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author | cpt |
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date | Mon, 05 Jun 2023 02:54:34 +0000 |
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children | e4207a7661e7 |
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<tool id="edu.tamu.cpt.xmfa.split" name="Split LCBs into smaller LCBs" version="@WRAPPER_VERSION@.0"> <description/> <macros> <import>macros.xml</import> <import>cpt-macros.xml</import> </macros> <expand macro="requirements"/> <command detect_errors="aggressive"><![CDATA[ 'python $__tool_directory__/lcb_split.py' @XMFA_INPUT@ --window_size '$window_size' --threshold '$threshold' > '$output' ]]></command> <inputs> <expand macro="xmfa_input"/> <param type="integer" name="window_size" value="10" label="Default window size generating smaller LCBs"/> <param type="float" name="threshold" value="0.7" min="0" max="1" label="Threshold at which a given genome is part of the new small LCBs"/> </inputs> <outputs> <data format="xmfa" name="output"/> </outputs> <help><![CDATA[ **What it does** Helps reduce large and non-sensical protein LCBs into real protein alignments. **WARNING** Probably does not work if you have - strand genes. Need to test. ]]></help> <!-- TODO --> <expand macro="citations"/> </tool>