arXivDaily arXiv每日学术速递 周一至周五更新
arXiv 1411.1997stat.MEq-bio.GNq-bio.MNstat.ML
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基于贝叶斯双聚类模型的差异基因共表达网络

Differential gene co-expression networks via Bayesian biclustering models

Chuan Gao, Shiwen Zhao, Ian C. McDowell, Christopher D. Brown, Barbara E. Engelhardt

摘要:

识别大数据矩阵中的潜在结构对于探索生物过程至关重要。在这里,我们考虑从基因表达数据中恢复基因共表达网络,其中每个网络编码由共享生物机制局部共调控的基因之间的关系。要做到这一点,我们开发了贝叶斯统计模型的双聚类推断子集的共调节基因的共变异可能只在一个子集的样品。我们的双聚类方法,BicMix,具有理想的属性,包括允许过完整的数据表示,计算易处理性,并共同建模未知的混杂因素和生物信号。与相关的双聚类方法相比,BicMix在不同的模拟场景中以更高的精度恢复潜在结构。此外,我们开发了一种方法来恢复基因共表达网络的估计稀疏双聚类矩阵。我们将BicMix应用于乳腺癌基因表达数据,并恢复了ER+和ER-样本之间存在差异的基因共表达网络。

英文摘要:

Identifying latent structure in large data matrices is essential for exploring biological processes. Here, we consider recovering gene co-expression networks from gene expression data, where each network encodes relationships between genes that are locally co-regulated by shared biological mechanisms. To do this, we develop a Bayesian statistical model for biclustering to infer subsets of co-regulated genes whose covariation may be observed in only a subset of the samples. Our biclustering method, BicMix, has desirable properties, including allowing overcomplete representations of the data, computational tractability, and jointly modeling unknown confounders and biological signals. Compared with related biclustering methods, BicMix recovers latent structure with higher precision across diverse simulation scenarios. Further, we develop a method to recover gene co-expression networks from the estimated sparse biclustering matrices. We apply BicMix to breast cancer gene expression data and recover a gene co-expression network that is differential across ER+ and ER- samples.

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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