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The Transcriptomic Toolbox: Resources for Interpreting Large Gene Expression Data within a Precision Medicine Context for Metabolic Disease Atherosclerosis

机译:转录组工具箱:用于在代谢疾病动脉粥样硬化的精确医学环境中解释大型基因表达数据的资源

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摘要

As one of the most widespread metabolic diseases, atherosclerosis affects nearly everyone as they age; arteries gradually narrow from plaque accumulation over time reducing oxygenated blood flow to central and periphery causing heart disease, stroke, kidney problems, and even pulmonary disease. Personalized medicine promises to bring treatments based on individual genome sequencing that precisely target the molecular pathways underlying atherosclerosis and its symptoms, but to date only a few genotypes have been identified. A promising alternative to this genetic approach is the identification of pathways altered in atherosclerosis by transcriptome analysis of atherosclerotic tissues to target specific aspects of disease. Transcriptomics is a potentially useful tool for both diagnostics and discovery science, exposing novel cellular and molecular mechanisms in clinical and translational models, and depending on experimental design to identify and test novel therapeutics. The cost and time required for transcriptome analysis has been greatly reduced by the development of next generation sequencing. The goal of this resource article is to provide background and a guide to appropriate technologies and downstream analyses in transcriptomics experiments generating ever-increasing amounts of gene expression data.
机译:动脉粥样硬化是最广泛的代谢疾病之一,随着年龄的增长几乎影响每个人。随着时间的流逝,动脉逐渐从斑块聚集处变窄,从而减少了充氧的血液流向中枢和外周,从而导致心脏病,中风,肾脏问题,甚至是肺部疾病。个性化医学有望带来基于个体基因组测序的治疗方法,这些治疗方法精确地针对动脉粥样硬化及其症状的分子途径,但迄今为止,仅发现了少数基因型。这种遗传方法的一种有前途的替代方法是通过对动脉粥样硬化组织进行转录组分析来确定疾病的特定方面,从而确定动脉粥样硬化中改变的途径。转录组学是诊断学和发现科学的潜在有用工具,可在临床和转化模型中揭示新颖的细胞和分子机制,并依赖于实验设计来识别和测试新颖的疗法。下一代测序技术的发展大大降低了转录组分析所需的成本和时间。本文的目的是为转录组学实验中适当的技术和下游分析提供背景和指南,以产生数量不断增加的基因表达数据。

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