Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies

PLoS ONE

Volumn 8, Issue 7, 2013, Pages

  Joshi, Peter K ^a   Prendergast, James ^b   Fraser, Ross M ^a   Huffman, Jennifer E ^b   Vitart, Veronique ^b   Hayward, Caroline ^b   McQuillan, Ruth ^a   Glodzik, Dominik ^a,b   Polašek, Ozren ^c,d   Hastie, Nicholas D ^b   Rudan, Igor ^a   Campbell, Harry ^a   Wright, Alan F ^b   Haley, Chris S ^b,e   Wilson, James F ^a,b   Navarro, Pau ^b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b UNIVERSITY OF EDINBURGH   (United Kingdom)

^c UNIVERSITY OF SPLIT   (Croatia)

^d UNIVERSITY OF SPLIT   (Croatia)

^e UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; EXOME; GENE FREQUENCY; GENETIC ASSOCIATION; SAMPLE SIZE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EUROPEAN CONTINENTAL ANCESTRY GROUP; EXOME; GENE FREQUENCY; GENOME, HUMAN; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84880483904     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0068604     Document Type: Article

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