Mercurial > repos > sanbi-uwc > vcf_to_alignment
annotate vcf_to_alignment.xml @ 2:a0c85f2d74a5 draft
planemo upload for repository https://github.com/sanbi-sa/tools-sanbi-uwc commit 9612f06b8c60520dc0a047ec072ced317c7796e4
author | sanbi-uwc |
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date | Wed, 01 Feb 2017 08:45:12 -0500 |
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1 <?xml version="1.0" encoding="utf-8" ?> |
2
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2 <tool id="vcf_to_alignment" name="Generate FASTA alignment from VCF collection" version="0.2"> |
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3 <description>Generate a multiple sequence alignment given a collection of variants and a reference sequence</description> |
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4 <requirements> |
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5 <requirement type="package" version="1.67">biopython</requirement> |
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6 <requirement type="package" version="0.6.8">pyvcf</requirement> |
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7 <requirement type="package" version="2.1.0">intervaltree</requirement> |
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8 </requirements> |
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9 <command detect_errors="aggressive"><![CDATA[ |
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10 #if str($reference.source) == 'history': |
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11 ln -s '${reference.history}' reference.fasta && |
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12 #end if |
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13 python $__tool_directory__/vcf_to_msa.py --vcf_files |
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14 #for $vcf_file in $vcf_inputs: |
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15 '${vcf_file.element_identifier}^^^${vcf_file}' |
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16 #end for |
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17 --reference_file |
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18 #if str($reference.source) == 'history': |
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planemo upload for repository https://github.com/sanbi-sa/tools-sanbi-uwc commit bc8fd85986b54f9d000e7d5869876fc9e479b6eb
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19 reference.fasta |
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20 #else |
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21 '${reference.builtin.fields.path}' |
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22 #end if |
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23 --output_file '${output_alignment}' |
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24 ]]> |
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25 </command> |
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26 <inputs> |
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27 <param name="vcf_inputs" type="data_collection" format="vcf" collection_type="list" label="Variants (VCF format)" /> |
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28 <conditional name="reference" label="Reference sequence source"> |
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29 <param name="source" type="select"> |
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30 <option value="history" selected="True">History</option> |
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31 <option value="builtin">Built-in</option> |
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32 </param> |
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33 <when value="history"> |
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34 <param name="history" type="data" format="fasta" label="Reference sequence" /> |
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35 </when> |
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36 <when value="builtin"> |
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37 <param name="builtin" type="select" label="Reference sequence (FASTA format)"> |
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38 <options from_data_table="all_fasta" /> |
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39 <validator type="no_options" message="No FASTA datasets are available for the selected input dataset" /> |
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40 </param> |
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41 </when> |
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42 </conditional> |
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43 </inputs> |
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44 <outputs> |
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45 <data name="output_alignment" format="fasta" label="Alignment ${on_string}" /> |
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46 </outputs> |
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47 <tests> |
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48 <test> |
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49 <param name="vcf_inputs"> |
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50 <collection type="list"> |
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51 <element name="vcf_inputs.vcf1" value="vcf1.vcf" /> |
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52 <element name="vcf_inputs.vcf2" value="vcf2.vcf" /> |
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53 <element name="vcf_inputs.vcf3" value="vcf3.vcf" /> |
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54 </collection> |
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55 </param> |
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56 <param name="history" value="reference.fasta" ftype="fasta" /> |
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57 <output name="output_alignment" value="output1.fasta" /> |
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58 </test> |
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59 </tests> |
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60 <help><![CDATA[ |
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61 Using the SNPs identified by the VCF files given as input, generates a sequence including the |
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62 SNPs by combining them with the reference and then combines the sequences into a FASTA |
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63 format alignment file. |
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64 ]]> |
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65 </help> |
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66 <citations></citations> |
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67 </tool> |