Dear,
Is there any possible could integrate ERCC spike-in control in RNAseq analysis workflow on Galaxy platform?
I apply Hisat2, featureCounts, and Deseq2 to do RNAseq analysis currently. However, I didn’t find any options to incorporate ERCC spike-in control to do the normalization between samples.
Would you give me some suggestions?
Thanks a lot!
Szu Shuo