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1 <tool id="extract_aln_ends.py" name="extract_aln_ends.py" version="0.1.0">
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2 <description>Extract alignment ends from sam file.</description>
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3 <macros>
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4 <import>macros.xml</import>
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5 </macros>
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6 <expand macro="requirements" />
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7 <expand macro="stdio" />
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8 <version_command>python extract_aln_ends.py --version</version_command>
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9 <command interpreter="python"><![CDATA[
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10 extract_aln_ends.py
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11 #if $positional_1 and $positional_1 is not None:
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12 $positional_1
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13 #end if
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14
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15 > $default]]></command>
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16 <inputs>
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17 <param area="false" label="Sam input." name="positional_1" type="data" format="sam"/>
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18 </inputs>
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19 <outputs>
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20 <data format="bed" hidden="false" name="default"/>
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21 </outputs>
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22 <tests>
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23 <test>
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24 <param name="positional_1" value="twomates.sam"/>
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25 <output name="default" file="tworeads_aln_ends.bed"/>
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26 </test>
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27 </tests>
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28 <help><![CDATA[
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29 Extract alignment ends from sam file.
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30
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31 The resulting bed file contains the outer coordinates of the alignments. The
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32 bed name field is set to the read id and the score field is set to the edit
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33 distance of the alignment. The crosslinked nucleotide is one nt upstream of the
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34 5'-end of the bed entries.
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35
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36 This tool only reports results for alignments that are properly aligned in FR
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37 ("forward-reverse") direction.
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38
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39 Input:
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40 * sam file containing alignments (paired-end sequencing)
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41
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42 Output:
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43 * bed6 file containing outer coordinates (sorted by read id)
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44
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45 Author: Daniel Maticzka
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46 Copyright: 2015
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47 License: Apache
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48 Email: maticzkd@informatik.uni-freiburg.de
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49 Status: Development
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50 ]]></help>
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51 <expand macro="citations" />
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52 </tool>
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