Mercurial > repos > iuc > delly_call
comparison macros.xml @ 0:e15927444573 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly commit 86ada42b811af0262618636f2d8d1788274f9884"
| author | iuc |
|---|---|
| date | Mon, 28 Sep 2020 07:43:20 +0000 |
| parents | |
| children | c027f82af2fb |
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| -1:000000000000 | 0:e15927444573 |
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| 1 <?xml version="1.0"?> | |
| 2 <macros> | |
| 3 <token name="@TOOL_VERSION@">0.8.3</token> | |
| 4 <token name="@DESCRIPTION@"></token> | |
| 5 <xml name="requirements"> | |
| 6 <requirements> | |
| 7 <requirement type="package" version="@TOOL_VERSION@">delly</requirement> | |
| 8 <requirement type="package" version="1.10.2">bcftools</requirement> | |
| 9 </requirements> | |
| 10 </xml> | |
| 11 <xml name="version_command"> | |
| 12 <version_command><![CDATA[delly -v 2>&1 | grep 'Delly version' | cut -f 3 -d ' ']]></version_command> | |
| 13 </xml> | |
| 14 <xml name="citations"> | |
| 15 <citations> | |
| 16 <citation type="doi">10.1093/bioinformatics/bts378</citation> | |
| 17 </citations> | |
| 18 </xml> | |
| 19 | |
| 20 <!-- | |
| 21 input | |
| 22 --> | |
| 23 | |
| 24 <xml name="exclude"> | |
| 25 <param argument="--exclude" type="data" format="tabular" optional="true" label="Select file with regions to exclude"/> | |
| 26 </xml> | |
| 27 <xml name="genome"> | |
| 28 <param argument="--genome" type="data" format="fasta" label="Select genome"/> | |
| 29 </xml> | |
| 30 <xml name="genoqual"> | |
| 31 <param name="genoqual" type="integer" value="5" label="Set minimum mapping quality for genotyping" help="(--geno-qual)"/> | |
| 32 </xml> | |
| 33 <xml name="minclip"> | |
| 34 <param argument="--minclip" type="integer" value="25" label="Set minimum clipping length"/> | |
| 35 </xml> | |
| 36 <xml name="maxreadsep"> | |
| 37 <param argument="--maxreadsep" type="integer" value="40" label="Set maximum read separation"/> | |
| 38 </xml> | |
| 39 <xml name="minrefsep"> | |
| 40 <param argument="--minrefsep" type="integer" value="25" label="Set minimum reference separation"/> | |
| 41 </xml> | |
| 42 <xml name="samples" token_format="bam" token_multiple="true" token_label="Select sample file(s)"> | |
| 43 <param name="samples" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/> | |
| 44 </xml> | |
| 45 <xml name="svtype"> | |
| 46 <param argument="--svtype" type="select" label="Select type(s) of structural variants to detect"> | |
| 47 <option value="ALL" selected="true">All types (ALL)</option> | |
| 48 <option value="DEL">Deletion (DEL)</option> | |
| 49 <option value="INS">Insertion (INS)</option> | |
| 50 <option value="DUP">Duplication (DUP)</option> | |
| 51 <option value="INV">Inversion (INV)</option> | |
| 52 <option value="BND">Translocation (BND)</option> | |
| 53 </param> | |
| 54 </xml> | |
| 55 <xml name="vcffile"> | |
| 56 <param argument="--vcffile" type="data" format="vcf,bcf" optional="true" label="Select genotyping file"/> | |
| 57 </xml> | |
| 58 | |
| 59 <!-- | |
| 60 output | |
| 61 --> | |
| 62 | |
| 63 <xml name="vcf"> | |
| 64 <data name="out_vcf" format="vcf" from_work_dir="result.vcf" label="${tool.name} on ${on_string}: Result (VCF)"> | |
| 65 <filter>'vcf' in oo['out']</filter> | |
| 66 </data> | |
| 67 </xml> | |
| 68 <xml name="bcf"> | |
| 69 <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)"> | |
| 70 <filter>'bcf' in oo['out']</filter> | |
| 71 </data> | |
| 72 </xml> | |
| 73 <xml name="dump"> | |
| 74 <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads"> | |
| 75 <filter>'dump' in oo['out']</filter> | |
| 76 </data> | |
| 77 </xml> | |
| 78 <xml name="log"> | |
| 79 <data name="out_log" format="txt" from_work_dir="log.txt" label="${tool.name} on ${on_string}: Log"> | |
| 80 <filter>'log' in oo['out']</filter> | |
| 81 </data> | |
| 82 </xml> | |
| 83 | |
| 84 <!-- | |
| 85 Help | |
| 86 --> | |
| 87 | |
| 88 <token name="@WID@"><![CDATA[ | |
| 89 Delly is an integrated structural variant (SV) prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome. | |
| 90 ]]></token> | |
| 91 <token name="@REFERENCES@"><![CDATA[ | |
| 92 More information are available on `github <https://github.com/dellytools/delly>`_. | |
| 93 ]]></token> | |
| 94 </macros> |
