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arXiv 2108.00290cs.LGq-bio.GN
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一种用于从转录组图谱中发现候选生物标志物的混合包络特征选择设计

A Hybrid Ensemble Feature Selection Design for Candidate Biomarkers Discovery from Transcriptome Profiles

Universidade Federal do Rio Grande do Sul(南里奥格兰德联邦大学);Hospital de Clínicas de Porto Alegre(阿雷格里港临床医院);Centro Universitário CESUCA(CESUCA大学中心)

Felipe Colombelli, Thayne Woycinck Kowalski, Mariana Recamonde-Mendoza

摘要:

通过特征选择(FS)方法,特别是使用在数据水平上具有扰动的集成FS(EFS)策略(即,均质,Hom-EFS)或方法水平(即,异构,Het-EFS)。在这里,我们提出了一种混合EFS(Hyb-EFS)设计,探索两种类型的扰动,以提高候选生物标志物的稳定性和预测能力。有了这个,Hyb-EFS旨在破坏良好性能与单个数据集,单个算法或两者的特定组合的关联,这对于基因组生物标志物的更好再现性特别有趣。我们调查了我们的方法与四种类型的癌症相关的微阵列数据的充分性,与其他合奏和单一FS方法进行了广泛的比较。在我们的实验中使用了五种FS方法:Wx,对称不确定性(SU),增益比(GR),特征方向(GeoDE)和ReliefF。我们观察到,Hyb-EFS和Het-EFS方法减弱了在不同数据集上大多数单个FS和Hom-EFS中观察到的巨大性能变化。此外,Hyb-EFS在我们的域中改进了Het-EFS的稳定性。比较由性能最好的选择器(Wx、GR和SU)组成的Hyb-EFS和Het-EFS,我们的混合方法超过了等效的异构设计和最好的Hom-EFS(Hom-Wx)。有趣的是,由我们的Hyb-EFS产生的排名达到了更高的生物可接受性,癌症相关基因和途径的富集程度非常高。因此,我们的实验表明,所提出的混合EFS设计在从微阵列数据中发现候选生物标志物中的潜力。最后,我们提供了一个开源框架来支持其他领域的类似分析,既可以作为用户友好的应用程序,也可以作为普通的Python包。

英文摘要:

The discovery of disease biomarkers from gene expression data has been greatly advanced by feature selection (FS) methods, especially using ensemble FS (EFS) strategies with perturbation at the data level (i.e., homogeneous, Hom-EFS) or method level (i.e., heterogeneous, Het-EFS). Here we proposed a Hybrid EFS (Hyb-EFS) design that explores both types of perturbation to improve the stability and the predictive power of candidate biomarkers. With this, Hyb-EFS aims to disrupt associations of good performance with a single dataset, single algorithm, or a specific combination of both, which is particularly interesting for better reproducibility of genomic biomarkers. We investigated the adequacy of our approach for microarray data related to four types of cancer, carrying out an extensive comparison with other ensemble and single FS approaches. Five FS methods were used in our experiments: Wx, Symmetrical Uncertainty (SU), Gain Ratio (GR), Characteristic Direction (GeoDE), and ReliefF. We observed that the Hyb-EFS and Het-EFS approaches attenuated the large performance variation observed for most single FS and Hom-EFS across distinct datasets. Also, the Hyb-EFS improved upon the stability of the Het-EFS within our domain. Comparing the Hyb-EFS and Het-EFS composed of the top-performing selectors (Wx, GR, and SU), our hybrid approach surpassed the equivalent heterogeneous design and the best Hom-EFS (Hom-Wx). Interestingly, the rankings produced by our Hyb-EFS reached greater biological plausibility, with a notably high enrichment for cancer-related genes and pathways. Thus, our experiments suggest the potential of the proposed Hybrid EFS design in discovering candidate biomarkers from microarray data. Finally, we provide an open-source framework to support similar analyses in other domains, both as a user-friendly application and a plain Python package.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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