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Evaluation of integrative clustering methods for the analysis of multi-omics data

机译:评价综合聚类方法分析多OMICS数据

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Recent advances in sequencing,mass spectrometry and cytometry technologies have enabled researchers to collect large-scale omics data from the same set of biological samples. The joint analysis of multiple omics offers the opportunity to uncover coordinated cellular processes acting across different omic layers. In this work, we present a thorough comparison of a selection of recent integrative clustering approaches, including Bayesian (BCC and MDI) and matrix factorization approaches (iCluster,moCluster, JIVE and iNMF). Based on simulations, the methods were evaluated on their sensitivity and their ability to recover both the correct number of clusters and the simulated clustering at the common and data-specific levels. Standard non-integrative approaches were also included to quantify the added value of integrative methods. For most matrix factorization methods and one Bayesian approach (BCC), the shared and specific structures were successfully recovered with high and moderate accuracy, respectively. An opposite behavior was observed on non-integrative approaches, i.e. high performances on specific structures only. Finally, we applied the methods on the Cancer Genome Atlas breast cancer data set to check whether results based on experimental data were consistent with those obtained in the simulations.
机译:测序,质谱和细胞仪技术的最新进展使研究人员能够从同一组生物样品集中收集大规模的OMICS数据。多个OMIC的联合分析提供了揭示跨越不同OMIC层的协调蜂窝过程的机会。在这项工作中,我们彻底比较了最近一系列综合聚类方法,包括贝叶斯(BCC和MDI)和矩阵分解方法(iCluster,Mocluster,Jive和Inmf)。基于仿真,评估其敏感性的方法及其在公共和数据特定级别恢复正确数量的群集和模拟聚类的能力。还包括标准的非综合方法,以量化整合方法的附加值。对于大多数矩阵分解方法和一个贝叶斯方法(BCC),共享和特定结构分别以高和中等的精度成功恢复。在非融合方法中观察到相反的行为,即仅对特定结构的高性能。最后,我们应用了癌症基因组阿特拉斯乳腺癌数据集的方法,以检查基于实验数据的结果是否与模拟中获得的结果一致。

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