Copy Number Data Analysis and Management Software

Data Analysis

oneClickCGH

oneClickCGH IcononeClickCGH® is our novel DNA Copy Number software package designed to facilitate array-based chromosomal analysis for Cytogenetics. It provides diagnosticians with fully automated data analysis, visualization and reporting capabilities necessary to process data from a routine Cytogenetic test. It is fully compatible with all commercial array CGH and SNP platforms. Its major advantages are compatibility with output of any major array platform, simplicity of workflow design, unprecedented interactivity of the interface and comprehensiveness of its reporting features. This is basically an end-to-end solution for array data interpretation in a clinical setting.

Interaction with detected DNA anomalies
Using annotation plots Interacting with report table Report document Analysis of gene significance

CGH Fusion

Cgh Fusion IconCGH Fusion® is our state-of-the-art aCGH software built with high-throughput chromosomal analysis in mind. It is the perfect tool for centralized processing of high volumes of array data produced by Cytogenetic tests. In-depth analytics and rich annotation facilities of CGH Fusion are designed to dramatically improve efficiency of DNA Copy Number analysis in a clinical lab. CGH Fusion can enhance Cytogenetic workflow by comparing data from different samples, for instance, originated from the same family. This software is compatible with all major array CGH and SNP technologies, which gives you the power of being able to compare results across different array platforms.
Anomaly frequency plot
Multi-sample comparison Using annotation plots for data interpretation Interacting with report table Report document

Data Management

cnTrack

cnTrack IconcnTrack® provides a secure and scalable way to store, retrieve and manage aCGH and SNP array data for Cytogenetics laboratories. But don't think of it as just a data repository - cnTrack can also help you organize laboratory-wide operations for analysis of array data in the most efficient manner. You can work across all major aCGH and SNP array platforms including Affymetrix, Agilent, Illumina, PerkinElmer, Roche-Nimblegen and custom arrays. State-of-the-art dataset analysis engine enables clinicians and researchers to construct, curate and visualize Copy Number Variant (CNV) profiles built on large sets of accumulated data and to re-use them in their routine array-based Cytogenetic tests. Seamless integration with infoQuant's Analysis Suite incorporating oneClickCGH® and CGH Fusion® makes cnTrack a powerful answer to everyday data management and interpretation needs of a Cytogenetics laboratory.
Personal data management space
Patient Information Querying legacy data Integrated Cytogenetic report Enterprise-wide Administration

Evaluations and Online Demonstrations

infoQuant provides 14 day evaluations as well as one-on-one online demonstrations for oneClickCGH and CGH Fusion.  An online demonstration is available for cnTrack

Please complete our evaluation request form to participate. 

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