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Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Array CGH for the detection of genomic copy number variants has replaced G-banded karyotype analysis. This paper describes the technology and its application in a clinical diagnostic service laboratory. DNA extracted from a patient’s sample (blood, saliva or other tissue types) is labeled with a flu...

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Pubblicato in:J Vis Exp
Autori principali: Ahn, Joo Wook, Coldwell, Michael, Bint, Susan, Mackie Ogilvie, Caroline
Natura: Artigo
Lingua:Inglês
Pubblicazione: MyJove Corporation 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4354656/
https://ncbi.nlm.nih.gov/pubmed/25742425
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3791/51718
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