Velsera (formerly PierianDx)
Powering the Business of Precision Medicine.
Overview
Velsera was formed by the merger of PierianDx, UgenTec, and BioStrand. The company offers an integrated platform that supports the entire clinical genomics workflow, including variant interpretation (Clinical Genomics Workspace), lab process automation, and business analytics. They aim to help labs scale their precision medicine operations.
✨ Key Features
- Clinical Genomics Workspace for variant interpretation
- Somatic and germline analysis
- Integrated knowledge base and guidelines
- Workflow automation and quality control
- Reimbursement and business analytics tools
🎯 Key Differentiators
- Comprehensive, end-to-end workflow from FASTQ to report
- Extensive, expertly curated clinical genomics knowledgebase
- Combination of software and professional services
Unique Value: Provides a single, integrated platform that streamlines the entire clinical genomics workflow for cancer testing, backed by a deep, evidence-based knowledgebase.
🎯 Use Cases (4)
✅ Best For
- Used by academic medical centers, cancer centers, and commercial labs
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Early-stage academic research not requiring clinical-grade reporting or operational tools
🏆 Alternatives
Offers a more complete, sample-to-report solution compared to point solutions, and a more structured, evidence-driven interpretation process than some AI-heavy platforms.
💻 Platforms
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Varies tier)
🔒 Compliance & Security
💰 Pricing
✓ 14-day free trial
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