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SLEPR: A Sample-Level Enrichment-Based Pathway Ranking Method — Seeking Biological Themes through Pathway-Level Consistency

机译:SLEPR:一种基于样品水平的富集途径排名方法—通过途径水平一致性寻求生物学主题

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摘要

Analysis of microarray and other high throughput data often involves identification of genes consistently up or down-regulated across samples as the first step in extraction of biological meaning. This gene-level paradigm can be limited as a result of valid sample fluctuations and biological complexities. In this report, we describe a novel method, SLEPR, which eliminates this limitation by relying on pathway-level consistencies. Our method first selects the sample-level differentiated genes from each individual sample, capturing genes missed by other analysis methods, ascertains the enrichment levels of associated pathways from each of those lists, and then ranks annotated pathways based on the consistency of enrichment levels of individual samples from both sample classes. As a proof of concept, we have used this method to analyze three public microarray datasets with a direct comparison with the GSEA method, one of the most popular pathway-level analysis methods in the field. We found that our method was able to reproduce the earlier observations with significant improvements in depth of coverage for validated or expected biological themes, but also produced additional insights that make biological sense. This new method extends existing analyses approaches and facilitates integration of different types of HTP data.
机译:微阵列和其他高通量数据的分析通常涉及鉴定样品中一致上调或下调的基因,这是提取生物学意义的第一步。由于有效的样品波动和生物学复杂性,这种基因水平的范例可能受到限制。在本报告中,我们描述了一种新颖的方法SLEPR,它通过依赖于路径级别的一致性来消除此限制。我们的方法首先从每个样本中选择样本水平的分化基因,捕获其他分析方法遗漏的基因,从每个列表中确定相关途径的富集水平,然后根据个体富集水平的一致性对注释途径进行排序来自两个样本类别的样本。作为概念证明,我们已使用此方法与GSEA方法(本领域最流行的途径水平分析方法之一)直接比较来分析三个公共微阵列数据集。我们发现,我们的方法能够重现早期的观察结果,并大大提高了已验证或预期的生物学主题的覆盖深度,而且还产生了具有生物学意义的其他见解。这种新方法扩展了现有的分析方法,并有助于集成不同类型的HTP数据。

著录项

  • 期刊名称 PLoS Clinical Trials
  • 作者

    Ming Yi; Robert M. Stephens;

  • 作者单位
  • 年(卷),期 2008(3),9
  • 年度 2008
  • 页码 e3288
  • 总页数 17
  • 原文格式 PDF
  • 正文语种
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 12:33:24

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