Closed MattCarlile05 closed 9 months ago
Hi, Thanks for letting us know. Could you share the .nextflow.log
or the tar that is output if you click report issue in the app anyway?
Hi, does the final report html get output and are these errors reported there?
We do get the final html report with no errors indicated. We only found the errors when we looked at the report html file located in the execution folder.
For each of your plasmids is there a plannotate annotated assembly in the report? From the log it looks like the workflow completed as expected, where did you see the text that you've pasted in the relevant log output? Was there any other error message with that?
There is a pLannotate assembly for each plasmid in the report. The errors are in 'NextFlow Workflow Report' html file located in the outputs execution folder.
oh would you be able to update the workflow to the latest version and let me know if it works? I noticed it says v0.3.1 - it may be an old bug.
Closing through lack of response, please open a new issue if it persists with the latest version v1.1.0
Operating System
macOS
Other Linux
No response
Workflow Version
v0.3.1
Workflow Execution
EPI2ME Desktop application
EPI2ME Version
v5.0.2
CLI command run
No response
Workflow Execution - CLI Execution Profile
None
What happened?
The assembly works fine but no final fastq file or gbk file generated.
I uploaded 4K reads, and used the default workflow parameters. I’ve run the workflow using the Epi2me labs Desktop and the Command line, in both cases with Docker. The assemblies look fine and the html reports looks good.
This has happened every time I have run the workflow, the log on Epi2me doesn't highlight an error - its only when you look at the execution log report that the errors 'Failed due to insufficient reads' and 'Failed to polish assembly with Medaka' are indicated.
Relevant log output
Application activity log entry
No response