Evidence map›Paper›PMID 18482828›Full record

ArticleGenomics2008

HapMap tagSNP transferability in multiple populations: general guidelines.

Jinchuan Xing, David J Witherspoon, W Scott Watkins, Yuhua Zhang, Whitney Tolpinrud, Lynn B Jorde

Abstract read
In one paragraph

Article in Genomics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Aging · 2020
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Jinchuan XingDepartment of Human Genetics, Eccles Institute of Human Genetics, University of Utah, Salt Lake City, UT 84112, USA.
David J Witherspoon
W Scott Watkins
Yuhua Zhang
Whitney Tolpinrud
Lynn B Jorde
University of Utah · US

Funding

POPULATION GENETICS OF MOBILE ELEMENTSR01GM059290 · NIGMS · UNIVERSITY OF UTAH · PI BATZER, MARK A, FESCHOTTE, CEDRIC · 1999 to 2018
$8.5M
The Angiotensinogen Gene and Human HypertensionR01HL070048 · NHLBI · UNIVERSITY OF UTAH · PI JORDE, LYNN · 2003 to 2006
$1.3M
NHLBI NIH HHS HL-070048NHLBI NIH HHS R01 HL070048NIGMS NIH HHS GM-59290NIGMS NIH HHS R01 GM059290
6 · The paper itself

Abstract

Linkage disequilibrium (LD) has received much attention recently because of its value in localizing disease-causing genes. Due to the extensive LD between neighboring loci in the human genome, it is believed that a subset of the single nucleotide polymorphisms in a region (tagSNPs) can be selected to capture most of the remaining SNP variants. In this study, we examined LD patterns and HapMap tagSNP transferability in more than 300 individuals. A South Indian sample and an African Mbuti Pygmy population sample were included to evaluate the performance of HapMap tagSNPs in geographically distinct and genetically isolated populations. Our results show that HapMap tagSNPs selected with r(2) >= 0.8 can capture more than 85% of the SNPs in populations that are from the same continental group. Combined tagSNPs from HapMap CEU and CHB+JPT serve as the best reference for the Indian sample. The HapMap YRI are a sufficient reference for tagSNP selection in the Pygmy sample. In addition to our findings, we reviewed over 25 recent studies of tagSNP transferability and propose a general guideline for selecting tagSNPs from HapMap populations.

Indexed as

Genome, HumanHuman Genome ProjectLinkage DisequilibriumPolymorphism, Single NucleotideAnimalsChromosome MappingGene FrequencyGenetic Diseases, InbornHumansRacial Groups

Identifiers

PMID18482828
PMCPMC2471876
OpenAlexW2076685939

What OpenQuestion holds

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Registered trials

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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.