CoLabs, University of California, San Francisco, California, USA; email:
Biomedical Informatics Program, University of California, San Francisco, California, USA.
Annu Rev Biomed Data Sci. 2023 Aug 10;6:313-337. doi: 10.1146/annurev-biodatasci-020422-050645. Epub 2023 May 9.
Single-cell RNA sequencing methods have led to improved understanding of the heterogeneity and transcriptomic states present in complex biological systems. Recently, the development of novel single-cell technologies for assaying additional modalities, specifically genomic, epigenomic, proteomic, and spatial data, allows for unprecedented insight into cellular biology. While certain technologies collect multiple measurements from the same cells simultaneously, even when modalities are separately assayed in different cells, we can apply novel computational methods to integrate these data. The application of computational integration methods to multimodal paired and unpaired data results in rich information about the identities of the cells present and the interactions between different levels of biology, such as between genetic variation and transcription. In this review, we both discuss the single-cell technologies for measuring these modalities and describe and characterize a variety of computational integration methods for combining the resulting data to leverage multimodal information toward greater biological insight.
单细胞 RNA 测序方法提高了我们对复杂生物系统中存在的异质性和转录组状态的理解。最近,新型单细胞技术的发展可用于检测其他模式,特别是基因组、表观基因组、蛋白质组和空间数据,从而使我们能够以前所未有的方式深入了解细胞生物学。虽然某些技术可以同时从同一细胞中收集多个测量值,即使在不同细胞中分别检测不同的模式时,我们也可以应用新的计算方法来整合这些数据。将计算整合方法应用于多模态配对和非配对数据中,可以获得有关存在细胞身份以及不同生物学层次之间相互作用的丰富信息,例如遗传变异与转录之间的相互作用。在这篇综述中,我们讨论了用于测量这些模式的单细胞技术,并描述和表征了多种用于组合这些数据的计算整合方法,以利用多模态信息获得更深入的生物学见解。