基于多模态图的半监督管道预测癌症生存。

Hamid Reza Hassanzadeh, John H Phan, May D Wang
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引用次数: 5

摘要

癌症生存预测是一个活跃的研究领域,可以帮助预防不必要的治疗,提高患者的生活质量。基因表达谱被广泛应用于癌症研究中,以发现信息丰富的生物标志物,帮助预测不同的临床终点预测。我们使用来自RNA深度测序(RNA-seq)的多种数据模式来预测癌症患者的生存。尽管在癌症肿瘤的表达谱中有丰富的可用信息,但在很大程度上,由于与高维表达谱相比数据样本的缺乏,实现上述目标仍然是一个巨大的挑战。因此,转录组数据模式的分析需要最先进的大数据分析技术,这些技术可以最大限度地利用所有可用数据来发现隐藏在大量噪声中的相关信息。在本文中,我们提出了一个管道,通过利用输入的结构(流形学习)和利用使用拉普拉斯支持向量机(一种基于图的半监督学习(GSSL)范例的未标记样本来预测癌症患者的生存。研究表明,在某些情况下,单一模型本身不会产生最佳精度,通过堆叠泛化策略将不同模型融合在一起,可以协同提高精度。我们将我们的方法应用于两个癌症数据集,并提出了有希望的结果。我们认为,类似的管道可以用于预测任务,其中标记的样本是昂贵的获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A Multi-Modal Graph-Based Semi-Supervised Pipeline for Predicting Cancer Survival.

A Multi-Modal Graph-Based Semi-Supervised Pipeline for Predicting Cancer Survival.

A Multi-Modal Graph-Based Semi-Supervised Pipeline for Predicting Cancer Survival.

Cancer survival prediction is an active area of research that can help prevent unnecessary therapies and improve patient's quality of life. Gene expression profiling is being widely used in cancer studies to discover informative biomarkers that aid predict different clinical endpoint prediction. We use multiple modalities of data derived from RNA deep-sequencing (RNA-seq) to predict survival of cancer patients. Despite the wealth of information available in expression profiles of cancer tumors, fulfilling the aforementioned objective remains a big challenge, for the most part, due to the paucity of data samples compared to the high dimension of the expression profiles. As such, analysis of transcriptomic data modalities calls for state-of-the-art big-data analytics techniques that can maximally use all the available data to discover the relevant information hidden within a significant amount of noise. In this paper, we propose a pipeline that predicts cancer patients' survival by exploiting the structure of the input (manifold learning) and by leveraging the unlabeled samples using Laplacian support vector machines, a graph-based semi supervised learning (GSSL) paradigm. We show that under certain circumstances, no single modality per se will result in the best accuracy and by fusing different models together via a stacked generalization strategy, we may boost the accuracy synergistically. We apply our approach to two cancer datasets and present promising results. We maintain that a similar pipeline can be used for predictive tasks where labeled samples are expensive to acquire.

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