view alleyoop.xml @ 7:5a26589d95ad draft default tip

"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/slamdunk commit b5aa6e762b55a9793dc7514efcda05eb2ccd529c"

<tool id="alleyoop" name="Alleyoop" version="@TOOL_VERSION@+galaxy@VERSION_SUFFIX@" profile="@PROFILE@">
    <description>- post-processing and QC of Slamdunk analyses</description>
    <macros>
        <import>macros.xml</import>
    </macros>
    <expand macro="requirements"/>
    <version_command>alleyoop --version</version_command>
    <command detect_errors="exit_code"><![CDATA[
#import re

#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

mkdir ./filter &&
#for $bam in $reads:
    #set $ext = ""
    #set $bam_name = re.sub('[^\w\-\.]', '_', str($bam.element_identifier))
    #if not $bam_name.endswith('.bam')
        #set $ext = ".bam"
    #end if
    ln -s '$bam' './filter/${bam_name}${ext}' &&
    ln -s '$bam.metadata.bam_index' './filter/${bam_name}${ext}.bai' &&
#end for

mkdir ./count &&
#for $tsv in $count_tsvs:
    #set $ext = ""
    #set $tsv_name = re.sub('[^\w\-\.]', '_', str($tsv.element_identifier))
    #if not $tsv_name.endswith('_tcount.tsv')
        #set $ext = "_tcount.tsv"
    #end if
    ln -s '$tsv' './count/${tsv_name}${ext}' &&
#end for

mkdir ./snp &&
#for $vcf in $variants:
    #set $ext = ""
    #set $vcf_name = re.sub('[^\w\-\.]', '_', str($vcf.element_identifier))
    #if not $vcf_name.endswith('_snp.vcf')
        #set $ext = "_snp.vcf"
    #end if
    ln -s '$vcf' './snp/${vcf_name}${ext}' &&
#end for

alleyoop summary -o ./summary.txt -t ./count ./filter/*bam &&

alleyoop rates -o ./stats -r reference.fa -mq $mq ./filter/*bam &&

alleyoop utrrates -o ./stats -r reference.fa -b $reference -t \${GALAXY_SLOTS:-1} -l $l -mq $mq ./filter/*bam &&

alleyoop tcperreadpos -o ./stats -r reference.fa -s ./snp -t \${GALAXY_SLOTS:-1} -l $l -mq $mq ./filter/*bam &&

alleyoop tcperutrpos -o ./stats -r reference.fa -s ./snp -t \${GALAXY_SLOTS:-1} -l $l -b $reference -mq $mq ./filter/*bam

#if $bams:
    && alleyoop read-separator -o ./splitbams -s ./snp -r reference.fa ./filter/*bam
#end if

