Evidence map›Paper›PMID 19700652›Full record

ArticleGenome research2009

Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations.

Yik-Ying Teo, Xueling Sim, Rick T H Ong, Adrian K S Tan, Jieming Chen, Erwin Tantoso, Kerrin S Small, Chee-Seng Ku, Edmund J D Lee, Mark Seielstad and 1 more

Abstract read
In one paragraph

Article in Genome research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed, 5 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

89 citing papers in PubMed, 5 syntheses or guidelines pooled it.

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29 more citing papers are in PubMed but not listed here.

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

11 authors.

Yik-Ying TeoCentre for Molecular Epidemiology, National University of Singapore, Singapore 117597.
Xueling Sim
Rick T H Ong
Adrian K S Tan
Jieming Chen
Erwin Tantoso
Kerrin S Small
Chee-Seng Ku
Edmund J D Lee
Mark Seielstad
Kee-Seng Chia

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Singapore Genome Variation Project (SGVP) provides a publicly available resource of 1.6 million single nucleotide polymorphisms (SNPs) genotyped in 268 individuals from the Chinese, Malay, and Indian population groups in Southeast Asia. This online database catalogs information and summaries on genotype and phased haplotype data, including allele frequencies, assessment of linkage disequilibrium (LD), and recombination rates in a format similar to the International HapMap Project. Here, we introduce this resource and describe the analysis of human genomic variation upon agglomerating data from the HapMap and the Human Genome Diversity Project, providing useful insights into the population structure of the three major population groups in Asia. In addition, this resource also surveyed across the genome for variation in regional patterns of LD between the HapMap and SGVP populations, and for signatures of positive natural selection using two well-established metrics: iHS and XP-EHH. The raw and processed genetic data, together with all population genetic summaries, are publicly available for download and browsing through a web browser modeled with the Generic Genome Browser.

Indexed as

Databases, GeneticChinaChromosome MappingGene FrequencyGenetics, PopulationGenetic VariationGenome, HumanGenome-Wide Association StudyGenomicsGenotypeHaplotypesHumansIndiaLinkage DisequilibriumMalaysiaPolymorphism, Single Nucleotide

Identifiers

PMID19700652
PMCPMC2775604

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.