Two-stage family-based designs for sequencing studies
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Link
http://link.springer.com/content/pdf/10.1186/1753-6561-8-S1-S32.pdf
Reference29 articles.
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3. Shi G, Rao DC: Optimum designs for next-generation sequencing to discover rare variants for common complex disease. Genet Epidemiol. 2011, 35: 572-579.
4. Feng T, Elston RC, Zhu X: Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS). Genet Epidemiol. 2011, 35: 398-409. 10.1002/gepi.20588.
5. Zhu X, Feng T, Li Y, Lu Q, Elston RC: Detecting rare variants for complex traits using family and unrelated data. Genet Epidemiol. 2010, 34: 171-187. 10.1002/gepi.20449.
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