| Abstract |
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Alterations in genomic DNA are a key feature of many constitutional disorders and cancer. The discovery of the underlying
regions of gene dosage has thus been essential in dissecting complex disease phenotypes and identifying targets for therapeutic
intervention and diagnostic testing. The development of array comparative genomic hybridization (aCGH) using bacterial artificial
chromosomes (BACs) as hybridization targets has facilitated the discovery and fine mapping of novel genomic alterations allowing
rapid identification of target genes.
In BAC aCGH, DNA samples are first labeled with fluorescent dyes through a random priming reaction with 100–400 ng of genomic
DNA. This probe is then co-hybridized to an array consisting of BAC clones, either tiling the genome (˜50 kbp resolution)
or spaced at intervals (e.g., 1 Mbp resolution). The resulting arrays are then imaged and the signal at each locus is compared
between a reference and test sample to determine the copy number status. The DNA samples to be analyzed may be derived from
either fresh, frozen, or formalin-fixed paraffin-embedded material, and sample requirements are currently significantly lower
than those for oligonucleotide platforms due to the high probe-binding capacity of BAC clone targets (˜150 kbp) compared to
oligonucleotides (25–80 bp). In this chapter, we describe in detail the technical procedure required to perform copy number
analysis of genomes with BAC aCGH.
Series: Methods in Molecular Biology | Volume: 556 | Pub. Date: Feb-01-2009 | Page Range: 7-19 | DOI: 10.1007/978-1-60327-192-9_2
Subject: Genetics/Genomics
Key Words: CGH - array CGH - bacterial artificial chromosomes - genomics - gene dosage - DNA copy number
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