| Literature DB >> 32135093 |
Xiaojie Qiu1, Arman Rahimzamani2, Li Wang3, Bingcheng Ren4, Qi Mao5, Timothy Durham6, José L McFaline-Figueroa6, Lauren Saunders1, Cole Trapnell7, Sreeram Kannan8.
Abstract
Here, we present Scribe (https://github.com/aristoteleo/Scribe-py), a toolkit for detecting and visualizing causal regulatory interactions between genes and explore the potential for single-cell experiments to power network reconstruction. Scribe employs restricted directed information to determine causality by estimating the strength of information transferred from a potential regulator to its downstream target. We apply Scribe and other leading approaches for causal network reconstruction to several types of single-cell measurements and show that there is a dramatic drop in performance for "pseudotime"-ordered single-cell data compared with true time-series data. We demonstrate that performing causal inference requires temporal coupling between measurements. We show that methods such as "RNA velocity" restore some degree of coupling through an analysis of chromaffin cell fate commitment. These analyses highlight a shortcoming in experimental and computational methods for analyzing gene regulation at single-cell resolution and suggest ways of overcoming it.Entities:
Keywords: RNA velocity; Scribe; causal network inference; coupled dynamics; gene regulatory network inference; pseudotime; real time; single-cell RNA-seq; single-cell trajectories; slam-seq
Mesh:
Substances:
Year: 2020 PMID: 32135093 PMCID: PMC7223477 DOI: 10.1016/j.cels.2020.02.003
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304