Open NowickiLab opened 1 year ago
Please advise how to code the common option for scenario (4), if I only have the assembled .fna files to be targeted that are saved locally, not in NCBI. Thank you!
You can connect all contig seqs into one complete genome by yourself. You can add 200 Ns between two contig seqs.
Please advise how to code the common option for scenario (4), if I only have the assembled .fna files to be targeted that are saved locally, not in NCBI. Thank you!