Hello,
I have two questions:
Is Z-scaled data or Pareto-scaled counts data from RNA-Seq appropriate as input into WGCNA (or the multiWGCNA package (if this is known))?
I have tried using multiWGCNA to analyze RNA-Seq data across two strains and two tissue types. I have rownames that correspond to ENSEMBL IDs but I'm getting the error:
error in .rownamesdf<-(x, value = value) : duplicate 'row.names' are not allowed.
I have checked that each row has a unique ID by using the function
rownames(df) = make.names(rownames(df), unique = TRUE)
and have separately added unique numbers to each ID to 'tag' it.
Please advise on why this might be happening if possible!
Best, shasabhi1
What function do you run to get the error?