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planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mothur commit a9d1e0debcd357d8080a1c6c5f1d206dd45a7a4d
author | iuc |
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date | Fri, 19 May 2017 05:03:09 -0400 |
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children | 82e91bb188b2 |
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<tool profile="16.07" id="mothur_make_sra" name="Make.sra" version="@WRAPPER_VERSION@.0"> <description>creates the necessary files for a NCBI submission</description> <macros> <import>macros.xml</import> </macros> <expand macro="requirements"/> <expand macro="stdio"/> <expand macro="version_command"/> <command><![CDATA[ @SHELL_OPTIONS@ ## create symlinks to input datasets ln -s "$project" project.dat && ln -s "$sff" sff.dat && ln -s "$oligos" oligos.dat && ln -s "$mimark" mimark.dat && ln -s "$fastq" fastq.dat && echo 'make.sra( project=project.dat, sff=sff.dat, oligos=oligos.dat, mimark=mimark.dat, #if $fastq: fastq=fastq.dat, #end if bdiffs=$bdiffs, pdiffs=$pdiffs, tdiffs=$tdiffs, ldiffs=$ldiffs, sdiffs=$sdiffs, checkorient=$checkorient, orientation=$orientation, platform=$platform, instrument=$instrument, libstrategy=$libstrategy, libselection=$libselection, libsource=$libsource, datatype=$datatype )' | sed 's/ //g' ## mothur trips over whitespace | mothur | tee mothur.out.log ]]></command> <inputs> <param name="project" type="data" format="tabular" label="Project file"/> <param name="sff" type="data" format="sff" label="sff - provide the original sff file"/> <param name="oligos" type="data" format="mothur.oligos" label="oligos - provide an oligos file to parse your sff or fastq file by. It is required and must contain barcodes and primers"/> <param name="mimark" type="data" format="txt" label="mimarks file - you can create the template for this file using the get.mimarkspackage command"/> <param name="fastq" type="data" optional="true" format="fastq" label="fastq - provide the original fastq file"/> <param name="bdiffs" type="integer" value="0" min="0" label="bdiffs - number of differences to allow in the barcode (must be > 0; default 0)"/> <param name="pdiffs" type="integer" value="0" min="0" label="pdiffs - number of differences to allow in the primer (must be > 0; default 0)"/> <param name="tdiffs" type="integer" value="0" min="0" label="tdiffs - total number of differences to allow in primer and barcode (must be > 0; default 0)"/> <param name="ldiffs" type="integer" value="0" min="0" label="ldiffs - total number of differences to allow in linker sequence (must be > 0; default 0)"/> <param name="sdiffs" type="integer" value="0" min="0" label="sdiffs - total number of differences to allow in spacer sequence (must be > 0; default 0)"/> <param name="checkorient" type="boolean" truevalue="true" falsevalue="false" checked="false" label="checkorient - will check for the reverse compliment of the barcode or primer in the sequence. The default is false."/> <param name="orientation" type="select" label="orientation - specify the sequence orientation"> <option value="forward" selected="true">forward</option> <option value="reverse">reverse</option> </param> <param name="platform" type="select" label="platform - specify platform you are using" help="This is a controlled vocabulary section in the XML file that will be generated"> <option value="_LS454" selected="true">454 (_LS454)</option> <option value="ILLUMINA">Illumina (ILLUMINA)</option> <option value="ION_TORRENT">Ion Torrent (ION_TORRENT)</option> <option value="PACBIO_SMRT">PacBio (PACBIO_SMRT)</option> </param> <param name="instrument" type="select" label="instrument - specify instrument" help="This is a controlled vocabulary section in the XML file that will be generated"> <option value="454_GS" selected="true">454_GS</option> <option value="454_GS_20">454_GS_20</option> <option value="454_GS_FLX">454_GS_FLX</option> <option value="454_GS_FLX_Titanium">454_GS_FLX_Titanium</option> <option value="454_GS_Junior">454_GS_Junior</option> <option value="Illumina_Genome_Analyzer">Illumina_Genome_Analyzer</option> <option value="Illumina_Genome_Analyzer_II">Illumina_Genome_Analyzer_II</option> <option value="Illumina_Genome_Analyzer_IIx">Illumina_Genome_Analyzer_IIx</option> <option value="Illumina_HiSeq_2000">Illumina_HiSeq_2000</option> <option value="Illumina_HiSeq_1000">Illumina_HiSeq_1000</option> <option value="Illumina_MiSeq">Illumina_MiSeq</option> <option value="PacBio_RS">PacBio_RS</option> <option value="Ion_Torrent_PGM">Ion_Torrent_PGM</option> <option value="unspecified">unspecified</option> </param> <param name="libstrategy" type="select" label="libstrategy - specify library strategy" help="This is a controlled vocabulary section in the XML file that will be generated"> <option value="AMPLICON" selected="true">AMPLICON</option> <option value="WGA">WGA</option> <option value="WGS">WGS</option> <option value="RNA-Seq">RNA-Seq</option> <option value="miRNA-Se">miRNA-Se</option> <option value="WCS">WCS</option> <option value="CLONE">CLONE</option> <option value="POOLCLONE">POOLCLONE</option> <option value="CLONEEND">CLONEEND</option> <option