New Product Watch | GenomeWeb

New Product Watch

InfoQuant last week launched oneClickCGH and CGH Fusion version 5.0. The London-based firm's new software packages allow the integration of loss-of-heterozygosity and copy number data with data from SNP arrays.
Specifically, oneClickCGH 5.0 provides integrated genome-wide CNV frequencies, the construction of interactive custom CNV tracks, gene significance analysis, integrated Progenetix CGH data, and allele-specific plots for LOH detection.

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