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Article

Evaluation of power of the Illumina HumanOmni5M-4v1 BeadChip to detect risk variants for human complex diseases.

European journal of human genetics : EJHG - 1 Jul 2016

Xing Chuanhua, Huang Jie, Hsu Yi-Hsiang, DeStefano Anita L, Heard-Costa Nancy L, Wolf Philip A, Seshadri Sudha, Kiel Douglas P, Cupples L Adrienne, Dupuis Josée

Abstract excerpt

Although emerging sequencing technologies can characterize all genetic variants, the cost is still high. Illumina released the HumanOmni5M-4v1 (Omni5) genotype array with ~4.3M assayed SNPs, a much denser array compared with other available arrays. The Omni5 balances both cost and array density. In this article, we illustrate the power of Omni5 to detect genetic associations. The Omni5 includes variants with a...

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Identifiers

PMID: 26577045
DOI: 10.1038/ejhg.2015.244
PMCID: PMC5070895

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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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