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

Bioinformatics

Volumn 30, Issue 15, 2014, Pages 2189-2196

  Bureau, Alexandre ^a,b   Younkin, Samuel G ^c   Parker, Margaret M ^c   Bailey Wilson, Joan E ^d   Marazita, Mary L ^e   Murray, Jeffrey C ^f   Mangold, Elisabeth ^g   Albacha Hejazi, Hasan ^h   Beaty, Terri H ^c   Ruczinski, Ingo ^c  

^a Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec   (Canada)

^b UNIVERSITÉ LAVAL   (Canada)

^c JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^d NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^e UNIVERSITY OF PITTSBURGH   (United States)

^f UNIVERSITY OF IOWA   (United States)

^g UNIVERSITY OF BONN   (Germany)

^h Hejazi Clinic   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE CONTROL STUDY; EXOME; FEMALE; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENETICS; GENOMICS; HUMAN; MALE; METHODOLOGY; MONTE CARLO METHOD; PEDIGREE; PROBABILITY; RARE DISEASE;

CASE-CONTROL STUDIES; EXOME; FEMALE; GENETIC LINKAGE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; HUMANS; MALE; MONTE CARLO METHOD; PEDIGREE; PROBABILITY; RARE DISEASES;

EID: 84904246839     PISSN: 13674803     EISSN: 14602059     Source Type: Journal    
DOI: 10.1093/bioinformatics/btu198     Document Type: Article

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