In recent years, the feasibility of performing large, genome-wide association studies (GWASs) has provided a powerful tool to identify susceptibility loci in complex diseases. GWASs utilize microarrays of several hundred thousand single-nucleotide polymorphisms (SNPs) to capture a significant amount
Searching for the missing heritability of complex diseases
✍ Scribed by Kari Hemminki; Asta Försti; Richard Houlston; Justo Lorenzo Bermejo
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 141 KB
- Volume
- 32
- Category
- Article
- ISSN
- 1059-7794
No coin nor oath required. For personal study only.
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