I have an existing dataset from nanopore run in fast5 format. I'm using GALAXY to convert it into fastq format. The tools which I've trialled from the tools list are : 1) extract fastq in tabular format from a set of fast5 files and 2) extract read in fasta or fastq format from nanopore files.
I got either 1 line or 0 bytes from these runs,,,no output.
Does anyone has any idea why? or which step did i miss or input the wrong thing?