Haplotype Imputation for Association Analysis
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Published:2013-11-11
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Volume:
Page:183-211
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ISSN:1431-8776
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Container-title:Design, Analysis, and Interpretation of Genome-Wide Association Scans
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language:
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Publisher
Springer New York
Reference42 articles.
1. Daly, M. J., Rioux, J., Schaffner, S., Hudson, T., & Lander, E. (2001). High-resolution haplotype structure in the human genome. Nature Genetics, 29, 229–232. 2. Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., et al. (2002). The structure of haplotype blocks in the human genome. Science, 296, 2225–2229. 3. Barrett, J. C., Fry, B., Maller, J., & Daly, M. J. (2005). Haploview: Analysis and visualization of LD and haplotype maps. Bioinformatics, 21, 263–265. 4. Nackley, A. G., Shabalina, S. A., Tchivileva, I. E., Satterfield, K., Korchynskyi, O., Makarov, S. S., et al. (2006). Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science, 314, 1930–1933. 5. Roten, L. T., Fenstad, M. H., Forsmo, S., Johnson, M. P., Moses, E. K., Austgulen, R., et al. (2011). A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2). Molecular Human Reproduction, 17, 439–446.
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