Clinical Diagnostics

cnTrack streamlines array data workflows for Cytogenetic labs

At its core cnTrack provides a secure and scalable way to analyze, store, retrieve and manage CGH/SNP array and sequencing (WGS or WES) data. It was designed to facilitate and monitor distributed data interpretation process involving multiple workstations in a large diagnostic or research laboratory.

Contact us to evaluate cnTrack for 30 days

Evaluation allows access for 3 staff members and unlimited data processing with no limitations.

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Clinical Diagnostics

cnTrack

  • Streamlined data interpretation and reporting
  • Well-defined yet scalable reporting pipeline
  • Platform-agnostic centralized data management
  • Full spectrum of data analytics
  • Ease of lab-wide distribution and access
Integrated Cytogenetic report
Integrated public annotation tracks

Collaborative Data Analysis

Genomius

  • Unprecedented ease of access and use
  • Compatibility across all platforms
  • Built-in data management
  • Highly interactive publication-grade plot
  • Power of collaboration between users

Desktop Analytics

CGH Fusion

  • Unsupervised batch processing
  • Centralized genomic variant analytics
  • Compatibility with major array platforms
  • Unprecedented level of data interaction
  • Custom-built CNV tracks
  • Power of data fusion across samples
Multi-sample comparison