Mercurial > repos > rnateam > mirdeep2
diff mirdeep2.xml @ 0:eaac585f172a draft
Imported from capsule None
author | rnateam |
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date | Tue, 27 Jan 2015 09:06:24 -0500 |
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children | b21be04f52e4 |
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--- /dev/null Thu Jan 01 00:00:00 1970 +0000 +++ b/mirdeep2.xml Tue Jan 27 09:06:24 2015 -0500 @@ -0,0 +1,196 @@ +<tool id="rbc_mirdeep2" name="MiRDeep2" version="2.0.0"> + <description> +<![CDATA[ +identification of novel and known miRNAs +]]> + </description> + <requirements> + <requirement type="package" version="2.0">mirdeep2</requirement> + <requirement type="package" version="2.0">mirdeep2_quantifier</requirement> + <requirement type="package" version="0.12.7">bowtie</requirement> + <requirement type="package" version="5.18.1">perl</requirement> + <requirement type="package" version="1.8.5">vienna_rna</requirement> + <requirement type="package" version="2.023">pdf_api2</requirement> + <requirement type="package" version="2.0">randfold</requirement> + </requirements> + + <command> +<![CDATA[ + miRDeep2.pl + + $reads + $genome + $mappings + + #if $mature_this + $mature_this + #else + none + #end if + + #if $mature_other + $mature_other + #else + none + #end if + + #if $precursors + $precursors + #else + none + #end if + + #if $species.value != 'all' + -t $species + #end if + + #if $star_sequences + -s $star_sequences + #end if + + #if $min_read_stack + -a $min_read_stack + #end if + + #if $min_read_stack + -a $min_read_stack + #end if + + -g $max_precursors_analyze + -b $min_score_cutoff + $disable_randfold + + ; cp result*.bed result.bed 2> /dev/null + ; cp result*.csv result.csv 2> /dev/null + ; cp mirdeep_runs/run*/output.mrd . 2> /dev/null + ; cp mirdeep_runs/run*/survey.csv . 2> /dev/null + + ## html output + ; + cp result*.html $html 2> /dev/null + + ## move pdf directory to be accessible from the new index.html + ; + mkdir -p $html.files_path 2> /dev/null + ; + cp -R pdfs* $html.files_path 2> /dev/null + +]]> + </command> + <stdio> + <!-- Anything other than zero is an error --> + <exit_code range="1:" /> + <exit_code range=":-1" /> + <!-- In case the return code has not been set propery check stderr too --> + <regex match="Error:" /> + <regex match="Exception:" /> + </stdio> + <inputs> + <param name="reads" format="fasta" type="data" label="Collapsed deep sequencing reads"> + <help> +<![CDATA[ +Reads in fasta format. The identifier should contain a prefix, a running +number and a '_x' to indicate the number of reads that have this sequence. +There should be no redundancy in the sequences. +]]> + </help> + </param> + <param name="genome" format="fasta" type="data" label="Genome" help="Genome contigs in fasta format. The identifiers should be unique."/> + <param name="mappings" format="tabular" type="data" label="Mappings" help="Reads mapped against genome. Mappings should be in ARF format."/> + <param name="mature_this" optional="true" format="fasta" type="data" label="Mature miRNA sequences for this species" + help="miRBase miRNA sequences in fasta format. These should be the known mature sequences for the species being analyzed."/> + <param name="mature_other" optional="true" format="fasta" type="data" label="Mature miRNA sequences for related species"> + <help> +<![CDATA[ +miRBase miRNA sequences in fasta format. These should be the pooled known +mature sequences for 1-5 species closely related to the species being analyzed. +]]> + </help> + </param> + <param name="precursors" optional="true" format="fasta" type="data" label="Precursor sequences" + help="miRBase miRNA precursor sequences in fasta format. These should be the known precursor sequences for the species being analyzed."