Hi to every one,
I'm running a pipeline in which i need as an input file Pacbio reads but unfortunately the pacbio reads available have a low coverage (around 7 that is 3 unit below the minimun accepted from the pipeline). Since in my lab they are doing some Nanopore sequencing I was thinking if after the fastq file correction ( i always used canu) i can merge corrected nanopore and Pacbio reads in the same file (using cat for instance).
This will increase a lot the power of my analysis.
Do you know if that is possible?