R: Coverage calculation and normalization to reads per million...
coverage.rpm
R Documentation
Coverage calculation and normalization to reads per million (rpm)
Description
Calculates the coverage values from a RangedData object (or anything with a defined coverage function associated) and returns the coverage normalized to reads per million, allowing the comparison of experiments with a different absolut number of reads.
Usage
coverage.rpm(data, scale=1e6, ...)
Arguments
data
RangedData (or compatible) with the reads information
scale
By default, a million (1e6), but you could change this value for abnormal high or low amount of reads
...
Additional arguments to be passed to coverage function
#Load the example dataset and get the coverage
data(nucleosome_htseq)
cov = coverage.rpm(nucleosome_htseq)
print(cov)
#Plot it
plot(as.vector(cov[["chr1"]]), type="l", ylab="coverage", xlab="position")
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.
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Type 'license()' or 'licence()' for distribution details.
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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.
Type 'q()' to quit R.
> library(nucleR)
Loading required package: ShortRead
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: BiocParallel
Loading required package: Biostrings
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: XVector
Loading required package: Rsamtools
Loading required package: GenomeInfoDb
Loading required package: GenomicRanges
Loading required package: GenomicAlignments
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")'.
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/nucleR/coverage.rpm.Rd_%03d_medium.png", width=480, height=480)
> ### Name: coverage.rpm
> ### Title: Coverage calculation and normalization to reads per million
> ### (rpm)
> ### Aliases: coverage.rpm
> ### Keywords: manip
>
> ### ** Examples
>
>
> #Load the example dataset and get the coverage
> data(nucleosome_htseq)
> cov = coverage.rpm(nucleosome_htseq)
>
> print(cov)
RleList of length 1
$chr1
numeric-Rle of length 8284 with 4589 runs
Lengths: 4 1 ... 3
Values : 55.5524693072607 277.762346536304 ... 222.209877229043
>
> #Plot it
> plot(as.vector(cov[["chr1"]]), type="l", ylab="coverage", xlab="position")
>
>
>
>
>
> dev.off()
null device
1
>