Description Usage Arguments Details Value Author(s) See Also Examples
This function applies a sliding mean window to intensities to reduce noise generated by experimental variation, as well as take advantage of the overlapping nature of array peptides to share signal.
1 | slidingMean(peptideSet, width = 9, verbose = FALSE, split.by.clade = TRUE)
|
peptideSet |
A |
width |
A |
verbose |
A |
split.by.clade |
A |
Peptide membership in the sliding mean window is determined by its position and the width argument. Two peptides are in the same window if the difference in their positions is less than or equal to width/2. A peptide's position is taken to be position(peptideSet).
A peptide's intensity is replaced by the mean of all peptide intensities within the peptide's sliding mean window.
When split.by.clade = TRUE, peptides are smoothed within clades defined by the clade column of the GRanges object occupying the featureRange slot of peptideSet. If set to FALSE, a peptide at a given position will borrow information from the neighboring peptides as well as the ones from other clades around this position.
A peptideSet
object with smoothed intensities.
Gregory Imholte
summarizePeptides
, normalizeArray
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 | ## This example curated from the vignette -- please see vignette("pepStat")
## for more information
if (require("pepDat")) {
## Get example GPR files + associated mapping file
dirToParse <- system.file("extdata/gpr_samples", package = "pepDat")
mapFile <- system.file("extdata/mapping.csv", package = "pepDat")
## Make a peptide set
pSet <- makePeptideSet(files = NULL, path = dirToParse,
mapping.file = mapFile, log=TRUE)
## Plot array images -- useful for quality control
plotArrayImage(pSet, array.index = 1)
plotArrayResiduals(pSet, array.index = 1, smooth = TRUE)
## Summarize peptides, using pep_hxb2 as the position database
data(pep_hxb2)
psSet <- summarizePeptides(pSet, summary = "mean", position = pep_hxb2)
## Normalize the peptide set
pnSet <- normalizeArray(psSet)
## Smooth
psmSet <- slidingMean(pnSet, width = 9)
## Make calls
calls <- makeCalls(psmSet, freq = TRUE, group = "treatment",
cutoff = .1, method = "FDR", verbose = TRUE)
## Produce a summary of the results
summary <- restab(psmSet, calls)
}
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Loading required package: Biobase
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Attaching package: 'BiocGenerics'
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clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
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lapply, lengths, mapply, match, mget, order, paste, pmax, pmax.int,
pmin, pmin.int, rank, rbind, rowMeans, rowSums, rownames, sapply,
setdiff, sort, table, tapply, union, unique, unsplit, which,
which.max, which.min
Welcome to Bioconductor
Vignettes contain introductory material; view with
'browseVignettes()'. To cite Bioconductor, see
'citation("Biobase")', and for packages 'citation("pkgname")'.
Loading required package: IRanges
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Attaching package: 'S4Vectors'
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Loading required package: pepDat
Warning message:
In library(package, lib.loc = lib.loc, character.only = TRUE, logical.return = TRUE, :
there is no package called 'pepDat'
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