comparison trycycler_consensus.xml @ 1:07039273d784 draft

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/trycycler commit e88166111fa3b6c57c870ea4cff6e012a1b1a912"

0:e01ad81e86b7

<tool id='trycycler_consensus' name='Trycycler consensus' version='@TOOL_VERSION@' profile='21.01'>
    <description>generate a consensus contig sequence for each cluster</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <expand macro='edam_ontology'/>
    <expand macro='requirements'/>
    <version_command>trycycler --version</version_command>
    <command detect_errors='exit_code'><![CDATA[
        mkdir -p 'selected_cluster' &&
        ln -s '${cluster_all_seqs}' 'selected_cluster/2_all_seqs.fasta' &&
        ln -s '${reconcile_msa}' 'selected_cluster/3_msa.fasta' &&

            #end if
            --min_aligned_len $min_aligned_len
            --min_read_cov $min_read_cov
            --threads \${GALAXY_SLOTS:-2} &&
            mv 'selected_cluster/7_final_consensus.fasta' $consensus
    ]]></command>
    <inputs>
        <param name='cluster_all_seqs' type='data' 
            format='fasta' label='Reconciled cluster' 
            help='Reconciled sequences file' />
        <param name='reconcile_msa' type='data' 
            format='fasta' label='Reconcile msa' 
            help='Multiple sequence alignment file' />
        <param name='partition_reads' type='data' 
            format='fastq' label='Partition reads' 
            help='Partitioned reads' />
        <param name='reads' type='data' 
            format='fastq,fastq.gz' label='Long-read datasets' 
            help='Long reads (FASTQ format) used to generate the assemblies' />
        <param argument='--linear' type='boolean' 
            truevalue='--linear' falsevalue='' 
            label='Input contigs are not circular' 
            help='Use this option if your input contigs are not circular. It will disable the circularisation-correction steps in Trycycler reconcile.' />
        <param argument='--min_aligned_len' type='integer' min='500' max='3500' 
            value='1000' label='Min bases aligned' 
            help='Reads with less than this many bases aligned (default = 1000) will be ignored.' />
        <param argument='--min_read_cov' type='integer' min='0' max='100' 
            value='90' label='Min read length covered by alignments' 
            help='Reads with less than this percentage of their length covered by alignments (default = 90.0) will be ignored.' />
    </inputs>
    <outputs>
        <data name='consensus' format='fasta' label='${tool.name} on ${on_string}'/>
    </outputs>
    <tests>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_01.fasta'/>
            <param name='reconcile_msa' value='aligned_cluster_01.fasta'/>
            <param name='partition_reads' value='partition_01.fastq'/>
            <param name='reads' value='reads.fastq.gz'/>
            <param name='min_aligned_len' value='1200'/>
            <param name='min_read_cov' value='95'/>
            <output name='consensus' file='consensus_sequence_01.fasta'/>
        </test>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_02.fasta'/>
            <param name='reconcile_msa' value='aligned_cluster_02.fasta'/>
            <param name='partition_reads' value='partition_01.fastq'/>
            <param name='reads' value='reads.fastq.gz'/>
            <param name='min_aligned_len' value='1100'/>
            <param name='min_read_cov' value='90'/>
            <output name='consensus' file='consensus_sequence_02.fasta'/>
        </test>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_03.fasta'/>
            <param name='reconcile_msa' value='aligned_cluster_03.fasta'/>
            <param name='partition_reads' value='partition_01.fastq'/>
            <param name='reads' value='reads.fastq.gz'/>
            <param name='min_aligned_len' value='1300'/>
            <param name='min_read_cov' value='97'/>
            <output name='consensus' file='consensus_sequence_03.fasta'/>
        </test>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_03.fasta'/>
            <param name='reconcile_msa' value='aligned_cluster_03.fasta'/>
            <param name='partition_reads' value='partition_01.fastq'/>
            <param name='reads' value='reads.fastq.gz'/>
            <param name='min_aligned_len' value='1000'/>
            <param name='min_read_cov' value='87'/>
            <output name='consensus' file='consensus_sequence_04.fasta'/>
        </test>
    </tests>
    <help><![CDATA[

