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Article

Inference of chromosome-specific copy numbers using population haplotypes.

BMC bioinformatics - 24 May 2011

Huang Yao-Ting, Wu Min-Han

Abstract excerpt

BACKGROUND: Using microarray and sequencing platforms, a large number of copy number variations (CNVs) have been identified in humans. In practice, because our human genome is a diploid, these platforms are limited to or more accurate for detecting total copy numbers rather than chromosome-specific copy numbers at each of the two homologous chromosomes. Nevertheless, the analysis of linkage disequilibrium (LD)...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 21605463
DOI: 10.1186/1471-2105-12-194
PMCID: PMC3128032

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