Sequence variants from whole genome sequencing a large group of Icelanders-Reference-Cited by-同舟云学术

Sequence variants from whole genome sequencing a large group of Icelanders

Published:2015-03-25 Issue:1 Volume:2 Page:
ISSN:2052-4463
Container-title:Scientific Data
language:en
Short-container-title:Sci Data

Author:

Gudbjartsson Daniel F,Sulem Patrick,Helgason Hannes,Gylfason Arnaldur,Gudjonsson Sigurjon A,Zink Florian,Oddson Asmundur,Magnusson Gisli,Halldorsson Bjarni V,Hjartarson Eirikur,Sigurdsson Gunnar Th.,Kong Augustine,Helgason Agnar,Masson Gisli,Magnusson Olafur Th.,Thorsteinsdottir Unnur,Stefansson Kari

Publisher

Springer Science and Business Media LLC

Subject

Library and Information Sciences,Statistics, Probability and Uncertainty,Computer Science Applications,Education,Information Systems,Statistics and Probability

Link

http://www.nature.com/articles/sdata201511.pdf

Reference27 articles.

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3. Hindorff, L. A. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl Acad. Sci. USA 106, 9362–9367 (2009).

4. Abecasis, G. R. et al. An integrated map of genetic variation from 1,092 human genomes. Nature 491, 56–65 (2012).

5. Tennessen, J. A. et al. Evolution and functional impact of rare coding variation from deep sequencing of human exomes. Science 337, 64–69 (2012).

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