Ingenuity Variant Analysis and iReport selected for Weill Cornell sequencing core facility

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 resequencing study, and Ingenuity iReport makes rich biology and networks underlying an RNA-Seq study really approachable and intuitive. Both solutions provide a unique combination of filtering, analytics, and deep expert-curated annotation content, so we can quickly prioritize variants and genes of interest."

"Cornell and the Mason laboratory are pioneering in clinical applications of NGS for the benefit of patients," stated Doug Bassett, Ph.D., Chief Scientific Officer and Chief Technology Officer, Ingenuity Systems. "It has been a pleasure working with Cornell researchers in the development of our new NGS product capabilities—and we are pleased to have these new products leveraged as part of their NGS core laboratory offering."

Source:

Ingenuity Systems

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
New study challenges traditional view of how the genetic code evolved