comparison flash.xml @ 0:a8e42976aa6b draft

planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/flash commit 48012d1879395ecf1b4e6cd962f325c372164a33

0:a8e42976aa6b

<?xml version="1.0"?>
<tool id="flash" name="FLASH" version="1.2.11">
    <description>adjust length of short reads</description>
    <requirements>
        <requirement type="package" version="1.2.11">flash</requirement>
    </requirements>
    <version_command>flash --version | head -n 1</version_command>
    <command detect_errors="aggressive">
        <![CDATA[
            flash --threads=\${GALAXY_SLOTS:-1}
                -m $min_overlap
                -M $max_overlap
                -x $max_mismatch_density
                $allow_outies
                '$forward' '$reverse'
        ]]>
    </command>
    <inputs>
        <param format="fastq" name="forward" type="data" label="Forward reads" />
        <param format="fastq" name="reverse" type="data" label="Reverse reads" />
        <param name="min_overlap" argument="--min-overlap" type="integer" optional="true" value="10" label="Minimum overlap" help="The minimum required overlap length between two reads to provide a confident overlap." />
        <param name="max_overlap" argument="--max-overlap" type="integer" optional="true" value="65" label="Maximum overlap" help="Maximum overlap length expected in approximately 90% of read pairs. Overlaps longer than the maximum overlap parameter are still considered as good overlaps, but the mismatch density is calculated over the first max_overlap bases in the overlapped region rather than the entire overlap." />
        <param name="max_mismatch_density" argument="--max-mismatch-density" type="float" optional="true" value="0.25" label="Maximum mismatch density" help="Maximum allowed ratio between the number of mismatched base pairs and the overlap length. Two reads will not be combined with a given overlap if that overlap results in a mismatched base density higher than this value." />
        <param name="allow_outies" argument="--allow-outies" type="boolean" truevalue="--allow-outies" falsevalue="" checked="false" label="Combine read pairs in both orientations" help="FLASH uses the same parameters when trying each orientation. If a read pair can be combined in either orientation, the better-fitting one will be chosen using the same scoring algorithm that FLASH normally uses." />
    </inputs>
    <outputs>
        <data format="fastq" name="merged_reads" from_work_dir="out.extendedFrags.fastq" label="${tool.name} on ${on_string}: Merged reads" />
        <data format="fastq" name="unmerged_reads_f" from_work_dir="out.notCombined_1.fastq" label="${tool.name} on ${on_string}: Unmerged forward reads" />
        <data format="fastq" name="unmerged_reads_r" from_work_dir="out.notCombined_2.fastq" label="${tool.name} on ${on_string}: Unmerged reverse reads" />
        <data format="tabular" name="hist" from_work_dir="out.hist" label="${tool.name} on ${on_string}: Unmerged reads tabular histogram" />
        <data format="txt" name="histogram" from_work_dir="out.histogram" label="${tool.name} on ${on_string}: Unmerged reads histogram" />
        <data format="tabular" name="hist_in" from_work_dir="out.hist.innie" label="${tool.name} on ${on_string}: Unmerged reads tabular histogram (in)" >
            <filter>allow_outies</filter>
        </data>
        <data format="tabular" name="hist_out" from_work_dir="out.hist.outie" label="${tool.name} on ${on_string}: Unmerged reads tabular histogram (out)" >
            <filter>allow_outies</filter>
        </data>
        <data format="txt" name="histogram_in" from_work_dir="out.histogram.innie" label="${tool.name} on ${on_string}: Unmerged reads histogram (in)" >
            <filter>allow_outies</filter>
        </data>
        <data format="txt" name="histogram_out" from_work_dir="out.histogram.outie" label="${tool.name} on ${on_string}: Unmerged reads histogram (out)" >
            <filter>allow_outies</filter>
        </data>
    </outputs>
    <tests>
        <test>
            <param name="forward" value="flash_forward_in1.fastq" />
            <param name="reverse" value="flash_reverse_in1.fastq" />
            <output name="merged_reads" file="flash_merged_out1.fastq" />
            <output name="unmerged_reads_f" file="flash_unmerged_f_out1.fastq" />
            <output name="unmerged_reads_r" file="flash_unmerged_r_out1.fastq" />
            <output name="hist" file="flash_hist_out1.tabular" />
            <output name="histogram" file="flash_hist_out1.txt" />
        </test>
        <test>
            <param name="forward" value="flash_forward_in2.fastq" />
            <param name="reverse" value="flash_reverse_in2.fastq" />
            <param name="allow_outies" value="true" />
            <output name="merged_reads" file="flash_merged_out2.fastq" />
            <output name="unmerged_reads_f" file="flash_unmerged_f_out2.fastq" />
            <output name="unmerged_reads_r" file="flash_unmerged_r_out2.fastq" />
            <output name="hist" file="flash_hist_out2.tabular" />
            <output name="histogram" file="flash_hist_out2.txt" />
            <output name="hist_in" file="flash_hist_in_out2.tabular" />
            <output name="histogram_in" file="flash_hist_in_out2.txt" />
            <output name="hist_out" file="flash_hist_out_out2.tabular" />
            <output name="histogram_out" file="flash_hist_out_out2.txt" />
        </test>
    </tests>
    <help>
<![CDATA[
FLASH (Fast Length Adjustment of SHort reads) is an accurate and fast tool
to merge paired-end reads that were generated from DNA fragments whose
lengths are shorter than twice the length of reads.  Merged read pairs result
in unpaired longer reads, which are generally more desired in genome
assembly and genome analysis processes.

Briefly, the FLASH algorithm considers all possible overlaps at or above a
minimum length between the reads in a pair and chooses the overlap that
results in the lowest mismatch density (proportion of mismatched bases in
the overlapped region).  Ties between multiple overlaps are broken by
considering quality scores at mismatch sites.  When building the merged
sequence, FLASH computes a consensus sequence in the overlapped region.
]]>
    </help>
    <citations>
        <citation type="doi">10.1093/bioinformatics/btr507</citation>
    </citations>
</tool>