Evidence map›Paper›PMID 24457334›Full record

ArticleNature protocols2014

A framework for parameter estimation and model selection from experimental data in systems biology using approximate Bayesian computation.

Juliane Liepe, Paul Kirk, Sarah Filippi, Tina Toni, Chris P Barnes, Michael P H Stumpf

Abstract read
In one paragraph

Article in Nature protocols, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing 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

97 citing papers in PubMed.

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  18. ADP release can explain spatially-dependent kinesin binding times.bioRxiv : the preprint server for biology · 2023
    Article
  19. Article
  20. Julia for biologists.Nature methods · 2023
    Review

37 more citing papers are in PubMed but not listed here.

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

6 authors.

Juliane LiepeDepartment of Life Sciences, Centre for Integrative Systems Biology and Bioinformatics, Imperial College, London, UK.
Paul KirkDepartment of Life Sciences, Centre for Integrative Systems Biology and Bioinformatics, Imperial College, London, UK.
Sarah FilippiDepartment of Life Sciences, Centre for Integrative Systems Biology and Bioinformatics, Imperial College, London, UK.
Tina ToniDepartment of Life Sciences, Centre for Integrative Systems Biology and Bioinformatics, Imperial College, London, UK.
Chris P BarnesDepartment of Cell and Developmental Biology, University College, London, UK.
Michael P H Stumpf1] Department of Life Sciences, Centre for Integrative Systems Biology and Bioinformatics, Imperial College, London, UK. [2] Institute of Chemical Biology, Imperial College, London, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/G007934/1Medical Research Council G1002092National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/K001949/1Wellcome Trust 086763Wellcome Trust 090433Wellcome Trust 090433/B/09/ZWellcome Trust 097319Wellcome Trust 097319/Z/11/Z
6 · The paper itself

Abstract

As modeling becomes a more widespread practice in the life sciences and biomedical sciences, researchers need reliable tools to calibrate models against ever more complex and detailed data. Here we present an approximate Bayesian computation (ABC) framework and software environment, ABC-SysBio, which is a Python package that runs on Linux and Mac OS X systems and that enables parameter estimation and model selection in the Bayesian formalism by using sequential Monte Carlo (SMC) approaches. We outline the underlying rationale, discuss the computational and practical issues and provide detailed guidance as to how the important tasks of parameter inference and model selection can be performed in practice. Unlike other available packages, ABC-SysBio is highly suited for investigating, in particular, the challenging problem of fitting stochastic models to data. In order to demonstrate the use of ABC-SysBio, in this protocol we postulate the existence of an imaginary reaction network composed of seven interrelated biological reactions (involving a specific mRNA, the protein it encodes and a post-translationally modified version of the protein), a network that is defined by two files containing 'observed' data that we provide as supplementary information. In the first part of the PROCEDURE, ABC-SysBio is used to infer the parameters of this system, whereas in the second part we use ABC-SysBio's relevant functionality to discriminate between two different reaction network models, one of them being the 'true' one. Although computationally expensive, the additional insights gained in the Bayesian formalism more than make up for this cost, especially in complex problems.

Indexed as

Bayes TheoremModels, BiologicalSoftwareSystems Biology

Identifiers

PMID24457334
PMCPMC5081097

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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.