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Studying copy number variations using a nanofluidic platform
Copy number variations (CNVs) in the human genome are conventionally detected using high-throughput scanning technologies, such as comparative genomic hybridization and high-density single nucleotide polymorphism (SNP) microarrays, or relatively low-throughput techniques, such as quantitative polyme...
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| Main Authors: | , , |
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| Format: | Artigo |
| Language: | Inglês |
| Published: |
Oxford University Press
2008
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2566873/ https://ncbi.nlm.nih.gov/pubmed/18710881 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkn518 |
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