Evidence map›Paper›PMID 41663695›Full record

ArticleMolecular systems biology2026

Dissecting reversible and irreversible single cell state transitions from gene regulatory networks.

Daniel A Ramirez, Mingyang Lu

Abstract read
In one paragraph

Article in Molecular systems biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

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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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Daniel A RamirezCenter for Theoretical Biological Physics, Northeastern University, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0003-3258-834X
Mingyang LuCenter for Theoretical Biological Physics, Northeastern University, Boston, MA, 02115, USA. m.lu@northeastern.edu.ORCID http://orcid.org/0000-0001-8158-0593

Funding

New Computational Systems Biology Methods for Modeling Gene Regulatory CircuitsR35GM128717 · NIGMS · NORTHEASTERN UNIVERSITY · PI Mingyang Lu · 2018 to 2026
$3.3M
HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM128717National Science Foundation (NSF) MCB-2114191
6 · The paper itself

Abstract

Understanding cell state transitions and their governing regulatory mechanisms remains one of the fundamental questions in biology. We develop a computational method, state transition inference using cross-cell correlations (STICCC), for predicting reversible and irreversible cell state transitions at single-cell resolution by using gene expression data and a set of gene regulatory interactions. The method is inspired by the fact that the gene expression time delays between regulators and targets can be exploited to infer past and future gene expression states. From applications to both simulated and experimental single-cell gene expression data, we show that STICCC-inferred vector fields capture basins of attraction and irreversible fluxes. By connecting regulatory information with systems' dynamical behaviors, STICCC reveals how network interactions influence reversible and irreversible state transitions. Compared to existing methods that infer pseudotime and RNA velocity, STICCC provides complementary insights into the gene regulation of cell state transitions.

Indexed as

Computational BiologyGene Regulatory NetworksSingle-Cell AnalysisAlgorithmsAnimalsGene Expression RegulationSingle-Cell Gene Expression AnalysisSystems BiologyCell State TransitionGene Regulatory Network (GRN)RNA VelocitySingle Cell RNA-seqSystems Biology

Identifiers

PMID41663695
PMCPMC13144439

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Registered trials

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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.