Mercurial > repos > crs4 > kggseq_variant_selection
comparison tool_dependencies.xml @ 10:124e64eea35b draft default tip
Fix shell command
author | crs4 |
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date | Mon, 11 Jun 2018 13:19:34 -0400 |
parents | 4088332e198a |
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9:4088332e198a | 10:124e64eea35b |
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2 <tool_dependency> | 2 <tool_dependency> |
3 <package name="kggseq" version="1.0_20180410"> | 3 <package name="kggseq" version="1.0_20180410"> |
4 <install version="1.0"> | 4 <install version="1.0"> |
5 <actions> | 5 <actions> |
6 <action type="download_by_url" target_filename="kggseq_archive-v1.0_20180410.tar.gz">https://github.com/crs4/kggseq_archive/archive/v1.0_20180410.tar.gz</action> | 6 <action type="download_by_url" target_filename="kggseq_archive-v1.0_20180410.tar.gz">https://github.com/crs4/kggseq_archive/archive/v1.0_20180410.tar.gz</action> |
7 <action type="shell_command">java -jar kggseq.jar --no-lib-check --resource-update --resource resources --buildver hg19 --vcf-file examples-lite/rare.disease.hg19.vcf</action> | |
7 <action type="shell_command">java -jar kggseq.jar --no-lib-check --resource-update --resource resources --buildver hg19 --db-filter 1kgeur201305,1kgeas201305,1kgafr201305,1kgsas201305,1kgamr201305,1kg201305,1kg201204,1kgafr201204,1kgeur201204,1kgamr201204,1kgasn201204,dbsnp135,dbsnp137,dbsnp138,dbsnp138nf,dbsnp141,ESP6500AA,ESP6500EA,exac,gadexome,gadgenome --genome-annot --db-gene refgene,gencode,knowngene,ensembl --db-score dbnsfp --superdup-annot --cosmic-annot --omim-annot --scsnv-annot --mouse-pheno --zebrafish-pheno --ddd-annot --mendel-causing-predict best --patho-gene-predict --dgv-cnv-annot --o-flanking-seq 10 --vcf-file examples-lite/rare.disease.hg19.vcf</action> | 8 <action type="shell_command">java -jar kggseq.jar --no-lib-check --resource-update --resource resources --buildver hg19 --db-filter 1kgeur201305,1kgeas201305,1kgafr201305,1kgsas201305,1kgamr201305,1kg201305,1kg201204,1kgafr201204,1kgeur201204,1kgamr201204,1kgasn201204,dbsnp135,dbsnp137,dbsnp138,dbsnp138nf,dbsnp141,ESP6500AA,ESP6500EA,exac,gadexome,gadgenome --genome-annot --db-gene refgene,gencode,knowngene,ensembl --db-score dbnsfp --superdup-annot --cosmic-annot --omim-annot --scsnv-annot --mouse-pheno --zebrafish-pheno --ddd-annot --mendel-causing-predict best --patho-gene-predict --dgv-cnv-annot --o-flanking-seq 10 --vcf-file examples-lite/rare.disease.hg19.vcf</action> |
8 <action type="move_directory_files"> | 9 <action type="move_directory_files"> |
9 <source_directory>.</source_directory> | 10 <source_directory>.</source_directory> |
10 <destination_directory>$INSTALL_DIR</destination_directory> | 11 <destination_directory>$INSTALL_DIR</destination_directory> |
11 </action> | 12 </action> |