Interpretation and Reporting of Sequence Variants in Cancer

Our convenient guide provides conceptual information for anybody involved in the variant interpretation process for sequence variants in cancer.

By downloading, you'll get instructions on the following topics:

  • Evidence collection
  • Determination of clinical impact
  • Evaluation of the strength of the clinical evidence
  • Classification of the variant
  • Polymorphisms, minor allele frequency, and the use of population databases
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Download the Guide