Object of class ExpressionSet holding the
normalized probe intensity data
probeAnno
Environment holding the genomic positions of probes
in the ExpressionSet
allChr
Character vector of all chromosomes in genome
test
character; one of one.sample or two.sample
grouping
factor vector of length equal to number of samples,
not required if test=one.sample
winHalfSize
Half the size of the window centered at a probe
position, in which all other probes contribute to the calculation of
the mean and standard deviation.
min.probes
integer; if less probes are in the sliding window,
NA instead of the mean and sd is returned. This is meant to avoid to
computing non-meaningful means and standard deviations. If unwanted,
set this to 1 or less
checkUnique
logical; indicates whether the uniqueness
indicator of probe matches from the probeAnno environment should be
used.
uniqueCodes
numeric; which numeric codes in the chromosome-wise
match-uniqueness elements of the probeAnno environment indicate
uniqueness?
verbose
logical; detailed progress output to STDOUT?
Value
An object of class ExpressionSet, holding the T statistics
values for the probes of the supplied ExpressionSet. The number of
results samples is the number of levels in the supplied factor
grouping.
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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Platform: x86_64-pc-linux-gnu (64-bit)
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> library(Ringo)
Loading required package: Biobase
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
Welcome to Bioconductor
Vignettes contain introductory material; view with
'browseVignettes()'. To cite Bioconductor, see
'citation("Biobase")', and for packages 'citation("pkgname")'.
Loading required package: RColorBrewer
Loading required package: limma
Attaching package: 'limma'
The following object is masked from 'package:BiocGenerics':
plotMA
Loading required package: Matrix
Loading required package: grid
Loading required package: lattice
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/Ringo/compute_sliding_t.Rd_%03d_medium.png", width=480, height=480)
> ### Name: computeSlidingT
> ### Title: Function to compute sliding T statistics on a tiling expression
> ### set
> ### Aliases: computeSlidingT
> ### Keywords: manip
>
> ### ** Examples
>
> exDir <- system.file("exData",package="Ringo")
> load(file.path(exDir,"exampleProbeAnno.rda"))
> load(file.path(exDir,"exampleX.rda"))
> tX <- computeSlidingT(exampleX, probeAnno=exProbeAnno,
+ allChr=c("9"), winHalfSize=400)
computing probe-wise mean and standard deviation in sliding window.
chr9 Suz12_vs_total ...
computing t-statistics...
preparing result...done.
> sampleNames(tX) <- "t-Stat_Suz12vsTotal"
> # if (interactive()){
> grid.newpage()
> plot(cbind2(exampleX, tX), exProbeAnno, chrom="9",
+ xlim=c(34318000,34321000), ylim=c(-2,8.5), gff=exGFF,
+ paletteName="Paired")
> # }
>
>
>
>
>
> dev.off()
null device
1
>