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Article

Minimal haplotype tagging.

Proceedings of the National Academy of Sciences of the United States of America - 19 Aug 2003

Sebastiani Paola, Lazarus Ross, Weiss Scott T, Kunkel Louis M, Kohane Isaac S, Ramoni Marco F

Abstract excerpt

The high frequency of single-nucleotide polymorphisms (SNPs) in the human genome presents an unparalleled opportunity to track down the genetic basis of common diseases. At the same time, the sheer number of SNPs also makes unfeasible genome-wide disease association studies. The haplotypic nature of the human genome, however, lends itself to the selection of a parsimonious set of SNPs, called haplotype tagging...

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Identifiers

PMID: 12900503
DOI: 10.1073/pnas.1633613100
PMCID: PMC187880

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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