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To explain how to go from raw whole-genome sequencing data to the files needed for input into regentrans (recombination-filtered variant alignment and phylogeny).
We outline exactly what commands they need to run.
And provide a toy example.
And very clear documentation on what the inputs etc. should be.
Still need to figure out the best way to tell people to run it if they don't have access to a cluster. Or maybe they do have one they can use?
Arianna also suggested creating the SNV distance matrix using this on the cluster since it can be computationally intensive to do locally in R: https://github.com/tseemann/snp-dists (should also update the intro vignette to include this as an option)
Maybe find cloud option?
Also mention at beginning that should split by MLST (maybe ARIBA or look into other options - Evan might know of others)
The text was updated successfully, but these errors were encountered:
To explain how to go from raw whole-genome sequencing data to the files needed for input into
regentrans
(recombination-filtered variant alignment and phylogeny).I think this is the best tool to direct them to:
https://github.com/tseemann/snippy
The text was updated successfully, but these errors were encountered: