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Article

The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.

Human heredity - 1 Jan 2006

Liu Wenlei, Zhao Wei, Chase Gary A

Abstract excerpt

OBJECTIVE: Single nucleotide polymorphisms (SNPs) serve as effective markers for localizing disease susceptibility genes, but current genotyping technologies are inadequate for genotyping all available SNP markers in a typical linkage/association study. Much attention has recently been paid to methods for selecting the minimal informative subset of SNPs in identifying haplotypes, but there has been little...

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Share to Chromosome Mapping
Share to Gene Frequency
Share to Genetic Linkage

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Haplotypes

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Share to Polymorphism, Single Nucleotide

Share to Selection, Genetic

Source

Identifiers

PMID: 16557026
DOI: 10.1159/000092141

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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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