We at the Clinical Genomics Centre (MSH/UHN) are pleased to announce a special seminar from Ingenuity Systems, the company which offers the well known Ingenuity Pathway Analysis software. Their upcoming talk will be focused on their new variant analysis software and it is titled:
"Interpreting Variants from the Human Genome, Exome and Targeted Panel Sequencing: A Rapid, Point-and-Click Approach"
Presented by David Dailey, NGS Specialist on Wednesday, November 6th, 12-1 pm at 60 Murray street, room L2-208.
For more information, please see the abstract and poster below.
Lunch will be served!
Classification and prioritization of variants is challenging, not just because of the number and uniqueness of variants of potential interest, but also due to the wide range of information sources useful to the prioritization process. Ingenuity has put its proven ability to capture published findings to bring together information on variant and gene function, pathways, processes and disease models within an intuitive system that enbles investigators and clinical researchers to ask many questions of their data and see the results in seconds, with direct access to the supporting findings to guide decisions on which variants to carry forward. Examples pertinant to rare disease, germline and somatic cancer, will be presented.