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Weill Cornell Medical College Selects Ingenuity® Variant Analysis™ and Ingenuity® iReport™ for Sequencing Core Facility
Date:3/19/2012

REDWOOD CITY, Calif., March 19, 2012 /PRNewswire/ -- Ingenuity Systems, a leading provider of information and analysis solutions for life science researchers, today announced that the Weill Cornell Medical College has chosen Ingenuity Variant Analysis and Ingenuity iReport for use in its sequencing core facility.  Variant Analysis will be used to identify causal variants from the output of whole genome and exome sequencing experiments and iReport will be used for the biological interpretation of RNA-Seq and other gene expression data.

The ability to rapidly and reliably identify causal variants and relevant pathways from NGS studies is imperative for realizing the full value of NGS platforms. The Ingenuity NGS offerings leverage the unique and proprietary Ingenuity® Knowledge Base to provide researchers with a rapid and evidence-backed biological analysis of their NGS experiments.

Ingenuity Variant Analysis offers a unique combination of filtering, analytics, and richly annotated content that allows researchers to identify and prioritize variants by drilling down to a small, targeted subset of compelling variants based both upon published biological evidence and the researcher's own knowledge of disease biology. Researchers working with RNA-Seq data can use Ingenuity iReport to quickly and accurately determine key affected pathways and biological processes, and understand the molecular and genetic basis of observed gene expression changes – all with peer-reviewed literature support. 

"Pathway analysis is essential for elucidating the molecular networks affected by rare variants and for discovering the compounding, perturbing effects within biological processes which encompass many genetic loci," stated Christopher Mason, Ph.D., Assistant Professor, Institute for Computational Biomedicine, Cornell University. "Ingenuity Variant Analysis enables us to rapidly identify the most compelling variants from an NGS resequen
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