The underrepresentation of non-Europeans in human genetic studies so far has limited the diversity of individuals in genomic datasets and led to reduced medical relevance for a large proportion of the world's population. Population-specific reference genome datasets as well as genome-wide association studies in diverse populations are needed to address this issue. Here we describe the pilot phase of the GenomeAsia 100K Project. This includes a whole-genome sequencing reference dataset from 1,739 individuals of 219 population groups and 64 countries across Asia. We catalogue genetic variation, population structure, disease associations and founder effects. We also explore the use of this dataset in imputation, to facilitate genetic studies i...
International audienceThe 1000 Genomes Project aims to provide a deep characterization of human geno...
In the last decade, an unprecedented increase in the availability of whole genome sequence (WGS) dat...
Abstract Background Genotype imputation from single-nucleotide polymorphism (SNP) genotype data usin...
The underrepresentation of non-Europeans in human genetic studies so far has limited the diversity o...
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic vari...
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic vari...
High-throughput sequencing technology enables population-level surveys of human genomic variation. H...
Underrepresentation of Asian genomes has hindered population and medical genetics research on Asians...
International audienceThe 1000 Genomes Project aims to provide a deep characterization of human geno...
In the last decade, an unprecedented increase in the availability of whole genome sequence (WGS) dat...
Abstract Background Genotype imputation from single-nucleotide polymorphism (SNP) genotype data usin...
The underrepresentation of non-Europeans in human genetic studies so far has limited the diversity o...
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic vari...
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic vari...
High-throughput sequencing technology enables population-level surveys of human genomic variation. H...
Underrepresentation of Asian genomes has hindered population and medical genetics research on Asians...
International audienceThe 1000 Genomes Project aims to provide a deep characterization of human geno...
In the last decade, an unprecedented increase in the availability of whole genome sequence (WGS) dat...
Abstract Background Genotype imputation from single-nucleotide polymorphism (SNP) genotype data usin...