破译
生物
表观遗传学
基因调控网络
计算生物学
DNA甲基化
系统生物学
推论
单细胞分析
基因组学
仿形(计算机编程)
基因
转录组
组学
计算机科学
基因组
细胞
数据集成
蛋白质组学
基因表达谱
基因表达
生物网络
功能基因组学
遗传学
人工智能
操作系统
作者
Mark Fiers,Liesbeth Minnoye,Sara Aibar,Carmen Bravo González-Blas,Zeynep Kalender Atak,Stein Aerts
摘要
Single-cell techniques are advancing rapidly and are yielding unprecedented insight into cellular heterogeneity. Mapping the gene regulatory networks (GRNs) underlying cell states provides attractive opportunities to mechanistically understand this heterogeneity. In this review, we discuss recently emerging methods to map GRNs from single-cell transcriptomics data, tackling the challenge of increased noise levels and data sparsity compared with bulk data, alongside increasing data volumes. Next, we discuss how new techniques for single-cell epigenomics, such as single-cell ATAC-seq and single-cell DNA methylation profiling, can be used to decipher gene regulatory programmes. We finally look forward to the application of single-cell multi-omics and perturbation techniques that will likely play important roles for GRN inference in the future.
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