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Change order of Bowtie2 output datasets to put aligned reads at top of history.
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@@ -145,6 +145,22 @@
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</inputs>
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<outputs>
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<data format="fastqsanger" name="output_unaligned_reads_l" label="${tool.name} on ${on_string}: unaligned reads (L)" >
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<filter>unalignedFile is True</filter>
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<actions>
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<action type="format">
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<option type="from_param" name="singlePaired.input1" param_attribute="ext" />
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</action>
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</actions>
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</data>
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<data format="fastqsanger" name="output_unaligned_reads_r" label="${tool.name} on ${on_string}: unaligned reads (R)">
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<filter>singlePaired['sPaired'] == "paired" and unalignedFile is True</filter>
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<actions>
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<action type="format">
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<option type="from_param" name="singlePaired.input1" param_attribute="ext" />
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</action>
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</actions>
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</data>
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<data format="bam" name="output" label="${tool.name} on ${on_string}: aligned reads">
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<actions>
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<conditional name="refGenomeSource.genomeSource">
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@@ -164,22 +180,6 @@
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</conditional>
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</actions>
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</data>
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<data format="fastqsanger" name="output_unaligned_reads_l" label="${tool.name} on ${on_string}: unaligned reads (L)" >
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<filter>unalignedFile is True</filter>
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<actions>
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<action type="format">
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<option type="from_param" name="singlePaired.input1" param_attribute="ext" />
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</action>
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</actions>
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</data>
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<data format="fastqsanger" name="output_unaligned_reads_r" label="${tool.name} on ${on_string}: unaligned reads (R)">
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<filter>singlePaired['sPaired'] == "paired" and unalignedFile is True</filter>
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<actions>
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<action type="format">
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<option type="from_param" name="singlePaired.input1" param_attribute="ext" />
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</action>
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</actions>
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</data>
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</outputs>
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<tests>
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