R: Get a Data Frame of GC Content from a 'SequenceSummary'...
getGC-methods
R Documentation
Get a Data Frame of GC Content from a SequenceSummary object
Description
An object that inherits from class SequenceSummary contains
base frequency data by position gathered by
readSeqFile. getGC
is an accessor function that reshapes the base frequency data into a
data frame and returns the GC content by position.
This accessor function is useful if you want to map variables to
custom ggplot2 aesthetics. Frequencies or proportions of all
bases (not just GC) can be accessed with getBase and
getBaseProp respectively.
Usage
getGC(x)
Arguments
x
an S4 object that inherits from SequenceSummary from
readSeqFile.
Value
getGC returns a data.frame with columns:
position
the position in the read.
gc
GC content per position in the read.
Methods
signature(x = "SequenceSummary")
getGC is an accessor function that works on any object read
in with readSeqFile; that is, objects that inherit from
SequenceSummary.
## Load a FASTQ file, with sequence hashing.
s.fastq <- readSeqFile(system.file('extdata', 'test.fastq',
package='qrqc'))
# A custom GC plot
d <- merge(getQual(s.fastq), getGC(s.fastq), by.x="position", by.y="position")
p <- ggplot(d) + geom_linerange(aes(x=position, ymin=lower,
ymax=upper, color=gc)) + scale_color_gradient(low="red",
high="blue") + scale_y_continuous("GC content")
p
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 'demo()' for some demos, 'help()' for on-line help, or
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> 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/getGC-methods.Rd_%03d_medium.png", width=480, height=480)
> ### Name: getGC-methods
> ### Title: Get a Data Frame of GC Content from a 'SequenceSummary' object
> ### Aliases: getGC getGC-methods getGC,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 GC plot
> d <- merge(getQual(s.fastq), getGC(s.fastq), by.x="position", by.y="position")
> p <- ggplot(d) + geom_linerange(aes(x=position, ymin=lower,
+ ymax=upper, color=gc)) + scale_color_gradient(low="red",
+ high="blue") + scale_y_continuous("GC content")
> p
>
>
>
>
>
> dev.off()
null device
1
>