Array comparative genomic hybridization (also microarray-based comparative genomic hybridization, matrix CGH, array CGH, aCGH) is a molecular cytogenetic technique for the detection of …

Array CGH is a genetic test that looks for extra or missing genetic material from your DNA. Differences in the amount of genetic material can sometimes cause health problems.

Researchers are now using array CGH (aCGH), to quickly scan through an entire genome for imbalances. Many human genetic disorders result from unbalanced chromosomal abnormalities, in …

What is array CGH? A technique used in molecular biology for the detection of genomic dosage changes (deletions or duplications) at a much higher level of resolution than karyotyping.

Comparative genomic hybridization (CGH) was developed to survey DNA copy-number variations across a whole genome.

The technique used in place of karyotyping is called array comparative genomic hybridization (array-CGH) which accurately identifies both the location and gene content of pathogenic chromosome …

This guide describes the Agilent recommended operational procedures to analyze DNA copy number variations using Agilent 60-mer oligonucleotide microarrays for array-based comparative genomic …

Array comparative genomic hybridization (aCGH), also called molecular karyotyping, is a technique that was developed for high resolution, genome-wide screening of segmental genomic copy number …

Array based comparative genomic hybridization (array CGH) has emerged as a powerful tool for detecting gene copy number variants implicated in many disease states.

In recent years, array-based Comparative Genomic Hybridization (aCGH) has been refined to determine chromosomal changes at progressively higher resolutions 1.