Wang Xuefei, Wu Xinchao, Hong Ni, Jin Wenfei
Shenzhen Key Laboratory of Gene Regulation and Systems Biology, School of Life Sciences, Southern University of Science and Technology, Shenzhen, China.
Biophys Rev. 2023 Jul 15;16(1):13-28. doi: 10.1007/s12551-023-01092-3. eCollection 2024 Feb.
With the rapid advance of single-cell sequencing technology, cell heterogeneity in various biological processes was dissected at different omics levels. However, single-cell mono-omics results in fragmentation of information and could not provide complete cell states. In the past several years, a variety of single-cell multimodal omics technologies have been developed to jointly profile multiple molecular modalities, including genome, transcriptome, epigenome, and proteome, from the same single cell. With the availability of single-cell multimodal omics data, we can simultaneously investigate the effects of genomic mutation or epigenetic modification on transcription and translation, and reveal the potential mechanisms underlying disease pathogenesis. Driven by the massive single-cell omics data, the integration method of single-cell multi-omics data has rapidly developed. Integration of the massive multi-omics single-cell data in public databases in the future will make it possible to construct a cell atlas of multi-omics, enabling us to comprehensively understand cell state and gene regulation at single-cell resolution. In this review, we summarized the experimental methods for single-cell multimodal omics data and computational methods for multi-omics data integration. We also discussed the future development of this field.
随着单细胞测序技术的迅速发展,不同生物学过程中的细胞异质性在不同组学水平上得到了解析。然而,单细胞单一组学会导致信息碎片化,无法提供完整的细胞状态。在过去几年中,已经开发了多种单细胞多组学技术,以联合分析来自同一单细胞的多种分子模式,包括基因组、转录组、表观基因组和蛋白质组。有了单细胞多组学数据,我们可以同时研究基因组突变或表观遗传修饰对转录和翻译的影响,并揭示疾病发病机制的潜在机制。在海量单细胞组学数据的推动下,单细胞多组学数据的整合方法迅速发展。未来整合公共数据库中的海量多组学单细胞数据将有可能构建多组学细胞图谱,使我们能够在单细胞分辨率下全面了解细胞状态和基因调控。在这篇综述中,我们总结了单细胞多组学数据的实验方法和多组学数据整合的计算方法。我们还讨论了该领域的未来发展。