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The PierianDx Knowledgebase is not a variant lookup table. It's built on the foundation of a powerful rules engine that accurately delivers the richest set of rationalized medical interpretations from our clinical customers and Genomic Interpretation Services team, as well as expertly curated genomic data, clinical practice guidelines, FDA therapeutics, and clinical trials.
In addition to expertly curated sources such as NCCN/ASCO guidelines, FDA therapies, clinical trials, and published literature, our partner sharing network allows for the comparison of classifications and interpretations across medical directors at one or more sites. This unique aspect of the PierianDx KnowledgeBase enables the use of real-world evidence to make knowledge assertions more rapidly and accurately.
The PierianDx Knowledgebase encompasses over 6 megabases of sequence coverage (six million genomic variants) and supports all variant types (eg. single nucleotide variants, insertions/deletions, copy number variants, and structural variants) for somatic cancer and germline applications, making it the most comprehensive genomic knowledgebase available.
All shared genomic interpretations in the PierianDx Knowledgebase are expertly curated by our clinical customers or Interpretation Services team with an acute focus on their impact for clinical care. Each interpretation has medical oversight by our board certified Medical Director or is signed out directly by a board certified molecular pathologist or clinical geneticist.
With real-time publishing of medical interpretations and weekly updates to industry guidelines, FDA therapies and clinical trials, the PierianDx Knowledgebase contains the most up-to-date and clinically actionable information for next generation sequencing data.
This webinar provides practical strategies for the analysis of complex genomic alterations such as co-occurring variants, splice-site mutations, and gene fusions.View Webinar →
Shalini Verma, MD, FCAP - Medical Director and Laboratory Director, PierianDx
Andy Bredemeyer, PhD - VP of Product, PierianDxView Webinar →
Learn about the benefits associated with integrating genomic medicine into clinical pathways, along with approaches for pilot programs and recommendations for developing a testing framework.
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