replikation / poreCov

SARS-CoV-2 workflow for nanopore sequence data
https://case-group.github.io/
GNU General Public License v3.0
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Run --nanopolish on already basecalled data #194

Closed hoelzer closed 2 years ago

hoelzer commented 2 years ago

The help of poreCov states that it is possible to skip basecalling when providing FASTQ files and a sequencing_summary.txt via --nanopolish. However, for me, this results in:

Please provide a fast5 dir for nanopolish [--fast5]

Code used:

nextflow run replikation/poreCov -r 0.11.7 -profile local,singularity --cores 16 --max_cores 240 --krakendb GRCh38.p13_SC2_2021-02-08.tar.gz -w work-run382 --fastq_pass fastq_pass --update --output results-run382-nanopolish --primerV V4.1 --nanopolish sequencing_summary_run21-382.txt -resume

Is there maybe just a check still active that prevents this combination of inputs from running?

replikation commented 2 years ago