Description Usage Arguments Value Examples
Get top x hub genes for each module.
1 | WGCNA_hubgene(cyt, top_hub_n = 20, prefix = "ehbio")
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cyt |
A list containing two elements (edgeData and nodeData) generated by
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top_hub_n |
A number to get top x hub genes. |
prefix |
prefix for output files. |
A dataframe containing selected hub genes.
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 | df = generateAbundanceDF(nSample=30, nGrp=3, sd=5)
datExpr <- WGCNA_dataFilter(df)
datExpr <- WGCNA_sampleClusterDetectOutlier(datExpr)
power <- WGCNA_softpower(datExpr)
net <- WGCNA_coexprNetwork(datExpr, power)
WGCNA_saveModuleAndMe(net, datExpr)
cyt <- WGCNA_cytoscape(net, power, datExpr)
hubgene <- WGCNA_hubgene(cyt)
#2
exprMat <- "test.file"
wgcnaL <- WGCNA_readindata(exprMat)
traitData <- 'trait.file'
wgcnaL <- WGCNA_readindata(exprMat, traitData)
datExpr <- wgcnaL$datExpr
WGCNA_dataCheck(datExpr)
datExpr <- WGCNA_dataFilter(datExpr)
datExpr <- WGCNA_sampleClusterDetectOutlier(datExpr)
# datExpr <- WGCNA_sampleClusterDetectOutlier(datExpr, traitColors=wgcnaL$traitColors)
power <- WGCNA_softpower(datExpr)
net <- WGCNA_coexprNetwork(datExpr, power)
MEs_col <- WGCNA_saveModuleAndMe(net, datExpr)
WGCNA_MEs_traitCorrelationHeatmap(MEs_col, traitData=wgcnaL$traitData)
cyt <- WGCNA_cytoscape(net, power, datExpr)
hubgene <- WGCNA_hubgene(cyt)
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