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Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans
BACKGROUND: High-resolution microarray technology is routinely used in basic research and clinical practice to efficiently detect copy number variants (CNVs) across the entire human genome. A new generation of arrays combining high probe densities with optimized designs will comprise essential tools...
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| Pubblicato in: | BMC Genomics |
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| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5402652/ https://ncbi.nlm.nih.gov/pubmed/28438122 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-3658-x |
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