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"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mitos commit 791f28c8a7194fdd1ecec05ad166932d461899b2"
author | iuc |
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date | Fri, 27 Mar 2020 17:53:04 -0400 |
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children | 1f4933f5a323 |
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<tool id="mitos" name="@MITOS_NAME@" version="@MITOS_VERSION@" profile="20.01"> <description>de-novo annotation of metazoan mitochondrial genomes</description> <macros> <import>macros.xml</import> <token name="@MITOS_NAME@">MITOS</token> <token name="@MITOS_VERSION@">1.0.5</token> </macros> <requirements> <requirement type="package" version="@MITOS_VERSION@">mitos</requirement> <requirement type="package">zip</requirement> </requirements> <version_command>python -c "import mitos; print(mitos.__version__)"</version_command> <command detect_errors="aggressive"><![CDATA[ mkdir outdir && runmitos.py --input '$input' --code $code --outdir outdir --refdir '$refdir.fields.path' #for tpe in ["prot", "trna", "rrna"] #if not $tpe in str($advanced.featuretypes).split(',') --no$tpe #end if #end for --finovl $advanced.finovl --evalue $advanced_prot.evalue --cutoff $advanced_prot.cutoff #set maxovl=float($advanced_prot.maxovl)/100.0 --maxovl $maxovl --clipfac $advanced_prot.clipfac #set fragovl=float($advanced_prot.fragovl)/100.0 --fragovl $fragovl --fragfac $advanced_prot.fragfac --ststrange $advanced_prot.ststrange #if "raw" in str($addoutputs).split(','): && zip -9 -y -r output.zip outdir/ > /dev/null #end if ]]></command> <inputs> <param argument="--input" label="sequence" type="data" format="fasta" help="a single sequence in fasta formated sequence"> <options options_filter_attribute="metadata.sequences"> <filter type="add_value" value="1"/> </options> </param> <param argument="--code" label="Genetic code" type="select"> <option value="2">Vertebrate (2)</option> <option value="4">Mold, Protozoan, Coelenteral (4)</option> <option value="5">Invertebrate (5)</option> <option value="9">Echinoderm, Flatworm (9)</option> <option value="13">Ascidian (13)</option> <option value="14">Alternative Flatworm (14)</option> </param> <param argument="--refdir" label="Reference data" type="select" help="contact the administrator of this Galaxy instance if you miss reference data"> <options from_data_table="mitos"> <filter type="static_value" value="mitos" column="2"/> </options> <validator message="No reference annotation is available for MITOS" type="no_options" /> </param> <param name="addoutputs" type="select" multiple="true" label="Outputs"> <option value="bed" selected="true">BED</option> <option value="mito" selected="false">mito</option> <option value="gff" selected="false">GFF file</option> <option value="seq" selected="false">SEQ</option> <option value="fas" selected="false">nucleotide FASTA</option> <option value="faa" selected="false">protein FASTA</option> <option value="geneorder" selected="false">geneorder</option> <option value="protein_plot" selected="false">Protein prediction plot</option> <option value="ncRNA_plot" selected="false">ncRNA prediction plot</option> <!--<option value="ncRNA_structure_ps_plots" selected="false">ncRNA structure plots - postscript</option>--> <option value="ncRNA_structure_svg_plots" selected="false">ncRNA structure plots - svg</option> <option value="raw" selected="false">zipped raw results</option> </param> <section name="advanced" title="Advanced options"> <param name="featuretypes" label="Feature types" help="Feature types that should be predicted by MITOS (--noprot,--notrna,--norrna)" type="select" multiple="true"> <option value="prot" selected="true">Protein coding genes</option> <option value="trna" selected="true">tRNAs</option> <option value="rrna" selected="true">rRNAs</option> </param> <param