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CNV-seq, a new method to detect copy number variation using high-throughput sequencing
BACKGROUND: DNA copy number variation (CNV) has been recognized as an important source of genetic variation. Array comparative genomic hybridization (aCGH) is commonly used for CNV detection, but the microarray platform has a number of inherent limitations. RESULTS: Here, we describe a method to det...
Tallennettuna:
| Päätekijät: | , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2009
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2667514/ https://ncbi.nlm.nih.gov/pubmed/19267900 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-10-80 |
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