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Comparison of Different Sampling Algorithms for Phenotype Prediction

机译:表型预测的不同采样算法的比较

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In this paper, we compare different sampling algorithms used for identifying the defective pathways in highly underdetermined phenotype prediction problems. The first algorithm (Fisher's ratio sampler) selects the most discriminatory genes and samples the high discriminatory genetic networks according to a prior probability that it is proportional to their individual Fisher's ratio. The second one (holdout sampler) is inspired by the bootstrapping procedure used in regression analysis and uses the minimum-scale signatures found in different random hold outs to establish the most frequently sampled genes. The third one is a pure random sampler which randomly builds networks of differentially expressed genes. In all these algorithms, the likelihood of the different networks is established via leave one out cross-validation (LOOCV). and the posterior analysis of the most frequently sampled genes serves to establish the altered biological pathways. These algorithms are compared to the results obtained via Bayesian Networks (BNs). We show the application of these algorithms to a microarray dataset concerning Triple Negative Breast Cancers. This comparison shows that the Random, Fisher's ratio and Holdout samplers are most effective than BNs, and all provide similar insights about the genetic mechanisms that are involved in this disease. Therefore, it can be concluded that all these samplers are good alternatives to Bayesian Networks which much lower computational demands. Besides this analysis confirms the insight that the altered pathways should be independent of the sampling methodology and the classifier that is used to infer them.
机译:在本文中,我们比较了在高度不确定的表型预测问题中用于识别缺陷途径的不同采样算法。第一种算法(费舍尔比率采样器)根据与它们各自的费舍尔比率成正比的先验概率来选择最具歧视性的基因,并对高判别性遗传网络进行采样。第二个样本(保持取样器)是从回归分析中使用的引导程序启发而来的,并使用在不同随机保持物中发现的最小尺度特征来建立最频繁采样的基因。第三个是纯随机采样器,可随机构建差异表达基因的网络。在所有这些算法中,通过留出交叉验证(LOOCV)来确定不同网络的可能性。对最常采样的基因进行后验分析有助于建立改变的生物学途径。将这些算法与通过贝叶斯网络(BN)获得的结果进行比较。我们展示了这些算法对涉及三阴性乳腺癌的微阵列数据集的应用。这种比较表明,Random,Fisher比率和Holdout采样器比BN最为有效,并且都对这种疾病涉及的遗传机制提供了相似的见解。因此,可以得出结论,所有这些采样器都是贝叶斯网络的良好选择,贝叶斯网络的计算需求低得多。除此之外,这一分析还证实了这样的见解,即改变后的途径应独立于抽样方法和用于推断它们的分类器。

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