Using high-resolution variant frequencies empowers clinical genome interpretation and enables investigation of genetic architecture

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AJHG-D-18-00517_R2_accepted.pdf (300.43 KB)

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Author(s)

Whiffin, Nicola

Roberts, Angharad M

Minikel, Eric

Zappala, Zach

Walsh, Roddy

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Type

Journal Article

Date Issued

2019-01-03

Date Acceptance

2019-01-01

Citation

American Journal of Human Genetics, 2019, 104 (1), pp.187-190

URI

http://hdl.handle.net/10044/1/67621

DOI

https://www.dx.doi.org/10.1016/j.ajhg.2018.11.012

ISSN

0002-9297

Publisher

Elsevier (Cell Press)

Start Page

187

End Page

190

Journal / Book Title

American Journal of Human Genetics

Volume

104

Issue

1

Copyright Statement

© 2019 Elsevier Ltd. All rights reserved. This manuscript is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Licence http://creativecommons.org/licenses/by-nc-nd/4.0/

Sponsor

Fondation Leducq

Fondation Leducq

British Heart Foundation

Wellcome Trust

Department of Health

Wellcome Trust

Royal Brompton & Harefield NHS Foundation Trust

Identifier

http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000454775500018&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202

Grant Number

11 CVD-01

11 CVD-01

RM/13/1/30157

100134/Z/12/Z

HICF-R6-373

107469/Z/15/Z

N/A

Subjects

Science & Technology

Life Sciences & Biomedicine

Genetics & Heredity

Publication Status

Published

Date Publish Online

2019-01-03