Imputation of the Rare HOXB13 G84E Mutation and Cancer Risk in a Large Population-Based Cohort

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...

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Bibliographic Details
Main Authors: Hoffmann, Thomas J., Sakoda, Lori C., Shen, Ling, Jorgenson, Eric, Habel, Laurel A., Liu, Jinghua, Kvale, Mark N., Asgari, Maryam M., Banda, Yambazi, Corley, Douglas, Kushi, Lawrence H., Quesenberry, Charles P., Schaefer, Catherine, Van Den Eeden, Stephen K., Risch, Neil, Witte, John S.
Format: Online
Language:English
Published: Public Library of Science 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309593/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309593/

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