Webinar: Learn about the most rapid way to go from human NGS data to biological interpretation

Register for an Ingenuity webinar that discusses how Ingenuity® Variant Analysis™ combines analytical tools and integrated content to help you rapidly identify a short list of compelling variants using selection criteria based both upon published biological evidence and your own knowledge of disease biology.

At AGBT, Ingenuity introduced Variant Analysis – a new application for researchers who need to identify causal variants from human resequencing data.  Not surprisingly, given the copious amounts of data now possible via next generation sequencing, biological interpretation of thousands of potentially deleterious variants has been 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. At last, there is a fast, easy-to-use application which allows you to leverage an extensive knowledge base of millions of expert-curated mutation and literature-based biomedical findings to empower real-time interactive filtering and rapid prioritization to quickly zero in on the few that are most compelling for follow-up.

To learn more about Variant Analysis and its impact on your research, join us for the webinar:

Rapid Biological Interpretation of Human NGS Data with Ingenuity Variant Analysis

In this webinar we will demonstrate the application of a context-rich knowledge base to discover cancer-driver variants and novel causal variants for human genetic disease, using a combination of causal analytics, genetic analysis at the variant/gene/pathway levels, and the ability to visualize how variants impact disease progression

Date: Wednesday, March 14, 2012, 7:00am PST
Speaker: Dan Richards, Sr. Director of Computational Biology, Ingenuity Systems

Click here to register

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