if(interactive()){
## loading TargetExperiment object
data(ampliPanel, package="TarSeqQC")
## Defining bam file, bed file and fasta file names and paths
setBamFile(ampliPanel)<-system.file("extdata", "mybam.bam",
package="TarSeqQC", mustWork=TRUE)
setFastaFile(ampliPanel)<-system.file("extdata", "myfasta.fa",
package="TarSeqQC", mustWork=TRUE)
# Exploring the nucleotide percentages compositions of the read counts for a
# particular amplicon
g<-plotNtdPercentage(ampliPanel,featureID="AMPL20")
g
}
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
'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.
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> library(TarSeqQC)
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: Rsamtools
Loading required package: Biostrings
Loading required package: XVector
Loading required package: ggplot2
Loading required package: plyr
Attaching package: 'plyr'
The following object is masked from 'package:XVector':
compact
The following object is masked from 'package:IRanges':
desc
The following object is masked from 'package:S4Vectors':
rename
Loading required package: openxlsx
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/TarSeqQC/TargetExperiment-plotNtdPercentage.Rd_%03d_medium.png", width=480, height=480)
> ### Name: plotNtdPercentage
> ### Title: Plot nucleotide read percentages for a particular feature.
> ### Aliases: plotNtdPercentage plotNtdPercentage,TargetExperiment-method
> ### plotNtdPercentage-methods
>
> ### ** Examples
>
> #if(interactive()){
> ## loading TargetExperiment object
> data(ampliPanel, package="TarSeqQC")
> ## Defining bam file, bed file and fasta file names and paths
> setBamFile(ampliPanel)<-system.file("extdata", "mybam.bam",
+ package="TarSeqQC", mustWork=TRUE)
> setFastaFile(ampliPanel)<-system.file("extdata", "myfasta.fa",
+ package="TarSeqQC", mustWork=TRUE)
> # Exploring the nucleotide percentages compositions of the read counts for a
> # particular amplicon
> g<-plotNtdPercentage(ampliPanel,featureID="AMPL20")
| | | 0% | |=================================== | 50% | |======================================================================| 100%
| | | 0% | |=================================== | 50% | |======================================================================| 100%
> g
> #}
>
>
>
>
>
> dev.off()
null device
1
>