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Repository table_annovar
Owner: devteam
Synopsis: Annotate a VCF file using ANNOVAR annotations to produce a tabular file that can be filtered
Please see the http://www.openbioinformatics.org/annovar/annovar_accessary.html#excel for details.
Content homepage: Non
Type: unrestricted
Revision: 8:d4e292ddda05
This revision can be installed: True
Times cloned / installed: 3087

Repository README files - may contain important installation or license information

ANNOVAR needs to be installed manually in the following way:

1a) If you already have ANNOVAR installed on your system, simply edit the tool-data/annovar.loc file to reflect locations of 
the perl scripts (annotate_variation.pl and convert2annovar.pl) and humandb directory (directory containing the annovar database files)

1b) If you do not have ANNOVAR installed, request annovar download and sign license here: 
http://www.openbioinformatics.org/annovar/annovar_download_form.php

i)  Once downloaded, install annovar per the installation instructions and note the installation path.

ii)  Then download all desired databases for all desired builds as follows:
annotate_variation.pl -downdb -buildver <build> [-webfrom annovar] <database> <humandb>

 where <humandb> is location where all database files should be stored
 and <database> is the database file to download, e.g. refGene (see bottom of document for all available database files at the time of writing this tool)
 and <build> can be hg18 or hg19 for humans, also other organisms available.

 list of all available databases can be found here: http://www.openbioinformatics.org/annovar/annovar_db.html

iii) edit the tool-data/annovar.loc file to reflect location of humandb folder

2) add the annovar scripts convert2annovar.pl and table_annovar.pl to your Galaxy user's path

3) restart galaxy instance for changes in .loc file to take effect
Dependencies of this repository

Name Version Type
SCRIPT_PATH set_environment

Contents of this repository

Name Description Version Minimum Galaxy Version
with functional information using ANNOVAR 0.2 16.01

Categories
Variant Analysis - Tools for single nucleotide polymorphism data such as WGA