Right now the workflow (due to aDNA traditions) is SE oriented. Typically users have PE data. The step of merging overlapping PE reads is not currently implemented (because in Anders' project all fastq-files were already merged by the aDNA SciLifeLab facility) but perhaps should be with e.g. fastp. Perhaps the whole Cutadapt step can be replaced with fastp?
Right now the workflow (due to aDNA traditions) is SE oriented. Typically users have PE data. The step of merging overlapping PE reads is not currently implemented (because in Anders' project all fastq-files were already merged by the aDNA SciLifeLab facility) but perhaps should be with e.g. fastp. Perhaps the whole Cutadapt step can be replaced with fastp?