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VARIABILITY SINGLE NUCLEOTIDE POLYMORPHISMS LINKING STOCHASTIC EPIGENETIC VARIATION AND COMMON DISEASE

机译:随机表型变异与常见疾病相关的单核苷酸多态性

摘要

Provided are methods and models for an alternative source of disease risk, which identifies not genetic variants for a phenotype per se, but variants for variability itself. Also provided are methods and models for a genome-scale, gene-specific analysis of DNA methylation in the same individuals over time, in order to identify a personalized epigenomic signature that may correlate with common genetic disease. Also provided are methods and models for simulating stochastic epigenetic variation as a driving force of development, evolutionary adaptation, and disease.
机译:提供了替代疾病风险来源的方法和模型,这些方法和模型不识别表型本身的遗传变异,而是识别变异性本身。还提供了用于随着时间的推移对同一个体中的DNA甲基化进行基因组规模,基因特异性分析的方法和模型,以鉴定可能与常见遗传疾病相关的个性化表观基因组特征。还提供了用于模拟随机表观遗传变异作为发展,进化适应和疾病驱动力的方法和模型。

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