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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
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