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Published 20 hours ago • verified publisher icon neherlab

Running workflow for new data

Open smb20200615 opened this issue 4 years ago • 0 comments

Do you have guidance on how to run your workflow on new genomes not available on RefSeq. I am interested in producing the all_genes_alignment file shown on the PanX website.

Many thanks in advance.

smb20200615 avatar Nov 24 '20 00:11 smb20200615