Do spike-In control normalization of RNAseq on Galaxy platform

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