Hi there,

In RNA-seq library prep, my samples were split on 2 plates (96 well), then pooled for sequencing. Now there are high variations (~10x) in the number of reads between the 2 plates. What would be the best approach to deal with the variation?

Thank you in advance!

Jay

# include your problematic code here with any corresponding output 
# please also include the results of running the following in an R session 

sessionInfo( )

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