Standardizing Genomic Testing into Clinical Pathways
With the rapid advancements of technology, incorporation of genetic testing into clinical pathways is leading the way to improve efficiency and safety, while lowering the long-term costs of healthcare.
This technical note delves into the engine that powers the rapid interpretation and reporting component of Clinical Genomics Workspace: The PierianDx Knowledgebase.
Evidence-based Categorization and Interpretation of Sequence Variants in Cancer
Our convenient guide provides conceptual information for anybody involved in the variant interpretation process for sequence variants in cancer.
5-Step Guide to Evidence-based Categorization of Somatic Variants
Our convenient infographic provides an overview of the key steps to interpreting and reporting sequence variants in cancer.
Moffitt Cancer Center Story
Learn how Moffitt Cancer Center built a world-class precision medicine program.
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