Summary: High-throughput sequencing technologies survey genetic variation at genome scale and are increasingly used to study the contribution of rare and low-frequency genetic variants to human traits. As part of the Cohorts arm of the UK10K project, genetic variants called from low-read depth (average 7) whole genome sequencing of 3621 cohort individuals were analysed for statistical associations with 64 different phenotypic traits of biomedical importance. Here, we de-scribe a novel genome browser based on the Biodalliance platform developed to provide inter-active access to the association results of the project. Availability and implementation: The browser is available a
Worldwide, hundreds of thousands of humans have had their genomes or exomes sequenced, and access to...
Summary: We describe an interactive package that provides graphical overviews of the results of whol...
Recent technological advances in the field of molecular biology have ushered in the genome wide asso...
UNLABELLED: High-throughput sequencing technologies survey genetic variation at genome scale and are...
Searching for Darwinian selection in natural populations has been the focus of a multitude of studie...
The 1000 Genomes Project (1000GP) represents the most comprehensive world-wide nucleotide variation ...
GWASs have identified numerous genetic variants associated with a wide variety of diseases, yet desp...
The UK Biobank project is a prospective cohort study with deep genetic and phenotypic data collected...
Motivation: The development of high-throughput sequencing technology has made it possible for more a...
Summary: Large biobanks linking phenotype to genotype have led to an explosion of genetic associatio...
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation ...
Genome-wide association analysis appears to be a promising way to identify heritable susceptibility ...
The study of human genetics was greatly facilitated by the sequencing of the first human genome in 2...
Genome and exome sequencing projects produce huge amount of data, which in turns can yield extensive...
International audienceGenome scans represent powerful approaches to investigate the action of natura...
Worldwide, hundreds of thousands of humans have had their genomes or exomes sequenced, and access to...
Summary: We describe an interactive package that provides graphical overviews of the results of whol...
Recent technological advances in the field of molecular biology have ushered in the genome wide asso...
UNLABELLED: High-throughput sequencing technologies survey genetic variation at genome scale and are...
Searching for Darwinian selection in natural populations has been the focus of a multitude of studie...
The 1000 Genomes Project (1000GP) represents the most comprehensive world-wide nucleotide variation ...
GWASs have identified numerous genetic variants associated with a wide variety of diseases, yet desp...
The UK Biobank project is a prospective cohort study with deep genetic and phenotypic data collected...
Motivation: The development of high-throughput sequencing technology has made it possible for more a...
Summary: Large biobanks linking phenotype to genotype have led to an explosion of genetic associatio...
The 1000 Genomes Project aims to provide a deep characterization of human genome sequence variation ...
Genome-wide association analysis appears to be a promising way to identify heritable susceptibility ...
The study of human genetics was greatly facilitated by the sequencing of the first human genome in 2...
Genome and exome sequencing projects produce huge amount of data, which in turns can yield extensive...
International audienceGenome scans represent powerful approaches to investigate the action of natura...
Worldwide, hundreds of thousands of humans have had their genomes or exomes sequenced, and access to...
Summary: We describe an interactive package that provides graphical overviews of the results of whol...
Recent technological advances in the field of molecular biology have ushered in the genome wide asso...