Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set-Reference-Cited by-同舟云学术

Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set

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

Author:

Yip Wai-Ki,De Gourab,Raby Benjamin A,Laird Nan

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-S21.pdf

Reference8 articles.

1. Laird NM, Lange C: Family-based methods for linkage and association analysis. Adv Genet. 2008, 60: 219-252.

2. 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.

3. Almasy LA, Dyer TD, Peralta JM, Kent JW, Charlesworth JC, Curran JE, Blangero J: Genetic Analysis Workshop 17 mini-exome simulation. BMC Proc. 2011, 5 (suppl 9): S2-10.1186/1753-6561-5-S9-S2.

4. Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES: Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet. 1996, 58: 1347-1363.

5. Zeegers MP, Rice JP, Rijsdijk FV, Abecasis GR, Sham PC: Regression-based sib pair linkage analysis for binary traits. Hum Hered. 2003, 55: 125-131. 10.1159/000072317.

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