Last data update: 2014.03.03
R: Add the information of the viewpoint fragments
addViewpointFrags R Documentation
Add the information of the viewpoint fragments
Description
addViewpointFrags
adds the genomic position and information of the
viewpoint primer fragments to colData
of the FourC
object.
Usage
addViewpointFrags(object, primerFragFile)
Arguments
object
A FourC
object.
primerFragFile
character string defining the file that contains the
information about the primer fragments. Defaults to
"primerFragments.rda"
which is the default output file
of findViewpointFragments
in the provided fragmentDir
.
Value
Updated FourC
object with information about the viewpoint
fragments added to colData
.
Author(s)
Felix A. Klein, felix.klein@embl.de
See Also
FourC
, findViewpointFragments
Examples
metadata <- list(projectPath=tempdir(),
fragmentDir="re_fragments",
referenceGenomeFile=system.file("extdata/dm3_chr2L_1-6900.fa",
package="FourCSeq"),
reSequence1="GATC",
reSequence2="CATG",
primerFile=system.file("extdata/primer.fa",
package="FourCSeq"),
bamFilePath=system.file("extdata/bam", package="FourCSeq"))
colData <- DataFrame(viewpoint = "testdata",
condition = factor(rep(c("WE_68h", "MESO_68h", "WE_34h"),
each=2),
levels = c("WE_68h", "MESO_68h", "WE_34h")),
replicate = rep(c(1, 2),
3),
bamFile = c("CRM_ap_ApME680_WE_6-8h_1_testdata.bam",
"CRM_ap_ApME680_WE_6-8h_2_testdata.bam",
"CRM_ap_ApME680_MESO_6-8h_1_testdata.bam",
"CRM_ap_ApME680_MESO_6-8h_2_testdata.bam",
"CRM_ap_ApME680_WE_3-4h_1_testdata.bam",
"CRM_ap_ApME680_WE_3-4h_2_testdata.bam"),
sequencingPrimer="first")
fc <- FourC(colData, metadata)
fc
fc <- addFragments(fc)
findViewpointFragments(fc)
fc <- addViewpointFrags(fc)
fc
Results
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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> library(FourCSeq)
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: ggplot2
Loading required package: DESeq2
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")'.
Loading required package: splines
Loading required package: LSD
Warning message:
replacing previous import 'ggplot2::Position' by 'BiocGenerics::Position' when loading 'ggbio'
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/FourCSeq/addViewpointFrags.Rd_%03d_medium.png", width=480, height=480)
> ### Name: addViewpointFrags
> ### Title: Add the information of the viewpoint fragments
> ### Aliases: addViewpointFrags
>
> ### ** Examples
>
> metadata <- list(projectPath=tempdir(),
+ fragmentDir="re_fragments",
+ referenceGenomeFile=system.file("extdata/dm3_chr2L_1-6900.fa",
+ package="FourCSeq"),
+ reSequence1="GATC",
+ reSequence2="CATG",
+ primerFile=system.file("extdata/primer.fa",
+ package="FourCSeq"),
+ bamFilePath=system.file("extdata/bam", package="FourCSeq"))
>
> colData <- DataFrame(viewpoint = "testdata",
+ condition = factor(rep(c("WE_68h", "MESO_68h", "WE_34h"),
+ each=2),
+ levels = c("WE_68h", "MESO_68h", "WE_34h")),
+ replicate = rep(c(1, 2),
+ 3),
+ bamFile = c("CRM_ap_ApME680_WE_6-8h_1_testdata.bam",
+ "CRM_ap_ApME680_WE_6-8h_2_testdata.bam",
+ "CRM_ap_ApME680_MESO_6-8h_1_testdata.bam",
+ "CRM_ap_ApME680_MESO_6-8h_2_testdata.bam",
+ "CRM_ap_ApME680_WE_3-4h_1_testdata.bam",
+ "CRM_ap_ApME680_WE_3-4h_2_testdata.bam"),
+ sequencingPrimer="first")
>
> fc <- FourC(colData, metadata)
> fc
class: FourC
dim: 0 6
metadata(8): projectPath fragmentDir ... bamFilePath version
assays(0):
rownames: NULL
rowData names(0):
colnames(6): testdata_WE_68h_1 testdata_WE_68h_2 ... testdata_WE_34h_1
testdata_WE_34h_2
colData names(5): viewpoint condition replicate bamFile
sequencingPrimer
>
> fc <- addFragments(fc)
>
> findViewpointFragments(fc)
>
> fc <- addViewpointFrags(fc)
> fc
class: FourC
dim: 2 6
metadata(8): projectPath fragmentDir ... bamFilePath version
assays(0):
rownames: NULL
rowData names(4): leftSize rightSize leftValid rightValid
colnames(6): testdata_WE_68h_1 testdata_WE_68h_2 ... testdata_WE_34h_1
testdata_WE_34h_2
colData names(16): viewpoint condition ... primerEnd primerSide
>
>
>
>
>
> dev.off()
null device
1
>