Hi everyone,
we want to establish a diagnostic tool in our institute of virology, where we extract RNA from a patients blood and than sequence it, maybe following this protocol. I understand everything until I have the reads in this case, however, I don't understand, how I would than map the generated reads.
Can you recommend an aligner for this purpose and where would you get a nice viral genome database? Or do I have to generate a giant fused genome for the alignment ?
Edited the title and the link
Thank you very much! That's exactly what I was looking for!
Is it possible to use Nanopore sequencing for that?
I guess as long as the reads are in .fastq format, DisCVR should work, however, I am not sure if it is thoroughly tested with ONT data.