Is it possible to use sub-workflows for IRIDA? Downstream of consensus we are doing the same analysis (pangolin & nextclade) for both Illumina and Nanopore.
List of variants (from Nextclade or summarised from ivar variants??) e.g. C241T,T445C,C3037T,C6286T,C11396T,C14408T,C21614T,G22205C,C22227T,A23403G,C26801G,C27944T,C28932T,G29645T
List of variant amino acids (from Nextclade) - e.g. N:A220V,ORF1a:L3711F,ORF1b:P314L,S:L18F,S:D215H,S:A222V,S:D614G
from QC report: pct_N_bases, pct_covered_bases, longest_no_N_run, num_aligned_reads
Is it possible to use sub-workflows for IRIDA? Downstream of consensus we are doing the same analysis (pangolin & nextclade) for both Illumina and Nanopore.