Evidence map›Paper›PMID 37260149›Full record

ArticleDevelopment (Cambridge, England)2023

A dynamical systems treatment of transcriptomic trajectories in hematopoiesis.

Simon L Freedman, Bingxian Xu, Sidhartha Goyal, Madhav Mani

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

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

15 citing papers in PubMed.

  1. Article
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  5. Review
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  7. Review
  8. Fluctuation structure predicts genome-wide perturbation outcomes.bioRxiv : the preprint server for biology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Simon L FreedmanIllumina, San Diego, CA 92122, USA.
Bingxian XuNSF-Simons Center for Quantitative Biology, Northwestern University, Evanston, IL 60208, USA.
Sidhartha GoyalDepartment of Physics, University of Toronto, Toronto, ON M5R 2M8, Canada.ORCID 0000-0002-7452-892X
Madhav ManiNSF-Simons Center for Quantitative Biology, Northwestern University, Evanston, IL 60208, USA.ORCID 0000-0002-5812-4167

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inspired by Waddington's illustration of an epigenetic landscape, cell-fate transitions have been envisioned as bifurcating dynamical systems, wherein exogenous signaling dynamics couple to the enormously complex signaling and transcriptional machinery of a cell to elicit qualitative transitions in its collective state. Single-cell RNA sequencing (scRNA-seq), which measures the distributions of possible transcriptional states in large populations of differentiating cells, provides an alternate view, in which development is marked by the variations of a myriad of genes. Here, we present a mathematical formalism for rigorously evaluating, from a dynamical systems perspective, whether scRNA-seq trajectories display statistical signatures consistent with bifurcations and, as a case study, pinpoint regions of multistability along the neutrophil branch of hematopoeitic differentiation. Additionally, we leverage the geometric features of linear instability to identify the low-dimensional phase plane in gene expression space within which the multistability unfolds, highlighting novel genetic players that are crucial for neutrophil differentiation. Broadly, we show that a dynamical systems treatment of scRNA-seq data provides mechanistic insights into the high-dimensional processes of cellular differentiation, taking a step toward systematic construction of mathematical models for transcriptomic dynamics.

Indexed as

HematopoiesisTranscriptomeCell DifferentiationGene Expression ProfilingModels, TheoreticalSingle-Cell AnalysisBifurcationDifferentiationPseudotimeSingle-cell RNA-seqWaddington

Identifiers

PMID37260149
PMCPMC10281553

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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.