Mercurial > repos > xuebing > sharplabtool
view tools/regVariation/delete_overlapping_indels.xml @ 2:c2a356708570
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author | xuebing |
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date | Fri, 09 Mar 2012 19:45:42 -0500 |
parents | 9071e359b9a3 |
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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>