.. class:: infomark

----                                                                                                    
                                                                                                        
.. class:: infomark

@PIPELINE@
    ]]></help>
    <expand macro='citations'/>
</tool>

1:07039273d784

<tool id='trycycler_consensus' name='Trycycler consensus' version='@TOOL_VERSION@' profile='20.01'>
    <description>generate a consensus contig sequence for each cluster</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <expand macro='edam_ontology' />
    <expand macro='requirements' />
    <version_command>trycycler --version</version_command>
    <command detect_errors='exit_code'><![CDATA[
        mkdir -p 'selected_cluster' &&
        ln -s '${cluster_all_seqs}' 'selected_cluster/2_all_seqs.fasta' &&
        ln -s '${reconcile_msa}' 'selected_cluster/3_msa.fasta' &&

            #end if
            --min_aligned_len $min_aligned_len
            --min_read_cov $min_read_cov
            --threads \${GALAXY_SLOTS:-2} &&
            mv 'selected_cluster/7_final_consensus.fasta' $consensus
    ]]>    </command>
    <inputs>
        <param name='cluster_all_seqs' type='data' format='fasta' label='Reconciled cluster' help='Reconciled sequences file' />
        <param name='reconcile_msa' type='data' format='fasta' label='Reconcile msa' help='Multiple sequence alignment file' />
        <param name='partition_reads' type='data' format='fastq' label='Partition reads' help='Partitioned reads' />
        <param name='reads' type='data' format='fastq,fastq.gz' label='Long-read datasets' help='Long reads (FASTQ format) used to generate the assemblies' />
        <param argument='--linear' type='boolean' truevalue='--linear' falsevalue='' label='Input contigs are not circular' help='Use this option if your input contigs are not circular. It will disable the circularisation-correction steps in Trycycler reconcile.' />
        <param argument='--min_aligned_len' type='integer' min='500' max='3500' value='1000' label='Min bases aligned' help='Reads with less than this many bases aligned (default = 1000) will be ignored.' />
        <param argument='--min_read_cov' type='integer' min='0' max='100' value='90' label='Min read length covered by alignments' help='Reads with less than this percentage of their length covered by alignments (default = 90.0) will be ignored.' />
    </inputs>
    <outputs>
        <data name='consensus' format='fasta' label='${tool.name} on ${on_string}' />
    </outputs>
    <tests>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_01.fasta' />
            <param name='reconcile_msa' value='aligned_cluster_01.fasta' />
            <param name='partition_reads' value='partition_01.fastq' />
            <param name='reads' value='reads.fastq.gz' />
            <param name='min_aligned_len' value='1200' />
            <param name='min_read_cov' value='95' />
            <output name='consensus' file='consensus_sequence_01.fasta' />
        </test>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_02.fasta' />
            <param name='reconcile_msa' value='aligned_cluster_02.fasta' />
            <param name='partition_reads' value='partition_01.fastq' />
            <param name='reads' value='reads.fastq.gz' />
            <param name='min_aligned_len' value='1100' />
            <param name='min_read_cov' value='90' />
            <output name='consensus' file='consensus_sequence_02.fasta' />
        </test>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_03.fasta' />
            <param name='reconcile_msa' value='aligned_cluster_03.fasta' />
            <param name='partition_reads' value='partition_01.fastq' />
            <param name='reads' value='reads.fastq.gz' />
            <param name='min_aligned_len' value='1300' />
            <param name='min_read_cov' value='97' />
            <output name='consensus' file='consensus_sequence_03.fasta' />
        </test>
        <test>
            <param name='cluster_all_seqs' value='reconciled_cluster_03.fasta' />
            <param name='reconcile_msa' value='aligned_cluster_03.fasta' />
            <param name='partition_reads' value='partition_01.fastq' />
            <param name='reads' value='reads.fastq.gz' />
            <param name='min_aligned_len' value='1000' />
            <param name='min_read_cov' value='87' />
            <output name='consensus' file='consensus_sequence_04.fasta' />
        </test>
    </tests>
    <help><![CDATA[

.. class:: infomark

----                                                                                                    
                                                                                                        
.. class:: infomark

@PIPELINE@
    ]]>    </help>
    <expand macro='citations' />
</tool>