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Because these tools draw in information from may disparate sources, they can be very difficult to install, configure, use, and maintain. For example, the vcf files from the 1000 Genomes project are arranged in a deep ftp tree by date of data generation. Large genome centers spend significant resources managing these tools. Our objective 

 

Pre-packaged programs

Annovar - one of the most powerful yet simple to run variant annotators available

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