Apr 112014
 
$ module load apps/annovar/529
apps/annovar/529/noarch
 |
 OK

$ ls $ANNOVARBIN
annotate_variation.pl  coding_change.pl 
convert2annovar.pl  retrieve_seq_from_fasta.pl
summarize_annovar.pl  table_annovar.pl 
variants_reduction.pl

$ ls $ANNOVARDIR
bin  db  example
$ module whatis apps/annovar/529/noarch

 apps/annovar/529 :

Title: ANNOVAR
 Summary: Functional annotation of genetic variants from high-throughput sequencing data
 License: NONFREE - Free for non-profit use; see http://www.openbioinformatics.org/annovar/annovar_faq.html#license
 Group: Bioinformatics
 URL: http://www.openbioinformatics.org/annovar/

Name: annovar
 Version: 529
 Module: apps/annovar/529/noarch
 Module path: /opt/gridware/etc/modules/apps/annovar/529/noarch
 Package path: /opt/gridware/pkg/apps/annovar/529/noarch

Repository: git+http://download.alces-software.com/git/packager-base@c0cb517
 Package: ext/annovar/@094f23e0
 Last update: 2012-09-20

Builder: root@headnode1.lampredi.cluster.local
 Build date: 2014-04-11T13:12:32
 Build parameters: tarball=/opt/gridware/ext/annovar-20130823.tar.gz
 Compiler: N/A

For further information, execute:
module help apps/annovar/529/noarch
$ module help apps/annovar/529/noarch

----------- Module Specific Help for 'apps/annovar/529/noarch' ---------------------------


                      ======== ANNOVAR ========                      
           Functional annotation of genetic variants from            
                   high-throughput sequencing data                   
                      ========================                      

This module sets up your environment for the use of the 'annovar'
application. This module sets up version '529' of the
application.


>> SYNOPSIS <1%) in the
    1000 Genome Project, or identify subset of non-synonymous SNPs
    with SIFT score>0.05, or many other annotations on specific
    mutations.
  * Other functionalities: Retrieve the nucleotide sequence in any
    user-specific genomic positions in batch, identify a candidate
    gene list for Mendelian diseases from exome data, identify a
    list of SNPs from 1000 Genomes that are in strong LD with a GWAS
    hit, and many other creative utilities.


>> LICENSING <> FURTHER INFORMATION <> GET STARTED <<

Please refer to the website for further details on usage of this
package.
$ module show apps/annovar/529/noarch

-------------------------------------------------------------------
/opt/gridware/etc/modules/apps/annovar/529/noarch:

module-whatis	 

            Title: ANNOVAR
          Summary: Functional annotation of genetic variants from high-throughput sequencing data
          License: NONFREE - Free for non-profit use; see http://www.openbioinformatics.org/annovar/annovar_faq.html#license
            Group: Bioinformatics
              URL: http://www.openbioinformatics.org/annovar/

             Name: annovar
          Version: 529
           Module: apps/annovar/529/noarch
      Module path: /opt/gridware/etc/modules/apps/annovar/529/noarch
     Package path: /opt/gridware/pkg/apps/annovar/529/noarch

       Repository: git+http://download.alces-software.com/git/packager-base@c0cb517
          Package: ext/annovar/@094f23e0
      Last update: 2012-09-20

          Builder: root@headnode1.lampredi.cluster.local
       Build date: 2014-04-11T13:12:32
 Build parameters: tarball=/opt/gridware/ext/annovar-20130823.tar.gz
         Compiler: N/A


For further information, execute:

	module help apps/annovar/529/noarch
 
module-conflict	 apps/annovar 
setenv		 ANNOVARDIR /opt/gridware/pkg/apps/annovar/529/noarch 
setenv		 ANNOVARBIN /opt/gridware/pkg/apps/annovar/529/noarch/bin 
prepend-path	 PATH /opt/gridware/pkg/apps/annovar/529/noarch/bin 
prepend-path	 MANPATH /opt/gridware/pkg/apps/annovar/529/noarch/share/man 
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 Posted by at 2:42 pm