期刊
EUROPEAN JOURNAL OF HUMAN GENETICS
卷 14, 期 2, 页码 139-148出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/sj.ejhg.5201531
关键词
array CGH; matrix CGH; cancer genome; cancer genetics; genetic disease; copy number alteration; array CGH software
资金
- NIDCR NIH HHS [R01 DE 015965-01] Funding Source: Medline
Array comparative genomic hybridization (arrayCGH) is a method used to detect segmental DNA copy number alterations. Recently, advances in this technology have enabled high-resolution examination for identifying genetic alterations and copy number variations on a genome-wide scale. This review describes the current genomic array platforms and CGH methodologies, highlights their applications for studying cancer genetics, constitutional disease and human variation, and discusses visualization and analytical software programs for computational interpretation of array CGH
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