/> + + <param name="species" type="select" label="Search in species" help="If not searching in a specific species all species in your files will be analyzed. (-t)"> + <option value="all">All species</option> + <option value="tni">tetraodon</option> + <option value="dps">d.pseudoobscura</option> + <option value="dya">d.yakuba</option> + <option value="ame">a.mellifera</option> + <option value="dmo">d.mojavensis</option> + <option value="cel">worm</option> + <option value="aga">a.gambiae</option> + <option value="cbr">c.briggsae</option> + <option value="cin">c.intestinalis</option> + <option value="mmu">mouse</option> + <option value="xtr">x.tropicalis</option> + <option value="eca">horse</option> + <option value="cfa">dog</option> + <option value="fru">fugu</option> + <option value="bta">cow</option> + <option value="der">d.erecta</option> + <option value="dgr">d.grimshawi</option> + <option value="gga">chicken</option> + <option value="spu">s.purpuratus</option> + <option value="bfl">lancelet</option> + <option value="ptr">chimp</option> + <option value="dse">d.sechellia</option> + <option value="dpe">d.persimilis</option> + <option value="dvi">d.virilis</option> + <option value="rno">rat</option> + <option value="dme">d.melanogaster</option> + <option value="lca">cat</option> + <option value="sja">c.japonica</option> + <option value="dan">d.ananassae</option> + <option value="hsa">human</option> + <option value="dsi">d.simulans</option> + </param> + <param name="star_sequences" format="fasta" type="data" optional="true" label="Star sequences" help="From miRBase in fasta format (optional) (-s)"/> + + <param name="min_read_stack" optional="true" type="integer" minvalue="0" label="Minimum read stack height"> + <help> +<![CDATA[ +minimum read stack height that triggers analysis. Using this option disables +automatic estimation of the optimal value and all detected precursors are analyzed. (-a) +]]> + </help> + </param> + <param name="max_precursors_analyze" type="integer" value="50000" label="Maximum precursors" + help="Maximum number of precursors to analyze when automatic excision gearing is used. If set to -1 all precursors will be analyzed. (-g)."/> + <param name="min_score_cutoff" type="integer" value="0" label="Minimum miRNA score" + help="Minimum score cut-off for predicted novel miRNAs to be displayed in the overview table. (-b)"/> + <param name="disable_randfold" type="boolean" truevalue="-c" falsevalue="" label="Disable randfold analysis" help="(-c)"/> + </inputs> + <outputs> + <data name="tab_results" format="tabular" from_work_dir="result.csv" label="Tabular output of ${tool.name} on ${on_string}"/> + <data format="html" name="html" label="${tool.name} on ${on_string} (html report)"/> + <data name="pred_acc" format="tabular" from_work_dir="survey.csv" label="Prediction accuracy output of ${tool.name} on ${on_string}"/> + <data name="bed_out" format="bed" from_work_dir="result.bed" label="Bed output of ${tool.name} on ${on_string}"/> + <data name="mrd_out" format="txt" from_work_dir="output.mrd" label="Text output of ${tool.name} on ${on_string}"/> + </outputs> + <tests> + <test> + <param name="reads" value="reads_collapsed.fa"/> + <param name="genome" value="cel_cluster.fa"/> + <param name="mappings" value="reads_collapsed_vs_genome.arf"/> + <param name="mature_this" value="mature_ref_this_species.fa"/> + <param name="mature_other" value="mature_ref_other_species.fa"/> + <param name="precursors" value="precursors_ref_this_species.fa"/> + + <output name="tab_results" file="result.csv" compare="sim_size"/> + <output name="prec_acc" file="survey.csv" compare="sim_size"/> + <output name="bed_out" file="result.bed" compare="sim_size"/> + <output name="mrd_out" file="output.mrd" compare="sim_size"/> + </test> + </tests> + <help> +<![CDATA[ +**What MiRDeep2 does** + +MiRDeep2 is a software package for identification of novel and known miRNAs in deep sequencing data. Furthermore, it can be used for miRNA expression profiling across samples. +]]> + </help> + <citations> + <citation type="doi">10.1093/nar/gkr688</citation> + <citation type="doi">10.1002/0471250953.bi1210s36</citation> + </citations> +</tool>