Releases
v2.0.0
bkille
released this
05 Jan 17:01
What's Changed
You can now pass a newline-separated file of paths to query sequences to -d
in addition to directories and command-line lists.
Adds --partition
flag, which splits recruited genomes into partitions of size --partition-size
(default 50).
Adds --no-recruit
option which skips the recruitment step, but still drops genomes if their size differs substantially from the reference.
Fixes multiple bugs in the output:
Output can now be parsed by BioPython's AlignIO module with the "mauve" format
LCBs no longer overlap
Ambiguous base pairs and small contigs no longer lead to incorrect coordinates
VCF now contains the correct reference allele.
FastANI now guarantees at least 100 segments (unless it requires a fragment length < 500)
Adds --min-ref-cov
option (default 90), which when used with --use-ani
, removes query genomes that do not cover at least 90% of the reference.
Output folder has been reorganized to separate logs and config files from the main output.
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