- Updated the Plasmidfinder database to use the January 18th 2023 release.
- Fixed an issue where the string "None" in the drug table would be parsed differently by different versions of pandas (#175).
- Upgraded to pandas version 2.
- Added the CGE-predicted phenotypes, PMID, Mechanism, and the Required Mutation columns to the Pointfinder output.
- The resfinder.tsv and pointfinder.tsv outputs now contain a Notes column.
- Updated the help description of the --mlst-scheme parameter to include a more useful link for available schemas.
- Switched to only officially supporting Python 3.7+ due to recent incompatibilities with Python 3.6 and some Python packages (numpy, biopython, and others).
- Adds the ability to handle "complex" pbp5 mutations. When appriopriate many pbp5 point mutations will be reported as a single mutation.
- Resfinder CGE-predicted phenotypes are now reported in the summary and detailed summary alongside existing predictions.
- Corrected a typo in the position for acrB in the PointFinder drug key table.
- Removed "enterobacteriaceae" from the list of supported PlasmindFinder databases.
- Changed the word sensitive to susceptible in outputs.
- Fixed a bug that occured when parsing some plasmid FASTA record IDs (PR 159).
- Fixed issue where sometimes the extraction of error messages from
makeblastdb
was crashing leading to less useful errors (PR 160).
- Updates to PointFinder database handling
- Adds the ability to handle promoters (regions with both promoter nucleotide information and non-promoter codon information)
- Adds handling of insertions and deletions in nucleotide and codon sequence
- Updates list of supported PointFinder species to
salmonella
,campylobacter
,enterococcus_faecalis
,enterococcus_faecium
,escherichia_coli
,helicobacter_pylori
.
- Switch name
e.coli
toescherichia_coli
in PointFinder gene-drug key to match organism name in PointFinder database.
- Fixed issue when using older version of pandas (#136) (0.8.0.dev0).
- Fixed up some Python warnings related to pandas (0.8.0.dev0).
- Adjusted
mlst
tests to account for differences in results for newer versions (0.8.0.dev0). - Drop support for Python 3.5 as it leads to issues with managing dependency versions (0.8.0.dev0).
- Switched from disallowing to generating a warning when the PointFinder organism is not one of the validated organisms (0.8.0.dev1).
- Updated ResFinder and PointFinder gene drug key to
072621
(0.8.0.dev2). - Updated default database commits to those corresponding to dates used by ResFinder (2022-05-24), PointFinder (2021-02-01), and PlasmidFinder (2021-11-29) (0.8.0.dev2).
- Fixed issue when multiple matches for same amino acid change to try and select the most specific amino acid change (0.8.0.dev2).
- Fixed up PlasmidFinder database handling to account for changes to PlasmidFinder database structure (0.8.0.dev2).
- Identical code to version
0.7.2
but made mainly to upload this version into Zenodo. - Migrated integration tests from TravisCI to GitHub Actions
- A few small fixes to
README.md
.
- Fixed
KeyError
issue with later versions of pandas (#115, thanks @javiertognarelli).
- Fix a bug so that the Sequence column in resfinder.tsv uses the isolate sequence instead of the reference sequence
- Added quality module that adds PASS/Fail column and detail information in Summary.tsv
- Added following new optional arguments for Search.py
- --genome-size-lower-bound
- --genome-size-upper-bound
- --minimum-N50-value
- --minimum-contig-length
- --unacceptable-number-contigs
- Add DNA column in Resfinder report
- Added --output-mlst in Search.py
- Added coloredlogs library to format the output
- Added support for MLST
- Renamed the following columns for clarification:
Plasmid Genes
toPlasmid
in Summary table.Gene
toPlasmid
in PlasmidFinder table.Gene
toGene/Plasmid
in Detailed Summary table.
- Add support for scanning against the PlasmidFinder database.
- Upgraded the testing package to use Green test runner.
- Added Detailed_Summary table which combines results from Resfinder, Pointfinder (optional), and Plasmidfinder.
- Added
--ignore-invalid-files
command and check for duplicate sequence ids.
- Add support for campylobacter from PointFinder database.
- Fix
read_table
deprecation warnings by replacingread_table
withread_csv
. - Handling issue with name of
16S
gene in PointFinder database for salmonella. - Refactoring and simplifying some of the git ResFinder/PointFinder database code.
- Added automated type checking with mypy.
- Exclusion of
aac(6')-Iaa
from results by default. Added ability to override this with--no-exclude-genes
or pass a custom list of genes to exclude from results with--exclude-genes-file
.
- Fix issue where
staramr
crashes if an input contig id is a number.
- Minor
- Updating default ResFinder/PointFinder databases to version from July 2018.
- Fix regex extracting gene/variant/accession values from ResFinder/PointFinder databases.
- Fixing a few entries in table mapping genes to phenotypes.
- Print stderr for errors with
makeblastdb
- Major
- Inclusion of predicted resistances to antimicrobial drugs thanks to gene/drug mappings from the NARMS/CIPARS Molecular Working Group. Resistance predictions are microbiological resistances and not clinical resistances (issue #4, #6).
- Adding a
staramr db restore-default
command to restore the defaultstaramr
database (issue #3). - Switched to using BLAST Tabular data + pandas to read BLAST results (issue #10).
- Inverted direction of BLAST (we now BLAST the AMR gene files against the input genomes).
- Minor
- Less verbose messages when encountering errors parsing the command-line options.
- Able to support adding options after a list of files (e.g.,
staramr search *.fasta -h
will print help docs). - Switched to including negative AMR results (samples with no AMR genes) by default. Must now use parameter
--exclude-negatives
to exclude them (issue #2). - Only print 2 decimals in Excel output (issue #5).
- Automatically adjust Excel cells to better fit text (issue #7).
- Many other coding improvements (issue #11, #13 and others).
- Initial release. Supports batch scanning against the ResFinder and PointFinder databases.