Agilent Alissa Clinical Informatics
One platform for your NGS data analysis and interpretation.
Overview
The Agilent Alissa platform provides a suite of tools to streamline the clinical genomics workflow. It supports various applications from hereditary disease and oncology to prenatal testing, enabling labs to manage their pipeline from raw data processing to the final clinical report in a secure and compliant environment.
✨ Key Features
- End-to-end workflow management
- Somatic and germline variant analysis
- Copy Number Variation (CNV) detection
- Integrated variant databases and annotation sources
- Customizable clinical reporting
🎯 Key Differentiators
- Single-vendor solution for both NGS and array CGH data analysis.
- Strong integration with Agilent's broader portfolio of lab solutions.
- Proven platform with a long history in the clinical diagnostics space (formerly Cartagenia).
Unique Value: Provides a unified and streamlined platform for labs to analyze, interpret, and report on both NGS and array CGH data, ensuring consistency and efficiency in clinical diagnostics.
🎯 Use Cases (4)
✅ Best For
- Used by clinical labs globally for diagnostic testing
💡 Check With Vendor
Verify these considerations match your specific requirements:
- Large-scale population genomics research (more clinically focused)
🏆 Alternatives
Its ability to handle both NGS and array data in a single, integrated workflow is a key advantage for labs that perform both types of testing.
💻 Platforms
✅ Offline Mode Available
🔌 Integrations
🛟 Support Options
- ✓ Email Support
- ✓ Phone Support
- ✓ Dedicated Support (Varies tier)
🔒 Compliance & Security
💰 Pricing
✓ 14-day free trial
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