Evidence map›Paper›PMID 37354494›Full record

ArticleBioinformatics (Oxford, England)2023

Modelling capture efficiency of single-cell RNA-sequencing data improves inference of transcriptome-wide burst kinetics.

Wenhao Tang, Andreas Christ Sølvsten Jørgensen, Samuel Marguerat, Philipp Thomas, Vahid Shahrezaei

Abstract read
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Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

24 citing papers in PubMed.

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  7. Intrinsic OASL expression governs heterogeneity in interferon induction during influenza A virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

5 authors.

Wenhao TangDepartment of Mathematics, Imperial College London, London SW7 2BX, United Kingdom.ORCID 0000-0002-4063-0846
Andreas Christ Sølvsten JørgensenDepartment of Mathematics, Imperial College London, London SW7 2BX, United Kingdom.
Samuel MargueratMRC London Institute of Medical Sciences (LMS), London W12 0NN, United Kingdom.ORCID 0000-0002-2402-3165
Philipp ThomasDepartment of Mathematics, Imperial College London, London SW7 2BX, United Kingdom.
Vahid ShahrezaeiDepartment of Mathematics, Imperial College London, London SW7 2BX, United Kingdom.ORCID 0000-0002-4013-5458

Funding

Medical Research Council MC_UP_1102/8Medical Research Council MR/T018429/1
6 · The paper itself

Abstract

motivationGene expression is characterized by stochastic bursts of transcription that occur at brief and random periods of promoter activity. The kinetics of gene expression burstiness differs across the genome and is dependent on the promoter sequence, among other factors. Single-cell RNA sequencing (scRNA-seq) has made it possible to quantify the cell-to-cell variability in transcription at a global genome-wide level. However, scRNA-seq data are prone to technical variability, including low and variable capture efficiency of transcripts from individual cells.

resultsHere, we propose a novel mathematical theory for the observed variability in scRNA-seq data. Our method captures burst kinetics and variability in both the cell size and capture efficiency, which allows us to propose several likelihood-based and simulation-based methods for the inference of burst kinetics from scRNA-seq data. Using both synthetic and real data, we show that the simulation-based methods provide an accurate, robust and flexible tool for inferring burst kinetics from scRNA-seq data. In particular, in a supervised manner, a simulation-based inference method based on neural networks proves to be accurate and useful when applied to both allele and nonallele-specific scRNA-seq data. AVAILABILITY AND IMPLEMENTATION: The code for Neural Network and Approximate Bayesian Computation inference is available at https://github.com/WT215/nnRNA and https://github.com/WT215/Julia_ABC, respectively.

Indexed as

Gene Expression ProfilingTranscriptomeBayes TheoremKineticsLikelihood FunctionsRNASequence Analysis, RNASingle-Cell AnalysisSoftwareRNA

Identifiers

PMID37354494
PMCPMC10318389

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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.