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Article

Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.

Genetic epidemiology - 1 May 2009

Zöllner Sebastian, Su Gang, Stewart William C L, Chen Yi, McInnis Melvin G, Burmeister Margit

Abstract excerpt

Copy number variations (CNVs) in the human genome provide exciting candidates for functional polymorphisms. Hence, we now assess association between CNV carrier status and diseases status by evaluating the signal intensity of SNP genotyping assays. Here, we present a novel statistical method desi...

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PMID: 19085946
DOI: 10.1002/gepi.20391

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19085946-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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