WGCNA to Cytoscape error
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zen • 0
@zen-22107
Last seen 4.2 years ago

Hello,

I am trying to make export files from WGCNA to Cytoscape for network analysis. I have 40 traits. WGCNA analysis identified 57 modules. I want to make a network figure using Cytoscape for all the traits how they are connected. I tried following code in HPC:

lnames = load(file = "dataInput.RData"); 
lnames=load(file = "SignedHybrid-networkConstruction-auto.RData");
softPower <- 7 ;
adjacency <- adjacency(datExpr, power = softPower) ;
TOM <- TOMsimilarity(adjacency) ;
modules = c("bisque4","black","blue","blue2","coral1","coral2","cyan","darkgrey","darkmagenta","darkred","darkseagreen4","darkslateblue","darkturquoise","darkviolet","firebrick4","green","greenyellow","grey","grey60","honeydew1","indianred4","ivory","lavendarblush3","lightcoral","lightcyan1","lightgreen","lightpink4","magenta","maroon","mediumorchid","mediumpurple2","mediumpurple3","navajowhite2","orangered4","palevioletred3","pink","plum1","plum2","plum3","purple","red","royalblue","salmon2","salmon4","skyblue","skyblue1","skyblue3","tan","thistle1 ","thistle2 ","thistle3","turquoise","violet","violetred","white","yellow","yellow4")
probes = colnames(datExpr) 
inModule = is.finite(match(moduleColors, modules));
modProbes = probes[inModule];
modTOM = TOM[inModule, inModule];
dimnames(modTOM) = list(modProbes, modProbes)
cyt = exportNetworkToCytoscape(modTOM,
                               edgeFile = paste("CytoscapeInput-edges0-", paste(modules, collapse="-"), ".txt", sep=""),
                               nodeFile = paste("CytoscapeInput-nodes0-", paste(modules, collapse="-"), ".txt", sep=""),
                               weighted = TRUE,
                               threshold = 0,
                               nodeNames = modProbes,
                               nodeAttr = moduleColors[inModule]);

But it gives error:

/apps/R/3.6/bin/launch_r: line 3:  3725 Killed singularity exec -B /apps,/opt/slurm,/var/run/munge:/run/munge "${HPC_SINGULARITY_IMAGE}" "$@"
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@peter-langfelder-4469
Last seen 28 days ago
United States

You gave way too little info - is this on a cluster? Do you have a log or R output file that shows where exactly the script was aborted? How big is the data? In my experience, jobs run on a cluster get killed mostly because they start consuming more resources than they requested. In this case the offender may be RAM, you may be trying to export a network to cytoscape that is too large (has too many genes).

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Thank you! Yes, it is on cluster. I do not have a log but the script was aborted at the last step to create cyt.

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Thank you! Yes, it is on cluster. I do not have a log but the script was aborted at the last step to create cyt.

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Well, you probably need to request more memory when you schedule the job. Check the number of genes that match the criteria you have for selection. Keep in mind that the necessary memory scales as the number of genes squared because the data for cytoscape is essentially a data frame where each row corresponds to a connection. If you have 10k genes, you have 100M connections (rows), or several character and numeric vectors of length 100M. That can easily take multiple gigabytes of memory.

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I see. Thank you for the detailed explanation!

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It is a duplicate comment.........

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Thank you......................

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