Mercurial > repos > iuc > deepvariant
comparison deepvariant.xml @ 1:b778a18bd878 draft
"planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/deepvariant commit ce3024e2098c50a93ea8a7fc120a40a570fd0c53"
author | iuc |
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date | Fri, 01 Oct 2021 07:46:42 +0000 |
parents | 7608209110d3 |
children | 98fe794d2ec0 |
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0:7608209110d3 | 1:b778a18bd878 |
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29 #if $regions_conditional.regions_option == 'region' | 29 #if $regions_conditional.regions_option == 'region' |
30 --regions $regions_conditional.region_literal | 30 --regions $regions_conditional.region_literal |
31 #else if $regions_conditional.regions_option == 'bed' | 31 #else if $regions_conditional.regions_option == 'bed' |
32 --regions region.bed | 32 --regions region.bed |
33 #end if | 33 #end if |
34 --call_variants_extra_args="use_openvino=true" ## Setting this will use OpenVINO on Intel CPUs, which empirically reduces call_variants runtime by 15%-25%. | 34 ##--call_variants_extra_args="use_openvino=true" ## Setting this will use OpenVINO on Intel CPUs, which empirically reduces call_variants runtime by 15%-25%. |
35 --num_shards=\${GALAXY_SLOTS:-2} | 35 --num_shards=\${GALAXY_SLOTS:-2} |
36 && gunzip './output.vcf.gz' | 36 && gunzip './output.vcf.gz' |
37 #if $output_gvcf | 37 #if $output_gvcf |
38 && gunzip './output.g.vcf.gz' | 38 && gunzip './output.g.vcf.gz' |
39 #end if | 39 #end if |
54 </when> | 54 </when> |
55 <when value="history"> | 55 <when value="history"> |
56 <param name="history_item" type="data" format="fasta" label="Reference genome" help="A reference genome in FASTA format" /> | 56 <param name="history_item" type="data" format="fasta" label="Reference genome" help="A reference genome in FASTA format" /> |
57 </when> | 57 </when> |
58 </conditional> | 58 </conditional> |
59 <param argument="--reads" type="data" format="BAM" label="BAM file" help="An aligned reads files for child and one or two parents in BAM format. The reads must be aligned to the reference genome" /> | 59 <param argument="--reads" type="data" format="BAM" label="BAM file" help="An aligned reads file in BAM format. The reads must be aligned to the reference genome" /> |
60 <param argument="--model_type" type="select" label="Model type" help="Type of model to use for variant calling"> | 60 <param argument="--model_type" type="select" label="Model type" help="Type of model to use for variant calling"> |
61 <option value="WGS">WGS: Illumina whole genome sequencing</option> | 61 <option value="WGS">WGS: Illumina whole genome sequencing</option> |
62 <option value="WES">WES: Illumina whole exome sequencing</option> | 62 <option value="WES">WES: Illumina whole exome sequencing</option> |
63 <option value="PACBIO">PacBio HiFi</option> | 63 <option value="PACBIO">PacBio HiFi</option> |
64 <option value="HYBRID_PACBIO_ILLUMINA">Hybrid PacBio HiFi-Illumina</option> | 64 <option value="HYBRID_PACBIO_ILLUMINA">Hybrid PacBio HiFi-Illumina</option> |