scanPAV
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Pipeline to detect PAVs (presence/absence variations) in genome comparison using whole genome alignment.
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scanPAV issues
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Hello Developers We used scanPav to compare genome A with B. We filtered them for more than 10 KB fragments which are present in A but absent in B. However,...
Dear Drs, Hope this email finds you well. I think I have followed the steps from the github but the outcome file contains a bit of error message. Please see...
Could you please tag a release? I would like to add the tool to Bioconda for easy installation.