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

id	sg-nus-scholar.10635-150629
record_format	dspace
spelling	sg-nus-scholar.10635-1506292024-11-10T00:33:57Z Using high-resolution variant frequencies to empower clinical genome interpretation 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. DUKE-NUS MEDICAL SCHOOL allele frequency clinical genomics ExAC inherited cardiovascular conditions variant interpretation 10.1038/gim.2017.26 Genetics in Medicine 19 10 1151-1158 GEMEF 2019-01-08T09:00:53Z 2019-01-08T09:00:53Z 2017 Article 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. (2017). Using high-resolution variant frequencies to empower clinical genome interpretation. Genetics in Medicine 19 (10) : 1151-1158. ScholarBank@NUS Repository. https://doi.org/10.1038/gim.2017.26 10983600 http://scholarbank.nus.edu.sg/handle/10635/150629 Nature Publishing Group Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	allele frequency clinical genomics ExAC inherited cardiovascular conditions variant interpretation
spellingShingle	allele frequency clinical genomics ExAC inherited cardiovascular conditions variant interpretation 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. Using high-resolution variant frequencies to empower clinical genome interpretation
description	10.1038/gim.2017.26
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL 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.
format	Article
author	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.
author_sort	Whiffin N.
title	Using high-resolution variant frequencies to empower clinical genome interpretation
title_short	Using high-resolution variant frequencies to empower clinical genome interpretation
title_full	Using high-resolution variant frequencies to empower clinical genome interpretation
title_fullStr	Using high-resolution variant frequencies to empower clinical genome interpretation
title_full_unstemmed	Using high-resolution variant frequencies to empower clinical genome interpretation
title_sort	using high-resolution variant frequencies to empower clinical genome interpretation
publisher	Nature Publishing Group
publishDate	2019
url	http://scholarbank.nus.edu.sg/handle/10635/150629
_version_	1821221250294349824

Using high-resolution variant frequencies to empower clinical genome interpretation

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