view sort.seqs.xml @ 10:437838af4988 draft default tip

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/mothur commit 7599ef16dc8b83ee49236ed5bb229260c969b0ab

<tool profile="16.07" id="mothur_sort_seqs" name="Sort.seqs" version="@WRAPPER_VERSION@.0">
    <description>put sequences in different files in the same order</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <expand macro="biotools"/>
    <expand macro="requirements"/>
    <expand macro="stdio"/>
    <expand macro="version_command"/>
    <command><![CDATA[
@SHELL_OPTIONS@

## create symlinks to input datasets
ln -s '$fasta_in' fasta_in.dat &&
ln -s '$qfile_in' qfile_in.dat &&
ln -s '$flow_in' flow_in.dat &&
ln -s '$name_in' name_in.dat &&
ln -s '$group_in' group_in.dat &&
ln -s '$tax_in' tax_in.dat &&
ln -s '$accnos' accnos.dat &&
ln -s '$count' count.dat &&

echo 'sort.seqs(
    #if $fasta_in:
        fasta=fasta_in.dat,
    #end if
    #if $qfile_in:
        qfile=qfile_in.dat,
    #end if
    #if $flow_in:
        flow=flow_in.dat,
    #end if
    #if $name_in:
        name=name_in.dat,
    #end if
    #if $group_in:
        group=group_in.dat,
    #end if
    #if $tax_in:
        taxonomy=tax_in.dat,
    #end if
    #if $accnos:
        accnos=accnos.dat,
    #end if
    #if $count:
        count=count.dat,
    #end if
    large=$large
)'
| sed 's/ //g'  ## mothur trips over whitespace
| mothur
| tee mothur.out.log
    ]]></command>
    <inputs>
        <param name="fasta_in" type="data" format="fasta" optional="true" label="fasta - sequences" help="format must be fasta"/>
        <param name="qfile_in" type="data" format="qual454" optional="true" label="qfile - sequence quality" help="format must be qual454"/>
        <param name="flow_in" type="data" format="mothur.sff.flow" optional="true" label="flow - sff flowgram" help="format must be mothur.sff.flow"/>
        <param name="group_in" type="data" format="mothur.groups" optional="true" label="groups - sequence groupings" help="format must be mothur.groups"/>
        <param name="name_in" type="data" format="mothur.names" optional="true" label="names - name reference" help="format must be mothur.names"/>
        <param name="tax_in" type="data" format="mothur.seq.taxonomy" optional="true" label="taxonomy - taxonomy reference" help="format must be mothur.seq.taxonomy"/>
        <param name="accnos" type="data" format="mothur.accnos" optional="true" label="accnos - sort" help="format must be mothur.accnos"/>
        <param name="count" type="data" format="mothur.count_table" optional="true" label="count - a count_table" help="format must be mothur.count_table (generated by count.seqs)"/>
        <param name="large" type="boolean" checked="false" truevalue="true" falsevalue="false" label="large - Datasets are large and may not fit in RAM"/>
        <expand macro="param-savelog"/>
    </inputs>
    <outputs>
        <expand macro="logfile-output"/>
        <data name="fasta_out" format_source="fasta_in" from_work_dir="fasta_in*.sorted.*" label="${tool.name} on ${on_string}: sorted.fasta">
            <filter>fasta_in</filter>
        </data>
        <data name="qfile_out" format_source="qfile_in" from_work_dir="qfile_in*.sorted.*" label="${tool.name} on ${on_string}: sorted.qfile">
            <filter>qfile_in</filter>
        </data>
        <data name="flow_out" format_source="flow_in" from_work_dir="flow_in*.sorted.*" label="${tool.name} on ${on_string}: sorted.flow">
            <filter>flow_in</filter>
        </data>
        <data name="group_out" format_source="group_in" from_work_dir="group_in*.sorted.*" label="${tool.name} on ${on_string}: sorted.group">
            <filter>group_in</filter>
        </data>
        <data name="name_out" format_source="name_in" from_work_dir="name_in*.sorted.*" label="${tool.name} on ${on_string}: sorted.name">
            <filter>name_in</filter>
        </data>
        <data name="taxonomy_out" format_source="tax_in" from_work_dir="tax_in*.sorted.*" label="${tool.name} on ${on_string}: sorted.taxonomy">
            <filter>tax_in</filter>
        </data>
    </outputs>
    <tests>
        <test>
            <param name="fasta_in" value="amazon.fasta" ftype="fasta"/>
            <output name="fasta_out" md5="0bc9320647234e8367c3b1b654f9302d" ftype="fasta"/>
            <param name="savelog" value="true"/>
            <expand macro="logfile-test"/>
        </test>
        <test>
            <param name="qfile_in" value="Mock_S280_L001_R1_001_small.trim.contigs.qual" ftype="qual454"/>
            <output name="qfile_out" md5="abed9d1811786c810a12fd00a376cee4" ftype="qual454"/>
            <param name="savelog" value="true"/>
            <expand macro="logfile-test"/>
        </test>
        <test>
            <param name="group_in" value="amazon.groups" ftype="mothur.groups"/>
            <output name="group_out" md5="fb60628ae445e7b06f9833f632b2cd0c" ftype="mothur.groups"/>
            <param name="savelog" value="true"/>
            <expand macro="logfile-test"/>
        </test>
        <test>
            <param name="fasta_in" value="amazon.fasta" ftype="fasta"/>
            <param name="count" value="amazon.count_table" ftype="mothur.count_table"/>
            <output name="fasta_out" md5="0bc9320647234e8367c3b1b654f9302d" ftype="fasta"/>
            <param name="savelog" value="true"/>
            <expand macro="logfile-test"/>
        </test>
        <test><!-- test with multiple file types input -->
            <param name="fasta_in" value="amazon.fasta" ftype="fasta"/>
            <param name="qfile_in" value="Mock_S280_L001_R1_001_small.trim.contigs.qual" ftype="qual454"/>
            <param name="group_in" value="amazon.groups" ftype="mothur.groups"/>
            <output name="fasta_out" md5="0bc9320647234e8367c3b1b654f9302d" ftype="fasta"/>
            <output name="qfile_out" md5="abed9d1811786c810a12fd00a376cee4" ftype="qual454"/>
            <output name="group_out" md5="fb60628ae445e7b06f9833f632b2cd0c" ftype="mothur.groups"/>
            <param name="savelog" value="true"/>
            <expand macro="logfile-test"/>
        </test>
    </tests>
    <help><![CDATA[

@MOTHUR_OVERVIEW@

**Command Documentation**

The sort.seqs_ command puts sequences from a fasta, name, group, quality, flow or taxonomy file in the same order.
You can provide an accnos file to indicate the order you want, otherwise mothur will use the order of the first file it reads.

.. _sort.seqs: https://www.mothur.org/wiki/Sort.seqs

    ]]></help>
    <expand macro="citations"/>
</tool>