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A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.
Genet Epidemiol. 2012 Nov;36(7):675-85. doi: 10.1002/gepi.21662. Epub 2012 Aug 3.
Genet Epidemiol. 2012.
PMID: 22865616
Free PMC article.
A flexible likelihood framework for detecting associations with secondary phenotypes in genetic studies using selected samples: application to sequence data.
Liu DJ, Leal SM.
Liu DJ, et al.
Eur J Hum Genet. 2012 Apr;20(4):449-56. doi: 10.1038/ejhg.2011.211. Epub 2011 Dec 14.
Eur J Hum Genet. 2012.
PMID: 22166943
Free PMC article.
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