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ToPASeq (version 1.6.0)

DEGraph: Function to use DEGraph method on microarray or RNA-Seq data

Description

DEGraph implements recent hypothesis testing methods which directly assess whether a particular gene network is differentially expressed between two conditions. In employs Graph Laplacian, Fourier transformation and multivariate T2-statistic

Usage

DEGraph(x, group, pathways, type, preparePaths=TRUE, norm.method=NULL, test.method=NULL, overall="biggest", useInteractionSigns=TRUE, EdgeAttrs=NULL, both.directions=TRUE, maxNodes=150, minEdges=0, commonTh=2, filterSPIA=FALSE, convertTo="none", convertBy=NULL)

Arguments

x
An ExpressionSet object or a gene expression data matrix or count matrix, rows refer to genes, columns to samples
group
Name or number of the phenoData column or a character vector or factor that contains required class assigments
pathways
A list of pathways in a form from graphite package or created by preparePathways()
type
Type of the data, "MA" for microarray and "RNASeq" for RNA-Seq
preparePaths
Logical, by default the pathways are transformed with preparePathways(). Use FALSE, if you have done this transformation separately
norm.method
Character, the method to normalize RNAseq data. If NULL then TMM-normalization is performed. Possible values are: "TMM", "DESeq2", "rLog", "none"
test.method
Character, the method for differentiall expression analysis of RNAseq data. If NULL then "voomlimma" is used. Possible values are: "DESeq2", "voomlimma", "vstlimma", "edgeR". This analysis is needed only for the visualization.
overall
Character, how should the overall p-value for a pathway be calculated. The possible values are: "mean", "min", "biggest". "biggest" returns the p-value of the biggest connected component.
useInteractionSigns
Logical, should types of interaction be included in the analysis?
EdgeAttrs
A list containing two data.frames. See makeDefaultEdgeData() for the details. The interactions are assigned signs according to the beta column of the second data.frame. The procedure is similar to the SPIA method
both.directions, maxNodes, minEdges, commonTh, filterSPIA, convertTo, convertBy
Arguments for the preparePathways()

Value

A list:
res
Results from analysis of individual pathways. The first column refers to the overall p-value for a pathway. Then groups of four columns follows. One group refers to one connected component and contains a pair of p-values (without and with Fourier transformation), graph and number of Fourier componets used in the test. The number of groups is equal to the highest number of components in analysed pathways. Components are sorted in the decreasing order of their nodes number.
topo.sig
NULL, present for the compatibility with outputs from other methods
degtest
A data.frame of gene-level statistics of all genes in the dataset

References

L. Jacob, P. Neuvial, and S. Dudoit. Gains in power from structured two-sample tests of means on graphs. Technical Report arXiv:q-bio/1009.5173v1, arXiv, 2010.

See Also

preparePathways

Examples

Run this code

if (require(DEGraph)) {
  data("Loi2008_DEGraphVignette")
  pathways<-pathways("hsapiens","biocarta")[1:10]
    DEGraph(exprLoi2008, classLoi2008, pathways, type="MA")
}
## Not run: 
# if (require(gageData)) {
# 
#  data(hnrnp.cnts)
#  hnrnp.cnts<-hnrnp.cnts[rowSums(hnrnp.cnts)>0,]
#  group<-c(rep("sample",4), rep("control",4))
#  pathways<-pathways("hsapiens","biocarta")[1:10]
#  #pathways<-lapply(pathways, function(p) as(p,"pathway"))
#  DEGraph(hnrnp.cnts, group, pathways, type="RNASeq", norm.method="TMM")
# }
# ## End(Not run)

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