Streamlined Genomic Analysis Platform for Precision Care
Pierian partners with clinicians and medical facilities to advance clinical genomics and modernize patient care.
The Pierian Clinical Sharing Network
Aggregates data driving new insights in genomics
Designed for Clinical Workflows
All shared genomic interpretations in our Genomics Knowledgebase are expertly curated by our team, and the database is expanded to include clinical customer interpretations.
Customers also rely on our Interpretation Services at times. As the number of interpretations build over time, the focus on clinical significance remains consistent.
Clinical Reporting and Sign-Out
Our board-certified medical directors oversee variant analyst services, sign out clinical reports, and support customers who have their own molecular pathologist or clinical geneticist to sign out. Our report template can be configured to meet your needs.
Select an option below to learn more.
Clinically Critical Summary Page
Summarize relevant biomarkers to associated tiers and therapies.
Provide underlying evidence supporting biomarker-therapy associations.
Clinical Trial Associations
Report clinical trials that are patient-specific.
Our API and HL7 interfaces enable seamless integration with your institution's electronic medical record (EMR), laboratory information system (LIS), and enterprise data warehouse (EDW). This ensures results are delivered in the most timely and usable format. Accessible genomic data can then be combined with other data sources and utilized more effectively across your organization.