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.
parsnp.tree is not created when using --use-fasttree with Parsnp. I looked through the parsnp python file and only the output of RAxML is renamed to parsnp.tree (via shutil.move). Though, the FastTree phylogeny is placed in <outputDirectory>/log/fasttree.out. It is not a terminating error.
I was able to replicate this not only with my test data, but also with the example mers_virus data within this repository.
Installation:
# Bioconda is added to my conda environment and this installs without error
conda create -n parsnp parsnp -y
conda activate parsnp
Commands:
# Using FastTree
## ERROR - parsnp.tree: newick format tree is missing!
parsnp -v -d genomes/ -r ref/England1.fna -o Parsnp2.0.3-fasttree -p 2 -c --use-fasttree
parsnp.tree
is not created when using--use-fasttree
with Parsnp. I looked through theparsnp
python file and only the output of RAxML is renamed to parsnp.tree (via shutil.move). Though, the FastTree phylogeny is placed in<outputDirectory>/log/fasttree.out
. It is not a terminating error.I was able to replicate this not only with my test data, but also with the example mers_virus data within this repository.
Installation:
Commands: