Mercurial > repos > iuc > delly_filter
comparison macros.xml @ 2:445e356988a7 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/delly commit d18d984264f54b45e94d97b5b97ed499a32a334a"
| author | iuc |
|---|---|
| date | Fri, 22 Jan 2021 14:28:59 +0000 |
| parents | c559b5bb484b |
| children | db71f8a3323a |
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| 1:c559b5bb484b | 2:445e356988a7 |
|---|---|
| 1 <?xml version="1.0"?> | 1 <?xml version="1.0"?> |
| 2 <macros> | 2 <macros> |
| 3 <token name="@TOOL_VERSION@">0.8.5</token> | 3 <token name="@TOOL_VERSION@">0.8.7</token> |
| 4 <token name="@VERSION_SUFFIX@">0</token> | 4 <token name="@VERSION_SUFFIX@">0</token> |
| 5 <xml name="requirements"> | 5 <xml name="requirements"> |
| 6 <requirements> | 6 <requirements> |
| 7 <requirement type="package" version="@TOOL_VERSION@">delly</requirement> | 7 <requirement type="package" version="@TOOL_VERSION@">delly</requirement> |
| 8 <requirement type="package" version="1.10.2">bcftools</requirement> | 8 <requirement type="package" version="1.10.2">bcftools</requirement> |
| 15 <citations> | 15 <citations> |
| 16 <citation type="doi">10.1093/bioinformatics/bts378</citation> | 16 <citation type="doi">10.1093/bioinformatics/bts378</citation> |
| 17 </citations> | 17 </citations> |
| 18 </xml> | 18 </xml> |
| 19 | 19 |
| 20 <!-- | 20 <!-- command --> |
| 21 command | |
| 22 --> | |
| 23 | 21 |
| 24 <token name="@BAM@"><![CDATA[ | 22 <token name="@BAM@"><![CDATA[ |
| 25 #for $i, $current in enumerate($samples) | 23 #for $i, $current in enumerate($input) |
| 26 ln -s '${current}' 'sample_${i}.bam' && | 24 ln -s '${current}' 'input_${i}.bam' && |
| 27 ln -s '${current.metadata.bam_index}' 'sample_${i}.bam.bai' && | 25 ln -s '${current.metadata.bam_index}' 'input_${i}.bam.bai' && |
| 28 #end for | 26 #end for |
| 29 ]]></token> | 27 ]]></token> |
| 30 <token name="@DUMP@"><![CDATA[ | 28 <token name="@DUMP@"><![CDATA[ |
| 31 #if 'dump' in $oo.out | 29 #if 'dump' in $oo.out |
| 32 && test -f 'dump.tsv.gz' && bgzip -d 'dump.tsv.gz' || echo 'No dump file.' | 30 && test -f 'dump.tsv.gz' && bgzip -d 'dump.tsv.gz' || echo 'No dump file.' |
| 41 #if 'vcf' in $oo.out | 39 #if 'vcf' in $oo.out |
| 42 && test -f 'result.bcf' && bcftools view 'result.bcf' > 'result.vcf' || echo 'No results.' | 40 && test -f 'result.bcf' && bcftools view 'result.bcf' > 'result.vcf' || echo 'No results.' |
| 43 #end if | 41 #end if |
| 44 ]]></token> | 42 ]]></token> |
| 45 | 43 |
| 46 <!-- | 44 <!-- input --> |
| 47 input | |
| 48 --> | |
| 49 | 45 |
| 46 <xml name="cnoffset" token_default=""> | |
| 47 <param name="cnoffset" type="float" min="0.0" max="1.0" value="@DEFAULT@" label="Set minimum CN offset" help="(--cn-offset)"/> | |
| 48 </xml> | |
| 49 <xml name="coverage" token_label=""> | |
| 50 <param argument="--coverage" type="integer" value="10" label="@LABEL@"/> | |
| 51 </xml> | |
| 50 <xml name="exclude"> | 52 <xml name="exclude"> |
| 51 <param argument="--exclude" type="data" format="tabular" optional="true" label="Select file with regions to exclude"/> | 53 <param argument="--exclude" type="data" format="tabular" optional="true" label="Select file with regions to exclude"/> |
| 52 </xml> | 54 </xml> |
| 53 <xml name="genome"> | 55 <xml name="genome"> |
| 54 <param argument="--genome" type="data" format="fasta" label="Select genome"/> | 56 <param argument="--genome" type="data" format="fasta" label="Select genome file"/> |
| 55 </xml> | 57 </xml> |
| 56 <xml name="genoqual"> | 58 <xml name="genoqual"> |
