom base plot
>   ggplot(getBase(s.fastq)) + geom_line(aes(x=position, y=frequency,
+     color=base)) + facet_grid(. ~ base) + scale_color_dna()
> 
> 
> 
> 
> 
> dev.off()
null device 
          1 
>