Last data update: 2014.03.03
R: Subsample short read alignment locations
laneSubsample R Documentation
Subsample short read alignment locations
Description
Subsamples data from multiple lanes on a per-chromosome
basis.
Usage
laneSubsample(lane1, lane2, fudge = 0.05)
Arguments
lane1, lane2
Two lanes of data, each of class
"GRanges"
.
fudge
A numeric fudge factor. For each chromosome, if the
difference in the sizes relative to the size of the first dataset is
less than fudge
, no subsampling is done.
Value
laneSubsample
returns a list similar to its input, but with the
larger dataset subsampled to be similar to the smaller one.
Author(s)
D. Sarkar
Examples
data(cstest)
## subsample to compare lanes
cstest.sub <- laneSubsample(cstest[[1]], cstest[[2]])
unlist(cstest.sub)
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
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Type 'q()' to quit R.
> library(chipseq)
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: GenomicRanges
Loading required package: GenomeInfoDb
Loading required package: ShortRead
Loading required package: BiocParallel
Loading required package: Biostrings
Loading required package: XVector
Loading required package: Rsamtools
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/chipseq/laneSubsample.Rd_%03d_medium.png", width=480, height=480)
> ### Name: laneSubsample
> ### Title: Subsample short read alignment locations
> ### Aliases: laneSubsample
> ### Keywords: manip utilities
>
> ### ** Examples
>
> data(cstest)
> ## subsample to compare lanes
> cstest.sub <- laneSubsample(cstest[[1]], cstest[[2]])
> unlist(cstest.sub)
GRanges object with 590770 ranges and 0 metadata columns:
seqnames ranges strand
<Rle> <IRanges> <Rle>
lane1 chr10 [3012941, 3012964] +
lane1 chr10 [3012978, 3013001] +
lane1 chr10 [3013071, 3013094] +
lane1 chr10 [3023240, 3023263] +
lane1 chr10 [3038377, 3038400] +
... ... ... ...
lane2 chr12 [121213126, 121213149] -
lane2 chr12 [121216905, 121216928] -
lane2 chr12 [121216967, 121216990] -
lane2 chr12 [121251805, 121251828] -
lane2 chr12 [121253426, 121253449] -
-------
seqinfo: 35 sequences from an unspecified genome
>
>
>
>
>
> dev.off()
null device
1
>