The future of the human SNP identification: Which individuals to sequence?

Proceedings of the National Academy of Sciences of the United States of America

Volumn 106, Issue 19, 2009, Pages

  Reichardt, Juergen K V ^a   Mehrian Shai, Ruty ^b  

^a UNIVERSITY OF SYDNEY   (Australia)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE PREDISPOSITION; GENE FREQUENCY; GENE SEQUENCE; GENETIC PREDISPOSITION; GENETIC VARIABILITY; GENOME; HIGH RISK POPULATION; HUMAN; LETTER; PHENOTYPE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

DATABASES, GENETIC; GENOME, HUMAN; GENOMICS; HUMANS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; POPULATION GROUPS; SEQUENCE ANALYSIS, DNA;

EID: 66049127618     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0903681106     Document Type: Letter

References (2)

1. Ionita-Laza I, Lange C, Laird NM (2009) Estimating the number of unseen variants in the human genome. Proc Natl Acad Sci USA 106:5008-5013.
2. Nebert DW (2000) Extreme discordant phenotype methodology: An intuitive approach to clinical pharmacogenetics. Eur J Pharmacol 410:107-120. (Pubitemid 32008137)