Where We Fit
Addressing the Scale and Complexity of Genomic Testing
We offer a complete, integrated solution to enable your precision medicine program – including a full range of software, support and services. We solve the dual challenges of scalability and complexity in NGS testing by providing your clinical lab with streamlined workflow, an extensive curated knowledgebase, comprehensive analysis, insightful interpretation, and precise reporting.
CLINICAL GENOMIC WORKSPACE
THE RIGHT WORKSPACE
PierianDx’s Clinical Genomics WorkSpace (CGW) is the industry’s leading integrated workspace for genomic analytics, classification, interpretation and reporting. Driven by our KnowledgeSpace, CGW provides end-to-end workflow from sample to report that seamlessly integrates with patient medical records and lab information systems.
Case Accessioning: a clinical genomic test is ordered for a patient either within CGW or by receipt of an order from upstream medical systems
Sequencing: primary data are acquired from sequencers to start the analytical process
Analysis: variants are called and annotated using validated pipelines and comprehensive genomic databases
Draft Report: medical interpretations and just-in-time curated information from our rapidly expanding medical knowledgebase are processed through a proprietary algorithm, which then produces a report highlighting the most relevant, clinically actionable information
Final Report: a fully featured, online editing system allows the medical professional to review, finalize, and sign out a report
Integration in Electronic Health Record: signed out report is messaged to the medical record for review by the treating physician
CGW CLINICAL WORKFLOW (IN RED)
PIERIANDX CLINICAL GENOMICS KNOWLEDGESPACE
You Source for Actionable Intelligence
PierianDx’s Clinical Genomics KnowledgeSpace automatically cultivates and curates billions of biomedical findings, expanding its intelligence with each use. Our KnowledgeSpace simplifies the complexity of genomic data by translating public data, highly curated data, PubMed, shared interpretations from our partners and other sources into easy-to-understand personal reports that clinicians can share with their patients.