Mercurial > repos > crs4 > kggseq_variant_selection

diff tool_dependencies.xml @ 8:eebc0adefae0 draft

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Updates to KGGSeq 1.0_20180410
author crs4
date Mon, 11 Jun 2018 12:41:24 -0400
parents ed0dbb61f0e1
children 4088332e198a
line wrap: on
line diff
--- a/tool_dependencies.xml	Mon Jun 11 12:40:53 2018 -0400
+++ b/tool_dependencies.xml	Mon Jun 11 12:41:24 2018 -0400
@@ -1,10 +1,10 @@
 <?xml version="1.0"?>
 <tool_dependency>
-  <package name="kggseq" version="1.0_20160707">
+  <package name="kggseq" version="1.0_20180410">
     <install version="1.0">
       <actions>
-        <action type="download_by_url" target_filename="kggseq_archive-v1.0_20160707.tar.gz">https://github.com/crs4/kggseq_archive/archive/v1.0_20160707.tar.gz</action>
-        <action type="shell_command">java -jar kggseq.jar --no-lib-check --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 --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 all  --patho-gene-predict --dgv-cnv-annot --o-flanking-seq 10  --vcf-file examples-lite/rare.disease.hg19.vcf</action>
+        <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>
+        <action type="shell_command">java -jar kggseq.jar --no-lib-check --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>
         <action type="move_directory_files">
           <source_directory>.</source_directory>
           <destination_directory>$INSTALL_DIR</destination_directory>