Evidence map›Paper›PMID 27549182›Full record

ArticleBMC systems biology2016

Inferring extrinsic noise from single-cell gene expression data using approximate Bayesian computation.

Oleg Lenive, Paul D W Kirk, Michael P H Stumpf

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Article in BMC systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

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13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

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  12. How to deal with parameters for whole-cell modelling.Journal of the Royal Society, Interface · 2017
    Review
  13. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Oleg LeniveICR, Sutton, SM2 5NG, UK.
Paul D W KirkMRC Biostatistics Unit, Cambridge Institute of Public Health, Cambridge, UK.
Michael P H StumpfImperial College, London, Centre for Integrative Systems Biology and Bioinformatics, London, SW7 2AZ, UK. m.stumpf@imperial.ac.uk.

Funding

Biotechnology and Biological Sciences Research CouncilMedical Research Council MC_UP_0801/1Medical Research Council MC_UU_00002/10Medical Research Council MR/M017672/1
6 · The paper itself

Abstract

backgroundGene expression is known to be an intrinsically stochastic process which can involve single-digit numbers of mRNA molecules in a cell at any given time. The modelling of such processes calls for the use of exact stochastic simulation methods, most notably the Gillespie algorithm. However, this stochasticity, also termed "intrinsic noise", does not account for all the variability between genetically identical cells growing in a homogeneous environment. Despite substantial experimental efforts, determining appropriate model parameters continues to be a challenge. Methods based on approximate Bayesian computation can be used to obtain posterior parameter distributions given the observed data. However, such inference procedures require large numbers of simulations of the model and exact stochastic simulation is computationally costly. In this work we focus on the specific case of trying to infer model parameters describing reaction rates and extrinsic noise on the basis of measurements of molecule numbers in individual cells at a given time point.

resultsTo make the problem computationally tractable we develop an exact, model-specific, stochastic simulation algorithm for the commonly used two-state model of gene expression. This algorithm relies on certain assumptions and favourable properties of the model to forgo the simulation of the whole temporal trajectory of protein numbers in the system, instead returning only the number of protein and mRNA molecules present in the system at a specified time point. The computational gain is proportional to the number of protein molecules created in the system and becomes significant for systems involving hundreds or thousands of protein molecules.

conclusionsWe employ this simulation algorithm with approximate Bayesian computation to jointly infer the model's rate and noise parameters from published gene expression data. Our analysis indicates that for most genes the extrinsic contributions to noise will be small to moderate but certainly are non-negligible.

Indexed as

Gene Expression ProfilingSingle-Cell AnalysisBayes TheoremComputational BiologyModels, GeneticStatistics as TopicApproximate Bayesian computationExtrinsic noiseGene expressionStochastic simulation

Identifiers

PMID27549182
PMCPMC4994381

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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.