A Genomic Data Fusion Framework to Exploit Rare and Common Variants for Association Discovery
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-19551-3_12
Reference10 articles.
1. Luo, L., Boerwinkle, E., Xiong, M.: Association studies for next-generation sequencing. Genome Research 21(7), 1099–1108 (2011)
2. Bansal, V., Libiger, O., Torkamani, A., Schork, N.J.: Statistical analysis strategies for association studies involving rare variants. Nat. Rev. Genet. 11(11), 773–785 (2010)
3. Li, Y., Byrnes, A.E., Li, M.: To Identify Associations with Rare Variants, Just WHaIT: Weighted Haplotype and Imputation-Based Tests. American Journal of Human Genetics 87(5), 728–773 (2010)
4. Dering, C., Hemmelmann, C., Pugh, E., Ziegler, A.: Statistical analysis of rare sequence variants: an overview of collapsing methods. Genetic Epidemiology 35(S1), S12–S17 (2011)
5. Price, A.L., et al.: Pooled association tests for rare variants in exon-resequencing studies. Am. J. Hum. Genet. 86(6), 832–838 (2010)
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