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Article

Markov Models for inferring copy number variations from genotype data on Illumina platforms.

Human heredity - 1 Jan 2009

Wang Hui, Veldink Jan H, Blauw Hylke, van den Berg Leonard H, Ophoff Roel A, Sabatti Chiara

Abstract excerpt

BACKGROUND/AIMS: Illumina genotyping arrays provide information on DNA copy number. Current methodology for their analysis assumes linkage equilibrium across adjacent markers. This is unrealistic, given the markers high density, and can result in reduced specificity. Another limitation of current methods is that they cannot be directly applied to the analysis of multiple samples with the goal of detecting copy...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19339782
DOI: 10.1159/000210445
PMCID: PMC2880724

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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