Evidence map›Paper›PMID 39570626›Full record

ArticleBioinformatics (Oxford, England)2024

OneSC: a computational platform for recapitulating cell state transitions.

Da Peng, Patrick Cahan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Da PengDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, United States.
Patrick CahanDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD 21205, United States.ORCID 0000-0003-3652-2540

Funding

From intra to intercellular regulatory networks that define cell type identityR35GM124725 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Patrick Cahan · 2017 to 2026
$4.5M
Targeting DKK-1 To Prevent Osteosarcoma MetastasisR01CA262802 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI LOEB, DAVID M. · 2021 to 2025
$3.3M
Maryland Stem Cell Research Foundation 2022-MSCRFL-5896NCI NIH HHS R01 CA262802NIGMS NIH HHS R35 GM124725NIH HHS NIH R35GM124725
6 · The paper itself

Abstract

motivationComputational modeling of cell state transitions has been a great interest of many in the field of developmental biology, cancer biology, and cell fate engineering because it enables performing perturbation experiments in silico more rapidly and cheaply than could be achieved in a lab. Recent advancements in single-cell RNA-sequencing (scRNA-seq) allow the capture of high-resolution snapshots of cell states as they transition along temporal trajectories. Using these high-throughput datasets, we can train computational models to generate in silico "synthetic" cells that faithfully mimic the temporal trajectories.

resultsHere we present OneSC, a platform that can simulate cell state transitions using systems of stochastic differential equations govern by a regulatory network of core transcription factors (TFs). Different from many current network inference methods, OneSC prioritizes on generating Boolean network that produces faithful cell state transitions and terminal cell states that mimic real biological systems. Applying OneSC to real data, we inferred a core TF network using a mouse myeloid progenitor scRNA-seq dataset and showed that the dynamical simulations of that network generate synthetic single-cell expression profiles that faithfully recapitulate the four myeloid differentiation trajectories going into differentiated cell states (erythrocytes, megakaryocytes, granulocytes, and monocytes). Finally, through the in silico perturbations of the mouse myeloid progenitor core network, we showed that OneSC can accurately predict cell fate decision biases of TF perturbations that closely match with previous experimental observations. AVAILABILITY AND IMPLEMENTATION: OneSC is implemented as a Python package on GitHub (https://github.com/CahanLab/oneSC) and on Zenodo (https://zenodo.org/records/14052421).

Indexed as

Cell DifferentiationAnimalsComputational BiologyComputer SimulationGene Regulatory NetworksMiceSequence Analysis, RNASingle-Cell AnalysisSoftwareTranscription FactorsTranscription Factors

Identifiers

PMID39570626
PMCPMC11630913

What Socratic holds

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LicenceCC BY
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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 Socratic graph.