Shu Hantao, Zhou Jingtian, Lian Qiuyu, Li Han, Zhao Dan, Zeng Jianyang, Ma Jianzhu
Institute for Interdisciplinary Information Sciences, Tsinghua University, Beijing, China.
Genomic Analysis Laboratory, The Salk Institute for Biological Studies, La Jolla, CA, USA.
Nat Comput Sci. 2021 Jul;1(7):491-501. doi: 10.1038/s43588-021-00099-8. Epub 2021 Jul 22.
Gene regulatory networks (GRNs) encode the complex molecular interactions that govern cell identity. Here we propose DeepSEM, a deep generative model that can jointly infer GRNs and biologically meaningful representation of single-cell RNA sequencing (scRNA-seq) data. In particular, we developed a neural network version of the structural equation model (SEM) to explicitly model the regulatory relationships among genes. Benchmark results show that DeepSEM achieves comparable or better performance on a variety of single-cell computational tasks, such as GRN inference, scRNA-seq data visualization, clustering and simulation, compared with the state-of-the-art methods. In addition, the gene regulations predicted by DeepSEM on cell-type marker genes in the mouse cortex can be validated by epigenetic data, which further demonstrates the accuracy and efficiency of our method. DeepSEM can provide a useful and powerful tool to analyze scRNA-seq data and infer a GRN.
基因调控网络(GRNs)编码了控制细胞身份的复杂分子相互作用。在此,我们提出了DeepSEM,这是一种深度生成模型,它可以联合推断GRNs以及单细胞RNA测序(scRNA-seq)数据的生物学意义表示。具体而言,我们开发了一种结构方程模型(SEM)的神经网络版本,以明确地对基因之间的调控关系进行建模。基准测试结果表明,与现有最先进的方法相比,DeepSEM在各种单细胞计算任务上,如GRN推断、scRNA-seq数据可视化、聚类和模拟,都取得了相当或更好的性能。此外,DeepSEM对小鼠皮层中细胞类型标记基因预测的基因调控可以通过表观遗传数据进行验证,这进一步证明了我们方法的准确性和效率。DeepSEM可以为分析scRNA-seq数据和推断GRN提供一个有用且强大的工具。