argument="--finovl" label="Final overlap (nt)" help="Maximum number of nucleotides by which genes of different types may overlap" type="integer" value="35" min="0"/> </section> <section name="advanced_prot" title="Advanced options for protein coding gene prediction"> <param argument="--evalue" label="BLAST E-value Exponent" help="Negation of the exponent of the E-value threshold used by BLAST, i.e. a value X gives an E-value of 10^(-X)" type="float" value="2" min="0"/> <param argument="--cutoff" label="Quality cutoff" help="Minimum allowed quality in % of the maximum quality value per reading frame" type="integer" value="50" min="0" max="100"/> <param argument="--maxovl" label="Maximum overlap" help="Maximum allowed overlap of proteins in percent of the smaller feature " type="integer" value="20" min="0" max="100"/> <param argument="--clipfac" label="Clipping factor" help="Clip overlapping proteins with the same name that differ by less than the specified factor" type="float" value="10" min="0"/> <param argument="--fragovl" label="Fragment overlap" help="Maximum allowed overlap of proteins in the query (in percent of the shorter query range) for two hits to be counted as fragments of the same gene" type="integer" value="20" min="0" max="100"/> <param argument="--fragfac" label="Fragment quality factor" help="Maximum factor by which fragments of the same protein may differ in their quality" type="float" value="10"/> <param argument="--ststrange" label="Start/stop range" help="Number of aminoacids searched for start and stop codon of proteins" type="integer" value="6"/> </section> </inputs> <outputs> <data name="bedout" format="bed" from_work_dir="outdir/result.bed"> <filter>"bed" in str(addoutputs)</filter> </data> <data name="mitoout" format="tabular" from_work_dir="outdir/result" label="${tool.name} on ${on_string}: mito"> <filter>"mito" in str(addoutputs)</filter> </data> <data name="gffout" format="gff" from_work_dir="outdir/result.gff" label="${tool.name} on ${on_string}: GFF"> <filter>"gff" in str(addoutputs)</filter> </data> <data name="seqout" format="txt" from_work_dir="outdir/result.seq" label="${tool.name} on ${on_string}: TBL"> <filter>"seq" in str(addoutputs)</filter> </data> <data name="fasout" format="fasta" from_work_dir="outdir/result.fas" label="${tool.name} on ${on_string}: nt FASTA"> <filter>"fas" in str(addoutputs)</filter> </data> <data name="faaout" format="fasta" from_work_dir="outdir/result.faa" label="${tool.name} on ${on_string}: aa FASTA"> <filter>"faa" in str(addoutputs)</filter> </data> <data name="geneorderout" format="fasta" from_work_dir="outdir/result.geneorder" label="${tool.name} on ${on_string}: geneorder"> <filter>"geneorder" in str(addoutputs)</filter> </data> <data name="protein_plot_out" format="pdf" from_work_dir="outdir/plots/prot.pdf" label="${tool.name} on ${on_string}: Protein prediction plot"> <filter>"protein_plot" in str(addoutputs)</filter> </data> <data name="ncRNA_plot_out" format="pdf" from_work_dir="outdir/plots/rna.pdf" label="${tool.name} on ${on_string}: ncRNA prediction plot"> <filter>"protein_plot" in str(addoutputs)</filter> </data> <!--<collection name="ncRNA_structure_plot_ps_out" type="list" label="${tool.name} on ${on_string}: ncRNA postscript structure plots"> <discover_datasets pattern="(?P<name>.+)\.ps" format="ps" directory="outdir/plots" /> <filter>"ncRNA_structure_ps_plots" in str(addoutputs)</filter> </collection>--> <collection name="ncRNA_structure_plot_svg_out" type="list" label="${tool.name} on ${on_string}: ncRNA svg structure plots"> <discover_datasets pattern="(?P<name>.+)\.svg" format="svg" directory="outdir/plots" /> <filter>"ncRNA_structure_svg_plots" in str(addoutputs)</filter> </collection> <data name="rawout" format="zip" from_work_dir="output.zip" label="${tool.name} on ${on_string}: raw data"> <filter>"raw" in str(addoutputs)</filter> </data> </outputs> <tests> <!