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Can we run on non complete genomes #27

Answered by lrvdijk
SilasK asked this question in Q&A
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In principle, it should work with drafty assemblies. In our experience, however, plasmids make everything harder. In drafty assemblies it's harder to detect which contigs belong to a plasmid. It may throw off StrainGST, e.g., reporting a reference only because a good chunk of a plasmid that happened to be present in that reference was detected. It also may throw off ANI estimates with StrainGR because plasmids tend to be more diverse, thus making it harder to define a "same strain" threshold. Even with this in mind, you could aggregate and do a weighted average (weighted by scaffold length) of the key metrics you're interested in.

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Converted from issue

This discussion was converted from issue #26 on February 27, 2023 20:24.