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Imputation of the Rare HOXB13 G84E Mutation and Cancer Risk in a Large Population-Based Cohort
Published Web Location
http://europepmc.org/articles/PMC4309593?pdf=renderNo data is associated with this publication.
Abstract
© 2015 Hoffmann et al.An efficient approach to characterizing the disease burden of rare genetic variants is to impute them into large well-phenotyped cohorts with existing genome-wide genotype data using large sequenced referenced panels. The success of t
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