    ]]></command>
    <inputs>
        <expand macro="reference_files"/>
        <param name="reads" type="data" format="sam,bam" multiple="True" label="Slamdunk BAM files"/>
        <param name="count_tsvs" type="data" format="tabular" multiple="True" label="Slamdunk Count TSV files"/>
        <param name="variants" type="data" format="vcf" multiple="True" label="Slamdunk VCF files"/>
        <param name="mq" argument="--min-basequality" type="integer" label="Minimum base quality"
                value="27" min="0"
                help="Minimum base quality for T>C conversions (default: 27)."/>
        <param name="l" argument="--max-read-length" type="integer" label="Read length"
            value="50" min="50" help="Maximum read length (before trimming)."/>
        <param name="bams" type="boolean" truevalue="True" falsevalue="False" checked="False" label="Output T>C separated BAM files?" help="If this option is set to Yes, the Alleyoop read-separator module will be run to output BAM files of separated T>C reads from non T>C reads. Default: No"/>
    </inputs>
    <outputs>
         <collection name="outputSummary" type="list" label="${tool.name} on ${on_string}: Summary tables">
            <discover_datasets pattern="(?P&lt;name&gt;.+)\.txt$" format="tabular" directory="." visible="false"/>
        </collection>
        <collection name="outputStats" type="list" label="${tool.name} on ${on_string}: Stats tables">
            <discover_datasets pattern="(?P&lt;name&gt;.+)\.csv$" format="tabular" directory="./stats" visible="false"/>
        </collection>
        <collection name="outputTCReads" type="list" label="${tool.name} on ${on_string}: TC Reads">
            <discover_datasets pattern="(?P&lt;name&gt;.+)_TCReads.bam$" format="bam" directory="./splitbams" visible="false"/>
            <filter>bams</filter>
        </collection>
        <collection name="outputbkgdReads" type="list" label="${tool.name} on ${on_string}: Background Reads">
            <discover_datasets pattern="(?P&lt;name&gt;.+)_backgroundReads.bam$" format="bam" directory="./splitbams" visible="false"/>
            <filter>bams</filter>
        </collection>
    </outputs>
    <tests>
        <!-- Ensure default output works -->
        <test expect_num_outputs="2">
            <param name="reference_source_selector" value="history"/>
            <param name="ref_file" ftype="fasta" value="ref.fa"/>
            <param name="reference" ftype="bed" value="actb.bed"/>
            <param name="reads" ftype="bam" value="reads1.bam,reads2.bam"/>
            <param name="count_tsvs" ftype="tabular" value="reads1_tcount.tsv,reads2_tcount.tsv"/>
            <param name="variants" ftype="vcf" value="reads1_snp.vcf,reads2_snp.vcf"/>
            <param name="l" value="100"/>
            <param name="mq" value="27"/>
            <output_collection name="outputSummary" count="2">
                <element name="summary" ftype="tabular" file="summary.txt" lines_diff="2"/>
            </output_collection>
            <output_collection name="outputStats" count="8">
                <element name="reads1_overallrates" ftype="tabular" file="reads1_overallrates.csv" lines_diff="2"/>
            </output_collection>
        </test>
        <!-- Ensure BAM output works -->
        <test expect_num_outputs="4">
            <param name="reference_source_selector" value="history"/>
            <param name="ref_file" ftype="fasta" value="ref.fa"/>
            <param name="reference" ftype="bed" value="actb.bed"/>
            <param name="reads" ftype="bam" value="reads1.bam,reads2.bam"/>
            <param name="count_tsvs" ftype="tabular" value="reads1_tcount.tsv,reads2_tcount.tsv"/>
            <param name="variants" ftype="vcf" value="reads1_snp.vcf,reads2_snp.vcf"/>
            <param name="l" value="100"/>
            <param name="mq" value="27"/>
            <param name="bams" value="True"/>
            <output_collection name="outputTCReads" count="2">
                <element name="reads1" ftype="bam" file="reads1_TCReads.bam" lines_diff="8"/>
            </output_collection>
            <output_collection name="outputbkgdReads" count="2">
                <element name="reads1" ftype="bam" file="reads1_backgroundReads.bam" lines_diff="8"/><!-- allow for diff in RG and PG lines -->
            </output_collection>
        </test>
    </tests>
    <help><![CDATA[
SLAMseq
=======

SLAMseq is a novel sequencing protocol that directly uncovers 4-thiouridine incorporation events in RNA by high-throughput sequencing. When combined with metabolic labeling protocols, SLAM-seq allows to study the intracellular RNA dynamics, from transcription, RNA processing to RNA stability.

Original publication: `Herzog et al., Nature Methods, 2017; doi:10.1038/nmeth.4435 <https://www.nature.com/nmeth/journal/vaop/ncurrent/full/nmeth.4435.html>`_

Alleyoop
========

Alleyoop (Additional sLamdunk heLpEr tools for anY diagnOstics Or Plots) is a collection of tools for post-processing and running diagnostics on Slamdunk analyses. This tool works on the output of the **Slamdunk** tool and requires all the inputs listed in the table below.

===============  ==========================================================================================================================================================
Parameter        Description
===============  ==========================================================================================================================================================
**Genome**       The reference fasta file (Genome assembly).
**Reference**    BED-file containing coordinates for 3' UTRs.
**Reads**        Slamdunk Filtered BAM files.
**Counts**       Slamdunk Count TSV files.
**Variants**     Slandunk VCF files.
**Read length**  Maximum length of reads (usually 50, 100, 150).
===============  ==========================================================================================================================================================

This tool runs the **Alleyoop** *summary*, *rates*, *utrrates*, *tcperreadpos* and *tcperutrpos* modules and outputs:

* Tab-separated *summary* files from the summary module with mapping and PCA statistics
* Tab-separated *stats* files from the rates, utrrates, tcperreadpos and tcperutrpos modules

Optionally, the *read-separator* module can be run to output BAM files of separated T>C and non T>C reads.

The summary and stats files can be summarised and visualised with MultiQC. An example MultiQC report can be seen here_. For information on these modules see the `Alleyoop documentation`_.

.. _`Alleyoop documentation`: http://t-neumann.github.io/slamdunk/docs.html#document-Alleyoop
.. _here: http://t-neumann.github.io/slamdunk/multiqc_example/multiqc_report.html

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