Hello, how are you? I have a problem during an analysis of phage therapy samples, when I get to the summary.seqs section, it indicates the following error:
mothur > summary.seqs(fasta=current, count=current)
Using /home/equiroz/Artemia/stability.trim.contigs.good.good.count_table as input file for the count parameter.
Using /home/equiroz/Artemia/stability.trim.contigs.good.unique.good.align as input file for the fasta parameter.
Using 64 processors.
[ERROR]: /home/equiroz/Artemia/stability.trim.contigs.good.unique.good.align is blank. Please correct.
Error in reading your fastafile, at position -1. Blank name.
Could someone give me some advice on this