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Mas-o-menos: a simple sign averaging method for discrimination in genomic data analysis

机译:Mas-o-menos:一种用于基因组数据分析的简单符号平均方法

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Motivation: The successful translation of genomic signatures into clinical settings relies on good discrimination between patient sub-groups. Many sophisticated algorithms have been proposed in the statistics and machine learning literature, but in practice simpler algorithms are often used. However, few simple algorithms have been formally described or systematically investigated. Results: We give a precise definition of a popular simple method we refer to as mas-o-menos, which calculates prognostic scores for discrimination by summing standardized predictors, weighted by the signs of their marginal associations with the outcome. We study its behavior theoretically, in simulations and in an extensive analysis of 27 independent gene expression studies of bladder, breast and ovarian cancer, altogether totaling 3833 patients with survival outcomes. We find that despite its simplicity, mas-o-menos can achieve good discrimination performance. It performs no worse, and sometimes better, than popular and much more CPU-intensive methods for discrimination, including lasso and ridge regression.
机译:动机:将基因组特征成功转化为临床背景取决于患者亚组之间的良好区分。在统计和机器学习文献中已经提出了许多复杂的算法,但是在实践中通常使用更简单的算法。但是,很少有简单的算法被正式描述或系统地研究过。结果:我们给出了一种称为mas-o-menos的流行简单方法的精确定义,该方法通过对标准化预测变量求和,并用其与结果的边际关联的符号加权,来计算歧视的预后评分。我们从理论上,在模拟和广泛分析27项膀胱癌,乳腺癌和卵巢癌独立基因表达研究中研究了其行为,总共对3833例患者进行了生存。我们发现,尽管其简单,但是mas-o-menos仍可以实现良好的辨别性能。它与流行的且占用大量CPU资源的判别方法(包括套索和岭回归)相比,性能更佳,有时甚至更好。

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