You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Hi Kris,
I have predicted viral scaffolds from 54 samples assemblies. I tried to use:
vRhyme -i fasta -r paired_reads_folder/*.fastq -t threads -o output_folder --method longest
But it shows an error:
Error. No file(s) for coverage information were identified. Check coverage inputs (c/b/s/r/u/v). Exiting.
The text was updated successfully, but these errors were encountered:
Hi Kris,
I also have the same error.
My log file contents:
Command: /opt/anaconda3/bin/vRhyme -i contigs.fasta -ccontigs.csv -t 10 --iter 10 -o output_folder --method longest
0.0 Initializing and validating vRhyme parameters
0.01 Running 'longest' dereplication: 97% identity and 70% coverage
0.17 No sequences were of sufficient similarity to dereplicate
0.17 Performing pairwise coverage comparisons
Error. No file(s) for coverage information were identified. Check coverage inputs (c/b/s/r/u/v). Exiting.
Hi Kris,
I have predicted viral scaffolds from 54 samples assemblies. I tried to use:
vRhyme -i fasta -r paired_reads_folder/*.fastq -t threads -o output_folder --method longest
But it shows an error:
Error. No file(s) for coverage information were identified. Check coverage inputs (c/b/s/r/u/v). Exiting.
The text was updated successfully, but these errors were encountered: