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An integrated map of genetic variation from 1,092 human genomes.

Abstract:

By characterizing the geographic and functional spectrum of human genetic variation, the 1000 Genomes Project aims to build a resource to help to understand the genetic contribution to disease. Here we describe the genomes of 1,092 individuals from 14 populations, constructed using a combination of low-coverage whole-genome and exome sequencing. By developing methods to integrate information across several algorithms and diverse data sources, we provide a validated haplotype map of 38 million...

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Publication status:
Published

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Publisher copy:
10.1038/nature11632

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Journal:
Nature
Volume:
491
Issue:
7422
Pages:
56-65
Publication date:
2012-11-01
DOI:
EISSN:
1476-4687
ISSN:
0028-0836
Source identifiers:
359975

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