view macros.xml @ 19:128ba8da994f draft default tip

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/nextclade commit c41319b6593caa0a11835f5e8bc48b1f1e316ff8
author iuc
date Sat, 08 Oct 2022 20:03:50 +0000
parents 07ab9bd68a02
children
line wrap: on
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<macros>
    <!-- same version number is used for nextclade and nextalign releases, even though they are distinct tools -->
    <token name="@TOOL_VERSION@">2.7.0</token>
    <xml name="citations">
        <citations>
            <citation type="bibtex">@online{nextclade,
                title={nextclade},
                year = 2021,
                url = {https://github.com/nextstrain/nextclade},
                urldate = {2021-03-26}
                }
            </citation>
            <yield/>
        </citations>
    </xml>
    <!--
        command
    -->
    <token name="@REF_FASTA@"><![CDATA[
    #if $reference_source.reference_source_selector == 'history':
        ln -f -s '$reference_source.ref_file' reference.fa &&
    #else:
        ln -f -s '$reference_source.ref_file.fields.path' reference.fa &&
    #end if
]]></token>
    <token name="@QUERY_FASTA@"><![CDATA[
    #if $input_fasta.is_of_type('fasta.gz')
        #set $query = 'query.fa.gz'
    #else
        #set $query = 'query.fa'
    #end if
    ln -s '$input_fasta' $query &&    
]]></token>
    <!--
        inputs
    -->
    <xml name="reference">
        <conditional name="reference_source">
            <param name="reference_source_selector" type="select" label="Choose the source for the reference genome">
                <option value="cached">Use a built-in genome</option>
                <option value="history">Use a genome from history</option>
            </param>
            <when value="cached">
                <param name="ref_file" type="select" label="Using reference genome" help="Select genome from the list">
                    <options from_data_table="all_fasta">
                        <filter type="sort_by" column="2"/>
                    </options>
                    <validator type="no_options" message="A built-in reference genome is not available for the build associated with the selected input file"/>
                </param>
            </when>
            <when value="history">
                <param name="ref_file" type="data" format="fasta" label="Use the following dataset as the reference sequence" help="You can upload a FASTA sequence to the history and use it as reference"/>
            </when>
        </conditional>
    </xml>
    <!--
        help
    -->
    <token name="@NEXTCLADE@"><![CDATA[
Nextclade is a tool that identifies differences between your sequences and a reference sequence, uses these differences to assign your sequences to clades, and reports potential sequence quality issues in your data.
You can use the tool to analyze sequences before you upload them to a database, or if you want to assign Nextstrain clades to a set of sequences.
]]></token>
    <xml name="column_metadata" tokens="dataset_name" token_extra_columns="">
        <!-- the columns in use are dependent on the dataset (i.e. database) - and extra columns seem to always be added in the same place -->
        <!-- note that the tool is assuming that the dataset columns remain static: this might be an incorrect assumption in the future -->
        <when value="@DATASET_NAME@">
            <action name="column_names" type="metadata" default="seqName,clade,@EXTRA_COLUMNS@qc.overallScore,qc.overallStatus,totalSubstitutions,totalDeletions,totalInsertions,totalFrameShifts,totalAminoacidSubstitutions,totalAminoacidDeletions,totalAminoacidInsertions,totalMissing,totalNonACGTNs,totalPcrPrimerChanges,substitutions,deletions,insertions,privateNucMutations.reversionSubstitutions,privateNucMutations.labeledSubstitutions,privateNucMutations.unlabeledSubstitutions,privateNucMutations.totalReversionSubstitutions,privateNucMutations.totalLabeledSubstitutions,privateNucMutations.totalUnlabeledSubstitutions,privateNucMutations.totalPrivateSubstitutions,frameShifts,aaSubstitutions,aaDeletions,aaInsertions,missing,nonACGTNs,pcrPrimerChanges,alignmentScore,alignmentStart,alignmentEnd,coverage,qc.missingData.missingDataThreshold,qc.missingData.score,qc.missingData.status,qc.missingData.totalMissing,qc.mixedSites.mixedSitesThreshold,qc.mixedSites.score,qc.mixedSites.status,qc.mixedSites.totalMixedSites,qc.privateMutations.cutoff,qc.privateMutations.excess,qc.privateMutations.score,qc.privateMutations.status,qc.privateMutations.total,qc.snpClusters.clusteredSNPs,qc.snpClusters.score,qc.snpClusters.status,qc.snpClusters.totalSNPs,qc.frameShifts.frameShifts,qc.frameShifts.totalFrameShifts,qc.frameShifts.frameShiftsIgnored,qc.frameShifts.totalFrameShiftsIgnored,qc.frameShifts.score,qc.frameShifts.status,qc.stopCodons.stopCodons,qc.stopCodons.totalStopCodons,qc.stopCodons.score,qc.stopCodons.status,isReverseComplement,failedGenes,warnings,errors"/>
        </when>
    </xml>
</macros>