@article {308415,
	title = {A global reference for human genetic variation.},
	journal = {Nature},
	volume = {526},
	year = {2015},
	note = {http://www.nature.com/nature/journal/v526/n7571/full/nature15393.html},
	month = {2015 Oct 1},
	pages = {68-74},
	abstract = {<p>The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set of individuals from multiple populations. Here we report completion of the project, having reconstructed the genomes of 2,504 individuals from 26 populations using a combination of low-coverage whole-genome sequencing, deep exome sequencing, and dense microarray genotyping. We characterized a broad spectrum of genetic variation, in total over 88 million variants (84.7 million single nucleotide polymorphisms (SNPs), 3.6 million short insertions/deletions (indels), and 60,000 structural variants), all phased onto high-quality haplotypes. This resource includes >99\% of SNP variants with a frequency of >1\% for a variety of ancestries. We describe the distribution of genetic variation across the global sample, and discuss the implications for common disease studies.</p>},
	keywords = {Datasets as Topic, Demography, Disease Susceptibility, Exome, Genetic Variation, Genetics, Medical, Genetics, Population, Genome, Human, Genome-Wide Association Study, Genomics, Genotype, Haplotypes, High-Throughput Nucleotide Sequencing, Humans, INDEL Mutation, Internationality, Physical Chromosome Mapping, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Rare Diseases, Reference Standards, Sequence Analysis, DNA},
	issn = {1476-4687},
	doi = {10.1038/nature15393},
	url = {http://www.ncbi.nlm.nih.gov/pubmed/26432245},
	author = {Auton, Adam and Brooks, Lisa D and Durbin, Richard M and Garrison, Erik P and Kang, Hyun Min and Korbel, Jan O and Marchini, Jonathan L and McCarthy, Shane and McVean, Gil A and Abecasis, Gon{\c c}alo R}
}
