log2 RSEM data with finite and non-negative

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1

Hello All

I am analyzing 1 RNAseq data which has been deposited in GEO as the RSEM upper quantile normalized data. I used limma-voom for DEGs between groups using galaxy. The error which I have got was:
[1] “Extracting counts”
Error in cpm.default(data$counts) :
library sizes should be finite and non-negative
Calls: cpm → cpm.default
Execution halted

Can anyone suggest me how to handle this data?

Thanks in advance

2

Anyone solve this problem yet? I have been confused with it too.
PS.it can well run on another coworker’s computer.