Description of feature
Currently different analysis software in ARG screening workflow use different input sequences.
For instance, AMRFinderPlus and RGI use nucleotide sequence as input whereas deeparg uses predicted protein sequences from the annotation step in the beginning of the pipeline.
Since all software accept both nucleotide and protein sequences, it would be really helpful to have a uniform input for all software which allows post-processing and comparison between predictions by different software based on sequence accession number.
https://nfcore.slack.com/archives/C02K5GX2W93/p1717515107461539
Description of feature
Currently different analysis software in ARG screening workflow use different input sequences.
For instance, AMRFinderPlus and RGI use nucleotide sequence as input whereas deeparg uses predicted protein sequences from the annotation step in the beginning of the pipeline.
Since all software accept both nucleotide and protein sequences, it would be really helpful to have a uniform input for all software which allows post-processing and comparison between predictions by different software based on sequence accession number.
https://nfcore.slack.com/archives/C02K5GX2W93/p1717515107461539