Comparative Genomic Hybridization (CGH)
What is CGH?
Comparative Genomic Hybridization (CGH) measures DNA copy number differences between a reference genome and a sample genome.
CGH is a molecular cytogenetic method of screening a tumor for genetic changes. Alterations are classified as DNA gains and losses and reveal a characteristic pattern that includes mutations at chromosomal and subchromosomal levels.
CGHView
CGHView™ is ASI's high-resolution CGH system with superb imaging capabilities and full karyotyping support. It is fully integrated with ASI’s robust Case Data Manager to easily generate statistics, compare cells and cases, print customized reports and manage data. As part of the CytoLabView suite, CGHView is an extension of FISHView Station. Upgrading to HiSKY, Karyotyping, and automatic scanning is seamless.
For information on additional capabilities such as powerful automated multi-layer imaging and timesaving image enhancement options - click here.
In the US, CGHView is not cleared for In Vitro Diagnostic procedures and is intended for research use only.
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