Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24

Genetic Epidemiology

Volumn 33, Issue 4, 2009, Pages 357-368

  Zöllner, Sebastian ^a,b   Su, Gang ^a   Stewart, William C L ^a   Chen, Yi ^a   McInnis, Melvin G ^b   Burmeister, Margit ^a,b,c  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

8q24; Association mapping; Copy number variation; Deletion; EM

Indexed keywords

ALLELE; ANALYTICAL ERROR; ARTICLE; BAYES THEOREM; BIPOLAR DISORDER; CHROMOSOME 8Q; CHROMOSOME DELETION; CONTROLLED STUDY; GENE DELETION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HYBRIDIZATION; MATHEMATICAL ANALYSIS; POLYMERASE CHAIN REACTION; PROBABILITY; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL ANALYSIS;

ALGORITHMS; BAYES THEOREM; BIPOLAR DISORDER; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 8; EPIDEMIOLOGIC METHODS; GENE DOSAGE; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; HETEROZYGOTE; HOMOZYGOTE; HUMANS; LINKAGE DISEQUILIBRIUM; MODELS, GENETIC; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE DELETION;

EID: 66249129714     PISSN: 07410395     EISSN: 10982272     Source Type: Journal    
DOI: 10.1002/gepi.20391     Document Type: Article

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