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"planemo upload for repository https://github.com/TGAC/earlham-galaxytools/tree/master/tools/lotus2 commit 187ff34ae1ea6f850882ef0fbbc80dbb3ffc2a24"
author | earlhaminst |
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date | Wed, 19 May 2021 02:38:24 +0000 |
parents | 478e767a0e7a |
children | cf56a6553385 |
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<tool id="lotus2" name="LotuS2" version="@VERSION@" profile="20.01"> <description>fast OTU processing pipeline</description> <macros> <token name="@VERSION@">2.05.1</token> <xml name="refDB_macro"> <param argument="-refDB" type="select" label="Reference Database"> <option value="SLV" selected="true">Silva LSU (23/28S) or SSU (16/18S) (SLV)</option> <option value="GG">Greengenes (GG)</option> <option value="UNITE">ITS focused on fungi (UNITE)</option> <option value="PR2">SSU focused on Protists (PR2)</option> <option value="beetax">Bee gut specific database and tax names (beetax)</option> <option value="HITdb">Human gut microbiota (HITdb)</option> </param> </xml> </macros> <requirements> <requirement type="package" version="@VERSION@">lotus2</requirement> </requirements> <version_command>lotus2 --version</version_command> <command detect_errors="exit_code"><![CDATA[ mkdir input && #if $inputs.paired_or_single == 'single': #for i, f in enumerate($inputs.input): #set ext = $f.ext.replace('sanger', '') ln -s '$f' 'input/input${i}.${ext}' && #end for #elif $inputs.paired_or_single == 'paired': #for i, f in enumerate($inputs.left_input): #set ext = $f.ext.replace('sanger', '') ln -s '$f' 'input/input${i}.1.${ext}' && #end for #for i, f in enumerate($inputs.right_input): #set ext = $f.ext.replace('sanger', '') ln -s '$f' 'input/input${i}.2.${ext}' && #end for #else: #for i, f in enumerate($inputs.pair_input): #set ext = $f.forward.ext.replace('sanger', '') ln -s '$f.forward' 'input/input${i}.1.${ext}' && #set ext = $f.reverse.ext.replace('sanger', '') ln -s '$f.reverse' 'input/input${i}.2.${ext}' && #end for #end if lotus2 -create_map mapping.txt -i input/ && cat mapping.txt && lotus2 -i input/ -o output -tmpDir tmp_folder -threads "\${GALAXY_SLOTS:-1}" -map mapping.txt -platform $platform #if $barcode: -barcode '$barcode' #end if #if $forwardPrimer: -forwardPrimer '$forwardPrimer' #end if #if $reversePrimer: -reversePrimer '$reversePrimer' #end if -clustering $clu_args.clustering -id $clu_args.id #if $clu_args.derepMin: -derepMin '$clu_args.derepMin' #end if -deactivateChimeraCheck $clu_args.deactivateChimeraCheck -chim_skew $clu_args.chim_skew -readOverlap $clu_args.readOverlap -taxAligner $tax_args.aligner_cond.taxAligner #if $tax_args.aligner_cond.taxAligner == '0': -rdp_thr $tax_args.aligner_cond.rdp_thr #elif $tax_args.aligner_cond.taxAligner == '3': -utax_thr $tax_args.aligner_cond.utax_thr #else: -refDB $tax_args.aligner_cond.refDB #end if -amplicon_type $tax_args.amplicon_type -tax_group $tax_args.tax_group -keepUnclassified $tax_args.keepUnclassified -useBestBlastHitOnly $tax_args.useBestBlastHitOnly -LCA_cover $tax_args.LCA_cover -LCA_frac $tax_args.LCA_frac -greengenesSpecies $tax_args.greengenesSpecies ; EXIT_VALUE=\$? ; tar -cvzf output.tar.gz output/ && exit \$EXIT_VALUE ]]></command> <inputs> <conditional name="inputs"> <param name="paired_or_single" type="select" label="Paired or Single-end data?"> <option value="single" selected="true">Single-end</option> <option value="paired">Paired-end</option> <option value="paired_collection">Paired-end collection</option> </param> <when value="single"> <param name="input" type="data" format="fastqsanger,fastqsanger.gz" multiple="true" label="Single-end reads" /> </when> <when value="paired"> <param name="left_input" type="data" format="fastqsanger,fastqsanger.gz" multiple="true" label="Left/Forward strand reads" /> <param name="right_input" type="data" format="fastqsanger,fastqsanger.gz" multiple="true" label="Right/Reverse strand reads" /> </when> <when value="paired_collection"> <param name="pair_input" type="data_collection" collection_type="list:paired" format="fastqsanger,fastqsanger.gz" label="List of paired reads" /> </when> </conditional> <param argument="-platform" type="select" label="Sequencing platform"> <option value="miSeq" selected="true">miSeq</option> <option value="hiSeq">hiSeq</option> <option value="454">454</option> <option value="PacBio">PacBio</option> </param> <param argument="-barcode" type="data" format="fastqsanger" optional="true" label="Barcode (MID) sequences (optional)" help="FASTQ file with barcodes (in the processed mi/hiSeq format), if provided by the sequencer" /> <param argument="-forwardPrimer" type="text" value="" label="Forward primer used to amplify DNA region" help="E.g. 16S primer fwd" /> <param argument="-reversePrimer" type="text" value="" label="Reverse primer used to amplify DNA region" help="E.g. 16S primer rev" /> <section name="clu_args" title="Clustering Options"> <param argument="-clustering" type="select" label="Clustering algorithm"> <option value="1">UPARSE</option> <option value="2">swarm</option> <option value="3">cd-hit</option> <option value="6">unoise3</option> <option