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I am running wf-clone-validation v1.7.1 locally. I am wondering how to get the linearization efficiency to be part of the report as it mentions in the Pipeline Overview (step 13)? I have run it with a sample and a plasmid reference, and added a "cut_site" column to my sample sheet but there are no stats generated in the report. Is there something else I need to add? How can I get the report to generate this stat? Thanks!
The text was updated successfully, but these errors were encountered:
Thanks for the response! I am running it on the Epi2Me app but can run it on the command line if that would be helpful for you. My sample sheet matches the example exactly and I am providing a full plasmid reference. Should these results be generated with the test data? If so, when I run the test data it is not generated either. I can provide the nextflow execution logs if that would be helpful. Is there a minimum length the cutsite needs to be? I provided strictly the recognition site for my restriction enzyme but in the sample sheet they look a bit longer than that. Thanks!
Hello,
I am running wf-clone-validation v1.7.1 locally. I am wondering how to get the linearization efficiency to be part of the report as it mentions in the Pipeline Overview (step 13)? I have run it with a sample and a plasmid reference, and added a "cut_site" column to my sample sheet but there are no stats generated in the report. Is there something else I need to add? How can I get the report to generate this stat? Thanks!
The text was updated successfully, but these errors were encountered: