Detecting sequence-sequence interactions for complex diseases

Current Genomics

Volumn 7, Issue 1, 2006, Pages 59-72

  Lin, Min ^a,b   Wu, Rongling ^a  

^a University of Florida ^*  (United States)

^b DUKE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Haplotype; Linkage disequilibrium; Quantitative trait nucleotide; Single nucleotide polymorphism

Indexed keywords

DNA; GENE PRODUCT; PROTEIN BAR1; PROTEIN BAR2; UNCLASSIFIED DRUG;

CHROMOSOME SIZE; CONTROLLED STUDY; DNA DETERMINATION; DNA SEQUENCE; DOMINANT GENE; GENE INTERACTION; GENE MAPPING; GENE REPRESSION; GENE STRUCTURE; GENE TECHNOLOGY; GENETIC ALGORITHM; GENETIC ANALYSIS; GENETIC ENHANCEMENT; GENETIC EPISTASIS; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; MAJOR CLINICAL STUDY; MAXIMUM LIKELIHOOD METHOD; NUCLEOTIDE SEQUENCE; OBESITY; PATHOGENESIS; QUANTITATIVE TRAIT LOCUS MAPPING; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL MODEL;

EID: 33746862227     PISSN: 13892029     EISSN: None     Source Type: Journal    
DOI: 10.2174/138920206776389775     Document Type: Review

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