From raw sequencer data to definitive clinical insights. Explore our deep-dive guides on NGS analysis, variant interpretation, and genomic software evaluation.
Our Learning Center is dedicated to providing high-fidelity educational content for clinical lab directors, bioinformaticians, and geneticists. Whether you are building a new diagnostic test or scaling an existing pipeline, our guides provide the technical foundation and strategic context needed for success.
Core concepts and workflows for processing next-generation sequencing data.
Standardizing variant interpretation with ACMG and AMP scoring frameworks.
How to move from genomic data to actionable insights. Covers evidence integration and classification standards.
Explore the software that automates ACMG and AMP scoring. Professional-grade interpretation built into VarSeq.
Buyer's guides and checklists for selecting and validating clinical software.
What to look for in NGS analysis software. A mid-funnel guide for laboratories actively evaluating new tools.
Cybersecurity, data warehousing, deployment architecture, and regulatory compliance for clinical labs and genome centers.
Somatic variant analysis, AMP guidelines, and precision oncology workflows.
Deep dive into somatic variant detection, AMP/ASCO/CAP tier classification, immunotherapy biomarkers, and the cancer analysis workflow.
Explore the clinical application of somatic analysis in cancer centers. AMP-guided interpretation and targeted therapy matching.
Stay current with the latest strategies in clinical genomics through our technical articles and expert webcasts.
Ready to apply these concepts to your laboratory? Request a personalized platform demo to see our interpretation workflows in action.