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From 'omes to biology

机译:从基因到生物学

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Technologies that have emerged from the genome project have dramatically increased our ability to generate data on the way in which organisms respond to their environments, how they execute their programmes of development and growth, and how these are altered in the development of disease states. However, our ability to analyse these large datasets has not kept pace with our ability to generate them and consequently new strategies must be developed to address the issues associated with their analysis. One approach that we have employed quite successfully is to look at data from microarrays (or proteomics or metabolomics experiments) not as independent datasets, but rather as elements of a much larger body of biological information across various scales that must be integrated with, and interpreted within, the context of such ancillary data. Here we outline the general approach and provide three examples from published studies of the way in which we have applied this strategy.
机译:基因组项目中出现的技术极大地提高了我们生成数据的能力,这些数据涉及生物对环境的反应方式,如何执行其发育和生长程序以及在疾病状态的发展中如何改变这些数据。但是,我们分析这些大型数据集的能力未能与我们生成它们的能力保持同步,因此必须开发新的策略来解决与分析相关的问题。我们已经非常成功地采用的一种方法是,将微阵列(或蛋白质组学或代谢组学实验)中的数据视为独立的数据集,而不是视为必须与之整合和解释的各种规模的更大范围生物信息的元素在此类辅助数据的上下文中。在这里,我们概述了通用方法,并提供了已发表的有关应用此策略的方法的三个示例。

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