Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates-Reference-Cited by-同舟云学术

Two-stage study designs combining genome-wide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates

Published:2011-11-29 Issue:S9 Volume:5 Page:
ISSN:1753-6561
Container-title:BMC Proceedings
language:en
Short-container-title:BMC Proc

Author:

Faye Laura L,Bull Shelley B

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://link.springer.com/content/pdf/10.1186/1753-6561-5-S9-S64.pdf

Reference11 articles.

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2. Garner C: Upward bias in odds ratio estimates from genome-wide association studies. Genet Epidemiol. 2007, 31: 288-295. 10.1002/gepi.20209.

3. Faye LL, Sun L, Dimitromanolakis A, Bull SB: A flexible genome-wide bootstrap method that accounts for ranking- and threshold-selection bias in GWAS interpretation and replication study design. Stat Med. 2011, 30 (15): 1898-1912. 10.1002/sim.4228. doi: 10.1002/sim.4228

4. Morris AP, Zeggini E: An evaluation of statistical approaches to rare variant analysis in genetic association studies. Genet Epidemiol. 2010, 34: 188-193. 10.1002/gepi.20450.

5. Dering C, Pugh E, Ziegler A: Statistical analysis of rare sequence variants: an overview of collapsing methods. Genet Epidemiol. 2011, X (suppl X): X-X.

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