Copy Number Data Analysis Software
infoQuant puts years of innovation in data analysis and commercial-grade software development behind its solutions for DNA Copy Number analytics. Our software were developed in close collaboration with specialists in Cytogenetics of major diagnostic and research laboratories and provide state-of-the-art yet intuitive data interpretation capabilities to array users. Watch a series of our recorded seminars on Copy Number and LOH analysis and our product videos for more information. A selection of white papers discussing analysis of array data acquired using real samples may help you get an in-depth overview of our software features and capabilities.
oneClickCGH oneClickCGH® is our novel Copy Number software package designed to facilitate array-based copy number analysis for Cytogenetics. It provides researchers and diagnosticians with fully automated data analysis, visualization and reporting capabilities necessary to process data from routine Cytogenetic tests based on 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. |
CGH Fusion CGH Fusion® is our state-of-the-art aCGH software that facilitates high-throughput multi-sample DNA Copy Number studies. This software is also compatible with all major array CGH and SNP platforms, which gives you the luxury of being able to analyze and compare data from multiple datasets generated with different array platforms in a single session. It is also a perfect tool for centralized processing of high volumes of raw data produced by array-based tests at a Cytogenetic laboratory. CGH Fusion can further enhance Cytogenetic workflow by comparing multiple samples, for instance, originated from the same family. |
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Software Comparison
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| Robust platform-specific detection of chromosomal anomalies and QC metrics |  |
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| Easy-to-use interactive data interpretation workflow designed for clinical Cytogenetics |
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| Integrated gene annotations, disorder associations and normal CNV tracks |
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| Wide variety of graphics-rich customizable report formats: PDF, Word, HTML and Excel |
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| Built-in interactive procedure for construction, editing and use of custom CNV tracks |
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| Support of all major array CGH and SNP platforms: Affymetrix, Agilent, BlueGnome, Illumina, OGT, PerkinElmer, Roche-Nimblegen, etc. |
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| Runs on OS X, Windows and Linux |
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| Batch-process data from hundreds or thousands of arrays with a click of a button (even across array platforms) | |
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| Build CNV frequency profiles for specific phenotypes or for normal samples using large datasets and re-use for reference in routine tests |
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| Compare probe-level data and detected anomalies across multiple samples in a single view |
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Evaluations and Online Demonstrations
infoQuant provides 14 day evaluations as well as one-on-one online demonstrations for oneClickCGH and CGH Fusion. Please complete our evaluation request form to participate.
