Array-Based Comparative Genomic Hybridization (aCGH).
Methods Mol Biol. 2017;1541:167-179.
Copy number variations (CNVs) in the genomes have been suggested to play important roles in human evolution, genetic diversity, and disease susceptibility. A number of assays have been developed for the detection of CNVs, including fluorescent in situ hybridization (FISH), array-based comparative genomic hybridization (aCGH), PCR-based assays, and next-generation sequencing (NGS). In this chapter, we describe a microarray method that has been used for the detection of genome-wide CNVs, loss of heterozygosity (LOH), and uniparental disomy (UPD) associated with constitutional and neoplastic disorders. Methods Mol Biol. 2017;1541:167-179.
Zhang, Chengsheng; Cerveira, Eliza; Romanovitch, Mallory; and Zhu, Qihui, "Array-Based Comparative Genomic Hybridization (aCGH)." (2017). Faculty Research 2017. 1.
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