This is an example of an link{AVASet-class} object containing the output of Roche's Amplicon Variant Analyzer Software.
It consists of 6 samples, 4 amplicons and 4 variants. The variants were previously filtered according to the amplicon coverage
(see setVariantFilter for details about filtering an AVASet object).
Usage
data(avaSetFiltered)
Format
Formal class 'AVASet'
Source
‘Next-generation sequencing technology reveals a characteristic
pattern of molecular mutations in 72.8
leukemia by detecting frequent alterations in TET2, CBL, RAS, and RUNX1’
(Kohlmann A et al., J Clin Oncol. 2010 Aug 20;28(24):3858-65. Epub 2010 Jul 19)
Examples
data(avaSetFiltered)
avaSetFiltered
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(R453Plus1Toolbox)
Loading required package: VariantAnnotation
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: GenomeInfoDb
Loading required package: stats4
Loading required package: S4Vectors
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: 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: Biostrings
Loading required package: XVector
Attaching package: 'VariantAnnotation'
The following object is masked from 'package:base':
tabulate
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/R453Plus1Toolbox/avaSetFiltered.Rd_%03d_medium.png", width=480, height=480)
> ### Name: avaSetFiltered
> ### Title: Amplicon Variant Analyzer data import
> ### Aliases: avaSetFiltered
> ### Keywords: datasets
>
> ### ** Examples
>
> data(avaSetFiltered)
> avaSetFiltered
Variants: (forward filter = 0.1)(reverse filter = 0.1)
AVASet (storageMode: list)
assayData: 4 features, 6 samples
element names: variantForwCount, totalForwCount, variantRevCount, totalRevCount
protocolData: none
phenoData
sampleNames: Sample_1 Sample_2 ... Sample_6 (6 total)
varLabels: SampleID MID1 ... Annotation (7 total)
varMetadata: labelDescription
featureData
featureNames: C1338 C1323 C1163 C1206
fvarLabels: name canonicalPattern ... referenceBases (7 total)
fvarMetadata: labelDescription
experimentData: use 'experimentData(object)'
Annotation:
Amplicons:
assayDataAmp:4 features, 6 samples
element names:forwCountrevCount
featureDataAmp:
An object of class 'AnnotatedDataFrame'
rowNames: TET2_E11.04 TET2_E06 TET2_E11.03 TET2_E04
varLabels: ampID primer1 ... targetStart (6 total)
varMetadata: labelDescription
Reference sequences:
class: AlignedRead
length: 4 reads; width: 339..346 cycles
chromosome: 4 4 4 4
position: 106162417 106196936 106196674 106164659
strand: + + + +
alignQuality: NumericQuality
alignData varLabels: name refSeqID gene
>
>
>
>
>
> dev.off()
null device
1
>