The method used to compute p-values. One of "pooled.ttest","ttest", "limma", "HotellingT2".
For "ttest" a Student t-test is applied for each gene pair. The variance is estimated locally for each gene pair.
For "pooled.ttest", a pooled variance is estimated from all gene pairs. The variance applied for each gene pair is the maximum of the pooled and the local variance estimate. This method obtains conservative p-values.
For "limma" mediates between the local and the global variance estimation in a Bayesian framework. The limma-package is applied to compute the p-values.
For "HotellingT2" Hotelling-T^2 statistics is computed jointly for all dimensions. It results in a single p-value summarizing all channels. For simplification the p-values are stored in a matrix of dimension genes x genes x screens x channels and the p-values are repeated for each channel. The same holds for q-values.
mixTemplateQuery
If a gene-pair is measured twice as template-query and as query-template, a single p-value is computed by combining all measurements, if mixTemplateQuery = TRUE.
Else a p-value is computed independently for both cases.
p.adjust.function
A function that corrects the p-values for multiple testing. Default method is the Benjamini-Hochberg method.
verbose
Either 0 (default, no output), 1 (minimum output), or 2 (outout)
Details
Computes p-values from a t-test, using the bioconductor package limma, or with a multidimensional Hotelling T^2 test.
Value
An object of class RNAinteract.
Author(s)
Bernd Fischer
References
~put references to the literature/web site here ~
See Also
RNAinteract-package
Examples
data("sgi")
sgi <- computePValues(sgi, method = "HotellingT2")
# Hotelling T^2 test will provide one p-value for all channels, PV will be the same
# for all channels in this case
PV <- getData(sgi, type="p.value", format="targetMatrix", channel="nrCells")
Results
R version 3.3.1 (2016-06-21) -- "Bug in Your Hair"
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Type 'q()' to quit R.
> library(RNAinteract)
Loading required package: abind
Loading required package: locfit
locfit 1.5-9.1 2013-03-22
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")'.
> png(filename="/home/ddbj/snapshot/RGM3/R_BC/result/RNAinteract/computePValues.Rd_%03d_medium.png", width=480, height=480)
> ### Name: computePValues
> ### Title: compute p-values
> ### Aliases: computePValues
> ### Keywords: manip htest multivariate
>
> ### ** Examples
>
> data("sgi")
> sgi <- computePValues(sgi, method = "HotellingT2")
> # Hotelling T^2 test will provide one p-value for all channels, PV will be the same
> # for all channels in this case
> PV <- getData(sgi, type="p.value", format="targetMatrix", channel="nrCells")
>
>
>
>
>
> dev.off()
null device
1
>