-- default options --> <test expect_num_outputs="1"> <param name="input" value="NC_012920.fasta"/> <param name="code" value="2"/> <param name="refdir" value="mitos1-refdata" /> <output name="bedout" file="NC_012920.bed" ftype="bed"/> <assert_command> <has_text text="--code 2"/> <has_text text="--finovl 35"/> <has_text text="--evalue 2.0"/> <has_text text="--cutoff 50"/> <has_text text="--maxovl 0.2"/> <has_text text="--clipfac 10.0"/> <has_text text="--fragovl 0.2"/> <has_text text="--fragfac 10.0"/> <has_text text="--ststrange 6"/> </assert_command> </test> <!-- default options, add outputs --> <test expect_num_outputs="11"> <param name="input" value="NC_012920.fasta"/> <param name="code" value="2"/> <param name="refdir" value="mitos1-refdata" /> <param name="addoutputs" value="bed,mito,gff,seq,fas,faa,raw,geneorder,protein_plot,ncRNA_plot,ncRNA_structure_svg_plots"/> <output name="bedout" file="NC_012920.bed" ftype="bed"/> <output name="mitoout" file="NC_012920.mito" ftype="tabular" /> <output name="gffout" file="NC_012920.gff" ftype="gff" /> <output name="seqout" file="NC_012920.seq" ftype="txt" /> <output name="fasout" file="NC_012920.fas" ftype="fasta" /> <output name="faaout" file="NC_012920.faa" ftype="fasta" /> <output name="rawout" ftype="zip"> <assert_contents> <has_archive_member path=".*/result.bed"/> </assert_contents> </output> <output name="geneorderout" file="NC_012920.geneorder" ftype="fasta" /> <output name="protein_plot_out" file="NC_012920_prot.pdf" ftype="pdf" compare="sim_size"/> <output name="ncRNA_plot_out" file="NC_012920_ncrna.pdf" ftype="pdf" compare="sim_size"/> <output_collection name="ncRNA_structure_plot_svg_out" type="list" count="24"> <element name="trnA-5586-5654" file="NC_012920_trnA.svg" ftype="svg" /> </output_collection> <assert_command> <has_text text="--code 2"/> <has_text text="--finovl 35"/> <has_text text="--evalue 2.0"/> <has_text text="--cutoff 50"/> <has_text text="--maxovl 0.2"/> <has_text text="--clipfac 10.0"/> <has_text text="--fragovl 0.2"/> <has_text text="--fragfac 10.0"/> <has_text text="--ststrange 6"/> </assert_command> </test> <!-- no rRNA, and advanced options --> <test expect_num_outputs="1"> <param name="input" value="NC_012920.fasta"/> <param name="code" value="2"/> <param name="refdir" value="mitos1-refdata" /> <param name="advanced|featuretypes" value="prot,trna" /> <param name="advanced|finovl" value="50" /> <output name="bedout" file="NC_012920.bed" ftype="bed" compare="sim_size"/> <assert_command> <has_text text="--code 2"/> <has_text text="--norrna"/> <has_text text="--finovl 50"/> </assert_command> </test> <!-- no rRNA, no tRNA; advanced protein options --> <test expect_num_outputs="1"> <param name="input" value="NC_012920.fasta"/> <param name="code" value="5"/> <param name="refdir" value="mitos1-refdata" /> <param name="advanced|featuretypes" value="prot" /> <param name="advanced_prot|evalue" value="3"/> <param name="advanced_prot|cutoff" value="40"/> <param name="advanced_prot|maxovl" value="30"/> <param name="advanced_prot|clipfac" value="5"/> <param name="advanced_prot|fragovl" value="15"/> <param name="advanced_prot|fragfac" value="11"/> <param name="advanced_prot|ststrange" value="12"/> <param name="addoutputs" value="bed"/> <output name="bedout" file="NC_012920.bed" ftype="bed" compare="sim_size"/> <assert_command> <has_text text="--code 5"/> <has_text text="--evalue 3"/> <has_text text="--cutoff 40"/> <has_text text="--maxovl 0.3"/> <has_text text="--clipfac 5.0"/> <has_text text="--fragovl 0.15"/> <has_text text="--fragfac 11.0"/> <has_text text="--ststrange 12"/> </assert_command> </test> </tests> <help> @COMMON_HELP@ <![CDATA[ ]]></help> <citations> <citation type="doi">10.1016/j.ympev.2012.08.023</citation> </citations> </tool>