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Measures for the degree of overlap of gene signatures and applications to TCGA

机译:衡量基因签名重叠程度的方法及其在TCGA中的应用

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摘要

For cancer and many other complex diseases, a large number of gene signatures have been generated. In this study, we use cancer as an example and note that other diseases can be analyzed in a similar manner. For signatures generated in multiple independent studies on the same cancer type and outcome, and for signatures on different cancer types, it is of interest to evaluate their degree of overlap. Many of the existing studies simply count the number (or percentage) of overlapped genes shared by two signatures. Such an approach has serious limitations. In this study, as a demonstrating example, we consider cancer prognosis data under the Cox model. Lasso, which is representative of a large number of regularization methods, is adopted for generating gene signatures. We examine two families of measures for quantifying the degree of overlap. The first family is based on the Cox-Lasso estimates at the optimal tunings, and the second family is based on estimates across the whole solution paths. Within each family, multiple measures, which describe the overlap from different perspectives, are introduced. The analysis of TCGA (The Cancer Genome Atlas) data on five cancer types shows that the degree of overlap varies across measures, cancer types and types of (epi)genetic measurements. More investigations are needed to better describe and understand the overlaps among gene signatures.
机译:对于癌症和许多其他复杂疾病,已经产生了大量的基因签名。在本研究中,我们以癌症为例,并注意可以以类似方式分析其他疾病。对于在相同癌症类型和结果的多个独立研究中生成的签名,以及对于不同癌症类型的签名,评估它们的重叠程度是很有意义的。许多现有研究仅计算两个特征共享的重叠基因的数量(或百分比)。这种方法具有严重的局限性。在本研究中,作为一个示例,我们考虑了Cox模型下的癌症预后数据。套索是代表大量正则化方法的代表,被用于生成基因签名。我们研究了两个系列的量化重叠程度的度量。第一个族基于最佳调整时的Cox-Lasso估计,第二个族基于整个解决方案路径上的估计。在每个家庭中,引入了多种措施,这些措施从不同角度描述了重叠。对五种癌症类型的TCGA(癌症基因组图谱)数据进行的分析表明,重叠程度随测量,癌症类型和(epi)遗传测量类型的不同而不同。为了更好地描述和理解基因标记之间的重叠,需要进行更多的研究。

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