Mercurial > repos > iuc > gemini
comparison gemini_load.xml @ 17:65f742e605ec draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/gemini commit 344140b8df53b8b7024618bb04594607a045c03a
| author | iuc |
|---|---|
| date | Mon, 04 May 2015 22:46:38 -0400 |
| parents | 9876fc2456ac |
| children |
comparison
equal
deleted
inserted
replaced
| 16:ae03de7a9fee | 17:65f742e605ec |
|---|---|
| 1 <tool id="gemini_@BINARY@" name="GEMINI @BINARY@" version="@VERSION@.0"> | 1 <tool id="gemini_@BINARY@" name="GEMINI @BINARY@" version="@VERSION@.0"> |
| 2 <description>Loading a VCF file into GEMINI</description> | 2 <description>Loading a VCF file into GEMINI</description> |
| 3 <expand macro="requirements" /> | |
| 4 <expand macro="version_command" /> | |
| 5 <macros> | 3 <macros> |
| 6 <import>gemini_macros.xml</import> | 4 <import>gemini_macros.xml</import> |
| 7 <token name="@BINARY@">load</token> | 5 <token name="@BINARY@">load</token> |
| 8 </macros> | 6 </macros> |
| 7 <expand macro="requirements" /> | |
| 8 <expand macro="stdio" /> | |
| 9 <expand macro="version_command" /> | |
| 9 <command> | 10 <command> |
| 10 <![CDATA[ | 11 <![CDATA[ |
| 11 ln -s "${ infile }" input.vcf && | 12 ln -s "${ infile }" input.vcf && |
| 12 | 13 |
| 13 gemini | 14 gemini |
| 14 --annotation-dir ${annotation_databases.fields.path} | 15 --annotation-dir ${annotation_databases.fields.path} |
| 15 @BINARY@ | 16 @BINARY@ |
| 16 -v input.vcf | 17 -v input.vcf |
| 17 #if str( $annotation_type ) != "None": | 18 #if str( $annotation_type ) != "None": |
| 18 -t $annotation_type | 19 -t $annotation_type |
| 31 --cores \${GALAXY_SLOTS:-4} | 32 --cores \${GALAXY_SLOTS:-4} |
| 32 | 33 |
| 33 "${ outfile }" | 34 "${ outfile }" |
| 34 ]]> | 35 ]]> |
| 35 </command> | 36 </command> |
| 36 <expand macro="stdio" /> | |
| 37 <inputs> | 37 <inputs> |
| 38 <param name="infile" type="data" format="vcf" label="VCF file to be loaded in the GEMINI database" help="Only build 37 (aka hg19) of the human genome is supported."> | 38 <param name="infile" type="data" format="vcf" label="VCF file to be loaded in the GEMINI database" help="Only build 37 (aka hg19) of the human genome is supported."> |
| 39 <options> | 39 <options> |
| 40 <filter type="add_value" value="hg19" /> | 40 <filter type="add_value" value="hg19" /> |
| 41 <filter type="add_value" value="Homo_sapiens_nuHg19_mtrCRS" /> | 41 <filter type="add_value" value="Homo_sapiens_nuHg19_mtrCRS" /> |
| 49 <option value="VEP">VEP annotated VCF file</option> | 49 <option value="VEP">VEP annotated VCF file</option> |
| 50 </param> | 50 </param> |
| 51 <param name="ped" type="data" format="tablar" optional="True" label="Sample information file in PED+ format" help="(-p)" /> | 51 <param name="ped" type="data" format="tablar" optional="True" label="Sample information file in PED+ format" help="(-p)" /> |
| 52 <expand macro="annotation_dir" /> | 52 <expand macro="annotation_dir" /> |
| 53 | 53 |
| 54 <param name="skip_gerp_bp" type="boolean" truevalue="--skip-gerp-bp" falsevalue="" checked="False" | 54 <param name="skip_gerp_bp" type="boolean" truevalue="--skip-gerp-bp" falsevalue="" checked="False" |
| 55 label="Do not load GERP scores at base pair resolution" help="(--skip-gerp-bp)"/> | 55 label="Do not load GERP scores at base pair resolution" help="(--skip-gerp-bp)"/> |
| 56 | 56 |
| 57 <param name="skip_cadd" type="boolean" truevalue="--skip-cadd" falsevalue="" checked="False" | 57 <param name="skip_cadd" type="boolean" truevalue="--skip-cadd" falsevalue="" checked="False" |
| 58 label="Do not load CADD scores" help="(--skip-cadd)"/> | 58 label="Do not load CADD scores" help="(--skip-cadd)"/> |
| 59 | 59 |
| 60 <param name="skip_gene_tables" type="boolean" truevalue="--skip-gene-tables" falsevalue="" checked="False" | 60 <param name="skip_gene_tables" type="boolean" truevalue="--skip-gene-tables" falsevalue="" checked="False" |
| 61 label="Do not load gene tables" help="(--skip-gene-tables)"/> | 61 label="Do not load gene tables" help="(--skip-gene-tables)"/> |
| 62 | 62 |
| 63 <param name="no_load_genotypes" type="boolean" truevalue="--no-load-genotypes" falsevalue="" checked="False" | 63 <param name="no_load_genotypes" type="boolean" truevalue="--no-load-genotypes" falsevalue="" checked="False" |
| 64 label="Genotypes exist in the file, but should not be stored" help="(--no-load-genotypes)"/> | 64 label="Genotypes exist in the file, but should not be stored" help="(--no-load-genotypes)"/> |
| 65 | 65 |
| 66 <param name="no_genotypes" type="boolean" truevalue="--no-load-genotypes" falsevalue="" checked="False" | 66 <param name="no_genotypes" type="boolean" truevalue="--no-load-genotypes" falsevalue="" checked="False" |
| 67 label="There are no genotypes in the file" help="e.g. some 1000G VCFs (--no-genotypes)"/> | 67 label="There are no genotypes in the file" help="e.g. some 1000G VCFs (--no-genotypes)"/> |
| 68 | 68 |
| 69 <param name="passonly" type="boolean" truevalue="--passonly" falsevalue="" checked="False" | 69 <param name="passonly" type="boolean" truevalue="--passonly" falsevalue="" checked="False" |
| 70 label="Keep only variants that pass all filters" help="e.g. some 1000G VCFs (--passonly)"/> | 70 label="Keep only variants that pass all filters" help="e.g. some 1000G VCFs (--passonly)"/> |
| 71 | 71 |
| 72 </inputs> | 72 </inputs> |
| 73 <outputs> | 73 <outputs> |
| 74 <data name="outfile" format="gemini.sqlite" /> | 74 <data name="outfile" format="gemini.sqlite" /> |
