Comments (3)
Set things up so that the number of haploid copies you expect in your summaries is the number that's given to PGGB. You'll need to investigate each assembly to see if it's haploid (collapsed) or diploid.
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Also I suggest renaming the FASTA sequences with PanSN format. If the assemblies are haploid collapsed then you'd have something like fish1#1#accession for each.
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Thank you Eric.
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Related Issues (20)
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- container creation failed
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