ArticleBMC evolutionary biology2009
SNP@Evolution: a hierarchical database of positive selection on the human genome.
Article in BMC evolutionary biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.
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Who cites it
19 citing papers in PubMed, 1 synthesis or guideline pooled it.
- The PLIN4 variant rs8887 modulates obesity related phenotypes in humans through creation of a novel miR-522 seed site.PloS one · 2011Pooled it
- Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmonary Function.Schizophrenia bulletin · 2015Article
- Genetic variation in taste receptor pseudogenes provides evidence for a dynamic role in human evolution.BMC evolutionary biology · 2014Article
- dbPSHP: a database of recent positive selection across human populations.Nucleic acids research · 2014Article
- Molecular adaptation of telomere associated genes in mammals.BMC evolutionary biology · 2013Article
- Patterns of nucleotide and haplotype diversity at ICAM-1 across global human populations with varying levels of malaria exposure.Human genetics · 2013Article
- EvoSNP-DB: A database of genetic diversity in East Asian populations.BMB reports · 2013Article
- Genetic variants at PSMD3 interact with dietary fat and carbohydrate to modulate insulin resistance.The Journal of nutrition · 2013Article
- Evolution of functionally diverse alleles associated with PTC bitter taste sensitivity in Africa.Molecular biology and evolution · 2012Article
- GWASdb: a database for human genetic variants identified by genome-wide association studies.Nucleic acids research · 2012Article
- Significant association of KIR2DL3-HLA-C1 combination with cerebral malaria and implications for co-evolution of KIR and HLA.PLoS pathogens · 2012Article
- Evolutionary dynamics of co-segregating gene clusters associated with complex diseases.PloS one · 2012Article
- A genome-wide survey for SNPs altering microRNA seed sites identifies functional candidates in GWAS.BMC genomics · 2011Article
- Haplo2Ped: a tool using haplotypes as markers for linkage analysis.BMC bioinformatics · 2011Article
- Evolutionary evidence of the effect of rare variants on disease etiology.Clinical genetics · 2011Review
- Genetic variation among major human geographic groups supports a peculiar evolutionary trend in PAX9.PloS one · 2011Article
- Selection and the cell cycle: positive Darwinian selection in a well-known DNA damage response pathway.Journal of molecular evolution · 2010Article
- Genome-wide association of serum bilirubin levels in Korean population.Human molecular genetics · 2010Article
- Evolutionary and functional analysis of celiac risk loci reveals SH2B3 as a protective factor against bacterial infection.American journal of human genetics · 2010Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundPositive selection is a driving force that has shaped the modern human. Recent developments in high throughput technologies and corresponding statistics tools have made it possible to conduct whole genome surveys at a population scale, and a variety of measurements, such as heterozygosity (HET), FST, and Tajima's D, have been applied to multiple datasets to identify signals of positive selection. However, great effort has been required to combine various types of data from individual sources, and incompatibility among datasets has been a common problem. SNP@Evolution, a new database which integrates multiple datasets, will greatly assist future work in this area. DESCRIPTION: As part of our research scanning for evolutionary signals in HapMap Phase II and Phase III datasets, we built SNP@Evolution as a multi-aspect database focused on positive selection. Among its many features, SNP@Evolution provides computed FST and HET of all HapMap SNPs, 5+ HapMap SNPs per qualified gene, and all autosome regions detected from whole genome window scanning. In an attempt to capture multiple selection signals across the genome, selection-signal enrichment strength (ES) values of HET, FST, and P-values of iHS of most annotated genes have been calculated and integrated within one frame for users to search for outliers. Genes with significant ES or P-values (with thresholds of 0.95 and 0.05, respectively) have been highlighted in color. Low diversity chromosome regions have been detected by sliding a 100 kb window in a 10 kb step. To allow this information to be easily disseminated, a graphical user interface (GBrowser) was constructed with the Generic Model Organism Database toolkit.
conclusionAvailable at http://bighapmap.big.ac.cn, SNP@Evolution is a hierarchical database focused on positive selection of the human genome. Based on HapMap Phase II and III data, SNP@Evolution includes 3,619,226/1,389,498 SNPs with their computed HET and FST, as well as qualified genes of 21,859/21,099 with ES values of HET and FST. In at least one HapMap population group, window scanning for selection signals has resulted in 1,606/10,138 large low HET regions. Among Phase II and III geographical groups, 660 and 464 regions show strong differentiation.
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