Parsnp was designed to align the core genome of hundreds to thousands of bacterial genomes within a few minutes to few hours. Input can be both draft assemblies and finished genomes, and output includes variant (SNP) calls, core genome phylogeny and multi-alignments. Parsnp leverages contextual information provided by multi-alignments surrounding SNP sites for filtration/cleaning, in addition to existing tools for recombination detection/filtration and phylogenetic reconstruction.
Hi~
I just installed parsnp and reported an error while running the program. The genome I used is the example you used: 49 MERS Coronavirus. The reported error is shown below:
Cannot open reference file !
Looking forward to your reply. Thank you very much
Hi~ I just installed parsnp and reported an error while running the program. The genome I used is the example you used: 49 MERS Coronavirus. The reported error is shown below:
Cannot open reference file !
Looking forward to your reply. Thank you very much