I am running Kraestnar atac-seq lab protocol, and before I purify I am trying to get a gel image from my library. But there is nothing showing up on the gel, could it be an amplification problem? For my samples I did not need to do more than 6 cycles on the qPCR for any samples.

and if anyone has ever followed this atac-seq protocol, tips would also be helpful!

Please help I am tired of wasting reagents and not getting any bands