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Genetics, statistics and human disease: analytical retooling for complexity

期刊

TRENDS IN GENETICS
卷 20, 期 12, 页码 640-647

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ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tig.2004.09.007

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资金

  1. NHLBI NIH HHS [HL 65234] Funding Source: Medline
  2. NIAID NIH HHS [AI 59694] Funding Source: Medline
  3. NIMH NIH HHS [T32 MH 64913] Funding Source: Medline
  4. NINDS NIH HHS [NS 32830] Funding Source: Medline
  5. PHS HHS [A619085] Funding Source: Medline

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Molecular biologists and geneticists alike now acknowledge that most common human diseases with a genetic component are likely to have complex etiologies. Yet despite this belief, many statistical geneticists continue applying, in slightly new and different ways, methodologies that were developed to dissect much simpler etiologies. In this article, we characterize, with examples, the various factors that can complicate genetic analysis and demonstrate their shared features and how they affect genetic analysis. We describe a variety of approaches that are currently available, revealing methodological gaps and suggesting new directions for method development. Finally, we propose a comprehensive two-step approach to analysis that systemically addresses the different genetic factors that are likely to underlie complex diseases.

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