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1 <tool id="gemini_@BINARY@" name="GEMINI @BINARY@" version="@VERSION@.0">
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2 <description>Loading a VCF file into GEMINI</description>
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3 <expand macro="requirements" />
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4 <expand macro="version_command" />
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5 <macros>
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6 <import>gemini_macros.xml</import>
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7 <token name="@BINARY@">load</token>
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8 </macros>
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9 <command>
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10 <![CDATA[
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11 gemini
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12 --annotation-dir ${annotation_databases.fields.path}
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13 @BINARY@
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14 -v "${ infile }"
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15 -t $annotation_type
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16
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17 #if $ped:
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18 -p $ped
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19 #end if
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20
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21 $skip_gerp_bp
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22 $skip_cadd
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23 $skip_gene_tables
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24 $no_load_genotypes
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25 $no_genotypes
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26 $passonly
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27 --cores \${GALAXY_SLOTS:-4}
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28
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29 "${ outfile }"
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30 ]]>
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31 </command>
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32 <expand macro="stdio" />
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33 <inputs>
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34 <param name="infile" type="data" format="vcf" label="VCF file to be loaded in the GEMINI database" />
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35
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36 <param name="annotation_type" type="select" label="The annotations to be used with the input vcf" help="(-t)">
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37 <option value="snpEff">snpEff annotated VCF file</option>
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38 <option value="VEP">VEP annotated VCF file</option>
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39 </param>
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40 <param name="ped" type="data" format="tablar" optional="True" label="Sample information file in PED+ format" help="(-p)" />
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41 <expand macro="annotation_dir" />
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42
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43 <param name="skip_gerp_bp" type="boolean" truevalue="--skip-gerp-bp" falsevalue="" checked="False"
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44 label="Do not load GERP scores at base pair resolution" help="(--skip-gerp-bp)"/>
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45
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46 <param name="skip_cadd" type="boolean" truevalue="--skip-cadd" falsevalue="" checked="False"
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47 label="Do not load CADD scores" help="(--skip-cadd)"/>
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48
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49 <param name="skip_gene_tables" type="boolean" truevalue="--skip-gene-tables" falsevalue="" checked="False"
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50 label="Do not load gene tables" help="(--skip-gene-tables)"/>
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51
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52 <param name="no_load_genotypes" type="boolean" truevalue="--no-load-genotypes" falsevalue="" checked="False"
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53 label="Genotypes exist in the file, but should not be stored" help="(--no-load-genotypes)"/>
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54
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55 <param name="no_genotypes" type="boolean" truevalue="--no-load-genotypes" falsevalue="" checked="False"
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56 label="There are no genotypes in the file" help="e.g. some 1000G VCFs (--no-genotypes)"/>
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57
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58 <param name="passonly" type="boolean" truevalue="--passonly" falsevalue="" checked="False"
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59 label="Keep only variants that pass all filters" help="e.g. some 1000G VCFs (--passonly)"/>
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60
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61 </inputs>
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62 <outputs>
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63 <data name="outfile" format="sqlite" label="${tool.name} on ${on_string}" />
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64 </outputs>
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65 <tests>
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66 <test>
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67 </test>
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68 </tests>
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69 <help>
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70 **What it does**
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71
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72 Before we can use GEMINI to explore genetic variation, we must first load our VCF file into the GEMINI database framework.
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73 We expect you to have first annotated the functional consequence of each variant in your VCF using either VEP or snpEff.
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74
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75 http://gemini.readthedocs.org/en/latest/content/loading.html
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76
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77 @CITATION@
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78 </help>
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79 <expand macro="citations"/>
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80 </tool>
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