A comparison of two collapsing methods in different approaches-Reference-Cited by-同舟云学术

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A comparison of two collapsing methods in different approaches

Published:2014-06 Issue:S1 Volume:8 Page:
ISSN:1753-6561
Container-title:BMC Proceedings
language:en
Short-container-title:BMC Proc

Author:

Dering Carmen,Schillert Arne,König Inke R,Ziegler Andreas

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

https://link.springer.com/content/pdf/10.1186/1753-6561-8-S1-S8.pdf

Reference10 articles.

1. Iyengar SK, Elston RC: The genetic basis of complex traits: rare variants or "common gene, common disease"?. Methods Mol Biol. 2007, 376: 71-84. 10.1007/978-1-59745-389-9_6.

2. Cohen JC, Kiss RS, Pertsemlidis A, Marcel YL, McPherson R, Hobbs HH: Multiple rare alleles contribute to low plasma levels of HDL cholesterol. Science. 2004, 305: 869-872. 10.1126/science.1099870.

3. Dering C, Hemmelmann C, Pugh E, Ziegler A: Statistical analysis of rare sequence variants: an overview of collapsing methods. Genet Epidemiol. 2011, 35 (suppl 1): S12-S17.

4. Asimit J, Zeggini E: Rare variant association analysis methods for complex traits. Annu Rev Genet. 2010, 44: 293-308. 10.1146/annurev-genet-102209-163421.

5. Bansal V, Libiger O, Torkamani A, Schork NJ: Statistical analysis strategies for association studies involving rare variants. Nat Rev Genet. 2010, 11: 773-785. 10.1038/nrg2867.

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic and clinical predictors of CD4 lymphocyte recovery during suppressive antiretroviral therapy: Whole exome sequencing and antiretroviral therapy response phenotypes;PLOS ONE;2019-08-15

2. Methods for Collapsing Multiple Rare Variants in Whole-Genome Sequence Data;Genetic Epidemiology;2014-08-11

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