Evidence map›Paper›PMID 19682379›Full record

ArticleJournal of biomedical science2009

TagSNP transferability and relative loss of variability prediction from HapMap to an admixed population.

Tulio C Lins, Breno S Abreu, Rinaldo W Pereira

Abstract readComparative Study
In one paragraph

Article in Journal of biomedical science, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Tulio C LinsPrograma de Pós-Graduação em Ciências Genômicas e Biotecnologia, Universidade Católica de Brasília, Brasília, DF, Brazil. lins.tulio@gmail.com
Breno S Abreu
Rinaldo W Pereira

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe application of a subset of single nucleotide polymorphisms, the tagSNPs, can be useful in capturing untyped SNPs information in a genomic region. TagSNP transferability from the HapMap dataset to admixed populations is of uncertain value due population structure, admixture, drift and recombination effects. In this work an empirical dataset from a Brazilian admixed sample was evaluated against the HapMap population to measure tagSNP transferability and the relative loss of variability prediction.

methodsThe transferability study was carried out using SNPs dispersed over four genomic regions: the PTPN22, HMGCR, VDR and CETP genes. Variability coverage and the prediction accuracy for tagSNPs in the selected genomic regions of HapMap phase II were computed using a prediction accuracy algorithm. Transferability of tagSNPs and relative loss of prediction were evaluated according to the difference between the Brazilian sample and the pooled and single HapMap population estimates.

resultsEach population presented different levels of prediction per gene. On average, the Brazilian (BRA) sample displayed a lower power of prediction when compared to HapMap and the pooled sample. There was a relative loss of prediction for BRA when using single HapMap populations, but a pooled HapMap dataset generated minor loss of variability prediction and lower standard deviations, except at the VDR locus at which loss was minor using CEU tagSNPs.

conclusionStudies that involve tagSNP selection for an admixed population should not be generally correlated with any specific HapMap population and can be better represented with a pooled dataset in most cases.

Indexed as

MarriagePolymorphism, Single NucleotideAfricaAlgorithmsAsia, EasternBrazilCholesterol Ester Transfer ProteinsChromosome MappingEthnicityEuropeGenetic VariationGenotypeHaplotypesHumansHydroxymethylglutaryl CoA ReductasesLinkage DisequilibriumCETP protein, humanCholesterol Ester Transfer ProteinsHydroxymethylglutaryl CoA ReductasesProtein Tyrosine Phosphatase, Non-Receptor Type 22PTPN22 protein, humanReceptors, Calcitriol

Identifiers

PMID19682379
PMCPMC2737315

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.