QuickStart Annovar
Functional annotation of genetic variants from high-though put sequencing data.
ANNOVAR is an efficient software tool to utilize update-to-date information to functionally annotate genetic variants detected from diverse genomes (including human genome hg18, hg19, hg38, as well as mouse, worm, fly, yeast and many others). Given a list of variants with chromosome, start position, end position, reference nucleotide, and observed nucleotides, ANNOVAR can perform gene-based, region-based or filter-based annotation as well as many other functionalities.
- 
                           Use Global Protect VPN: Whether on or Off-Campus Be sure vpn-groups selected when you connect. 
- 
                           Start an SSH Session $ ssh your_netid@hpc.kennesaw.edu 
- 
                           Check The Current Version(s) Available $ module avail Annovar ------------- /data/Apps/Modules/Software -------------- 
 ANNOVAR/2016Feb01
- 
                           Load the Module $ module load Annovar 
- 
                           For More Information on Annovar ÁñÁ«»ÆÊÓÆµ . 