| 57 <param name="genoqual" type="integer" value="5" label="Set minimum mapping quality for genotyping" help="(--geno-qual)"/> | 59 <param name="genoqual" type="integer" value="5" label="Set minimum mapping quality for genotyping" help="(--geno-qual)"/> |
| 58 </xml> | 60 </xml> |
| 61 <xml name="input" token_format="" token_multiple="false" token_label=""> | |
| 62 <param name="input" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/> | |
| 63 </xml> | |
| 64 <xml name="maxreadsep" token_default=""> | |
| 65 <param argument="--maxreadsep" type="integer" value="@DEFAULT@" label="Set maximum read separation"/> | |
| 66 </xml> | |
| 67 <xml name="maxsize" token_default="" token_label=""> | |
| 68 <param argument="--maxsize" type="integer" value="@DEFAULT@" label="@LABEL@"/> | |
| 69 </xml> | |
| 59 <xml name="minclip"> | 70 <xml name="minclip"> |
| 60 <param argument="--minclip" type="integer" value="25" label="Set minimum clipping length"/> | 71 <param argument="--minclip" type="integer" value="25" label="Set minimum clipping length"/> |
| 61 </xml> | 72 </xml> |
| 62 <xml name="maxreadsep" token_default="40"> | 73 <xml name="mincliquesize"> |
| 63 <param argument="--maxreadsep" type="integer" value="@DEFAULT@" label="Set maximum read separation"/> | 74 <param name="mincliquesize" type="integer" value="2" label="Set minimum paired-end/single-read clique size" help="(--min-clique-size)"/> |
| 64 </xml> | 75 </xml> |
| 65 <xml name="maxsize" token_default="1000000"> | 76 <xml name="minrefsep" token_default=""> |
| 66 <param argument="--maxsize" type="integer" value="@DEFAULT@" label="Set maximum SV size"/> | |
| 67 </xml> | |
| 68 <xml name="mincliquesize"> | |
| 69 <param name="mincliquesize" type="integer" value="2" label="Set minimum min. PE/SR clique size" help="(--min-clique-size)"/> | |
| 70 </xml> | |
| 71 <xml name="minrefsep" token_default="25"> | |
| 72 <param argument="--minrefsep" type="integer" value="@DEFAULT@" label="Set minimum reference separation"/> | 77 <param argument="--minrefsep" type="integer" value="@DEFAULT@" label="Set minimum reference separation"/> |
| 73 </xml> | 78 </xml> |
| 74 <xml name="minsize"> | 79 <xml name="minsize" token_default="" token_label=""> |
| 75 <param argument="--minsize" type="integer" value="0" label="Set minimum SV size"/> | 80 <param argument="--minsize" type="integer" value="@DEFAULT@" label="@LABEL@"/> |
| 76 </xml> | 81 </xml> |
| 77 <xml name="samples" token_format="bam" token_multiple="true" token_label="Select sample file(s)"> | 82 <xml name="pass"> |
| 78 <param name="samples" type="data" format="@FORMAT@" multiple="@MULTIPLE@" label="@LABEL@"/> | 83 <param argument="--pass" type="boolean" truevalue="--pass" falsevalue="" label="Filter sites for PASS?"/> |
| 84 </xml> | |
| 85 <xml name="ploidy"> | |
| 86 <param argument="--ploidy" type="integer" value="2" label="Set baseline ploidy"/> | |
| 87 </xml> | |
| 88 <xml name="samples"> | |
| 89 <param argument="--samples" type="data" format="tabular" label="Select sample file" help="Two-column sample file listing sample name and tumor or control."/> | |
| 79 </xml> | 90 </xml> |
| 80 <xml name="svtype"> | 91 <xml name="svtype"> |
| 81 <param argument="--svtype" type="select" label="Select type(s) of structural variants to detect"> | 92 <param argument="--svtype" type="select" label="Select type(s) of structural variants to detect"> |
| 82 <option value="ALL" selected="true">All types (ALL)</option> | 93 <option value="ALL" selected="true">All types (ALL)</option> |
| 83 <option value="DEL">Deletion (DEL)</option> | 94 <option value="DEL">Deletion (DEL)</option> |
