Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives-Reference-Cited by-同舟云学术

Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives

Published:2014-04-16 Issue:15 Volume:30 Page:2189-2196
ISSN:1460-2059
Container-title:Bioinformatics
language:en
Short-container-title:

Author:

Bureau Alexandre,Younkin Samuel G.,Parker Margaret M.,Bailey-Wilson Joan E.,Marazita Mary L.,Murray Jeffrey C.,Mangold Elisabeth,Albacha-Hejazi Hasan,Beaty Terri H.,Ruczinski Ingo

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Link

http://academic.oup.com/bioinformatics/article-pdf/30/15/2189/17146172/btu198.pdf

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3. Design considerations for massively parallel sequencing studies of complex human disease;Feng;PLoS One,2011

4. Rare and common variants: twenty arguments;Gibson;Nat. Rev. Genet.,2012

5. Disease gene identification strategies for exome sequencing;Gilissen;Eur. J. Hum. Genet.,2012

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