Identifying causal variants at loci with multiple signals of association.

Hormozdiari, Farhad; Kostem, Emrah; Kang, Eun Yong; Pasaniuc, Bogdan; Eskin, Eleazar

Hormozdiari, Farhad; Kostem, Emrah; Kang, Eun Yong; Pasaniuc, Bogdan; Eskin, Eleazar.

Hormozdiari F; Department of Computer Science, University of California, Los Angeles, California 90095.
Kostem E; Department of Computer Science, University of California, Los Angeles, California 90095.
Kang EY; Department of Computer Science, University of California, Los Angeles, California 90095.
Pasaniuc B; Department of Human Genetics, University of California, Los Angeles, California 90095 Department of Pathology and Laboratory Medicine, University of California, Los Angeles, California 90095.
Eskin E; Department of Computer Science, University of California, Los Angeles, California 90095 Department of Human Genetics, University of California, Los Angeles, California 90095 eeskin@cs.ucla.edu.

Genetics ; 198(2): 497-508, 2014 Oct.

Article en En | MEDLINE | ID: mdl-25104515

Asunto(s)

Estudios de Asociación Genética; Estudios de Casos y Controles; Quitinasas/genética; Enfermedad de la Arteria Coronaria/genética; Predisposición Genética a la Enfermedad; Humanos; Desequilibrio de Ligamiento; Modelos Genéticos; Polimorfismo de Nucleótido Simple; Sitios de Carácter Cuantitativo

Palabras clave

association studies; causal variants; fine mapping

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estudios de Asociación Genética Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2014 Tipo del documento: Article

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