A Hybrid Likelihood Model for Sequence-Based Disease Association Studies

PLoS Genetics

Volumn 9, Issue 1, 2013, Pages

  Chen, Yun Ching ^a   Carter, Hannah ^a   Parla, Jennifer ^b   Kramer, Melissa ^b   Goes, Fernando S ^c   Pirooznia, Mehdi ^c   Zandi, Peter P ^c   McCombie, W Richard ^b   Potash, James B ^d   Karchin, Rachel ^a  

^a Johns Hopkins University   (United States)

^b Simons Center for Quantitative Biology   (United States)

^c JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF IOWA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOGEN ACTIVATED PROTEIN KINASE; TRIACYLGLYCEROL;

ALLELE; ANGPTL3 GENE; ANGPTL4 GENE; ANGPTL5 GENE; ARTICLE; BIPOLAR DISORDER; BURDEN OR MUTATION POSITION TEST; CONTROLLED STUDY; DISEASE ASSOCIATION; GENE; GENE CLUSTER; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; SEQUENCE ANALYSIS; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL MODEL; SYSTEMATIC ERROR; VALIDATION PROCESS;

CASE-CONTROL STUDIES; COMPUTER SIMULATION; EXOME; GENETIC ASSOCIATION STUDIES; GENOME, HUMAN; HUMANS; LIKELIHOOD FUNCTIONS; MITOGEN-ACTIVATED PROTEIN KINASE KINASES; MODELS, GENETIC; MODELS, THEORETICAL; POLYMORPHISM, SINGLE NUCLEOTIDE; PROBABILITY; SIGNAL TRANSDUCTION;

EID: 84873493453     PISSN: 15537390     EISSN: 15537404     Source Type: Journal    
DOI: 10.1371/journal.pgen.1003224     Document Type: Article

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