Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Whole-genome patterns of common DNA variation in three human populations.

Science (New York, N.Y.) - 18 Feb 2005

Hinds David A, Stuve Laura L, Nilsen Geoffrey B, Halperin Eran, Eskin Eleazar, Ballinger Dennis G, Frazer Kelly A, Cox David R

Abstract excerpt

Individual differences in DNA sequence are the genetic basis of human variability. We have characterized whole-genome patterns of common human DNA variation by genotyping 1,586,383 single-nucleotide polymorphisms (SNPs) in 71 Americans of European, African, and Asian ancestry. Our results indicate that these SNPs capture most common genetic variation as a result of linkage disequilibrium, the correlation among...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Algorithms
Share to Black or African American

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

Share to Databases, Genetic

Share to Genome, Human

Share to Multifactorial Inheritance

Share to Recombination, Genetic

Share to Selection, Genetic

Share to White People

Source

Identifiers

PMID: 15718463
DOI: 10.1126/science.1105436

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole-genome patterns of common DNA variation in three human populations.PMID 15718463Read ↗

SNP and haplotype variation in the human genome.Semantic proximity Read ↗

Worldwide human relationships inferred from genome-wide patterns of variation.Semantic proximity Read ↗

Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans.Semantic proximity Read ↗

The human functional genome defined by genetic diversitySemantic proximity Read ↗

The structure of common genetic variation in United States populations.Semantic proximity Read ↗

Integrating common and rare genetic variation in diverse human populations.Semantic proximity Read ↗

Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes.Semantic proximity Read ↗

Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation.Semantic proximity Read ↗

Human genome sequence variation and the influence of gene history, mutation and recombination.Semantic proximity Read ↗

Global distribution of genomic diversity underscores rich complex history of continental human populations.Semantic proximity Read ↗

DNA variability of human genes.Semantic proximity Read ↗

Genetic determinants of phenotypic diversity in humans.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.