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Evaluating methods for combining rare variant data in pathway-based tests of genetic association.
BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S48. doi: 10.1186/1753-6561-5-S9-S48.
BMC Proc. 2011.
PMID: 22373429
Free PMC article.
Evaluating methods for the analysis of rare variants in sequence data.
Luedtke A, Powers S, Petersen A, Sitarik A, Bekmetjev A, Tintle NL.
Luedtke A, et al. Among authors: bekmetjev a.
BMC Proc. 2011 Nov 29;5 Suppl 9(Suppl 9):S119. doi: 10.1186/1753-6561-5-S9-S119.
BMC Proc. 2011.
PMID: 22373354
Free PMC article.
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Comparing gene set analysis methods on single-nucleotide polymorphism data from Genetic Analysis Workshop 16.
Tintle NL, Borchers B, Brown M, Bekmetjev A.
Tintle NL, et al. Among authors: bekmetjev a.
BMC Proc. 2009 Dec 15;3 Suppl 7(Suppl 7):S96. doi: 10.1186/1753-6561-3-s7-s96.
BMC Proc. 2009.
PMID: 20018093
Free PMC article.
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Incorporating duplicate genotype data into linear trend tests of genetic association: methods and cost-effectiveness.
Borchers B, Brown M, McLellan B, Bekmetjev A, Tintle NL.
Borchers B, et al. Among authors: bekmetjev a.
Stat Appl Genet Mol Biol. 2009;8(1):Article24. doi: 10.2202/1544-6115.1433. Epub 2009 May 5.
Stat Appl Genet Mol Biol. 2009.
PMID: 19492982
Free PMC article.
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The cost-effectiveness of reclassification sampling for prevalence estimation.
Bekmetjev A, VanBruggen D, McLellan B, DeWinkle B, Lunderberg E, Tintle N.
Bekmetjev A, et al.
PLoS One. 2012;7(2):e32058. doi: 10.1371/journal.pone.0032058. Epub 2012 Feb 13.
PLoS One. 2012.
PMID: 22348146
Free PMC article.
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