Evidence map›Paper›PMID 38123534›Full record

ArticleNature communications2023

Deciphering driver regulators of cell fate decisions from single-cell transcriptomics data with CEFCON.

Peizhuo Wang, Xiao Wen, Han Li, Peng Lang, Shuya Li, Yipin Lei, Hantao Shu, Lin Gao, Dan Zhao, Jianyang Zeng

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Peizhuo WangInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China.ORCID 0000-0003-1026-4715
Xiao WenCAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, 100101, Beijing, China.ORCID 0000-0001-9367-8803
Han LiInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China.ORCID 0000-0002-7380-6174
Peng LangInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China.
Shuya LiInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China.
Yipin LeiInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China.
Hantao ShuInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China.ORCID 0000-0002-7306-5644
Lin GaoSchool of Computer Science and Technology, Xidian University, 710071, Xi'an, Shaanxi Province, China.ORCID 0000-0001-6396-0787
Dan ZhaoInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China. zhaodan2018@tsinghua.edu.cn.ORCID 0000-0003-0195-6031
Jianyang ZengInstitute for Interdisciplinary Information Sciences, Tsinghua University, 100084, Beijing, China. zengjy@westlake.edu.cn.ORCID 0000-0003-0950-7716
Tsinghua University · CNWestlake University · CNChinese Academy of Sciences · CNXidian University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 32270640National Natural Science Foundation of China (National Science Foundation of China) T2125007
6 · The paper itself

Abstract

Single-cell technologies enable the dynamic analyses of cell fate mapping. However, capturing the gene regulatory relationships and identifying the driver factors that control cell fate decisions are still challenging. We present CEFCON, a network-based framework that first uses a graph neural network with attention mechanism to infer a cell-lineage-specific gene regulatory network (GRN) from single-cell RNA-sequencing data, and then models cell fate dynamics through network control theory to identify driver regulators and the associated gene modules, revealing their critical biological processes related to cell states. Extensive benchmarking tests consistently demonstrated the superiority of CEFCON in GRN construction, driver regulator identification, and gene module identification over baseline methods. When applied to the mouse hematopoietic stem cell differentiation data, CEFCON successfully identified driver regulators for three developmental lineages, which offered useful insights into their differentiation from a network control perspective. Overall, CEFCON provides a valuable tool for studying the underlying mechanisms of cell fate decisions from single-cell RNA-seq data.

Indexed as

Gene Expression ProfilingGene Expression RegulationAnimalsCell DifferentiationCell LineageGene Regulatory NetworksMiceSingle-Cell Analysis

Identifiers

PMID38123534
PMCPMC10733330
OpenAlexW4390011121

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.