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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...
Tallennettuna:
| Julkaisussa: | J Vis Exp |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MyJove Corporation
2015
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| Aiheet: | |
| Linkit: | 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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