Hi,
I have nanopore metagenomic samples and I am looking to detect the presence of 4 known L. monocytogenes strains (reference genomes available).
I have seen it suggested to:
- Use a single reference genome for mapping
- Then rely on StrainPhlAn’s marker gene knowledge to differentiate between the strains
My understanding however is that StrainPhlAn reconstructs a single consensus sequence per species per sample from marker genes, meaning:
-
If a sample contains multiple strains simultaneously, the output would be a chimeric consensus rather than detection of individual strains — is this correct?
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Is StrainPhlAn designed for reference-based detection of specific known strains, or primarily for phylogenetic comparison of the
dominant strain across samples?
Thanks!