| 95 <option value="DUP">Duplication (DUP)</option> | |
| 84 <option value="INS">Insertion (INS)</option> | 96 <option value="INS">Insertion (INS)</option> |
| 85 <option value="DUP">Duplication (DUP)</option> | |
| 86 <option value="INV">Inversion (INV)</option> | 97 <option value="INV">Inversion (INV)</option> |
| 87 <option value="BND">Translocation (BND)</option> | 98 <option value="BND">Translocation (BND)</option> |
| 88 </param> | 99 </param> |
| 89 </xml> | 100 </xml> |
| 90 <xml name="vcffile"> | 101 <xml name="vcffile"> |
| 91 <param argument="--vcffile" type="data" format="vcf,bcf" optional="true" label="Select genotyping file"/> | 102 <param argument="--vcffile" type="data" format="bcf,vcf" optional="true" label="Select genotyping file"/> |
| 92 </xml> | 103 </xml> |
| 93 | 104 |
| 94 <!-- | 105 <!-- output --> |
| 95 output | |
| 96 --> | |
| 97 | 106 |
| 107 <xml name="bcf"> | |
| 108 <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)"> | |
| 109 <filter>'bcf' in oo['out']</filter> | |
| 110 </data> | |
| 111 </xml> | |
| 98 <xml name="vcf"> | 112 <xml name="vcf"> |
| 99 <data name="out_vcf" format="vcf" from_work_dir="result.vcf" label="${tool.name} on ${on_string}: Result (VCF)"> | 113 <data name="out_vcf" format="vcf" from_work_dir="result.vcf" label="${tool.name} on ${on_string}: Result (VCF)"> |
| 100 <filter>'vcf' in oo['out']</filter> | 114 <filter>'vcf' in oo['out']</filter> |
| 101 </data> | |
| 102 </xml> | |
| 103 <xml name="bcf"> | |
| 104 <data name="out_bcf" format="bcf" from_work_dir="result.bcf" label="${tool.name} on ${on_string}: Result (BCF)"> | |
| 105 <filter>'bcf' in oo['out']</filter> | |
| 106 </data> | 115 </data> |
| 107 </xml> | 116 </xml> |
| 108 <xml name="dump"> | 117 <xml name="dump"> |
| 109 <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads"> | 118 <data name="out_dump" format="tabular" from_work_dir="dump.tsv" label="${tool.name} on ${on_string}: SV-reads"> |
| 110 <filter>'dump' in oo['out']</filter> | 119 <filter>'dump' in oo['out']</filter> |
| 114 <data name="out_log" format="txt" label="${tool.name} on ${on_string}: Log"> | 123 <data name="out_log" format="txt" label="${tool.name} on ${on_string}: Log"> |
| 115 <filter>'log' in oo['out']</filter> | 124 <filter>'log' in oo['out']</filter> |
| 116 </data> | 125 </data> |
| 117 </xml> | 126 </xml> |
| 118 | 127 |
| 119 <!-- | 128 <!-- help --> |
| 120 Help | |
| 121 --> | |
| 122 | 129 |
| 123 <token name="@WID@"><![CDATA[ | 130 <token name="@WID@"><![CDATA[ |
| 124 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. | 131 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. |
| 132 | |
| 133 Short-read SV calling | |
| 134 | |
| 135 - *call* to discover and genotype structural variants | |
| 136 - *merge* structural variants across VCF/BCF files and within a single VCF/BCF file | |
| 137 - *filter* somatic or germline structural variants | |
| 138 | |
| 139 Long-read SV calling | |
| 140 | |
| 141 - *lr* for long-read SV discovery | |
| 142 | |
| 143 Copy-number variant calling | |
| 144 | |
| 145 - *cnv* to discover and genotype copy-number variants | |
| 146 - *classify* somatic or germline copy-number variants | |
| 125 ]]></token> | 147 ]]></token> |
| 126 <token name="@REFERENCES@"><![CDATA[ | 148 <token name="@REFERENCES@"><![CDATA[ |
| 127 More information are available on `GitHub <https://github.com/dellytools/delly>`_. | 149 More information are available on `GitHub <https://github.com/dellytools/delly>`_. |
| 128 ]]></token> | 150 ]]></token> |
| 129 </macros> | 151 </macros> |
