## Abstract A combination of common and rare variants is thought to contribute to genetic susceptibility to complex diseases. Recently, nextβgeneration sequencers have greatly lowered sequencing costs, providing an opportunity to identify rare disease variants in large genetic epidemiology studies.
β¦ LIBER β¦
A General Framework for Detecting Disease Associations with Rare Variants in Sequencing Studies
β Scribed by Dan-Yu Lin; Zheng-Zheng Tang
- Book ID
- 113423087
- Publisher
- American Society of Human Genetics
- Year
- 2011
- Tongue
- English
- Weight
- 326 KB
- Volume
- 89
- Category
- Article
- ISSN
- 0002-9297
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