Open dieunelderilus opened 3 years ago
Hi @dieunelderilus,
I noticed in your command above you have a ~
in front of barcode01
, I suspect that this is not correct?
Hi @cjw85,
Sorry it was a mistake, I have noticed that, u have removed the ~
, and I still have the same error message. Please see bellow
(pipeline-umi-amplicon) [qlk5@biolinux fastq_pass]$ snakemake -j 16 reads --config input_fastq=barcode01/ reference_fasta=cds.fa
Building DAG of jobs... MissingRuleException: No rule to produce reads (if you use input functions make sure that they don't raise unexpected exceptions).
Hello @cjw85 I had created an empty 'Snakefile' in working directory while troubleshooting. After deleting it I am getting a different error message:
snakemake -j 16 reads --config input_fastq=barcode01/ reference_fasta=cds.fa
Error: no Snakefile found, tried Snakefile, snakefile, workflow/Snakefile, workflow/snakefile.
Hello, I am trying to run the pipeline-umi-amplicon on the fastq files generated my minion sequencing. However, I am finding a strange error . Here the command line and error found:
snakemake -j 16 reads --config input_fastq=~barcode01/ reference_fasta=cds.fa
error found: Building DAG of jobs... MissingRuleException: No rule to produce reads (if you use input functions make sure that they don't raise unexpected exceptions).
Please any help or suggestions? Cheers, ~DD