AMRfior 0.3.1

AMRfior: A toolkit that uses BLAST, BWA, Bowtie2, DIAMOND, and Minimap2 to search DNA and protein sequences against AMR databases (DNA and AA) such as CARD/RGI and ResFinder.

AMRfíor (pronounced AMR "feer", sounds like beer)

This toolkit utilises a combined approach that uses BLAST, BWA, Bowtie2, DIAMOND, and Minimap2 to search DNA and protein sequences against AMR databases (DNA and AA) such as CARD/RGI and ResFinder.

Requirements:

- python >=3.10
- samtools >=1.19.2
- blast >=2.17.0
- diamond >=2.1.13
- bowtie2 >=2.5.4
- bwa >=0.7.19
- minimap2 >=2.30
- seqtk >=1.4

Menu:

AMRfíor v0.3.1 - The Multi-Tool AMR Gene Detection Toolkit.

options:
  -h, --help            show this help message and exit

Required selection:
  -i INPUT, --input INPUT
                        Input FASTA/FASTAQ file(s) with sequences to analyse -
                        Separate FASTQ R1 and R2 with a comma for Paired-FASTQ
                        or single file path for Single-FASTA - .gz files
                        accepted
  -st {Single-FASTA,Paired-FASTQ}, --sequence-type {Single-FASTA,Paired-FASTQ}
                        Specify the input Sequence Type: Single-FASTA or
                        Paired-FASTQ (R1+R2) - Will convert Paired-FASTQ to
                        single combined FASTA for BLAST and DIAMOND analyses
                        (SLOW)
  -o OUTPUT, --output OUTPUT
                        Output directory for results

Output selection:
  --report_fasta {None,all,detected,detected-all}
                        Specify whether to output sequences that "mapped" to
                        genes."all" should only be used for deep
                        investigation/debugging."detected" will report the
                        reads that passed detection thresholds for each
                        detected gene."detected-all" will report all reads for
                        each detected gene. (default: None)

Tool selection:
  --tools {blastn,blastx,diamond,bowtie2,bwa,minimap2,all} [{blastn,blastx,diamond,bowtie2,bwa,minimap2,all} ...]
                        Specify which tools to run - "all" will run all tools
                        (default: all except blastx/n as it is very slow!!)

Database selection:
  --databases {resfinder,card,ncbi,user-provided} [{resfinder,card,ncbi,user-provided} ...]
                        Specify which AMR gene databases to use (default:
                        resfinder and card) -If "user-provided" is selected,
                        please ensure the path contains the appropriate
                        databases set up as per the documentation and specify
                        the path with --user-db-path.
  --user-db-path USER_DB_PATH
                        Path to the directory containing user-provided
                        databases (required if --databases includes "user-
                        provided")

Query threshold Parameters:
  --q-min-cov QUERY_MIN_COVERAGE, --query-min-coverage QUERY_MIN_COVERAGE
                        Minimum coverage threshold in percent (default: 40.0)

Gene Detection Parameters:
  --d-min-cov DETECTION_MIN_COVERAGE, --detection-min-coverage DETECTION_MIN_COVERAGE
                        Minimum coverage threshold in percent (default: 80.0)
  --d-min-id DETECTION_MIN_IDENTITY, --detection-min-identity DETECTION_MIN_IDENTITY
                        Minimum identity threshold in percent (default: 80.0)
  --d-min-base-depth DETECTION_MIN_BASE_DEPTH, --detection-min-base-depth DETECTION_MIN_BASE_DEPTH
                        Minimum average base depth for detection -
                        calculated against regions of the detected gene with
                        at least one read hit (default: 1.0)
  --d-min-reads DETECTION_MIN_NUM_READS, --detection-min-num-reads DETECTION_MIN_NUM_READS
                        Minimum number of reads required for detection
                        (default: 1)

Mode Selection:
  --dna-only            Run only DNA-based tools
  --protein-only        Run only protein-based tools
  --sensitivity {default,conservative,sensitive,very-sensitive}
                        Preset sensitivity levels - default means each tool
                        uses its own default settings and very-sensitive
                        applies DIAMONDs --ultra-sensitive and Bowtie2s
                        --very-sensitive-local presets

Tool-Specific Parameters:
  --minimap2-preset {sr,map-ont,map-pb,map-hifi}
                        Minimap2 preset: sr=short reads, map-ont=Oxford
                        Nanopore, map-pb=PacBio, map-hifi=PacBio HiFi
                        (default: sr)

Runtime Parameters:
  -t THREADS, --threads THREADS
                        Number of threads to use (default: 4)
  --no_cleanup
  -v, --verbose

Examples:
  # Basic usage with default tools (runs DNA & protein tools)
  AMRfior -i reads.fasta -st Single-FASTA -o results/

  # Select specific tools and output detected FASTA sequences
  AMRfior -i reads.fasta -st Single-FASTA -o results/     --tools diamond bowtie2     --report_fasta detected

  # Custom thresholds, paired-fastq input, threads and dna-only mode
  AMRfior -i reads_R1.fastq,reads_R2.fastq -st Paired-FASTQ -o results/     -t 16 --d-min-cov 90 --d-min-id 85     --dna-only