value="7" selected="true">dada2</option> </param> <param argument="-id" type="float" min="0" max="1" value="0.97" label="Clustering threshold for OTUs" /> <param argument="-derepMin" type="text" value="" label="Minimum size of dereplicated raw reads" help="E.g. 4:1,4:2,3:3 . See http://lotus2.earlham.ac.uk/images/Derep_options.pdf for how to specify this parameter" /> <param argument="-deactivateChimeraCheck" type="select" label="Chimera check"> <option value="0" selected="true">OTU chimera checks</option> <option value="1">No chimera check at all</option> <option value="2">Deactivate deNovo chimera check</option> <option value="3">Deactivate ref based chimera check</option> </param> <param argument="-chim_skew" type="integer" min="0" value="2" label="Skew in chimeric fragment abundance" /> <param argument="-readOverlap" type="integer" min="0" value="300" label="Maximum number of basepairs that two reads are overlapping" /> </section> <section name="tax_args" title="Taxonomy Options"> <conditional name="aligner_cond"> <param argument="-taxAligner" type="select" label="Taxonomy aligner"> <option value="0" selected="true">Deactivated (just use RDP)</option> <option value="1">Blast</option> <option value="2">Use LAMBDA to search against a 16S reference database for taxonomic profiling of OTUs</option> <option value="3">Use UTAX with custom databases</option> <option value="4">Use VSEARCH to align OTUs to custom databases</option> </param> <when value="0"> <param argument="-rdp_thr" type="float" min="0" max="1" value="0.8" label="Confidence threshold for RDP"/> </when> <when value="1"> <expand macro="refDB_macro" /> </when> <when value="2"> <expand macro="refDB_macro" /> </when> <when value="3"> <param argument="-utax_thr" type="float" min="0" max="1" value="0.8" label="Confidence threshold for UTAX"/> </when> <when value="4"> <expand macro="refDB_macro" /> </when> </conditional> <param argument="-amplicon_type" type="select" label="Amplicon type"> <option value="LSU">LSU Large subunit (23S/28S)</option> <option value="SSU" selected="true">SSU small subunit (16S/18S)</option> <option value="ITS">ITS internal transcribed spacer</option> <option value="ITS1">ITS1</option> <option value="ITS2">ITS2</option> </param> <param argument="-tax_group" type="select" label="Tax group"> <option value="bacteria" selected="true">bacterial 16S rDNA annnotation</option> <option value="fungi">fungal 18S/23S/ITS annotation</option> </param> <param argument="-keepUnclassified" type="boolean" truevalue="1" falsevalue="0" checked="true" label="Keep unclassified OTUs" help="Includes unclassified OTUs (i.e. no match in RDP/Blast database) in OTU and taxa abundance matrix calculations" /> <param argument="-useBestBlastHitOnly" type="boolean" truevalue="1" falsevalue="0" checked="false" label="Use best blast hit only" help="If selected, do not use LCA (lowest common ancestor) to determine most likely taxonomic level (not recommended)" /> <param argument="-LCA_cover" type="float" min="0" max="1" value="0.9" label="Minimum horizontal coverage of an OTU sequence against ref DB"/> <param argument="-LCA_frac" type="float" min="0" max="1" value="0.9" label="Minimum fraction of reads with identical taxonomy"/> <param argument="-greengenesSpecies" type="boolean" truevalue="1" falsevalue="0" checked="false" label="Create greengenes output labels instead of OTU" /> </section> </inputs> <outputs> <data name="otu" format="tabular" label="${tool.name} on ${on_string}: OTU abundance matrix" from_work_dir="output/OTU.txt" /> <data name="otu_biom" format="biom" label="${tool.name} on ${on_string}: biom-formatted OTU abundance matrix" from_work_dir="output/OTU.biom" /> <data name="otu_fna" format="fasta" label="${tool.name} on ${on_string}: FASTA-formatted extended OTU seed sequences" from_work_dir="output/OTU.fna" /> <data name="OTUphylo_nwk" format="newick" label="${tool.name} on ${on_string}: Newick-formatted phylogenetic tree between sequences" from_work_dir="output/OTUphylo.nwk" /> <data name="hiera_blast" format="tabular" label="${tool.name} on ${on_string}: OTU taxonomy assignments based on Blastn" from_work_dir="output/hiera_BLAST.txt" /> <data name="hiera_rdp" format="tabular" label="${tool.name} on ${on_string}: OTU taxonomy assignments based on RDP classifier" from_work_dir="output/hiera_RDP.txt" /> <data name="primary" format="tar" label="${tool.name} on ${on_string}: All output files" from_work_dir="output.tar.gz" /> </outputs> <tests> <test> <param name="paired_or_single" value="single"/> <param name="input" value="Anh_sample1.fastq.gz,Anh_sample2.fastq.gz" ftype="fastqsanger.gz"/> <param name="platform" value="454" /> <param name="clustering" value="3" /> <output name="otu" file="OTU.txt" compare="sim_size" /> <output name="otu_fna" file="OTU.fna" compare="sim_size" /> <output name="hiera_rdp" file="hiera_RDP.txt" compare="sim_size" /> </test> </tests> <help><![CDATA[ If you have separate FASTA and quality files, these can be combined in a FASTQ file using the "Combine FASTA and QUAL into FASTQ" tool. Documentation can be found at `<http://lotus2.earlham.ac.uk/>`_. ]]></help> <citations> <citation type="doi">10.1186/s40168-021-01012-1</citation> </citations> </tool>