This insights paper delves into the best practices for analyzing gene fusions, splice-site variants, co-occurring variants, CNVs, TMB, and MSI within the context of somatic cancer.
Insights Paper
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.
Technical Note
PierianDx Knowledgebase
This technical note delves into the engine that powers the rapid interpretation and reporting component of Clinical Genomics Workspace: The PierianDx Knowledgebase.
Technical Note
Clinical Genomics Workspace Compliance, Privacy, and Information Security
To support our customers who must comply with the necessarily stringent requirements of working in a healthcare setting, PierianDx has adopted an unwavering focus on privacy and security. Learn about the comprehensive approach we take that helps keep sensitive data private and secure.
Reference Guide
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.
Insights Paper
Moffitt Cancer Center Story
Learn how Moffitt Cancer Center built a world-class precision medicine program.
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