Whole-genome patterns of common DNA variation in three human populations

Science

Volumn 307, Issue 5712, 2005, Pages 1072-1079

  Hinds, David A ^a   Stuve, Laura L ^a   Nilsen, Geoffrey B ^a   Halperin, Eran ^b   Eskin, Eleazar ^c   Ballinger, Dennis G ^a   Frazer, Kelly A ^a   Cox, David R ^a  

^a Perlegen Sciences Inc   (United States)

^b INTERNATIONAL COMPUTER SCIENCE INSTITUTE   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DATA REDUCTION; GENETIC ENGINEERING; HUMAN ENGINEERING;

DNA VARIATIONS; HUMAN POPULATIONS; SINGLE-NUCLEOTIDE POLYMORPHISM (SNP); WHOLE-GENOME PATTERNS;

DNA SEQUENCES;

DNA;

GENOME;

ARTICLE; CORRELATION ANALYSIS; DNA SEQUENCE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC VARIABILITY; GENOME ANALYSIS; GENOTYPE; HAPLOTYPE; HUMAN; PHENOTYPIC VARIATION; POPULATION GENETICS; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

AFRICAN AMERICANS; ALGORITHMS; ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHROMOSOME MAPPING; DATABASES, GENETIC; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MULTIFACTORIAL INHERITANCE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECOMBINATION, GENETIC; RISK FACTORS; SELECTION (GENETICS); VARIATION (GENETICS);

EID: 13844313862     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.1105436     Document Type: Article

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