Chapter title |
Array-Based Comparative Genomic Hybridization (aCGH).
|
---|---|
Chapter number | 15 |
Book title |
Cancer Cytogenetics
|
Published in |
Methods in molecular biology, January 2017
|
DOI | 10.1007/978-1-4939-6703-2_15 |
Pubmed ID | |
Book ISBNs |
978-1-4939-6701-8, 978-1-4939-6703-2
|
Authors |
Chengsheng Zhang M.D., Ph.D., Eliza Cerveira, Mallory Romanovitch, Qihui Zhu, Chengsheng Zhang |
Editors |
Thomas S.K. Wan |
Abstract |
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. |
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