Releases: raufs/skDER
Releases · raufs/skDER
v1.2.8
v1.2.7
- Update granet to make it deterministic and also introduce the
--random-seed
option to allow changing the layout if desired. - Fix indentation issues in help function and slight updates to logging and messages in CiDDER and skDER.
- Create
CiDDER_Results.txt
file in CiDDER to capture the order in which representative genomes are selected.
Full Changelog: v1.2.6...v1.2.7
v1.2.6
- Make "greedy" mode the default algorithm in skder
- Correct stumbling on gzipped files with new method to calculate N50s introduced in v1.2.4.
- Introduce granet - for creating network visuals of genomes and where representative genomes selected fall.
- Update help functions of skder and cidder to include citation notice for skani and CD-HIT, respectively.
What's Changed
Full Changelog: v1.2.5...v1.2.6
v1.2.5
- In skDER, set the default value of
-p
- controlling additional arguments to pass toskani triangle
- from nothing (-s 90.0
to increase the screening parameter's value to 90.0 from the default value of 80.0. - Add support for providing directory paths, as well as files, to the
-g/--genomes
argument where the directories contain genome files to (also) include in skder/cidder analyses. - Begin development of Docker-based installation support - including convenience bash wrapper (still progress).
What's Changed
New Contributors
Full Changelog: v1.2.4...v1.2.5
v1.2.4
- Introduce
mgecut
- a program that can use PhiSpy or geNomad to predict MGEs in genomes and filter them out prior to genomic dereplication. - Integrate
mgecut
usage intoskder
andcidder
. - Switch to simple python implementation of N50 adapted from: https://gist.github.com/dinovski/2bcdcc770d5388c6fcc8a656e5dbe53c instead of using pyfastx.
Full Changelog: v1.2.3...v1.2.4
v1.2.3
v1.2.2
- Add memory option for CD-HIT usage in cidder and set default to unlimited.
- Cosmetic changes to code / comments / help-function
Full Changelog: v1.2.1...v1.2.2
v1.2.1
v1.2.0
- Introduce CiDDER - a CD-HIT based dereplication program to ensure you properly sample the pangenome space of a species/genus.
- Introduce new option to skDER to test a bunch of cutoffs for ANI and AF and generate a heatmap on the number of representative genomes that results from different combinations. E.g. useful if you want to limit your analysis to X genomes but don't know what ANI/AF cutoffs to use.
Full Changelog: v1.1.1...v1.2.0