Description Usage Arguments Value Examples
Export WGCNA resullt for cytoscape input edges and nodes.
1 2 3 4 5 6 7 8 | WGCNA_cytoscape(
net,
power,
datExpr,
TOM_plot = NULL,
prefix = "ehbio",
fulledge = F
)
|
net |
|
power |
soft-thresholding power for network construction. |
datExpr |
Expression data. A matrix (preferred) or
data frame in which columns are genes and rows ar samples. NAs are
allowed, but not too many. See |
TOM_plot |
Get TOM plot and save to file given here like 'tomplot.pdf'. |
prefix |
prefix for output files. |
fulledge |
Output all edges (very large). Default FALSE. Only output edges whithin modules. |
A list with edgeData and nodeData as two elements.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 | 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)
#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)
|
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