Markov models for inferring copy number variations from genotype data on illumina platforms

Human Heredity

Volumn 68, Issue 1, 2009, Pages 1-22

  Wang, Hui ^a   Veldink, Jan H ^e   Blauw, Hylke ^e   Van Den Berg, Leonard H ^e   Ophoff, Roel A ^b,c,e   Sabatti, Chiara ^b,d  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b Department of Human Genetics ^*  (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e UTRECHT UNIVERSITY   (Netherlands)

Author keywords

Disequilibrium association; Linkage

Indexed keywords

DNA;

ARTICLE; CHROMOSOME DELETION; DNA DETERMINATION; DNA POLYMORPHISM; GENE DELETION; GENE DUPLICATION; GENE IDENTIFICATION; GENE LOCATION; GENE LOCUS; GENE NUMBER; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC TRAIT; GENETIC VARIABILITY; GENOME; GENOTYPE; HUMAN; PROBABILITY; TUMOR GENE; TUMOR SUPPRESSOR GENE; X CHROMOSOME; GENE DOSAGE; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM;

GENE DELETION; GENE DOSAGE; GENOTYPE; HUMANS; LINKAGE DISEQUILIBRIUM; MARKOV CHAINS; POLYMORPHISM, GENETIC;

EID: 63349099666     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000210445     Document Type: Article

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