Open gianfilippo opened 2 years ago
Hi,
I am just learning how to process Nanopore sequencing data. I am starting from a FASTQ file and trying to understand the artic pipeline.
Could you please explain me how align_trim assigns the read groups ?
Thanks
Hi, I am not a developer, but I also had the same question. According to the artc docs here, during alignment post-processing, it would do "using the derived amplicon, assign each read a read group based on the primer pool".
Hi,
I am just learning how to process Nanopore sequencing data. I am starting from a FASTQ file and trying to understand the artic pipeline.
Could you please explain me how align_trim assigns the read groups ?
Thanks