Closed vmelichar closed 1 month ago
I found out a solution to my problem. The input directory has to have a specific structure (dirs named barcodeXX
where XX
is a 2 digit number). I did not know that because I had just one sample in one fastq file. Might be helpful to state this in the usage doc.
Hi, I am glad you could already find a solution to your problem. Thank you for raising the issue. I will update the doc in the next release and/or add a singleplex sample where no barcode subdirectory is necessary.
When checking your config file, I saw that you specified the newest v5 models for Medaka. I am currently preparing a new release of the pipeline supporting the newest version of Medaka and v5 models. Currently, the latest supported model is v4.3. The new release should be available by the end of next week.
Kind regards, Stephan
Hi,
I am trying to run the pipeline but came across a problem. On the test data, it works as expected (using the conda profile). But on my actual data, it stops after the first step and does nothing else. I would appreciate any help. Thanks.
This is the command:
nextflow run genepi/umi-pipeline-nf -r v0.2.1 -c custom_copy.config -params-file params.yaml -profile custom,conda -with-conda environment.yml -name umi 1_2 -resume
This is the custom_copy.config file:
This is the params.yaml file:
And this is the nextflox log file: