Improved imputation of common and uncommon SNPs with a new reference set

Nature Genetics

Volumn 44, Issue 1, 2012, Pages 6-7

  Wang, Zhaoming ^a,b   Jacobs, Kevin B ^a,b   Yeager, Meredith ^a,b   Hutchinson, Amy ^a,b   Sampson, Joshua ^b   Chatterjee, Nilanjan ^b   Albanes, Demetrius ^b   Berndt, Sonja I ^b   Chung, Charles C ^b   Diver, W Ryan ^c   Gapstur, Susan M ^c   Teras, Lauren R ^c   Haiman, Christopher A ^d   Henderson, Brian E ^d   Stram, Daniel ^d   Deng, Xiang ^a,b   Hsing, Ann W ^b   Virtamo, Jarmo ^e   Eberle, Michael A ^f   Stone, Jennifer L ^f   Purdue, Mark P ^b   Taylor, Phil ^b   Tucker, Margaret ^b   Chanock, Stephen J ^b   more..

^a NATIONAL CANCER INSTITUTE   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

^c AMERICAN CANCER SOCIETY   (United States)

^d UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^e NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^f NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACCURACY; COMPUTER MODEL; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC DATABASE; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE MAP; HUMAN; INFORMATION PROCESSING; LETTER; PRIORITY JOURNAL; REFERENCE DATABASE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

DATA INTERPRETATION, STATISTICAL; EUROPEAN CONTINENTAL ANCESTRY GROUP; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOMICS; GENOTYPE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; REFERENCE STANDARDS;

EID: 84555190223     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.1044     Document Type: Letter

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