Imputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohort.
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 this approach hinges on the accuracy of rare variant imputation, wh...
Main Authors: | , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2015-01-01
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Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC4309593?pdf=render |