Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data

PLoS ONE

Volumn 4, Issue 4, 2009, Pages

  Jiang, Haiyan ^a   Orr, Andrew ^a   Guernsey, Duane L ^a   Robitaille, Johane ^a   Asselin, Géraldine ^b   Samuels, Mark E ^c,d   Dubé, Marie Pierre ^b,c  

^a DALHOUSIE UNIVERSITY   (Canada)

^b MONTREAL HEART INSTITUTE   (Canada)

^c UNIVERSITÉ DE MONTRÉAL   (Canada)

^d UNIVERSITY OF MONTREAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; DIMETHYLALLYLTRANSFERASE; DOPAMINE 2 RECEPTOR; POLYCYSTIN 1; POLYCYSTIN 2; SARCOGLYCAN; TORSION DYSTONIA PROTEIN; UNCLASSIFIED DRUG;

ANALYTICAL ERROR; ARTICLE; CANADA; CORNEA DYSTROPHY; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE; HAPLOTYPE; HOMOZYGOSITY; HUMAN; KIDNEY FAILURE; LINKAGE ANALYSIS; MATHEMATICAL ANALYSIS; MICROSATELLITE MARKER; MONOGENIC DISORDER; MYOCLONUS DYSTONIA; PATHOGENESIS; POPULATION GENETICS; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; ALGORITHM; CHROMOSOME MAP; CONGENITAL CORNEA DYSTROPHY; DYSTONIC DISORDER; FEMALE; GENETICS; HOMOZYGOTE; MALE; METHODOLOGY; PEDIGREE; RETINA DEGENERATION; STATISTICS; VALIDATION STUDY;

ALGORITHMS; CHROMOSOME MAPPING; CORNEAL DYSTROPHIES, HEREDITARY; DYSTONIC DISORDERS; FEMALE; GENOTYPE; HAPLOTYPES; HOMOZYGOTE; HUMANS; MALE; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINAL DEGENERATION;

EID: 65449170412     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0005280     Document Type: Article

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