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Array Comparative Genomic Hybridization (aCGH) is a powerful tool which can be used to detect chromosomal aberrations in a rapid yet reliable manner. Our genomic expertise in this area has allowed us to develop a best-in-class proprietary platform which has been thoroughly tested and proven to be a superior choice for microarray CGH analysis.

Overview of aCGH

Overview of aCGH TechnologyArray Comparative Genomic Hybridization (aCGH) involves a process whereby differentially labeled test and reference DNA samples are hybridized to normal chromosomes, and flourescence ratios along the length of the chromosome provide a cytogenetic representation of copy-number variations.

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Expertise

Technological ExpertiseHaving processed in excess of 4,000 samples, our time-tested methods yield highly accurate and reproducible results.

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Applications of aCGH

Applications of Array Comparative Genomic HybridizationArray CGH is used in a variety of disciplines to provide researchers and clinicians with insight into genotype-phenotype relationships.

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Find a BAC Clone

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Search by gene, chromosome location, or by clone ID to quickly locate the BAC clone you're looking for.

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Diseases assayed

Syndrome Coverage

View our list of 200+ diseases and syndromes covered on our Human ACCUArray™.

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