"Hey, thank you very much for this cool tool. I'm working on amplicon sequencing derived from public data with taxa at the genus level. According to the instructions, the only mandatory input is the abundance table. However, I'm interested in finding contamination associated with this data. My idea is to use the contaminants reference, as my dataset doesn't have any controls. If I run the following command, the decontamination step is not performed:
grimer -i fungi.genus.raw.csv --transpose -f ","
Since my table is at the genus level and the contaminants.yaml contains NCBI accessions, how can I perform decontamination?
Thanks in advance,
Ailton."