Clinical Diagnostics

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. Using cnTrack, laboratory team can standardize and control their work across all major including ThermoFisher, Agilent, Roche, Illumina and more. Seamless integration of our analytical and visualization software CGH Fusion into cnTrack ensures precise and reliable DNA variant analysis in a high-throughput environment.

Features

Streamlined data interpretation and reporting

cnTrack is designed to accelerate DNA variant (Copy Number, LOH etc) reporting/interpretation in a modern diagnostic laboratory. It easily adapts to any existing array- or sequencing-based platform and any workflow a laboratory may have in place. By integrating all necessary components of Cytogenetic analysis such as clinical data (including connection to Shire, OMNILAB, STARLIMS etc), anomaly detection, data visualization, case reporting and sample management cnTrack has been proven to significantly reduce per-sample processing time and increase throughput.

Well-defined yet scalable reporting pipeline

The centerpiece of cnTrack web-based interface is a snapshot of laboratory's reporting pipeline. It can be customized for any particular user role to make distributed data analysis and variant interpretation more efficient. This snapshot feature ensures that all lab members see their immediate tasks and are aware of any urgent cases. Transparency of cnTrack interface facilitates timely detection and management of any possible bottlenecks in the workflow. cnTrack can be set up for use just by a few users or by dozens across the lab with the number of users adjusted as needed.

Platform-agnostic centralized data management

We built cnTrack to be truly platform agnostic: it accepts data generated by all major commercial array and sequencing platforms and can be used on any computer or device that has an Internet browser. Users can store and analyze data produced by major array platforms such as ThermoFisher, Agilent, Roche, Illumina and more. Import of sequencing data is also available. cnTrack is also agnostic with respect to database technology (Oracle, SQL Server etc) used on its backend for better integration with existing institution infrastructure.

Full spectrum of data analytics

Being integrated with our powerful DNA variant analytics software CGH Fusion, cnTrack delivers full power of Copy Number and LOH analysis to every licensed PC. Data from dozens or even hundreds of samples can be analyzed for chromosomal changes within minutes and then taken through clinical reporting pipeline.

Ease of lab-wide distribution and access

Based on a web-based technology cnTrack does not have any significant performance requirements with respect to user hardware. Cross-laboratory installation effort is also very minimal as most of system’s data management capabilities are delivered via Internet browser. Such light-client approach do data management aspect of cnTrack provides its users with a wide spectrum of infrastructural options. All elements of cnTrack can be installed on a secure server inside institution’s firewall. Alternatively, to avoid server maintenance costs, our clients can choose to keep cnTrack’s database core on a secure cloud managed by