" "
Satellite Banner
Informatics
Scientific Community
 
Become a Member | Sign in
Home>News>This Article
  News
Return

Ingenuity Systems Delivers Integrated Workflow in Ion Reporter™ Software Suite and Ingenuity Variant Analysis Offerings

Published: Sunday, October 14, 2012
Last Updated: Sunday, October 14, 2012
Bookmark and Share
Ingenuity and Ion Torrent to offer a promotional solution bundle for exome sequencing by the end of 2012

Ingenuity Systems, a leading provider of information and analysis solutions for life science researchers, has demonstrated the integration of Ingenuity Variant Analysis with Ion Reporter™ Software at Ion World 2012. The combined solutions enable users to get one-click access to Variant Analysis to interpret their variants from all human DNA variation workflows.

Integration includes automated user registration and data transfer, allowing researchers to work with Variant Analysis directly from within Ion Reporter. The interactive filter cascade in Variant Analysis provides a streamlined data analysis workflow to identify and prioritize variants.

"Ingenuity Variant Analysis is a natural extension of our cloud-based Ion Reporter Software," said Mike Lelivelt, Ph.D., Director of Bioinformatics at Life Technologies. "Ion Reporter builds a pipeline to do variant calling, mapping, identification and annotation. Variant Analysis extends that pipeline to help researchers identify, prioritize and report the most biologically interesting causal variants for follow-up."

Ion Reporter Software has been developed to simplify bioinformatics data analysis, annotation, reporting, and archiving of semiconductor sequencing data. Ingenuity Variant Analysis combines analytical tools and integrated content to help researchers rapidly identify and prioritize variants by drilling down to a small, targeted subset of compelling variants based on algorithms powered by the Ingenuity Knowledge Base of millions of findings from the biomedical literature and the researcher's own knowledge of disease biology.

"I've been impressed by the capabilities in Ingenuity Variant Analysis to set and adjust rich filters and test new hypotheses with a simple point and click," said Dr. Christopher E. Mason, Assistant Professor, Weill Cornell Medical College. "Increasing access to the unique content and intuitive user interface makes it easier for researchers to get insights from their data, since it allows you to move from a variant file to a hypothesis in a matter of minutes."

Special bundles - Exome Analysis

Ingenuity and Ion Torrent plan to offer a promotional solution bundle for exome sequencing, including the relevant combination of Ion Torrent reagents, Ion Reporter for data processing, and Ingenuity Variant Analysis for additional data interpretation.  The solution bundle will be available by the end of 2012.


Further Information

Join For Free

Access to this exclusive content is for Technology Networks Premium members only.

Join Technology Networks Premium for free access to:

  • Exclusive articles
  • Presentations from international conferences
  • Over 3,000+ scientific posters on ePosters
  • More than 4,400+ scientific videos on LabTube
  • 35 community eNewsletters


Sign In



Forgotten your details? Click Here
If you are not a member you can join here

*Please note: By logging into TechnologyNetworks.com you agree to accept the use of cookies. To find out more about the cookies we use and how to delete them, see our privacy policy.


Scientific News
New Database for Sharing MS Clinical Trial Data
A new database containing nearly 2500 patient records from the placebo arms of nine multiple sclerosis (MS) clinical trials is now available for research by qualified investigators.
‘Precision Prevention’ for Colorectal Cancer
New risk prediction model — not yet ready for clinical use — incorporates genetic, lifestyle and environmental risk factors.
Characterizing Cancerous Genomic Variations
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
Uncovering Hidden Genomic Alterations that Drive Cancers
Tested on large tumor genomics database, REVEALER method allows researchers to connect genomics to cell function.
Spotting DNA Repair Genes Gone Awry
Ludwig researchers develop a two-pronged approach for identifying genes responsible for fixing DNA damage that can trigger cancer when compromised.
Interpreting “Dark Matter” DNA
Scientists at the Gladstone Institutes have invented a new way to read and interpret the human genome.
A Programming Language for Living Cells
New language lets researchers design novel biological circuits.
The Epigenetics of Childhood Cancer
Qlucore software enables researchers to more easily study the genetic influences behind childhood cancer.
Mining Whole Exome Data to Improve Cancer Therapies
New tool interprets the raw data of whole exome tumor sequencing and then matches the cancer’s unique genetics to FDA-approved targeted treatments.
Pittcon 2016: Accelerating Innovation And Enhancing Productivity With Technology
Collaboration and externalization of data highlight evolving lab operations.
Scroll Up
Scroll Down
SELECTBIO

SELECTBIO Market Reports
Go to LabTube
Go to eposters
 
Access to the latest scientific news
Exclusive articles
Upload and share your posters on ePosters
Latest presentations and webinars
View a library of 1,800+ scientific and medical posters
3,000+ scientific and medical posters
A library of 2,500+ scientific videos on LabTube
4,400+ scientific videos
Close
Premium CrownJOIN TECHNOLOGY NETWORKS PREMIUM FOR FREE!