One concern is that my dataset includes both complete geneome and contig level genome(90 % of my dataset are contig level). Finally I'd like to construct phylogenetic tree.
In this case, are there any problems regarding using a lot of contig level genomes?
I would exclude poor quality draft assemblies that are likely to be contaminated/generated from low coverage data, but otherwise we have not encountered problems with this approach (e.g. here).
Hi, thank you for this great tools.
I'd like to detect recombination regions using gubbins. I'm going to use Snippy to create whole genome sequence alignment file for gubbins.
% snippy-clean_full_aln core.full.aln > clean.full.aln % run_gubbins.py -p gubbins clean.full.aln
One concern is that my dataset includes both complete geneome and contig level genome(90 % of my dataset are contig level). Finally I'd like to construct phylogenetic tree. In this case, are there any problems regarding using a lot of contig level genomes?
Best regards,