Using high-resolution variant frequencies to empower clinical genome interpretation

Using high-resolution variant frequencies to empower clinical genome interpretation

10.1038/gim.2017.26

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Bibliographic Details
Main Authors: Whiffin N., Minikel E., Walsh R., O'Donnell-Luria A.H., Karczewski K., Ing A.Y., Barton P.J.R., Funke B., Cook S.A., Macarthur D., Ware J.S.
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: Nature Publishing Group 2019
Subjects:
allele frequency
clinical genomics
ExAC
inherited cardiovascular conditions
variant interpretation
Online Access:http://scholarbank.nus.edu.sg/handle/10635/150629
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Institution: National University of Singapore

Internet

http://scholarbank.nus.edu.sg/handle/10635/150629

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