4.7 Article

Inferring Causal Gene Regulatory Networks from Coupled Single-Cell Expression Dynamics Using Scribe

期刊

CELL SYSTEMS
卷 10, 期 3, 页码 265-+

出版社

CELL PRESS
DOI: 10.1016/j.cels.2020.02.003

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资金

  1. US National Institutes of Health (NIH) [DP2 HD088158]
  2. Paul G. Allen Frontiers Group (Allen Discovery Center grant)
  3. W.M. Keck Foundation
  4. Alfred P. Sloan Foundation Research Fellowship
  5. NIH [1R01HG008164]
  6. NSF [1651236]
  7. NSF CCF award [1703403]

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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.

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