Closed watsonar closed 4 years ago
Upon further reflection, I hereby rescind this request, because why would genomes be in fastq format anyway? The answer is, they almost certainly wouldn't be, and you are accidentally using short read files like a ding dong.
Hello. :)
When running the pangenomics workflow from a
fasta.txt
file containing paths to external genomes, these genomes must be in fasta format, and cannot be in fastq format. I was wondering if we could add anfq2fa
step to the pangenomics workflow before theanvi_script_reformat_fasta
step, so that we could use fastq format input genomes.Thank you all so much for everything that you do, Andrea