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author | iuc |
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date | Tue, 29 Nov 2016 14:52:34 -0500 |
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<tool id="abricate" name="ABRicate" version="0.1.0"> <requirements> <requirement type="package" version="0.3">abricate</requirement> <requirement type="package" version="5.18.1">perl</requirement> <requirement type="package" version="2.2.31">blast+</requirement> </requirements> <version_command>abricate --version</version_command> <command detect_errors="exit_code"><![CDATA[ abricate "$fasta_input" #if $settings.advanced == "advanced" $settings.no_header #if $settings.min_dna_id --minid=$settings.min_dna_id #end if #if $settings.cull_limit --cull=$settings.cull_limit #end if #end if > "$report" ]]></command> <inputs> <param name="fasta_input" type="data" format="fasta" label="Select fasta file" help="Specify fasta file to screen for antibiotic resistant genes"/> <conditional name="settings"> <param name="advanced" type="select" label="Specify advanced parameters"> <option value="simple" selected="true">No, use program defaults.</option> <option value="advanced">Yes, see full parameter list.</option> </param> <when value="simple"> </when> <when value="advanced"> <param name="no_header" type="boolean" label="Suppress header" truevalue="--noheader" falsevalue="" help="Suppress output file's column headings" optional="true" /> <param name="min_dna_id" type="integer" label="Minimum DNA identity" value="75" min="0" max="100" help="Minimum DNA identity (default 75, must be between 0-100)" optional="true" /> <param name="cull_limit" type="integer" label="Culling limit" value="1" min="0" help="Culling limit (encompassing hits) (default 1, must be a positive number)" optional="true"> <validator type="in_range" message="This value must be greater than or equal to 0" min="0" max="2147483647"/> </param> </when> </conditional> </inputs> <outputs> <data format="tabular" name="report" label="${tool.name} on ${on_string} report file"/> </outputs> <tests> <!-- Basic test - will produce no results. --> <test> <param name="fasta_input" value="Acetobacter.fna"/> <param name="advanced" value="simple"/> <output name="report" ftype="tabular" file="output_noresults.txt" /> </test> <!-- Basic test - will produce results. --> <test> <param name="fasta_input" value="MRSA0252.fna"/> <param name="advanced" value="simple"/> <output name="report" ftype="tabular" file="output_mrsa.txt" compare="contains"/> </test> <!-- Advanced test - No header. --> <test> <param name="fasta_input" value="MRSA0252.fna"/> <param name="advanced" value="advanced"/> <param name="no_header" value="True"/> <output name="report" ftype="tabular" file="output_noheader.txt" compare="contains"/> </test> <!-- Advanced test - Cull limit 100 --> <test> <param name="fasta_input" value="MRSA0252.fna"/> <param name="advanced" value="advanced"/> <param name="cull_limit" value="100"/> <output name="report" ftype="tabular" file="output_cull100.txt" compare="contains"/> </test> <!-- Advanced test - Min DNA ID 100 --> <test> <param name="fasta_input" value="MRSA0252.fna"/> <param name="advanced" value="advanced"/> <param name="min_dna_id" value="100"/> <output name="report" ftype="tabular" file="output_minid100.txt" compare="contains"/> </test> </tests> <help><![CDATA[ **What it does** Given a FASTA contig file, ABRicate will perform a mass screening of contigs and identify the presence of antibiotic resistance genes. The database of these genes is built from ResFinder. **Output** ABRicate will produce a tab-seperated output file with the following outputs: +---------------+------------------------------------------------+ | Column | Description | +===============+================================================+ | FILE | The filename this hit came from | +---------------+------------------------------------------------+ | SEQUENCE | The sequence in the filename | +---------------+------------------------------------------------+ | START | Start coordinate in the sequence | +---------------+------------------------------------------------+ | END | End coordinate | +---------------+------------------------------------------------+ | GENE | ABR gene | +---------------+------------------------------------------------+ | COVERAGE | What proportion of the gene is in our sequence | +---------------+------------------------------------------------+ | COVERAGE_MAP | A visual represenation | +---------------+------------------------------------------------+ | GAPS | Was there any gaps in the | | | alignment - possible pseudogene? | +---------------+------------------------------------------------+ | %COVERAGE | Proportion of gene covered | +---------------+------------------------------------------------+ | %IDENTITY | Proportion of exact nucleotide matches | +---------------+------------------------------------------------+ **Example Output** :: #FILE SEQUENCE START END GENE COVERAGE COVERAGE_MAP GAPS %COVERAGE %IDENTITY Processing: 6008.fna Found 12 ABR genes in 6008.fna Klebsiella.fna NC_021232.1 872545 872964 fosA 1-420/420 =============== 0 100.00 100.00 Klebsiella.fna NC_021232.1 1381252 1382427 oqxA 1-1176/1176 =============== 0 100.00 99.32 Klebsiella.fna NC_021232.1 2584899 2585759 blaSHV1 1-861/861 =============== 0 100.00 99.88 ]]></help> <citations> <citation type="bibtex"> @UNPUBLISHED{Seemann2016, author = "Seemann T", title = "ABRicate: mass screening of contigs for antiobiotic resistance genes", year = "2016", note = "https://github.com/tseemann/abricate"} </citation> </citations> </tool>