I am working on genome assembly. I already run an assembly using PacBio hifi reads and hifiasm software. However, I want to improve more my assembly. I am wondering if I can use a Nanopore data and Pilón software for polishing. Could it increase the error rate for my data?.
If you have Hifi reads your error rate should already be quite good, therefore polishing with potentially longer and slightly more error-prone Nanonopore reads might not do any good. You might rather try to improve contingency. Do you have Hi-C data available? If you already have the Nanopore reads, I would try to use the Nanopore reads for gap-closure and scaffolding. Possibly, generate a hybrid assembly using both technologies to complement each other e.g. with the Flye assembler.