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癌症基因谱数据的荟萃分析。

Meta-analysis of cancer gene-profiling data.

作者信息

Yang Xinan, Sun Xiao

机构信息

Division of Bioinformatics, State Key Laboratory of Bioelectronics (Chien-Shiung Wu Laboratory), Southeast University, Nanjing, China.

出版信息

Methods Mol Biol. 2010;576:409-26. doi: 10.1007/978-1-59745-545-9_21.

Abstract

DNA microarray profiles are plagued by the issue of large number of variables but small number of samples and are often notorious for their low signal-to-noise ratio for clinical applications. Therefore, a great need for meta-analysis techniques is emerging to yield more valid and informative results than each experiment separately. By exploring the power of several studies in one single analysis, meta-analysis of many cancer gene-profiling data increases the statistical power to detect differentially expressed genes and allows assessment of heterogeneity. OrderedList is such a method that was specially proposed for cancer gene expression data meta-analysis. It is superior to other methods in that it does not rely on strong effects of differential gene expression in a single study but on consistent regulated genes across multiple studies. This chapter introduces the R implementation of this methodology on real data sets to identify biomarkers for adenocarcinoma lung cancer.

摘要

DNA微阵列图谱受到变量多但样本少这一问题的困扰,并且在临床应用中,其低信噪比常常声名狼藉。因此,对于荟萃分析技术的巨大需求正在出现,以产生比单独的每个实验更有效和更具信息性的结果。通过在一次单一分析中探索多项研究的效力,对许多癌症基因谱数据进行荟萃分析可提高检测差异表达基因的统计效力,并允许评估异质性。有序列表(OrderedList)就是这样一种专门为癌症基因表达数据荟萃分析而提出的方法。它优于其他方法,因为它不依赖于单个研究中差异基因表达的强效应,而是依赖于多个研究中一致调控的基因。本章介绍了该方法在真实数据集上的R实现,以识别肺腺癌的生物标志物。

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