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Article

Single-nucleotide polymorphism genotyping for disease association studies.

Methods in molecular medicine - 1 Jan 2005

Fornage Myriam, Doris Peter A

Abstract excerpt

The Human Genome Project has led to the discovery of millions of DNA sequence variants in the human genome. The majority of these variants are single-nucleotide polymorphisms (SNPs). Availability of an ultra-high-density SNP map, combined with improvement in genotyping technologies and efficient...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 16028683
DOI: 10.1385/1-59259-850-1:159

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-16028683-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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