R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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> library(geneRxCluster)
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
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/geneRxCluster/gRxPlotClumps.Rd_%03d_medium.png", width=480, height=480)
> ### Name: gRxPlotClumps
> ### Title: gRxPlotClumps
> ### Aliases: gRxPlotClumps
>
> ### ** Examples
>
> x.seqnames <- rep(letters[1:3],each=50)
> x.starts <- c(seq(1,length=50),seq(1,by=2,length=50),seq(1,by=3,length=50))
> x.lens <- rep(c(5,10,15,20,25),each=2)
> x.group <- rep(rep(c(TRUE,FALSE),length=length(x.lens)),x.lens)
> ## add a bit of fuzz:
> x.group <- 1==rbinom(length(x.group),1,pr=ifelse(x.group,.8,.2))
> x.kvals <- as.integer(sort(unique(x.lens)))
> x.res <- gRxCluster(x.seqnames,x.starts,x.group,x.kvals)
> gRxPlotClumps(x.res)
Using highest starts as seglens
> rm( x.seqnames, x.starts, x.lens, x.group, x.kvals, x.res)
>
>
>
>
>
> dev.off()
null device
1
>