Is anyone aware of a tool (GUI or python/R/bash package) to explore eventalign nanopore data (or fast5 raw data) with the corresponding alignment to a reference genome? Kind of like viewing how reads in a bam file align against a reference as with IGV except looking at how the current signal aligns to the reference. TIA!
*edit so I found this, any others out there? https://github.com/hiruna72/squigualiser