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2011
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2025
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The 1000 Genomes Project: data management and community access.
Not available
S-EPMC3340611
|
biostudies-literature
Cite
Mapping copy number variation by population-scale genome sequencing.
Not available
S-EPMC3077050
|
biostudies-literature
Cite
Probing CP symmetry and weak phases with entangled double-strange baryons.
Not available
S-EPMC9159954
|
biostudies-literature
Cite
Demographic history and rare allele sharing among human populations.
Not available
S-EPMC3142009
|
biostudies-literature
Cite
Diversity of human copy number variation and multicopy genes.
Not available
S-EPMC3020103
|
biostudies-literature
Cite
A map of human genome variation from population-scale sequencing.
Not available
S-EPMC3042601
|
biostudies-literature
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A second generation human haplotype map of over 3.1 million SNPs.
Not available
S-EPMC2689609
|
biostudies-literature
Cite
Integrative annotation of variants from 1092 humans: application to cancer genomics.
Not available
S-EPMC3947637
|
biostudies-literature
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A global reference for human genetic variation.
Not available
S-EPMC4750478
|
biostudies-literature
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Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel.
Not available
S-EPMC4338501
|
biostudies-literature
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