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Machine learning models to search relevant genetic signatures in clinical context

机译:机器学习模型可在临床环境中搜索相关的遗传特征

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Clinicians are interested in the estimation of robust and relevant genetic signatures from gene sequencing data. Many machine learning approaches have been proposed trying to address well-known issues of this complex task (feature or gene selection, classification or model selection, and prediction assessment). Addressing this problem often requires a deep knowledge of these methods and some of them demand high computational resources that may not be affordable. In this paper, an exhaustive study that includes different types of feature selection methods and classifiers is presented, providing clinicians an useful insight of the most suitable methods for this purpose. Predictions assessment is performed using a bootstrap cross-validation strategy as an honest validation scheme. The results of this study for six benchmark datasets show that filter or embedded methods are preferred, in general, to wrapper methods according to their better statistical significant results, in terms of accuracy, and lower demand for computational resources.
机译:临床医生对根据基因测序数据评估可靠且相关的遗传特征感兴趣。已经提出了许多机器学习方法来尝试解决这一复杂任务的众所周知的问题(特征或基因选择,分类或模型选择以及预测评估)。解决此问题通常需要对这些方法有深入的了解,其中一些方法需要大量的计算资源,而这些资源可能无法承受。在本文中,我们进行了详尽的研究,其中包括不同类型的特征选择方法和分类器,从而为临床医生提供了最有用的,最适合此目的的方法的见解。预测评估是使用引导交叉验证策略作为诚实验证方案来执行的。这项针对六个基准数据集的研究结果表明,一般而言,过滤器或嵌入式方法比包装器方法更可取,因为它们具有更好的统计显着性,准确性和较低的计算资源需求。

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