Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)
Genomewide association studies (GWAS) have proven a powerful hypothesis-free method to identify common disease-associated variants. Even quite large GWAS, however, have only at best identified moderate proportions of the genetic variants contributing to disease heritability. To provide cost-effective genotyping of common and rare variants to map the remaining heritability and to fine-map established loci, the Metabochip Consortium has developed a 200,000 SNP chip that has been produced in very large numbers for a fraction of the cost of GWAS chips. This chip provides a powerful tool for genetic studies of metabolic, cardiovascular and anthropometric traits (Voight et al., in press PLoS Genetics).
- Type: Other
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
Dataset ID | Description | Technology | Samples |
---|---|---|---|
EGAD00010000230 | - Illuminus | 2943 | |
EGAD00010000232 | - Illuminus | 2975 | |
EGAD00010000234 | Illumina HumanExome-12v1_A-GenCall, zCall | 12241 | |
EGAD00010000236 | - Illuminus, GenoSNP | 3125 |
Publications | Citations |
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The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet 8: 2012 e1002793 |
355 |
Search for new loci and low-frequency variants influencing glioma risk by exome-array analysis.
Eur J Hum Genet 24: 2016 717-724 |
7 |
Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia.
Blood 128: 2016 2319-2326 |
60 |