Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans

Abstract 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 essenti...

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Váldodahkkit:	Rajini R. Haraksingh, Alexej Abyzov, Alexander Eckehart Urban
Materiálatiipa:	Artigo
Giella:	Inglês
Almmustuhtton:	BMC 2017-04-01
Ráidu:	BMC Genomics
Fáttát:	Copy Number Variation (CNV) Array Comparative Genome Hybridization (aCGH) SNP array
Liŋkkat:	http://link.springer.com/article/10.1186/s12864-017-3658-x
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