WEBINAR: Identifying Clinically Relevant Variants from Human Resequencing Data

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Do you want to extract valuable insights from your human DNA resequencing studies - faster? Learn more by joining our webinar on November 16: "Rapid Identification of Clinically Relevant Variants from Human Resequencing Data"   Biological interpretation of thousands of potentially deleterious variants is a bottleneck in extracting valuable insights from DNA resequencing studies, often requiring months of effort after completion of the reference genome alignment and variant calling steps.  Register for this webinar to learn how to use Ingenuity Variant Analysis to rapidly analyze human resequencing data in just minutes.  Dan Richards, Vice President of Biomedical Informatics, will present the application of a context-rich knowledgebase in combination with causal analytics, statistical and genetic analysis at the variant, gene and pathway levels to discover clinically relevant cancer driver variants and novel causal variants for human genetic disease.  Dan will also highlight key new features including:   •       Multi-family pedigree support to select for variants consistent with Mendelian inheritance •       Statistical burden tests to find genes or pathways that have significantly more deleterious variants in one group than another •       Disease models that identify diseases consistent with clinical features and deleterious variants in medical genomes Also, for a very limited time only* you can sign up for a two week free trial of Variant Analysis.  Click here to get started! * Variant Analysis free trial is only available to new users who register and upload data on or before November 30, 2012.     Copyright ©2012 Ingenuity, Inc. All Rights Reserved. Ingenuity, Inc., 1700 Seaport Blvd. Third Floor Redwood City, CA, 94063 www.ingenuity.com

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