The interval of the experiment's viewpoint, consisting of a start and end coordinate
readLength
The experiment's read length (in base pairs)
pointsOfInterest
Points of interest to be marked in a near-cis visualization
rawReads
Reads of the 4C-seq experiment, aligned and stored as an GAlignments object
Details
A Data4Cseq object contains basic information for the corresponding 4C-seq experiment, including the viewpoint chromosome, the viewpoint region and reads from the experiment. See Data4Cseq-class for more details. The constructor collects the basic data; fragment data or normalized read counts are added later.
Fragments at the experiment's viewpoint are usually vastly overrepresented due to self-ligation; chooseNearCisFragments offers the option to discard all fragments in the specified viewpoint region. The specified viewpoint interval of a Data4Cseq object is supposed to correspond to the positions of the biological primers on the genome, but can also be increased in size if more fragments around the viewpoint should be removed.
Value
An instance of the Data4Cseq class.
Author(s)
Carolin Walter
See Also
Data4Cseq-class
Examples
# create a Data4Cseq object with a minimum of data
liverData = Data4Cseq(viewpointChromosome = "10", viewpointInterval = c(20879870, 20882209), readLength = 54)
liverData
# create a Data4Cseq object, including possible points of interest and raw reads
bamFile <- system.file("extdata", "fetalLiverShort.bam", package="Basic4Cseq")
liverReads <- readGAlignments(bamFile)
pointsOfInterestFile <- system.file("extdata", "fetalLiverVP.bed", package="Basic4Cseq")
liverData = Data4Cseq(viewpointChromosome = "10", viewpointInterval = c(20879870, 20882209), readLength = 54, pointsOfInterest = readPointsOfInterestFile(pointsOfInterestFile), rawReads = liverReads)
liverData
Results
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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> library(Basic4Cseq)
Loading required package: Biostrings
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: XVector
Loading required package: GenomicAlignments
Loading required package: GenomeInfoDb
Loading required package: GenomicRanges
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: Rsamtools
Loading required package: caTools
Attaching package: 'caTools'
The following object is masked from 'package:IRanges':
runmean
The following object is masked from 'package:S4Vectors':
runmean
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/Basic4Cseq/Data4Cseq.Rd_%03d_medium.png", width=480, height=480)
> ### Name: Data4Cseq
> ### Title: Creating a Data4Cseq object
> ### Aliases: Data4Cseq
> ### Data4Cseq,character,numeric,numeric,data.frame,GAlignments-method
> ### Data4Cseq,character,numeric,numeric,missing,missing-method
> ### Keywords: Data4Cseq
>
> ### ** Examples
>
> # create a Data4Cseq object with a minimum of data
> liverData = Data4Cseq(viewpointChromosome = "10", viewpointInterval = c(20879870, 20882209), readLength = 54)
> liverData
4C-seq experiment data
Type: Data4Cseq
Viewpoint: 10 : 20879870 - 20882209
Read length: 30
Number of reads: 0
Number of total fragments: 0
Number of near-cis fragments: 0
Points of interest: 0
>
> # create a Data4Cseq object, including possible points of interest and raw reads
> bamFile <- system.file("extdata", "fetalLiverShort.bam", package="Basic4Cseq")
> liverReads <- readGAlignments(bamFile)
> pointsOfInterestFile <- system.file("extdata", "fetalLiverVP.bed", package="Basic4Cseq")
> liverData = Data4Cseq(viewpointChromosome = "10", viewpointInterval = c(20879870, 20882209), readLength = 54, pointsOfInterest = readPointsOfInterestFile(pointsOfInterestFile), rawReads = liverReads)
> liverData
4C-seq experiment data
Type: Data4Cseq
Viewpoint: 10 : 20879870 - 20882209
Read length: 54
Number of reads: 2185
Number of total fragments: 0
Number of near-cis fragments: 0
Points of interest: 2
>
>
>
>
>
> dev.off()
null device
1
>