Last data update: 2014.03.03

R: Build a genome wide cut site map for a Restriction Enzyme...
buildREmapR Documentation

Build a genome wide cut site map for a Restriction Enzyme (RE)

Description

Build a genome-wide cut map for a Restriction Enzyme (RE)

Usage

buildREmap(REpatternFilePath, format = "fasta", BSgenomeName, outfile)

Arguments

REpatternFilePath

File path storing the recognition pattern of a RE

format

format of the pattern file, either "fasta" (the default) or "fastq

BSgenomeName

BSgenome object, please refer to available.genomes in BSgenome package for details

outfile

temporary output file for writing the matched chromosome location to

Value

Output REmap as a RangedData

Author(s)

Lihua Julie Zhu

Examples

	library(REDseq)
	REpatternFilePath = system.file("extdata", "examplePattern.fa", package="REDseq")
	library(BSgenome.Celegans.UCSC.ce2)
	buildREmap( REpatternFilePath, BSgenomeName=Celegans, outfile=tempfile())

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.
Type 'q()' to quit R.

> library(REDseq)
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: BSgenome.Celegans.UCSC.ce2
Loading required package: BSgenome
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: GenomicRanges
Loading required package: Biostrings
Loading required package: XVector
Loading required package: rtracklayer
Loading required package: multtest
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")'.

Loading required package: ChIPpeakAnno
Loading required package: grid
Loading required package: VennDiagram
Loading required package: futile.logger

No methods found in "IRanges" for requests: %in%
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/REDseq/buildREmap.Rd_%03d_medium.png", width=480, height=480)
> ### Name: buildREmap
> ### Title: Build a genome wide cut site map for a Restriction Enzyme (RE)
> ### Aliases: buildREmap
> ### Keywords: misc
> 
> ### ** Examples
> 
> 	library(REDseq)
> 	REpatternFilePath = system.file("extdata", "examplePattern.fa", package="REDseq")
> 	library(BSgenome.Celegans.UCSC.ce2)
> 	buildREmap( REpatternFilePath, BSgenomeName=Celegans, outfile=tempfile())
>>> Finding all hits in sequences chrI ...
>>> DONE searching
>>> Finding all hits in sequences chrII ...
>>> DONE searching
>>> Finding all hits in sequences chrIII ...
>>> DONE searching
>>> Finding all hits in sequences chrIV ...
>>> DONE searching
>>> Finding all hits in sequences chrV ...
>>> DONE searching
>>> Finding all hits in sequences chrX ...
>>> DONE searching
>>> Finding all hits in sequences chrM ...
>>> DONE searching
RangedData with 87959 rows and 2 value columns across 7 spaces
                          space               ranges   |      strand     score
                       <factor>            <IRanges>   | <character> <numeric>
ExampleRE.+.chrI.1            I       [ 1899,  1903]   |           +         1
ExampleRE.+.chrI.2            I       [ 6356,  6360]   |           +         1
ExampleRE.+.chrI.3            I       [ 6775,  6779]   |           +         1
ExampleRE.+.chrI.4            I       [ 6866,  6870]   |           +         1
ExampleRE.+.chrI.5            I       [11431, 11435]   |           +         1
ExampleRE.+.chrI.6            I       [11975, 11979]   |           +         1
ExampleRE.+.chrI.7            I       [12241, 12245]   |           +         1
ExampleRE.+.chrI.8            I       [13311, 13315]   |           +         1
ExampleRE.+.chrI.9            I       [14083, 14087]   |           +         1
...                         ...                  ... ...         ...       ...
ExampleRE.+.chrX.15068        X [17706097, 17706101]   |           +         1
ExampleRE.+.chrX.15069        X [17709329, 17709333]   |           +         1
ExampleRE.+.chrX.15070        X [17710564, 17710568]   |           +         1
ExampleRE.+.chrX.15071        X [17711033, 17711037]   |           +         1
ExampleRE.+.chrX.15072        X [17712037, 17712041]   |           +         1
ExampleRE.+.chrX.15073        X [17712181, 17712185]   |           +         1
ExampleRE.+.chrX.15074        X [17714984, 17714988]   |           +         1
ExampleRE.+.chrX.15075        X [17716980, 17716984]   |           +         1
ExampleRE.+.chrX.15076        X [17717264, 17717268]   |           +         1
> 
> 
> 
> 
> 
> dev.off()
null device 
          1 
>