Rank-based transcriptional signatures

Mario Lauria
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引用次数: 19

Abstract

We have developed a method for the definition and the analysis of gene expression signatures for diagnostic purposes. Our approach relies on construction of a reference map of transcriptional signatures, from both healthy controls and affected patients, using the respective mRNA or miRNA profiles. Subsequently, disease diagnosis can be performed by determining the relative map position of an individual’s transcriptional signature. Our approach addresses simultaneously the scarce repeatability issue and the high sensitivity of expression profiling methods to protocol variations, thereby providing a novel approach to RNA signature definition and analysis. Specifically, our method requires only that the relative position of RNA species be accurate in a ranking by value, not their absolute values. Furthermore, our method makes no assumptions on which RNA species must be included in the signature and, by considering a large subset (or even the whole set) of known RNAs, our approach can tolerate a moderate number of erroneous inversions in the ranking. The diagnostic power of our method has been convincingly demonstrated in an open scientific competition (sbv IMPROVER Diagnostic Signature Challenge), scoring second place overall, and first place in one sub-challenge. In addition, we report the application of our method to published miRNA expression profile data sets, quantifying its performance in terms of predictive capability and robustness to batch effects, compared with current state-of-the-art methods.
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基于排名的转录签名
我们已经开发了一种用于诊断目的的基因表达特征的定义和分析方法。我们的方法依赖于构建来自健康对照和受影响患者的转录特征参考图,使用各自的mRNA或miRNA谱。随后,可以通过确定个体转录特征的相对图谱位置来进行疾病诊断。我们的方法同时解决了表达谱方法对协议变化的高敏感性和缺乏可重复性的问题,从而为RNA特征定义和分析提供了一种新的方法。具体来说,我们的方法只要求RNA物种的相对位置在按值排序时准确,而不要求它们的绝对值。此外,我们的方法没有假设哪些RNA物种必须包含在签名中,并且通过考虑已知RNA的一个大子集(甚至整个集合),我们的方法可以容忍排名中的适度数量的错误反转。我们的方法的诊断能力已经在一个公开的科学竞赛(sbv IMPROVER诊断签名挑战赛)中得到了令人信服的证明,获得了总第二名和一个子挑战的第一名。此外,我们报告了我们的方法在已发表的miRNA表达谱数据集上的应用,与当前最先进的方法相比,量化了其在预测能力和批效应鲁棒性方面的性能。
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