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galaxy/tools/regVariation/delete_overlapping_indels.xml
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<tool id="delete_overlapping_indels" name="Delete Overlapping Indels" version="1.0.0">
<description>from a chromosome indels file</description>
<command interpreter="perl">
delete_overlapping_indels.pl $inputFile1 $inputIndelStartColumnNumber2 $inputIndelEndColumnNumber3 $outputFile1
</command>
<inputs>
<param format="tabular" name="inputFile1" type="data" label="Select indels file"/>
<param type="data_column" name="inputIndelStartColumnNumber2" data_ref="inputFile1" accept_default="true" label="Choose the indel start coordinate column number" />
<param type="data_column" name="inputIndelEndColumnNumber3" data_ref="inputFile1" accept_default="true" label="Choose the the indel end coordinate column number" />
</inputs>
<outputs>
<data format="tabular" name="outputFile1"/>
</outputs>
<tests>
<test>
<param name="inputFile1" value="indels1.tabular" />
<param name="inputIndelStartColumnNumber2" value="5" />
<param name="inputIndelEndColumnNumber3" value="6" />
<output name="outputFile1" file="non_overlapping_indels1.tabular" />
</test>
</tests>
<help>
.. class:: infomark
**What it does**
This program detects overlapping indels in a chromosome and keeps all non-overlapping indels. As for overlapping indels, the first encountered one is kept and all others are removed.
It requires three inputs:
- The first input is a TABULAR format file containing coordinates of indels in blocks extracted from multi-alignment.
- The second input is an integer number representing the number of the column where indel start coordinates are stored in the input file.
- The third input is an integer number representing the number of the column where indel end coordinates are stored in the input file.
- The output is a TABULAR format file containing all non-overlapping indels in the input file, and the first encountered indel of overlapping ones.
Note: The number of the first column is 1.
**Example**
Let us have the following insertions in the human genome. The start and end coordinates of insertions are on columns 5 and 6 respectively::
3 hg18.chr22_insert 3 hg18.chr22 14508610 14508612 3924 - panTro2.chr2b 132518950 132518951 3910 + rheMac2.chr17 14311798 14311799 3896 +
7 hg18.chr22_insert 13 hg18.chr22 14513678 14513690 348 - panTro2.chr2b 132517876 132517877 321 + rheMac2.chr17 14274462 14274463 337 +
7 hg18.chr22_insert 6 hg18.chr22 14513688 14513699 348 - panTro2.chr2b 132517879 132517880 321 + rheMac2.chr17 14274465 14274466 337 +
25 hg18.chr22_insert 9 hg18.chr22 14529501 14529509 385 - panTro2.chr22 14528775 14528776 376 - rheMac2.chr9 42869449 42869450 375 -
36 hg18.chr22_insert 4 hg18.chr22 14566316 14566319 540 - panTro2.chr2b 132492077 132492078 533 + rheMac2.chr10 59230438 59230439 533 -
40 hg18.chr22_insert 7 hg18.chr22 14508610 14508616 2337 - panTro2.chr2b 132487750 132487751 2313 + rheMac2.chr10 59128305 59128306 2332 +
41 hg18.chr22_insert 4 hg18.chr22 14571556 14571559 2483 - panTro2.chr2b 132485878 132485879 2481 + rheMac2.chr10 59126094 59126095 2508 +
By removing the overlapping indels which, we get::
3 hg18.chr22_insert 3 hg18.chr22 14508610 14508612 3924 - panTro2.chr2b 132518950 132518951 3910 + rheMac2.chr17 14311798 14311799 3896 +
7 hg18.chr22_insert 13 hg18.chr22 14513678 14513690 348 - panTro2.chr2b 132517876 132517877 321 + rheMac2.chr17 14274462 14274463 337 +
25 hg18.chr22_insert 9 hg18.chr22 14529501 14529509 385 - panTro2.chr22 14528775 14528776 376 - rheMac2.chr9 42869449 42869450 375 -
36 hg18.chr22_insert 4 hg18.chr22 14566316 14566319 540 - panTro2.chr2b 132492077 132492078 533 + rheMac2.chr10 59230438 59230439 533 -
41 hg18.chr22_insert 4 hg18.chr22 14571556 14571559 2483 - panTro2.chr2b 132485878 132485879 2481 + rheMac2.chr10 59126094 59126095 2508 +
</help>
</tool>