Do spike-In control normalization of RNAseq on Galaxy platform

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

I also need that. I performed RNAseq in human cells with spike-in 1/20 drosophila cells. I know how to run DEseq2 without spike-in, but don’t know how to run with spike-in. Really eager to know. Hope someone can help. appreciate it.