Evidence map›Paper›PMID 41131798›Full record

ArticleBioinformatics (Oxford, England)2025

Scalable inference and identifiability of kinetic parameters for transcriptional bursting from single cell data.

Junhao Gu, Nandor Laszik, Christopher E Miles, Jun Allard, Timothy L Downing, Elizabeth L Read

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Junhao GuDepartment of Chemical & Biomolecular Engineering, University of California, Irvine, Irvine, CA, 92617, United States.
Nandor LaszikNSF Simons Center for Multiscale Cell Fate, University of California, Irvine, Irvine, CA, 92697, United States.
Christopher E MilesNSF Simons Center for Multiscale Cell Fate, University of California, Irvine, Irvine, CA, 92697, United States.ORCID 0000-0001-5494-403X
Jun AllardNSF Simons Center for Multiscale Cell Fate, University of California, Irvine, Irvine, CA, 92697, United States.ORCID 0000-0002-2758-4515
Timothy L DowningNSF Simons Center for Multiscale Cell Fate, University of California, Irvine, Irvine, CA, 92697, United States.
Elizabeth L ReadDepartment of Chemical & Biomolecular Engineering, University of California, Irvine, Irvine, CA, 92617, United States.ORCID 0000-0002-9186-284X

Funding

National Science Foundation DMS1763272National Science Foundation EF2022182National Science Foundation CAREER DMS-2339241Simons Foundation 594598
6 · The paper itself

Abstract

motivationStochastic gene expression and cell-to-cell heterogeneity have attracted increased interest in recent years, enabled by advances in single-cell measurement technologies. These studies are also increasingly complemented by quantitative biophysical modeling, often using the framework of stochastic biochemical kinetic models. However, inferring parameters for such models (i.e., the kinetic rates of biochemical reactions) remains a technical and computational challenge, particularly doing so in a manner that can leverage high-throughput single-cell sequencing data.

resultsIn this work, we develop a chemical master equation model reference library-based computational pipeline to infer kinetic parameters describing noisy mRNA distributions from single-cell RNA sequencing data, using the commonly applied stochastic telegraph model. The approach fits kinetic parameters via steady-state distributions, as measured across a population of cells in snapshot data. Our pipeline also serves as a tool for comprehensive analysis of parameter identifiability, in both a priori (studying model properties in the absence of data) and a posteriori (in the context of a particular dataset) use-cases. The pipeline can perform both of these tasks, i.e. inference and identifiability analysis, in an efficient and scalable manner, and also serves to disentangle contributions to uncertainty in inferred parameters from experimental noise versus structural properties of the model. We found that for the telegraph model, the majority of the parameter space is not practically identifiable from single-cell RNA sequencing data, and low experimental capture rates worsen the identifiability. Our methodological framework could be extended to other data types in the fitting of small biochemical network models. AVAILABILITY AND IMPLEMENTATION: All code relevant to this work is available at https://github.com/Read-Lab-UCI/TelegraphLikelihoodInfer, archival DOI: https://doi.org/10.5281/zenodo.16915450.

Indexed as

Computational BiologySingle-Cell AnalysisTranscription, GeneticAlgorithmsHumansKineticsRNA, MessengerSequence Analysis, RNAStochastic ProcessesRNA, Messenger

Identifiers

PMID41131798
PMCPMC12646643

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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.