Rare-variant association methods
β Scribed by Bahcall, Orli
- Book ID
- 118008712
- Publisher
- Nature Publishing Group
- Year
- 2012
- Tongue
- English
- Weight
- 66 KB
- Volume
- 44
- Category
- Article
- ISSN
- 1061-4036
- DOI
- 10.1038/ng.2458
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## Abstract We summarize the work done by the contributors to Group 13 at Genetic Analysis Workshop 17 (GAW17) and provide a synthesis of their data analyses. The Group 13 contributors used a variety of approaches to test associations of both rare variants and common singleβnucleotide polymorphisms
## Abstract Nextβgeneration sequencing technology allows investigation of both common and rare variants in humans. Exomes are sequenced on the population level or in families to further study the genetics of human diseases. Genetic Analysis Workshop 17 (GAW17) provided exomic data from the 1000 Gen