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Updated: Apr 16, 2026

Detection of Copy Number Alterations Using Single Cell Sequencing
Published on: February 17, 2017
Hardy-Weinberg equilibrium revisited for inferences on genotypes featuring allele and copy-number variations
Andreas Recke1, Klaus-Günther Recke2, Saleh Ibrahim2
11] Lübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany [2] Department of Dermatology, Allergology and Venereology, University of Lübeck, Lübeck, Germany.
Abstract:
Copy number variations represent a substantial source of genetic variation and are associated with a plethora of physiological and pathophysiological conditions. Joint copy number and allelic variations (CNAVs) are difficult to analyze and require new strategies to unravel the properties of genotype distributions. We developed a Bayesian hidden Markov model (HMM) approach that allows dissecting intrinsic properties and metastructures of the distribution of CNAVs within populations, in particular haplotype phases of genes with varying copy numbers. As a key feature, this approach incorporates an extension of the Hardy-Weinberg equilibrium, allowing both a comprehensive and parsimonious model design. We demonstrate the quality of performance and applicability of the HMM approach with a real data set describing the Fcγ receptor (FcγR) gene region. Our concept, using a dynamic process to analyze a static distribution, establishes the basis for a novel understanding of complex genomic data sets.
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Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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