value="FINISHING">FINISHING</option> <option value="ChIP-Seq">ChIP-Seq</option> <option value="MNase-Seq">MNase-Seq</option> <option value="DNase-Hypersensitivity">DNase-Hypersensitivity</option> <option value="Bisulfite-Seq">Bisulfite-Seq</option> <option value="Tn-Seq">Tn-Seq</option> <option value="EST">EST</option> <option value="FL-cDNA">FL-cDNA</option> <option value="CTS">CTS</option> <option value="MRE-Seq">MRE-Seq</option> <option value="MeDIP-Seq">MeDIP-Seq</option> <option value="MBD-Seq">MBD-Seq</option> <option value="OTHER">OTHER</option> </param> <param name="libsource" type="select" label="libsource - specify library source" help="This is a controlled vocabulary section in the XML file that will be generated"> <option value="METAGENOMIC" selected="true">METAGENOMIC</option> <option value="GENOMIC">GENOMIC</option> <option value="TRANSCRIPTOMIC">TRANSCRIPTOMIC</option> <option value="METATRANSCRIPTOMIC">METATRANSCRIPTOMIC</option> <option value="SYNTHETIC">SYNTHETIC</option> <option value="VIRAL_RNA">VIRAL_RNA</option> <option value="OTHER">OTHER</option> </param> <param name="libselection" type="select" label="libselection - specify library selection" help="This is a controlled vocabulary section in the XML file that will be generated"> <option value="PCR" selected="true">PCR</option> <option value="RANDOM">RANDOM</option> <option value="RANDOM_PCR">RANDOM_PCR</option> <option value="RT-PCR">RT-PCR</option> <option value="HMPR">HMPR</option> <option value="MF">MF</option> <option value="CF-S">CF-S</option> <option value="CF-H">CF-H</option> <option value="CF-T">CF-T</option> <option value="CF-M">CF-M</option> <option value="MDA">MDA</option> <option value="MSLL">MSLL</option> <option value="cDNA">cDNA</option> <option value="ChIP">ChIP</option> <option value="MNase">MNase</option> <option value="Hybrid_Selection">Hybrid_Selection</option> <option value="Reduced_Representation">Reduced_Representation</option> <option value="Restriction_Digest">Restriction_Digest</option> <option value="5-methylcytidine_antibody">5-methylcytidine_antibody</option> <option value="MBD2_protein_methyl-CpG_binding_domain">MBD2_protein_methyl-CpG_binding_domain</option> <option value="CAGE">CAGE</option> <option value="RACE">RACE</option> <option value="size_fractionation">size_fractionation</option> <option value="Padlock_probes_capture_method">Padlock_probes_capture_method</option> <option value="other">other</option> </param> <param name="datatype" type="select" label="datatype - specify datatype" help="This is a controlled vocabulary section in the XML file that will be generated"> <option value="METAGENOME" selected="true">METAGENOME</option> <option value="GENOME_SEQUENCING">GENOME_SEQUENCING</option> <option value="METAGENOMIC_ASSEMBLY">METAGENOMIC_ASSEMBLY</option> <option value="ASSEMBLY">ASSEMBLY</option> <option value="TRANSCRIPTOME">TRANSCRIPTOME</option> <option value="PROTEOMIC">PROTEOMIC</option> <option value="MAP">MAP</option> <option value="CLONE_ENDS">CLONE_ENDS</option> <option value="TARGETED_LOCI">TARGETED_LOCI</option> <option value="RANDOM_SURVEY">RANDOM_SURVEY</option> <option value="EXOME">EXOME</option> <option value="VARIATION">VARIATION</option> <option value="EPIGENOMICS">EPIGENOMICS</option> <option value="PHENOTYPE">PHENOTYPE</option> <option value="GENOTYPE">GENOTYPE</option> <option value="OTHER">OTHER</option> </param> </inputs> <outputs> <expand macro="logfile-output"/> <data name="fasta_out" format="fasta" from_work_dir="sff*.fasta" label="${tool.name} on ${on_string}: fasta"/> <data name="qual_out" format="qual" from_work_dir="sff*.qual" label="${tool.name} on ${on_string}: qual"/> <data name="flow_out" format="mothur.sff.flow" from_work_dir="sff*.flow" label="${tool.name} on ${on_string}: flow"/> <data name="scrap_sff" format="sff" from_work_dir="sff*.scrap.sff" label="${tool.name} on ${on_string}: scrap sff"/> <data name="submission_xml" format="xml" from_work_dir="submission.xml" label="${tool.name} on ${on_string}: submission.xml"/> </outputs> <tests> <test><!-- test with defauts --> <param name="project" value="makesra.project" ftype="tabular"/> <param name="sff" value="Fasting_Example1.sff" ftype="sff"/> <param name="oligos" value="GQY1XT001.oligos" ftype="mothur.oligos"/> <param name="mimark" value="biosample.tsv" ftype="tabular"/> <output name="fasta_out" md5="212fa15e1ed077cecb65ee87f17ef2e1" ftype="fasta"/> <output name="qual_out" md5="ffcc4831369139055e1b8e9add9a59c0" ftype="qual"/> <output name="flow_out" md5="34b17477f98ab19c1ff755a61848d968" ftype="mothur.sff.flow"/> <output name="scrap_sff" ftype="sff"> <assert_contents> <has_text text="FLP3FBN01ELBSX"/> </assert_contents> </output> <output name="submission_xml" ftype="xml"> <assert_contents> <has_text text="Submission"/> <has_text text="Attribute"/> <has_text text="BioProject"/> </assert_contents> </output> <expand macro="logfile-test"/> </test> </tests> <help> <![CDATA[ @MOTHUR_OVERVIEW@ **Command Documentation** The make.sra_ creates the necessary files for a NCBI submission. .. _make.sra: https://www.mothur.org/wiki/Make.sra ]]> </help> <citations> <citation type="doi">10.1128/AEM.01541-09</citation> </citations> </tool>