Group file if already start with contigs

Hi Pat

I had posted that in a new trhead (uncategorized) and now I changed it to Commands in Mothur ( I need help working with MrDNA service sequences, providing R1 and R2 files both with barcodes?

I have the fastqs but with reads with barcode, both fwd and rev, in both R1 and R2 files and I don’t know how to use the make.contigs command.
I also have a full fasta file with the contigs to start at screen.seqs but I don’t know how to creat the groups file in that case.

I’d very much appreciate help to start following the SOP and process the sequences.

Thank you!

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