Methodology for the analysis of rare genetic variation in genome-wide association and re-sequencing studies of complex human traits
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics,Molecular Biology,Biochemistry,General Medicine
Link
http://academic.oup.com/bfg/article-pdf/13/5/362/679193/elu012.pdf
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1. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
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5. Common SNPs explain a large proportion of the heritability for human height
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