Open ericgonzalezs opened 1 year ago
Hi @ericgonzalezs
Yes you can use "flagger_end_to_end_no_variant_calling_no_ref.wdl" using the instructions mentioned here: https://github.com/mobinasri/flagger#running-pipeline-with-wdl It ignores incorporation coverage biases in HSats.
Hi,
I would like to run this pipeline in a plant genome. I would like to skip the step4 "incorporation coverage biases in HSats". How I could achieve this if I want to run "flagger_end_to_end_no_variant_calling_no_ref.wdl"?.
Many thanks.