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Array Comparative Genomic Hybridization is a technique for identifying genomic regions with copy number alterations. Deletions, duplications, and other types of chromosome instability are associated with genetic diseases and somatic alterations in cancer. CGH Explorer™ utilizes genomic DNA from
both reference and test genome that are labeled with fluorescent dyes.
The genomic samples competitively hybridize with an array of probes arranged
on a substrate. The hybridized slide can be scanned evaluating the signal
intensity CGH Explorer™ is an easy-to-use software tool for analyzing two color copy number alteration arrays from multiple platforms, including Agilent Technologies, Illumina, AffyMetrix, NimbleGen, BioRobotics, Combimetrix and others. The software performs raw image analysis and gridding eliminating image biases to significantly improving analysis accuracy. Simple, user-friendly interface and automation features speed analysis providing final results within a few mouse clicks. CGH Explorer™ features:
Recap Window following data processing permits rapid review of critical analysis and quality control. All panels, such as Raw Image, Quality Control, Feature Statistics, Log Plot can be evaluated in a single glance.
CGH Explorer™ automatically corrects image biases and filters out all low quality features. Two-channel images are aligned, features are placed into the grid, local adjustments are made, feature quality is assessed and intensities are extracted for each channel.
Quality is assessed for the whole chip and each feature. Using the control probe intensity the program calculates the uniformity and alignment parameters. Mulitple statistics and charts are available for analysis assesment. Graphic display are linked,clicking on a individual feature, other windows will scroll to and highlight the appropriate location to allow for easy inspection.
CGH Explorer interfaces with an integrated genetic database assisting with the quick identification of information such as gene and known Copy Number Variations. Comparative analysis of multiple projects can be conducted.
Along with the standard copy number variation report, the statistical and quality information about each array feature is available. Chromosome Alteration Report Array Features The information about each array feature is collected in the table. This includes the statistical parameters, genomic information for the probe, quality control parameters, and the overall quality score. Automated Processing Batch processing of several projects can speed up analysis and free up time by minimizing the need for user intervention. The data processing results are saved in project files that can be loaded and evaluated at a later time. |
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