A Journey into the Unknown: Exploring the Clinical Diagnostic Path from Targeted Panel to Whole Exome Sequencing

  • During this presentation, you will:

    • Gain exposure to NGS panel trends observed by Ambry Genetics
    • Examine pathogenic results observed in patients not meeting diagnostic criteria for single gene testing or a hereditary cancer syndrome
    • Compare the strengths, limitations, and differences between multi-gene panels and whole exome sequencing
    • Assess the utility of whole exome sequencing in suspected hereditary cancer syndromes
    • Review novel gene analysis interpretation and positive results attributed to previously uncharacterized genes.
  • Wed, June 22, 2016
  • 3:21pm PDT
  • Duration: 1 hour and 3 minutes
  • C.E.U. --
  • P.A.C.E. --

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